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Nicholas Schork

Title(s)Adjunct Professor, Psychiatry
SchoolHealth Sciences
Address9500 Gilman Drive #0603
La Jolla CA 92093
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    Collapse Research 
    Collapse Research Activities and Funding
    Integrative Omics to enhance therapeutics development for healthy aging
    NIH/NIA UH2AG064706Sep 15, 2019 - Aug 31, 2021
    Role: Principal Investigator
    Integrative Resource to Develop Translational Strategies to Promote Longevity
    NIH/NIA U24AG051129Sep 15, 2015 - May 31, 2020
    Role: Principal Investigator
    The Bipolar Genome Study
    NIH/NIMH R01MH094483Jul 1, 2012 - Apr 30, 2015
    Role: Principal Investigator
    Functional genomic tools for in vivo study of P. vivax
    NIH/NIAID R21AI085374Jun 15, 2010 - Nov 30, 2012
    Role: Principal Investigator
    Biomarkers of Autism at 12 months: From Brain Overgrowth to Genes
    NIH/NIMH P50MH081755Aug 6, 2007 - Jun 30, 2014
    Role: Co-Investigator
    Genomics for Transplantation: Discovery and Biomarkers
    NIH U19AI063603Sep 1, 2004 - Aug 31, 2016
    Role: Co-Investigator
    Longevity Consortium
    NIH/NIA U19AG023122Dec 1, 2003 - May 31, 2023
    Role: Co-Principal Investigator
    FAMILY BLOOD PRESSURE PROGRAM
    NIH/NHLBI U01HL064777Sep 29, 2000 - Nov 30, 2001
    Role: Principal Investigator
    Sympathetic Neuroeffector Junctions &Blood Pressure
    NIH P01HL058120Jun 1, 1999 - May 31, 2012
    Role: Co-Investigator
    High Performance Computing for Biomedical Research
    NIH P41RR006009Sep 1, 1990 - Jul 31, 2013
    Role: Co-Investigator

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Transcriptomic evidence that von Economo neurons are regionally specialized extratelencephalic-projecting excitatory neurons. Nat Commun. 2020 03 03; 11(1):1172. Hodge RD, Miller JA, Novotny M, Kalmbach BE, Ting JT, Bakken TE, Aevermann BD, Barkan ER, Berkowitz-Cerasano ML, Cobbs C, Diez-Fuertes F, Ding SL, McCorrison J, Schork NJ, Shehata SI, Smith KA, Sunkin SM, Tran DN, Venepally P, Yanny AM, Steemers FJ, Phillips JW, Bernard A, Koch C, Lasken RS, Scheuermann RH, Lein ES. PMID: 32127543.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    2. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addict Biol. 2020 Feb 16; e12880. Munn-Chernoff MA, Johnson EC, Chou YL, Coleman JRI, Thornton LM, Walters RK, Yilmaz Z, Baker JH, Hübel C, Gordon S, Medland SE, Watson HJ, Gaspar HA, Bryois J, Hinney A, Leppä VM, Mattheisen M, Ripke S, Yao S, Giusti-Rodríguez P, Hanscombe KB, Adan RAH, Alfredsson L, Ando T, Andreassen OA, Berrettini WH, Boehm I, Boni C, Boraska Perica V, Buehren K, Burghardt R, Cassina M, Cichon S, Clementi M, Cone RD, Courtet P, Crow S, Crowley JJ, Danner UN, Davis OSP, de Zwaan M, Dedoussis G, Degortes D, DeSocio JE, Dick DM, Dikeos D, Dina C, Dmitrzak-Weglarz M, Docampo E, Duncan LE, Egberts K, Ehrlich S, Escaramís G, Esko T, Estivill X, Farmer A, Favaro A, Fernández-Aranda F, Fichter MM, Fischer K, Föcker M, Foretova L, Forstner AJ, Forzan M, Franklin CS, Gallinger S, Giegling I, Giuranna J, Gonidakis F, Gorwood P, Gratacos Mayora M, Guillaume S, Guo Y, Hakonarson H, Hatzikotoulas K, Hauser J, Hebebrand J, Helder SG, Herms S, Herpertz-Dahlmann B, Herzog W, Huckins LM, Hudson JI, Imgart H, Inoko H, Janout V, Jiménez-Murcia S, Julià A, Kalsi G, Kaminská D, Karhunen L, Karwautz A, Kas MJH, Kennedy JL, Keski-Rahkonen A, Kiezebrink K, Kim YR, Klump KL, Knudsen GPS, La Via MC, Le Hellard S, Levitan RD, Li D, Lilenfeld L, Lin BD, Lissowska J, Luykx J, Magistretti PJ, Maj M, Mannik K, Marsal S, Marshall CR, Mattingsdal M, McDevitt S, McGuffin P, Metspalu A, Meulenbelt I, Micali N, Mitchell K, Monteleone AM, Monteleone P, Nacmias B, Navratilova M, Ntalla I, O'Toole JK, Ophoff RA, Padyukov L, Palotie A, Pantel J, Papezova H, Pinto D, Rabionet R, Raevuori A, Ramoz N, Reichborn-Kjennerud T, Ricca V, Ripatti S, Ritschel F, Roberts M, Rotondo A, Rujescu D, Rybakowski F, Santonastaso P, Scherag A, Scherer SW, Schmidt U, Schork NJ, Schosser A, Seitz J, Slachtova L, Slagboom PE, Slof-Op't Landt MCT, Slopien A, Sorbi S, Swiatkowska B, Szatkiewicz JP, Tachmazidou I, Tenconi E, Tortorella A, Tozzi F, Treasure J, Tsitsika A, Tyszkiewicz-Nwafor M, Tziouvas K, van Elburg AA, van Furth EF, Wagner G, Walton E, Widen E, Zeggini E, Zerwas S, Zipfel S, Bergen AW, Boden JM, Brandt H, Crawford S, Halmi KA, Horwood LJ, Johnson C, Kaplan AS, Kaye WH, Mitchell J, Olsen CM, Pearson JF, Pedersen NL, Strober M, Werge T, Whiteman DC, Woodside DB, Grove J, Henders AK, Larsen JT, Parker R, Petersen LV, Jordan J, Kennedy MA, Birgegård A, Lichtenstein P, Norring C, Landén M, Mortensen PB, Polimanti R, McClintick JN, Adkins AE, Aliev F, Bacanu SA, Batzler A, Bertelsen S, Biernacka JM, Bigdeli TB, Chen LS, Clarke TK, Degenhardt F, Docherty AR, Edwards AC, Foo JC, Fox L, Frank J, Hack LM, Hartmann AM, Hartz SM, Heilmann-Heimbach S, Hodgkinson C, Hoffmann P, Hottenga JJ, Konte B, Lahti J, Lahti-Pulkkinen M, Lai D, Ligthart L, Loukola A, Maher BS, Mbarek H, McIntosh AM, McQueen MB, Meyers JL, Milaneschi Y, Palviainen T, Peterson RE, Ryu E, Saccone NL, Salvatore JE, Sanchez-Roige S, Schwandt M, Sherva R, Streit F, Strohmaier J, Thomas N, Wang JC, Webb BT, Wedow R, Wetherill L, Wills AG, Zhou H, Boardman JD, Chen D, Choi DS, Copeland WE, Culverhouse RC, Dahmen N, Degenhardt L, Domingue BW, Frye MA, Gäebel W, Hayward C, Ising M, Keyes M, Kiefer F, Koller G, Kramer J, Kuperman S, Lucae S, Lynskey MT, Maier W, Mann K, Männistö S, Müller-Myhsok B, Murray AD, Nurnberger JI, Preuss U, Räikkönen K, Reynolds MD, Ridinger M, Scherbaum N, Schuckit MA, Soyka M, Treutlein J, Witt SH, Wodarz N, Zill P, Adkins DE, Boomsma DI, Bierut LJ, Brown SA, Bucholz KK, Costello EJ, de Wit H, Diazgranados N, Eriksson JG, Farrer LA, Foroud TM, Gillespie NA, Goate AM, Goldman D, Grucza RA, Hancock DB, Harris KM, Hesselbrock V, Hewitt JK, Hopfer CJ, Iacono WG, Johnson EO, Karpyak VM, Kendler KS, Kranzler HR, Krauter K, Lind PA, McGue M, MacKillop J, Madden PAF, Maes HH, Magnusson PKE, Nelson EC, Nöthen MM, Palmer AA, Penninx BWJH, Porjesz B, Rice JP, Rietschel M, Riley BP, Rose RJ, Shen PH, Silberg J, Stallings MC, Tarter RE, Vanyukov MM, Vrieze S, Wall TL, Whitfield JB, Zhao H, Neale BM, Wade TD, et al. PMID: 32064741.
      View in: PubMed   Mentions: 1     Fields:    
    3. Circulating tumor DNA as an early cancer detection tool. Pharmacol Ther. 2020 03; 207:107458. Campos-Carrillo A, Weitzel JN, Sahoo P, Rockne R, Mokhnatkin JV, Murtaza M, Gray SW, Goetz L, Goel A, Schork N, Slavin TP. PMID: 31863816.
      View in: PubMed   Mentions:    Fields:    
    4. Multi-Omic Biological Age Estimation and Its Correlation With Wellness and Disease Phenotypes: A Longitudinal Study of 3,558 Individuals. J Gerontol A Biol Sci Med Sci. 2019 Nov 13; 74(Supplement_1):S52-S60. Earls JC, Rappaport N, Heath L, Wilmanski T, Magis AT, Schork NJ, Omenn GS, Lovejoy J, Hood L, Price ND. PMID: 31724055.
      View in: PubMed   Mentions:    Fields:    
    5. Genetic Support for Longevity-Enhancing Drug Targets: Issues, Preliminary Data, and Future Directions. J Gerontol A Biol Sci Med Sci. 2019 Nov 13; 74(Supplement_1):S61-S71. McCorrison J, Girke T, Goetz LH, Miller RA, Schork NJ. PMID: 31724058.
      View in: PubMed   Mentions:    Fields:    
    6. Gut Microbiome-Based Metagenomic Signature for Non-invasive Detection of Advanced Fibrosis in Human Nonalcoholic Fatty Liver Disease. Cell Metab. 2019 Sep 03; 30(3):607. Loomba R, Seguritan V, Li W, Long T, Klitgord N, Bhatt A, Dulai PS, Caussy C, Bettencourt R, Highlander SK, Jones MB, Sirlin CB, Schnabl B, Brinkac L, Schork N, Chen CH, Brenner DA, Biggs W, Yooseph S, Venter JC, Nelson KE. PMID: 31484056.
      View in: PubMed   Mentions: 3     Fields:    
    7. Artificial intelligence and machine learning in clinical development: a translational perspective. NPJ Digit Med. 2019; 2:69. Shah P, Kendall F, Khozin S, Goosen R, Hu J, Laramie J, Ringel M, Schork N. PMID: 31372505.
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    8. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nat Genet. 2019 08; 51(8):1207-1214. Watson HJ, Yilmaz Z, Thornton LM, Hübel C, Coleman JRI, Gaspar HA, Bryois J, Hinney A, Leppä VM, Mattheisen M, Medland SE, Ripke S, Yao S, Giusti-Rodríguez P, Hanscombe KB, Purves KL, Adan RAH, Alfredsson L, Ando T, Andreassen OA, Baker JH, Berrettini WH, Boehm I, Boni C, Perica VB, Buehren K, Burghardt R, Cassina M, Cichon S, Clementi M, Cone RD, Courtet P, Crow S, Crowley JJ, Danner UN, Davis OSP, de Zwaan M, Dedoussis G, Degortes D, DeSocio JE, Dick DM, Dikeos D, Dina C, Dmitrzak-Weglarz M, Docampo E, Duncan LE, Egberts K, Ehrlich S, Escaramís G, Esko T, Estivill X, Farmer A, Favaro A, Fernández-Aranda F, Fichter MM, Fischer K, Föcker M, Foretova L, Forstner AJ, Forzan M, Franklin CS, Gallinger S, Giegling I, Giuranna J, Gonidakis F, Gorwood P, Mayora MG, Guillaume S, Guo Y, Hakonarson H, Hatzikotoulas K, Hauser J, Hebebrand J, Helder SG, Herms S, Herpertz-Dahlmann B, Herzog W, Huckins LM, Hudson JI, Imgart H, Inoko H, Janout V, Jiménez-Murcia S, Julià A, Kalsi G, Kaminská D, Kaprio J, Karhunen L, Karwautz A, Kas MJH, Kennedy JL, Keski-Rahkonen A, Kiezebrink K, Kim YR, Klareskog L, Klump KL, Knudsen GPS, La Via MC, Le Hellard S, Levitan RD, Li D, Lilenfeld L, Lin BD, Lissowska J, Luykx J, Magistretti PJ, Maj M, Mannik K, Marsal S, Marshall CR, Mattingsdal M, McDevitt S, McGuffin P, Metspalu A, Meulenbelt I, Micali N, Mitchell K, Monteleone AM, Monteleone P, Munn-Chernoff MA, Nacmias B, Navratilova M, Ntalla I, O'Toole JK, Ophoff RA, Padyukov L, Palotie A, Pantel J, Papezova H, Pinto D, Rabionet R, Raevuori A, Ramoz N, Reichborn-Kjennerud T, Ricca V, Ripatti S, Ritschel F, Roberts M, Rotondo A, Rujescu D, Rybakowski F, Santonastaso P, Scherag A, Scherer SW, Schmidt U, Schork NJ, Schosser A, Seitz J, Slachtova L, Slagboom PE, Slof-Op 't Landt MCT, Slopien A, Sorbi S, Swiatkowska B, Szatkiewicz JP, Tachmazidou I, Tenconi E, Tortorella A, Tozzi F, Treasure J, Tsitsika A, Tyszkiewicz-Nwafor M, Tziouvas K, van Elburg AA, van Furth EF, Wagner G, Walton E, Widen E, Zeggini E, Zerwas S, Zipfel S, Bergen AW, Boden JM, Brandt H, Crawford S, Halmi KA, Horwood LJ, Johnson C, Kaplan AS, Kaye WH, Mitchell JE, Olsen CM, Pearson JF, Pedersen NL, Strober M, Werge T, Whiteman DC, Woodside DB, Stuber GD, Gordon S, Grove J, Henders AK, Juréus A, Kirk KM, Larsen JT, Parker R, Petersen L, Jordan J, Kennedy M, Montgomery GW, Wade TD, Birgegård A, Lichtenstein P, Norring C, Landén M, Martin NG, Mortensen PB, Sullivan PF, Breen G, Bulik CM. PMID: 31308545.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    9. Power and Design Issues in Crossover-Based N-Of-1 Clinical Trials with Fixed Data Collection Periods. Healthcare (Basel). 2019 Jul 02; 7(3). Wang Y, Schork NJ. PMID: 31269712.
      View in: PubMed   Mentions:
    10. Rare variant phasing using paired tumor:normal sequence data. BMC Bioinformatics. 2019 May 27; 20(1):265. Buckley AR, Ideker T, Carter H, Schork NJ. PMID: 31132991.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    11. Association Between Improvement in Baseline Mood and Long-Term Use of a Mindfulness and Meditation App: Observational Study. JMIR Ment Health. 2019 May 08; 6(5):e12617. Athanas AJ, McCorrison JM, Smalley S, Price J, Grady J, Campistron J, Schork NJ. PMID: 31066704.
      View in: PubMed   Mentions:
    12. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nat Genet. 2019 05; 51(5):793-803. Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, Pers TH, Holmans PA, Richards AL, Abbott L, Agerbo E, Akil H, Albani D, Alliey-Rodriguez N, Als TD, Anjorin A, Antilla V, Awasthi S, Badner JA, Bækvad-Hansen M, Barchas JD, Bass N, Bauer M, Belliveau R, Bergen SE, Pedersen CB, Bøen E, Boks MP, Boocock J, Budde M, Bunney W, Burmeister M, Bybjerg-Grauholm J, Byerley W, Casas M, Cerrato F, Cervantes P, Chambert K, Charney AW, Chen D, Churchhouse C, Clarke TK, Coryell W, Craig DW, Cruceanu C, Curtis D, Czerski PM, Dale AM, de Jong S, Degenhardt F, Del-Favero J, DePaulo JR, Djurovic S, Dobbyn AL, Dumont A, Elvsåshagen T, Escott-Price V, Fan CC, Fischer SB, Flickinger M, Foroud TM, Forty L, Frank J, Fraser C, Freimer NB, Frisén L, Gade K, Gage D, Garnham J, Giambartolomei C, Pedersen MG, Goldstein J, Gordon SD, Gordon-Smith K, Green EK, Green MJ, Greenwood TA, Grove J, Guan W, Guzman-Parra J, Hamshere ML, Hautzinger M, Heilbronner U, Herms S, Hipolito M, Hoffmann P, Holland D, Huckins L, Jamain S, Johnson JS, Juréus A, Kandaswamy R, Karlsson R, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M, Koller AC, Kupka R, Lavebratt C, Lawrence J, Lawson WB, Leber M, Lee PH, Levy SE, Li JZ, Liu C, Lucae S, Maaser A, MacIntyre DJ, Mahon PB, Maier W, Martinsson L, McCarroll S, McGuffin P, McInnis MG, McKay JD, Medeiros H, Medland SE, Meng F, Milani L, Montgomery GW, Morris DW, Mühleisen TW, Mullins N, Nguyen H, Nievergelt CM, Adolfsson AN, Nwulia EA, O'Donovan C, Loohuis LMO, Ori APS, Oruc L, Ösby U, Perlis RH, Perry A, Pfennig A, Potash JB, Purcell SM, Regeer EJ, Reif A, Reinbold CS, Rice JP, Rivas F, Rivera M, Roussos P, Ruderfer DM, Ryu E, Sánchez-Mora C, Schatzberg AF, Scheftner WA, Schork NJ, Shannon Weickert C, Shehktman T, Shilling PD, Sigurdsson E, Slaney C, Smeland OB, Sobell JL, Søholm Hansen C, Spijker AT, St Clair D, Steffens M, Strauss JS, Streit F, Strohmaier J, Szelinger S, Thompson RC, Thorgeirsson TE, Treutlein J, Vedder H, Wang W, Watson SJ, Weickert TW, Witt SH, Xi S, Xu W, Young AH, Zandi P, Zhang P, Zöllner S, Adolfsson R, Agartz I, Alda M, Backlund L, Baune BT, Bellivier F, Berrettini WH, Biernacka JM, Blackwood DHR, Boehnke M, Børglum AD, Corvin A, Craddock N, Daly MJ, Dannlowski U, Esko T, Etain B, Frye M, Fullerton JM, Gershon ES, Gill M, Goes F, Grigoroiu-Serbanescu M, Hauser J, Hougaard DM, Hultman CM, Jones I, Jones LA, Kahn RS, Kirov G, Landén M, Leboyer M, Lewis CM, Li QS, Lissowska J, Martin NG, Mayoral F, McElroy SL, McIntosh AM, McMahon FJ, Melle I, Metspalu A, Mitchell PB, Morken G, Mors O, Mortensen PB, Müller-Myhsok B, Myers RM, Neale BM, Nimgaonkar V, Nordentoft M, Nöthen MM, O'Donovan MC, Oedegaard KJ, Owen MJ, Paciga SA, Pato C, Pato MT, Posthuma D, Ramos-Quiroga JA, Ribasés M, Rietschel M, Rouleau GA, Schalling M, Schofield PR, Schulze TG, Serretti A, Smoller JW, Stefansson H, Stefansson K, Stordal E, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Werge T, Nurnberger JI, Wray NR, Di Florio A, Edenberg HJ, Cichon S, Ophoff RA, Scott LJ, Andreassen OA, Kelsoe J, Sklar P. PMID: 31043756.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    13. Fine mapping and subphenotyping implicates ADRA1B gene variants in psoriasis susceptibility in a Chinese population. Epigenomics. 2019 02; 11(4):455-467. Fan X, Wang H, Sun L, Zheng X, Yin X, Zuo X, Peng Q, Standish KA, Cheng H, Zhang Y, Wang Z, Xiao F, Yang S, Zhang X, Schork NJ. PMID: 30785334.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    14. Combinatorial interactions of genetic variants in human cardiomyopathy. Nat Biomed Eng. 2019 02; 3(2):147-157. Deacon DC, Happe CL, Chen C, Tedeschi N, Manso AM, Li T, Dalton ND, Peng Q, Farah EN, Gu Y, Tenerelli KP, Tran VD, Chen J, Peterson KL, Schork NJ, Adler ED, Engler AJ, Ross RS, Chi NC. PMID: 30923642.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    15. An investigation of indirect effects of personality features on anorexia nervosa severity through interoceptive dysfunction in individuals with lifetime anorexia nervosa diagnoses. Int J Eat Disord. 2019 02; 52(2):200-205. Duffy ME, Rogers ML, Joiner TE, Bergen AW, Berrettini W, Bulik CM, Brandt H, Crawford S, Crow S, Fichter M, Halmi K, Kaplan AS, Klump KL, Lilenfeld L, Magistretti PJ, Mitchell J, Schork NJ, Strober M, Thornton LM, Treasure J, Woodside B, Kaye WH, Keel PK. PMID: 30636025.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    16. Artificial Intelligence and Personalized Medicine. Cancer Treat Res. 2019; 178:265-283. Schork NJ. PMID: 31209850.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    17. Single-nucleus and single-cell transcriptomes compared in matched cortical cell types. PLoS One. 2018; 13(12):e0209648. Bakken TE, Hodge RD, Miller JA, Yao Z, Nguyen TN, Aevermann B, Barkan E, Bertagnolli D, Casper T, Dee N, Garren E, Goldy J, Graybuck LT, Kroll M, Lasken RS, Lathia K, Parry S, Rimorin C, Scheuermann RH, Schork NJ, Shehata SI, Tieu M, Phillips JW, Bernard A, Smith KA, Zeng H, Lein ES, Tasic B. PMID: 30586455.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    18. Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. Eur Neuropsychopharmacol. 2019 01; 29(1):156-170. Budde M, Friedrichs S, Alliey-Rodriguez N, Ament S, Badner JA, Berrettini WH, Bloss CS, Byerley W, Cichon S, Comes AL, Coryell W, Craig DW, Degenhardt F, Edenberg HJ, Foroud T, Forstner AJ, Frank J, Gershon ES, Goes FS, Greenwood TA, Guo Y, Hipolito M, Hood L, Keating BJ, Koller DL, Lawson WB, Liu C, Mahon PB, McInnis MG, McMahon FJ, Meier SM, Mühleisen TW, Murray SS, Nievergelt CM, Nurnberger JI, Nwulia EA, Potash JB, Quarless D, Rice J, Roach JC, Scheftner WA, Schork NJ, Shekhtman T, Shilling PD, Smith EN, Streit F, Strohmaier J, Szelinger S, Treutlein J, Witt SH, Zandi PP, Zhang P, Zöllner S, Bickeböller H, Falkai PG, Kelsoe JR, Nöthen MM, Rietschel M, Schulze TG, Malzahn D. PMID: 30503783.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    19. Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics. Int J Bipolar Disord. 2018 Nov 11; 6(1):24. Breuer R, Mattheisen M, Frank J, Krumm B, Treutlein J, Kassem L, Strohmaier J, Herms S, Mühleisen TW, Degenhardt F, Cichon S, Nöthen MM, Karypis G, Kelsoe J, Greenwood T, Nievergelt C, Shilling P, Shekhtman T, Edenberg H, Craig D, Szelinger S, Nurnberger J, Gershon E, Alliey-Rodriguez N, Zandi P, Goes F, Schork N, Smith E, Koller D, Zhang P, Badner J, Berrettini W, Bloss C, Byerley W, Coryell W, Foroud T, Guo Y, Hipolito M, Keating B, Lawson W, Liu C, Mahon P, McInnis M, Murray S, Nwulia E, Potash J, Rice J, Scheftner W, Zöllner S, McMahon FJ, Rietschel M, Schulze TG. PMID: 30415424.
      View in: PubMed   Mentions:
    20. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. Am J Hum Genet. 2018 11 01; 103(5):691-706. Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, Van der Most PJ, Tanaka T, Naderi E, Rose LM, Wu Y, Karlsson R, Barbalic M, Lin H, Pool R, Zhu G, Macé A, Sidore C, Trompet S, Mangino M, Sabater-Lleal M, Kemp JP, Abbasi A, Kacprowski T, Verweij N, Smith AV, Huang T, Marzi C, Feitosa MF, Lohman KK, Kleber ME, Milaneschi Y, Mueller C, Huq M, Vlachopoulou E, Lyytikäinen LP, Oldmeadow C, Deelen J, Perola M, Zhao JH, Feenstra B, Amini M, Lahti J, Schraut KE, Fornage M, Suktitipat B, Chen WM, Li X, Nutile T, Malerba G, Luan J, Bak T, Schork N, Del Greco M F, Thiering E, Mahajan A, Marioni RE, Mihailov E, Eriksson J, Ozel AB, Zhang W, Nethander M, Cheng YC, Aslibekyan S, Ang W, Gandin I, Yengo L, Portas L, Kooperberg C, Hofer E, Rajan KB, Schurmann C, den Hollander W, Ahluwalia TS, Zhao J, Draisma HHM, Ford I, Timpson N, Teumer A, Huang H, Wahl S, Liu Y, Huang J, Uh HW, Geller F, Joshi PK, Yanek LR, Trabetti E, Lehne B, Vozzi D, Verbanck M, Biino G, Saba Y, Meulenbelt I, O'Connell JR, Laakso M, Giulianini F, Magnusson PKE, Ballantyne CM, Hottenga JJ, Montgomery GW, Rivadineira F, Rueedi R, Steri M, Herzig KH, Stott DJ, Menni C, Frånberg M, St Pourcain B, Felix SB, Pers TH, Bakker SJL, Kraft P, Peters A, Vaidya D, Delgado G, Smit JH, Großmann V, Sinisalo J, Seppälä I, Williams SR, Holliday EG, Moed M, Langenberg C, Räikkönen K, Ding J, Campbell H, Sale MM, Chen YI, James AL, Ruggiero D, Soranzo N, Hartman CA, Smith EN, Berenson GS, Fuchsberger C, Hernandez D, Tiesler CMT, Giedraitis V, Liewald D, Fischer K, Mellström D, Larsson A, Wang Y, Scott WR, Lorentzon M, Beilby J, Ryan KA, Pennell CE, Vuckovic D, Balkau B, Concas MP, Schmidt R, Mendes de Leon CF, Bottinger EP, Kloppenburg M, Paternoster L, Boehnke M, Musk AW, Willemsen G, Evans DM, Madden PAF, Kähönen M, Kutalik Z, Zoledziewska M, Karhunen V, Kritchevsky SB, Sattar N, Lachance G, Clarke R, Harris TB, Raitakari OT, Attia JR, van Heemst D, Kajantie E, Sorice R, Gambaro G, Scott RA, Hicks AA, Ferrucci L, Standl M, Lindgren CM, Starr JM, Karlsson M, Lind L, Li JZ, Chambers JC, Mori TA, de Geus EJCN, Heath AC, Martin NG, Auvinen J, Buckley BM, de Craen AJM, Waldenberger M, Strauch K, Meitinger T, Scott RJ, McEvoy M, Beekman M, Bombieri C, Ridker PM, Mohlke KL, Pedersen NL, Morrison AC, Boomsma DI, Whitfield JB, Strachan DP, Hofman A, Vollenweider P, Cucca F, Jarvelin MR, Jukema JW, Spector TD, Hamsten A, Zeller T, Uitterlinden AG, Nauck M, Gudnason V, Qi L, Grallert H, Borecki IB, Rotter JI, März W, Wild PS, Lokki ML, Boyle M, Salomaa V, Melbye M, Eriksson JG, Wilson JF, Penninx BWJH, Becker DM, Worrall BB, Gibson G, Krauss RM, Ciullo M, Zaza G, Wareham NJ, Oldehinkel AJ, Palmer LJ, Murray SS, Pramstaller PP, Bandinelli S, Heinrich J, Ingelsson E, Deary IJ, Mägi R, Vandenput L, van der Harst P, Desch KC, Kooner JS, Ohlsson C, Hayward C, Lehtimäki T, Shuldiner AR, Arnett DK, Beilin LJ, Robino A, Froguel P, Pirastu M, Jess T, Koenig W, Loos RJF, Evans DA, Schmidt H, Smith GD, Slagboom PE, Eiriksdottir G, Morris AP, Psaty BM, Tracy RP, Nolte IM, Boerwinkle E, Visvikis-Siest S, Reiner AP, Gross M, Bis JC, Franke L, Franco OH, Benjamin EJ, Chasman DI, Dupuis J, Snieder H, Dehghan A, Alizadeh BZ. PMID: 30388399.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    21. Accelerating the Drug Delivery Pipeline for Acute and Chronic Pancreatitis: Summary of the Working Group on Drug Development and Trials in Recurrent Acute Pancreatitis at the National Institute of Diabetes and Digestive and Kidney Diseases Workshop. Pancreas. 2018 Nov/Dec; 47(10):1193-1199. Lowe ME, Goodman MT, Coté GA, Glesby MJ, Haupt M, Schork NJ, Singh VK, Andersen DK, Pandol SJ, Uc A, Whitcomb DC. PMID: 30325857.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    22. Report: NIA workshop on translating genetic variants associated with longevity into drug targets. Geroscience. 2018 12; 40(5-6):523-538. Schork NJ, Raghavachari N. PMID: 30374935.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    23. Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas. Genome Med. 2018 09 14; 10(1):69. Buckley AR, Ideker T, Carter H, Harismendy O, Schork NJ. PMID: 30217226.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    24. Genetic risks and clinical rewards. Nat Genet. 2018 09; 50(9):1210-1211. Schork AJ, Schork MA, Schork NJ. PMID: 30158681.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    25. Transcriptomic and morphophysiological evidence for a specialized human cortical GABAergic cell type. Nat Neurosci. 2018 09; 21(9):1185-1195. Boldog E, Bakken TE, Hodge RD, Novotny M, Aevermann BD, Baka J, Bordé S, Close JL, Diez-Fuertes F, Ding SL, Faragó N, Kocsis ÁK, Kovács B, Maltzer Z, McCorrison JM, Miller JA, Molnár G, Oláh G, Ozsvár A, Rózsa M, Shehata SI, Smith KA, Sunkin SM, Tran DN, Venepally P, Wall A, Puskás LG, Barzó P, Steemers FJ, Schork NJ, Scheuermann RH, Lasken RS, Lein ES, Tamás G. PMID: 30150662.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    26. Network Rewiring in Cancer: Applications to Melanoma Cell Lines and the Cancer Genome Atlas Patients. Front Genet. 2018; 9:228. Ding KF, Finlay D, Yin H, Hendricks WPD, Sereduk C, Kiefer J, Sekulic A, LoRusso PM, Vuori K, Trent JM, Schork NJ. PMID: 30042785.
      View in: PubMed   Mentions:
    27. Personalized medicine: motivation, challenges, and progress. Fertil Steril. 2018 06; 109(6):952-963. Goetz LH, Schork NJ. PMID: 29935653.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    28. Link between gut-microbiome derived metabolite and shared gene-effects with hepatic steatosis and fibrosis in NAFLD. Hepatology. 2018 09; 68(3):918-932. Caussy C, Hsu C, Lo MT, Liu A, Bettencourt R, Ajmera VH, Bassirian S, Hooker J, Sy E, Richards L, Schork N, Schnabl B, Brenner DA, Sirlin CB, Chen CH, Loomba R. PMID: 29572891.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    29. A loop-counting method for covariate-corrected low-rank biclustering of gene-expression and genome-wide association study data. PLoS Comput Biol. 2018 05; 14(5):e1006105. Rangan AV, McGrouther CC, Kelsoe J, Schork N, Stahl E, Zhu Q, Krishnan A, Yao V, Troyanskaya O, Bilaloglu S, Raghavan P, Bergen S, Jureus A, Landen M. PMID: 29758032.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    30. The big data revolution and human genetics. Hum Mol Genet. 2018 05 01; 27(R1):R1. Schork NJ. PMID: 29672687.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    31. Randomized clinical trials and personalized medicine: A commentary on deaton and cartwright. Soc Sci Med. 2018 08; 210:71-73. Schork NJ. PMID: 29786513.
      View in: PubMed   Mentions: 1     Fields:    
    32. Comparison of phasing strategies for whole human genomes. PLoS Genet. 2018 04; 14(4):e1007308. Choi Y, Chan AP, Kirkness E, Telenti A, Schork NJ. PMID: 29621242.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    33. Effective discovery of rare variants by pooled target capture sequencing: A comparative analysis with individually indexed target capture sequencing. Mutat Res. 2018 05; 809:24-31. Ryu S, Han J, Norden-Krichmar TM, Schork NJ, Suh Y. PMID: 29677560.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    34. Cell type discovery and representation in the era of high-content single cell phenotyping. BMC Bioinformatics. 2017 12 21; 18(Suppl 17):559. Bakken T, Cowell L, Aevermann BD, Novotny M, Hodge R, Miller JA, Lee A, Chang I, McCorrison J, Pulendran B, Qian Y, Schork NJ, Lasken RS, Lein ES, Scheuermann RH. PMID: 29322913.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    35. Nonlinear mixed effects dose response modeling in high throughput drug screens: application to melanoma cell line analysis. Oncotarget. 2018 Jan 12; 9(4):5044-5057. Ding KF, Petricoin EF, Finlay D, Yin H, Hendricks WPD, Sereduk C, Kiefer J, Sekulic A, LoRusso PM, Vuori K, Trent JM, Schork NJ. PMID: 29435161.
      View in: PubMed   Mentions:    Fields:    
    36. Mixed-methods quantitative-qualitative study of 29 nonagenarians and centenarians in rural Southern Italy: focus on positive psychological traits. Int Psychogeriatr. 2018 01; 30(1):31-38. Scelzo A, Di Somma S, Antonini P, Montross LP, Schork N, Brenner D, Jeste DV. PMID: 29229012.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    37. Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk. J Community Genet. 2018 Jul; 9(3):217-225. Broady KM, Ormond KE, Topol EJ, Schork NJ, Bloss CS. PMID: 29130150.
      View in: PubMed   Mentions:
    38. Precision medicine for suicidality: from universality to subtypes and personalization. Mol Psychiatry. 2017 09; 22(9):1250-1273. Niculescu AB, Le-Niculescu H, Levey DF, Phalen PL, Dainton HL, Roseberry K, Niculescu EM, Niezer JO, Williams A, Graham DL, Jones TJ, Venugopal V, Ballew A, Yard M, Gelbart T, Kurian SM, Shekhar A, Schork NJ, Sandusky GE, Salomon DR. PMID: 28809398.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    39. Integrated Genomic Medicine: A Paradigm for Rare Diseases and Beyond. Adv Genet. 2017; 97:81-113. Schork NJ, Nazor K. PMID: 28838357.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    40. Single-Subject Studies in Translational Nutrition Research. Annu Rev Nutr. 2017 08 21; 37:395-422. Schork NJ, Goetz LH. PMID: 28715990.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    41. Nonalcoholic fatty liver disease with cirrhosis increases familial risk for advanced fibrosis. J Clin Invest. 2017 Jun 30; 127(7):2697-2704. Caussy C, Soni M, Cui J, Bettencourt R, Schork N, Chen CH, Ikhwan MA, Bassirian S, Cepin S, Gonzalez MP, Mendler M, Kono Y, Vodkin I, Mekeel K, Haldorson J, Hemming A, Andrews B, Salotti J, Richards L, Brenner DA, Sirlin CB, Loomba R. PMID: 28628033.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCTClinical Trials
    42. Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls. BMC Genomics. 2017 06 12; 18(1):458. Buckley AR, Standish KA, Bhutani K, Ideker T, Lasken RS, Carter H, Harismendy O, Schork NJ. PMID: 28606096.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    43. Comprehensive analysis of treatment response phenotypes in rheumatoid arthritis for pharmacogenetic studies. Arthritis Res Ther. 2017 05 12; 19(1):90. Standish KA, Huang CC, Curran ME, Schork NJ. PMID: 28494788.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCTClinical Trials
    44. Gut Microbiome-Based Metagenomic Signature for Non-invasive Detection of Advanced Fibrosis in Human Nonalcoholic Fatty Liver Disease. Cell Metab. 2017 May 02; 25(5):1054-1062.e5. Loomba R, Seguritan V, Li W, Long T, Klitgord N, Bhatt A, Dulai PS, Caussy C, Bettencourt R, Highlander SK, Jones MB, Sirlin CB, Schnabl B, Brinkac L, Schork N, Chen CH, Brenner DA, Biggs W, Yooseph S, Venter JC, Nelson KE. PMID: 28467925.
      View in: PubMed   Mentions: 52     Fields:    Translation:HumansCells
    45. Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun; 174(4):413-426. Jia P, Zhao Z, Hulgan T, Bush WS, Samuels DC, Bloss CS, Heaton RK, Ellis RJ, Schork N, Marra CM, Collier AC, Clifford DB, Gelman BB, Sacktor N, Morgello S, Simpson DM, McCutchan JA, Barnholtz-Sloan JS, Franklin DR, Rosario D, Letendre SL, Grant I, Kallianpur AR. PMID: 28447399.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    46. Analysis of variability in high throughput screening data: applications to melanoma cell lines and drug responses. Oncotarget. 2017 Apr 25; 8(17):27786-27799. Ding KF, Finlay D, Yin H, Hendricks WPD, Sereduk C, Kiefer J, Sekulic A, LoRusso PM, Vuori K, Trent JM, Schork NJ. PMID: 28212541.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    47. Clickotine, A Personalized Smartphone App for Smoking Cessation: Initial Evaluation. JMIR Mhealth Uhealth. 2017 Apr 25; 5(4):e56. Iacoviello BM, Steinerman JR, Klein DB, Silver TL, Berger AG, Luo SX, Schork NJ. PMID: 28442453.
      View in: PubMed   Mentions: 8     Fields:    
    48. Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun; 174(4):435-450. Peng Q, Schork NJ, Wilhelmsen KC, Ehlers CL. PMID: 28436151.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    49. Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites. Nat Genet. 2017 Apr; 49(4):568-578. Long T, Hicks M, Yu HC, Biggs WH, Kirkness EF, Menni C, Zierer J, Small KS, Mangino M, Messier H, Brewerton S, Turpaz Y, Perkins BA, Evans AM, Miller LA, Guo L, Caskey CT, Schork NJ, Garner C, Spector TD, Venter JC, Telenti A. PMID: 28263315.
      View in: PubMed   Mentions: 41     Fields:    Translation:Humans
    50. Genome-wide association study of paliperidone efficacy. Pharmacogenet Genomics. 2017 01; 27(1):7-18. Li Q, Wineinger NE, Fu DJ, Libiger O, Alphs L, Savitz A, Gopal S, Cohen N, Schork NJ. PMID: 27846195.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    51. PRODUCTION OF A PRELIMINARY QUALITY CONTROL PIPELINE FOR SINGLE NUCLEI RNA-SEQ AND ITS APPLICATION IN THE ANALYSIS OF CELL TYPE DIVERSITY OF POST-MORTEM HUMAN BRAIN NEOCORTEX. Pac Symp Biocomput. 2017; 22:564-575. Aevermann B, McCorrison J, Venepally P, Hodge R, Bakken T, Miller J, Novotny M, Tran DN, Diezfuertes F, Christiansen L, Zhang F, Steemers F, Lasken RS, Lein ED, Schork N, Scheuermann RH. PMID: 27897007.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    52. Identification of novel loci affecting circulating chromogranins and related peptides. Hum Mol Genet. 2017 01 01; 26(1):233-242. Benyamin B, Maihofer AX, Schork AJ, Hamilton BA, Rao F, Schmid-Schönbein GW, Zhang K, Mahata M, Stridsberg M, Schork NJ, Biswas N, Hook VY, Wei Z, Montgomery GW, Martin NG, Nievergelt CM, Whitfield JB, O'Connor DT. PMID: 28011710.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    53. Patient perspectives on whole-genome sequencing for undiagnosed diseases. Per Med. 2017 01; 14(1):17-25. Boeldt DL, Cheung C, Ariniello L, Darst BF, Topol S, Schork NJ, Philis-Tsimikas A, Torkamani A, Fortmann AL, Bloss CS. PMID: 29749824.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    54. Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population. J Psychiatry Neurosci. 2016 10; 41(6):413-421. Yin X, Wineinger NE, Wang K, Yue W, Norgren N, Wang L, Yao W, Jiang X, Wu B, Cui Y, Shen C, Cheng H, Zhou F, Chen G, Zuo X, Zheng X, Fan X, Wang H, Wang L, Lee J, Lam M, Tai ES, Zhang Z, Huang Q, Sun L, Xu J, Yang S, Wilhelmsen KC, Liu J, Schork NJ, Zhang X. PMID: 27091718.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    55. Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans. Hum Mol Genet. 2016 10 01; 25(19):4350-4368. Evans DS, Avery CL, Nalls MA, Li G, Barnard J, Smith EN, Tanaka T, Butler AM, Buxbaum SG, Alonso A, Arking DE, Berenson GS, Bis JC, Buyske S, Carty CL, Chen W, Chung MK, Cummings SR, Deo R, Eaton CB, Fox ER, Heckbert SR, Heiss G, Hindorff LA, Hsueh WC, Isaacs A, Jamshidi Y, Kerr KF, Liu F, Liu Y, Lohman KK, Magnani JW, Maher JF, Mehra R, Meng YA, Musani SK, Newton-Cheh C, North KE, Psaty BM, Redline S, Rotter JI, Schnabel RB, Schork NJ, Shohet RV, Singleton AB, Smith JD, Soliman EZ, Srinivasan SR, Taylor HA, Van Wagoner DR, Wilson JG, Young T, Zhang ZM, Zonderman AB, Evans MK, Ferrucci L, Murray SS, Tranah GJ, Whitsel EA, Reiner AP, Sotoodehnia N. PMID: 27577874.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    56. Conservation of Distinct Genetically-Mediated Human Cortical Pattern. PLoS Genet. 2016 07; 12(7):e1006143. Peng Q, Schork A, Bartsch H, Lo MT, Panizzon MS, Westlye LT, Kremen WS, Jernigan TL, Le Hellard S, Steen VM, Espeseth T, Huentelman M, Håberg AK, Agartz I, Djurovic S, Andreassen OA, Dale AM, Schork NJ, Chen CH. PMID: 27459196.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    57. Shared genetic effects between hepatic steatosis and fibrosis: A prospective twin study. Hepatology. 2016 11; 64(5):1547-1558. Cui J, Chen CH, Lo MT, Schork N, Bettencourt R, Gonzalez MP, Bhatt A, Hooker J, Shaffer K, Nelson KE, Long MT, Brenner DA, Sirlin CB, Loomba R. PMID: 27315352.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    58. Mission critical: the need for proteomics in the era of next-generation sequencing and precision medicine. Hum Mol Genet. 2016 Oct 01; 25(R2):R182-R189. Cayer DM, Nazor KL, Schork NJ. PMID: 27439388.
      View in: PubMed   Mentions: 3     Fields:    
    59. Epigenomic Diversity in a Global Collection of Arabidopsis thaliana Accessions. Cell. 2016 Jul 14; 166(2):492-505. Kawakatsu T, Huang SC, Jupe F, Sasaki E, Schmitz RJ, Urich MA, Castanon R, Nery JR, Barragan C, He Y, Chen H, Dubin M, Lee CR, Wang C, Bemm F, Becker C, O'Neil R, O'Malley RC, Quarless DX, Schork NJ, Weigel D, Nordborg M, Ecker JR. PMID: 27419873.
      View in: PubMed   Mentions: 68     Fields:    Translation:AnimalsCells
    60. p53-Dependent DNA damage response sensitive to editing-defective tRNA synthetase in zebrafish. Proc Natl Acad Sci U S A. 2016 07 26; 113(30):8460-5. Song Y, Shi Y, Carland TM, Lian S, Sasaki T, Schork NJ, Head SR, Kishi S, Schimmel P. PMID: 27402763.
      View in: PubMed   Mentions: 3     Fields:    Translation:AnimalsCells
    61. Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Hum Mol Genet. 2016 08 01; 25(15):3383-3394. Hou L, Bergen SE, Akula N, Song J, Hultman CM, Landén M, Adli M, Alda M, Ardau R, Arias B, Aubry JM, Backlund L, Badner JA, Barrett TB, Bauer M, Baune BT, Bellivier F, Benabarre A, Bengesser S, Berrettini WH, Bhattacharjee AK, Biernacka JM, Birner A, Bloss CS, Brichant-Petitjean C, Bui ET, Byerley W, Cervantes P, Chillotti C, Cichon S, Colom F, Coryell W, Craig DW, Cruceanu C, Czerski PM, Davis T, Dayer A, Degenhardt F, Del Zompo M, DePaulo JR, Edenberg HJ, Étain B, Falkai P, Foroud T, Forstner AJ, Frisén L, Frye MA, Fullerton JM, Gard S, Garnham JS, Gershon ES, Goes FS, Greenwood TA, Grigoroiu-Serbanescu M, Hauser J, Heilbronner U, Heilmann-Heimbach S, Herms S, Hipolito M, Hitturlingappa S, Hoffmann P, Hofmann A, Jamain S, Jiménez E, Kahn JP, Kassem L, Kelsoe JR, Kittel-Schneider S, Kliwicki S, Koller DL, König B, Lackner N, Laje G, Lang M, Lavebratt C, Lawson WB, Leboyer M, Leckband SG, Liu C, Maaser A, Mahon PB, Maier W, Maj M, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, McInnis MG, McKinney R, Mitchell PB, Mitjans M, Mondimore FM, Monteleone P, Mühleisen TW, Nievergelt CM, Nöthen MM, Novák T, Nurnberger JI, Nwulia EA, Ösby U, Pfennig A, Potash JB, Propping P, Reif A, Reininghaus E, Rice J, Rietschel M, Rouleau GA, Rybakowski JK, Schalling M, Scheftner WA, Schofield PR, Schork NJ, Schulze TG, Schumacher J, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Simhandl C, Slaney CM, Smith EN, Squassina A, Stamm T, Stopkova P, Streit F, Strohmaier J, Szelinger S, Tighe SK, Tortorella A, Turecki G, Vieta E, Volkert J, Witt SH, Wright A, Zandi PP, Zhang P, Zollner S, McMahon FJ. PMID: 27329760.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    62. Single nucleotide polymorphisms in the REG-CTNNA2 region of chromosome 2 and NEIL3 associated with impulsivity in a Native American sample. Genes Brain Behav. 2016 07; 15(6):568-77. Ehlers CL, Gizer IR, Bizon C, Slutske W, Peng Q, Schork NJ, Wilhelmsen KC. PMID: 27167163.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    63. Towards understanding and predicting suicidality in women: biomarkers and clinical risk assessment. Mol Psychiatry. 2016 06; 21(6):768-85. Levey DF, Niculescu EM, Le-Niculescu H, Dainton HL, Phalen PL, Ladd TB, Weber H, Belanger E, Graham DL, Khan FN, Vanipenta NP, Stage EC, Ballew A, Yard M, Gelbart T, Shekhar A, Schork NJ, Kurian SM, Sandusky GE, Salomon DR, Niculescu AB. PMID: 27046645.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    64. Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. Brain Imaging Behav. 2016 Mar; 10(1):272-82. Eicher JD, Montgomery AM, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst T, Frazier J, Kaufmann WE, Keating B, Kenet T, Kennedy D, Mostofsky S, Murray SS, Sowell ER, Bartsch H, Kuperman JM, Brown TT, Hagler DJ, Dale AM, Jernigan TL, Gruen JR. PMID: 25953057.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    65. Whole-genome mutational burden analysis of three pluripotency induction methods. Nat Commun. 2016 Feb 19; 7:10536. Bhutani K, Nazor KL, Williams R, Tran H, Dai H, Džakula Ž, Cho EH, Pang AWC, Rao M, Cao H, Schork NJ, Loring JF. PMID: 26892726.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    66. Using single nuclei for RNA-seq to capture the transcriptome of postmortem neurons. Nat Protoc. 2016 Mar; 11(3):499-524. Krishnaswami SR, Grindberg RV, Novotny M, Venepally P, Lacar B, Bhutani K, Linker SB, Pham S, Erwin JA, Miller JA, Hodge R, McCarthy JK, Kelder M, McCorrison J, Aevermann BD, Fuertes FD, Scheuermann RH, Lee J, Lein ES, Schork N, McConnell MJ, Gage FH, Lasken RS. PMID: 26890679.
      View in: PubMed   Mentions: 40     Fields:    Translation:HumansCells
    67. Normalizing sleep quality disturbed by psychiatric polypharmacy and sleep apnea: a comprehensive patient-centered N-of-1 study. F1000Res. 2016; 5:132. Magnuson V, Wang Y, Schork N. PMID: 28781744.
      View in: PubMed   Mentions:    Fields:    
    68. The Combined Effect of Common Genetic Risk Variants on Circulating Lipoproteins Is Evident in Childhood: A Longitudinal Analysis of the Cardiovascular Risk in Young Finns Study. PLoS One. 2016; 11(1):e0146081. Buscot MJ, Magnussen CG, Juonala M, Pitkänen N, Lehtimäki T, Viikari JS, Kähönen M, Hutri-Kähönen N, Schork NJ, Raitakari OT, Thomson RJ. PMID: 26731281.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    69. Partial Least Squares Regression Can Aid in Detecting Differential Abundance of Multiple Features in Sets of Metagenomic Samples. Front Genet. 2015; 6:350. Libiger O, Schork NJ. PMID: 26734061.
      View in: PubMed   Mentions:
    70. Variants Near CCK Receptors are Associated With Electrophysiological Responses to Pre-pulse Startle Stimuli in a Mexican American Cohort. Twin Res Hum Genet. 2015 Dec; 18(6):727-37. Norden-Krichmar TM, Gizer IR, Phillips E, Wilhelmsen KC, Schork NJ, Ehlers CL. PMID: 26608796.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    71. Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies. PLoS One. 2015; 10(10):e0139355. Coombes B, Basu S, Guha S, Schork N. PMID: 26436424.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    72. Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies. BMC Bioinformatics. 2015 Sep 22; 16:304. Standish KA, Carland TM, Lockwood GK, Pfeiffer W, Tatineni M, Huang CC, Lamberth S, Cherkas Y, Brodmerkel C, Jaeger E, Smith L, Rajagopal G, Curran ME, Schork NJ. PMID: 26395405.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    73. Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults. J Gerontol A Biol Sci Med Sci. 2015 Nov; 70(11):1418-24. Tranah GJ, Yaffe K, Katzman SM, Lam ET, Pawlikowska L, Kwok PY, Schork NJ, Manini TM, Kritchevsky S, Thomas F, Newman AB, Harris TB, Coleman AL, Gorin MB, Helzner EP, Rowbotham MC, Browner WS, Cummings SR. PMID: 26328603.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    74. Heritability of Hepatic Fibrosis and Steatosis Based on a Prospective Twin Study. Gastroenterology. 2015 Dec; 149(7):1784-93. Loomba R, Schork N, Chen CH, Bettencourt R, Bhatt A, Ang B, Nguyen P, Hernandez C, Richards L, Salotti J, Lin S, Seki E, Nelson KE, Sirlin CB, Brenner D. PMID: 26299412.
      View in: PubMed   Mentions: 43     Fields:    Translation:Humans
    75. Understanding and predicting suicidality using a combined genomic and clinical risk assessment approach. Mol Psychiatry. 2015 Nov; 20(11):1266-85. Niculescu AB, Levey DF, Phalen PL, Le-Niculescu H, Dainton HD, Jain N, Belanger E, James A, George S, Weber H, Graham DL, Schweitzer R, Ladd TB, Learman R, Niculescu EM, Vanipenta NP, Khan FN, Mullen J, Shankar G, Cook S, Humbert C, Ballew A, Yard M, Gelbart T, Shekhar A, Schork NJ, Kurian SM, Sandusky GE, Salomon DR. PMID: 26283638.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    76. Large-scale genomics unveil polygenic architecture of human cortical surface area. Nat Commun. 2015 Jul 20; 6:7549. Chen CH, Peng Q, Schork AJ, Lo MT, Fan CC, Wang Y, Desikan RS, Bettella F, Hagler DJ, Westlye LT, Kremen WS, Jernigan TL, Le Hellard S, Steen VM, Espeseth T, Huentelman M, Håberg AK, Agartz I, Djurovic S, Andreassen OA, Schork N, Dale AM. PMID: 26189703.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    77. Anxiety is related to indices of cortical maturation in typically developing children and adolescents. Brain Struct Funct. 2016 07; 221(6):3013-25. Newman E, Thompson WK, Bartsch H, Hagler DJ, Chen CH, Brown TT, Kuperman JM, McCabe C, Chung Y, Libiger O, Akshoomoff N, Bloss CS, Casey BJ, Chang L, Ernst TM, Frazier JA, Gruen JR, Kennedy DN, Murray SS, Sowell ER, Schork N, Kenet T, Kaufmann WE, Mostofsky S, Amaral DG, Dale AM, Jernigan TL. PMID: 26183468.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    78. Modeling the 3D geometry of the cortical surface with genetic ancestry. Curr Biol. 2015 Aug 03; 25(15):1988-92. Fan CC, Bartsch H, Schork AJ, Chen CH, Wang Y, Lo MT, Brown TT, Kuperman JM, Hagler DJ, Schork NJ, Jernigan TL, Dale AM. PMID: 26166778.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    79. A weighted polygenic risk score using 14 known susceptibility variants to estimate risk and age onset of psoriasis in Han Chinese. PLoS One. 2015; 10(5):e0125369. Yin X, Cheng H, Lin Y, Wineinger NE, Zhou F, Sheng Y, Yang C, Li P, Li F, Shen C, Yang S, Schork NJ, Zhang X. PMID: 25933357.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    80. The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. Neuroimage. 2016 Jan 01; 124(Pt B):1149-1154. Jernigan TL, Brown TT, Hagler DJ, Akshoomoff N, Bartsch H, Newman E, Thompson WK, Bloss CS, Murray SS, Schork N, Kennedy DN, Kuperman JM, McCabe C, Chung Y, Libiger O, Maddox M, Casey BJ, Chang L, Ernst TM, Frazier JA, Gruen JR, Sowell ER, Kenet T, Kaufmann WE, Mostofsky S, Amaral DG, Dale AM. PMID: 25937488.
      View in: PubMed   Mentions: 48     Fields:    Translation:Humans
    81. Personalized medicine: Time for one-person trials. Nature. 2015 Apr 30; 520(7549):609-11. Schork NJ. PMID: 25925459.
      View in: PubMed   Mentions: 128     Fields:    Translation:Humans
    82. Dysregulation of soluble epoxide hydrolase and lipidomic profiles in anorexia nervosa. Mol Psychiatry. 2016 Apr; 21(4):537-46. Shih PB, Yang J, Morisseau C, German JB, Zeeland AA, Armando AM, Quehenberger O, Bergen AW, Magistretti P, Berrettini W, Halmi KA, Schork N, Hammock BD, Kaye W. PMID: 25824304.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    83. Family income, parental education and brain structure in children and adolescents. Nat Neurosci. 2015 May; 18(5):773-8. Noble KG, Houston SM, Brito NH, Bartsch H, Kan E, Kuperman JM, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Murray SS, Casey BJ, Chang L, Ernst TM, Frazier JA, Gruen JR, Kennedy DN, Van Zijl P, Mostofsky S, Kaufmann WE, Kenet T, Dale AM, Jernigan TL, Sowell ER. PMID: 25821911.
      View in: PubMed   Mentions: 132     Fields:    Translation:Humans
    84. A genome sequencing program for novel undiagnosed diseases. Genet Med. 2015 Dec; 17(12):995-1001. Bloss CS, Zeeland AA, Topol SE, Darst BF, Boeldt DL, Erikson GA, Bethel KJ, Bjork RL, Friedman JR, Hwynn N, Patay BA, Pockros PJ, Scott ER, Simon RA, Williams GW, Schork NJ, Topol EJ, Torkamani A. PMID: 25790160.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    85. Scripps Genome ADVISER: Annotation and Distributed Variant Interpretation SERver. PLoS One. 2015; 10(2):e0116815. Pham PH, Shipman WJ, Erikson GA, Schork NJ, Torkamani A. PMID: 25706643.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    86. Rare variants in neuronal excitability genes influence risk for bipolar disorder. Proc Natl Acad Sci U S A. 2015 Mar 17; 112(11):3576-81. Ament SA, Szelinger S, Glusman G, Ashworth J, Hou L, Akula N, Shekhtman T, Badner JA, Brunkow ME, Mauldin DE, Stittrich AB, Rouleau K, Detera-Wadleigh SD, Nurnberger JI, Edenberg HJ, Gershon ES, Schork N, Price ND, Gelinas R, Hood L, Craig D, McMahon FJ, Kelsoe JR, Roach JC. PMID: 25730879.
      View in: PubMed   Mentions: 38     Fields:    Translation:HumansCells
    87. DCAF4, a novel gene associated with leucocyte telomere length. J Med Genet. 2015 Mar; 52(3):157-62. Mangino M, Christiansen L, Stone R, Hunt SC, Horvath K, Eisenberg DT, Kimura M, Petersen I, Kark JD, Herbig U, Reiner AP, Benetos A, Codd V, Nyholt DR, Sinnreich R, Christensen K, Nassar H, Hwang SJ, Levy D, Bataille V, Fitzpatrick AL, Chen W, Berenson GS, Samani NJ, Martin NG, Tishkoff S, Schork NJ, Kyvik KO, Dalgård C, Spector TD, Aviv A. PMID: 25624462.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    88. Gene expression analysis of head and neck squamous cell carcinoma survival and recurrence. Oncotarget. 2015 Jan 01; 6(1):547-55. Zhi X, Lamperska K, Golusinski P, Schork NJ, Luczewski L, Kolenda T, Golusinski W, Masternak MM. PMID: 25575813.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    89. Protective variant associated with alcohol dependence in a Mexican American cohort. BMC Med Genet. 2014 Dec 21; 15:136. Norden-Krichmar TM, Gizer IR, Wilhelmsen KC, Schork NJ, Ehlers CL. PMID: 25527893.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    90. Molecular Mechanism for Hypertensive Renal Disease: Differential Regulation of Chromogranin A Expression at 3'-Untranslated Region Polymorphism C+87T by MicroRNA-107. J Am Soc Nephrol. 2015 Aug; 26(8):1816-25. Zhang K, Mir SA, Hightower CM, Miramontes-Gonzalez JP, Maihofer AX, Chen Y, Mahata SK, Nievergelt CM, Schork NJ, Freedman BI, Vaingankar SM, O'Connor DT. PMID: 25392232.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    91. Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene. Psychoneuroendocrinology. 2015 Jan; 51:459-71. Nievergelt CM, Maihofer AX, Mustapic M, Yurgil KA, Schork NJ, Miller MW, Logue MW, Geyer MA, Risbrough VB, O'Connor DT, Baker DG. PMID: 25456346.
      View in: PubMed   Mentions: 43     Fields:    Translation:Humans
    92. Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample. Am J Med Genet B Neuropsychiatr Genet. 2014 Dec; 165B(8):673-83. Peng Q, Gizer IR, Libiger O, Bizon C, Wilhelmsen KC, Schork NJ, Ehlers CL. PMID: 25270064.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    93. Functional expression of dental plaque microbiota. Front Cell Infect Microbiol. 2014; 4:108. Peterson SN, Meissner T, Su AI, Snesrud E, Ong AC, Schork NJ, Bretz WA. PMID: 25177549.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    94. Characterization of genetic variation in the VGLL4 gene in anorexia nervosa. Psychiatr Genet. 2014 Aug; 24(4):183-4. Clarke TK, Crist RC, Doyle GA, Weiss AR, Brandt H, Crawford S, Crow S, Fichter MM, Halmi KA, Johnson C, Kaplan AS, La Via M, Mitchell JE, Strober M, Rotondo A, Treasure J, Woodside DB, Keel P, Klump KL, Lilenfeld L, Plotnicov K, Magistretti PJ, Bergen AW, Kaye WH, Schork NJ, Berrettini WH. PMID: 24983835.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    95. Admixture and clinical phenotypic variation. Hum Hered. 2014; 77(1-4):73-86. Goetz LH, Uribe-Bruce L, Quarless D, Libiger O, Schork NJ. PMID: 25060271.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    96. Influence of individual differences in disease perception on consumer response to direct-to-consumer genomic testing. Clin Genet. 2015 Mar; 87(3):225-32. Boeldt DL, Schork NJ, Topol EJ, Bloss CS. PMID: 24798746.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    97. A high resolution case study of a patient with recurrent Plasmodium vivax infections shows that relapses were caused by meiotic siblings. PLoS Negl Trop Dis. 2014 Jun; 8(6):e2882. Bright AT, Manary MJ, Tewhey R, Arango EM, Wang T, Schork NJ, Yanow SK, Winzeler EA. PMID: 24901334.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansAnimals
    98. Genetic risk prediction and neurobiological understanding of alcoholism. Transl Psychiatry. 2014 May 20; 4:e391. Levey DF, Le-Niculescu H, Frank J, Ayalew M, Jain N, Kirlin B, Learman R, Winiger E, Rodd Z, Shekhar A, Schork N, Kiefer F, Kiefe F, Wodarz N, Müller-Myhsok B, Dahmen N, Nöthen M, Sherva R, Farrer L, Smith AH, Kranzler HR, Rietschel M, Gelernter J, Niculescu AB. PMID: 24844177.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimals
    99. Mechanisms of linezolid resistance among coagulase-negative staphylococci determined by whole-genome sequencing. mBio. 2014 May 13; 5(3):e00894-14. Tewhey R, Gu B, Kelesidis T, Charlton C, Bobenchik A, Hindler J, Schork NJ, Humphries RM. PMID: 24915435.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    100. Expression levels of insulin-like growth factors 1 and 2 in head and neck squamous cell carcinoma. Growth Horm IGF Res. 2014 Aug; 24(4):137-41. Zhi X, Lamperska K, Golusinski P, Schork NJ, Luczewski L, Golusinski W, Masternak MM. PMID: 24802266.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    101. Candidate SNP associations of optimism and resilience in older adults: exploratory study of 935 community-dwelling adults. Am J Geriatr Psychiatry. 2014 Oct; 22(10):997-1006.e5. Rana BK, Darst BF, Bloss C, Shih PA, Depp C, Nievergelt CM, Allison M, Parsons JK, Schork N, Jeste DV. PMID: 24791650.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    102. Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia. Ann Neurol. 2014 Apr; 75(4):542-9. Chen YZ, Friedman JR, Chen DH, Chan GC, Bloss CS, Hisama FM, Topol SE, Carson AR, Pham PH, Bonkowski ES, Scott ER, Lee JK, Zhang G, Oliveira G, Xu J, Scott-Van Zeeland AA, Chen Q, Levy S, Topol EJ, Storm D, Swanson PD, Bird TD, Schork NJ, Raskind WH, Torkamani A. PMID: 24700542.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    103. Correlation analysis of genetic admixture and social identification with body mass index in a Native American community. Am J Hum Biol. 2014 May-Jun; 26(3):347-60. Norden-Krichmar TM, Gizer IR, Libiger O, Wilhelmsen KC, Ehlers CL, Schork NJ. PMID: 24757035.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    104. A genome-wide association study of anorexia nervosa. Mol Psychiatry. 2014 Oct; 19(10):1085-94. Boraska V, Franklin CS, Floyd JA, Thornton LM, Huckins LM, Southam L, Rayner NW, Tachmazidou I, Klump KL, Treasure J, Lewis CM, Schmidt U, Tozzi F, Kiezebrink K, Hebebrand J, Gorwood P, Adan RA, Kas MJ, Favaro A, Santonastaso P, Fernández-Aranda F, Gratacos M, Rybakowski F, Dmitrzak-Weglarz M, Kaprio J, Keski-Rahkonen A, Raevuori A, Van Furth EF, Slof-Op 't Landt MC, Hudson JI, Reichborn-Kjennerud T, Knudsen GP, Monteleone P, Kaplan AS, Karwautz A, Hakonarson H, Berrettini WH, Guo Y, Li D, Schork NJ, Komaki G, Ando T, Inoko H, Esko T, Fischer K, Männik K, Metspalu A, Baker JH, Cone RD, Dackor J, DeSocio JE, Hilliard CE, O'Toole JK, Pantel J, Szatkiewicz JP, Taico C, Zerwas S, Trace SE, Davis OS, Helder S, Bühren K, Burghardt R, de Zwaan M, Egberts K, Ehrlich S, Herpertz-Dahlmann B, Herzog W, Imgart H, Scherag A, Scherag S, Zipfel S, Boni C, Ramoz N, Versini A, Brandys MK, Danner UN, de Kovel C, Hendriks J, Koeleman BP, Ophoff RA, Strengman E, van Elburg AA, Bruson A, Clementi M, Degortes D, Forzan M, Tenconi E, Docampo E, Escaramís G, Jiménez-Murcia S, Lissowska J, Rajewski A, Szeszenia-Dabrowska N, Slopien A, Hauser J, Karhunen L, Meulenbelt I, Slagboom PE, Tortorella A, Maj M, Dedoussis G, Dikeos D, Gonidakis F, Tziouvas K, Tsitsika A, Papezova H, Slachtova L, Martaskova D, Kennedy JL, Levitan RD, Yilmaz Z, Huemer J, Koubek D, Merl E, Wagner G, Lichtenstein P, Breen G, Cohen-Woods S, Farmer A, McGuffin P, Cichon S, Giegling I, Herms S, Rujescu D, Schreiber S, Wichmann HE, Dina C, Sladek R, Gambaro G, Soranzo N, Julia A, Marsal S, Rabionet R, Gaborieau V, Dick DM, Palotie A, Ripatti S, Widén E, Andreassen OA, Espeseth T, Lundervold A, Reinvang I, Steen VM, Le Hellard S, Mattingsdal M, Ntalla I, Bencko V, Foretova L, Janout V, Navratilova M, Gallinger S, Pinto D, Scherer SW, Aschauer H, Carlberg L, Schosser A, Alfredsson L, Ding B, Klareskog L, Padyukov L, Courtet P, Guillaume S, Jaussent I, Finan C, Kalsi G, Roberts M, Logan DW, Peltonen L, Ritchie GR, Barrett JC, Estivill X, Hinney A, Sullivan PF, Collier DA, Zeggini E, Bulik CM. PMID: 24514567.
      View in: PubMed   Mentions: 76     Fields:    Translation:Humans
    105. Chip-based direct genotyping of coding variants in genome wide association studies: utility, issues and prospects. Gene. 2014 Apr 25; 540(1):104-9. Nievergelt CM, Wineinger NE, Libiger O, Pham P, Zhang G, Baker DG, Schork NJ. PMID: 24521671.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    106. Genetic implication of a novel thiamine transporter in human hypertension. J Am Coll Cardiol. 2014 Apr 22; 63(15):1542-55. Zhang K, Huentelman MJ, Rao F, Sun EI, Corneveaux JJ, Schork AJ, Wei Z, Waalen J, Miramontes-Gonzalez JP, Hightower CM, Maihofer AX, Mahata M, Pastinen T, Ehret GB, Schork NJ, Eskin E, Nievergelt CM, Saier MH, O'Connor DT. PMID: 24509276.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    107. Utility of network integrity methods in therapeutic target identification. Front Genet. 2014; 5:12. Peng Q, Schork NJ. PMID: 24550933.
      View in: PubMed   Mentions:
    108. Association between traumatic brain injury and risk of posttraumatic stress disorder in active-duty Marines. JAMA Psychiatry. 2014 Feb; 71(2):149-57. Yurgil KA, Barkauskas DA, Vasterling JJ, Nievergelt CM, Larson GE, Schork NJ, Litz BT, Nash WP, Baker DG. PMID: 24337530.
      View in: PubMed   Mentions: 36     Fields:    Translation:Humans
    109. Common variants explain a large fraction of the variability in the liability to psoriasis in a Han Chinese population. BMC Genomics. 2014 Jan 30; 15:87. Yin X, Wineinger NE, Cheng H, Cui Y, Zhou F, Zuo X, Zheng X, Yang S, Schork NJ, Zhang X. PMID: 24479639.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    110. Treatment responses to tooth whitening in twins. Twin Res Hum Genet. 2014 Feb; 17(1):23-6. Corby PM, Biesbrock A, Gerlach R, Corby AL, Moreira A, Schork NJ, Bretz WA. PMID: 24429255.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    111. Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. Hum Mol Genet. 2014 May 01; 23(9):2498-510. Yoneyama S, Guo Y, Lanktree MB, Barnes MR, Elbers CC, Karczewski KJ, Padmanabhan S, Bauer F, Baumert J, Beitelshees A, Berenson GS, Boer JM, Burke G, Cade B, Chen W, Cooper-Dehoff RM, Gaunt TR, Gieger C, Gong Y, Gorski M, Heard-Costa N, Johnson T, Lamonte MJ, McDonough C, Monda KL, Onland-Moret NC, Nelson CP, O'Connell JR, Ordovas J, Peter I, Peters A, Shaffer J, Shen H, Smith E, Speilotes L, Thomas F, Thorand B, Monique Verschuren WM, Anand SS, Dominiczak A, Davidson KW, Hegele RA, Heid I, Hofker MH, Huggins GS, Illig T, Johnson JA, Kirkland S, König W, Langaee TY, McCaffery J, Melander O, Mitchell BD, Munroe P, Murray SS, Papanicolaou G, Redline S, Reilly M, Samani NJ, Schork NJ, Van Der Schouw YT, Shimbo D, Shuldiner AR, Tobin MD, Wijmenga C, Yusuf S, Hakonarson H, Lange LA, Demerath EW, Fox CS, North KE, Reiner AP, Keating B, Taylor KC. PMID: 24345515.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    112. Direct-to-consumer pharmacogenomic testing is associated with increased physician utilisation. J Med Genet. 2014 Feb; 51(2):83-9. Bloss CS, Schork NJ, Topol EJ. PMID: 24343916.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    113. A pharmacological network for lifespan extension in Caenorhabditis elegans. Aging Cell. 2014 Apr; 13(2):206-15. Ye X, Linton JM, Schork NJ, Buck LB, Petrascheck M. PMID: 24134630.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansAnimals
    114. The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING). Neuropsychology. 2014 Jan; 28(1):1-10. Akshoomoff N, Newman E, Thompson WK, McCabe C, Bloss CS, Chang L, Amaral DG, Casey BJ, Ernst TM, Frazier JA, Gruen JR, Kaufmann WE, Kenet T, Kennedy DN, Libiger O, Mostofsky S, Murray SS, Sowell ER, Schork N, Dale AM, Jernigan TL. PMID: 24219608.
      View in: PubMed   Mentions: 39     Fields:    Translation:Humans
    115. Mitochondrial DNA sequence associations with dementia and amyloid-ß in elderly African Americans. Neurobiol Aging. 2014 Feb; 35(2):442.e1-8. Tranah GJ, Yokoyama JS, Katzman SM, Nalls MA, Newman AB, Harris TB, Cesari M, Manini TM, Schork NJ, Cummings SR, Liu Y, Yaffe K. PMID: 24140124.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    116. Human heart rate: heritability of resting and stress values in twin pairs, and influence of genetic variation in the adrenergic pathway at a microribonucleic acid (microrna) motif in the 3'-UTR of cytochrome b561 [corrected]. J Am Coll Cardiol. 2014 Feb 04; 63(4):358-68. Zhang K, Deacon DC, Rao F, Schork AJ, Fung MM, Waalen J, Schork NJ, Nievergelt CM, Chi NC, O'Connor DT. PMID: 24140660.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    117. Genome-wide association study of shared components of reading disability and language impairment. Genes Brain Behav. 2013 Nov; 12(8):792-801. Eicher JD, Powers NR, Miller LL, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst T, Frazier J, Kaufmann WE, Keating B, Kenet T, Kennedy D, Mostofsky S, Murray SS, Sowell ER, Bartsch H, Kuperman JM, Brown TT, Hagler DJ, Dale AM, Jernigan TL, St Pourcain B, Davey Smith G, Ring SM, Gruen JR. PMID: 24024963.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    118. Evidence for the role of EPHX2 gene variants in anorexia nervosa. Mol Psychiatry. 2014 Jun; 19(6):724-32. Scott-Van Zeeland AA, Bloss CS, Tewhey R, Bansal V, Torkamani A, Libiger O, Duvvuri V, Wineinger N, Galvez L, Darst BF, Smith EN, Carson A, Pham P, Phillips T, Villarasa N, Tisch R, Zhang G, Levy S, Murray S, Chen W, Srinivasan S, Berenson G, Brandt H, Crawford S, Crow S, Fichter MM, Halmi KA, Johnson C, Kaplan AS, La Via M, Mitchell JE, Strober M, Rotondo A, Treasure J, Woodside DB, Bulik CM, Keel P, Klump KL, Lilenfeld L, Plotnicov K, Topol EJ, Shih PB, Magistretti P, Bergen AW, Berrettini W, Kaye W, Schork NJ. PMID: 23999524.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    119. Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation. PLoS Genet. 2013 Aug; 9(8):e1003622. Paliwal A, Temkin AM, Kerkel K, Yale A, Yotova I, Drost N, Lax S, Nhan-Chang CL, Powell C, Borczuk A, Aviv A, Wapner R, Chen X, Nagy PL, Schork N, Do C, Torkamani A, Tycko B. PMID: 24009515.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    120. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet. 2013 Sep 05; 93(3):545-54. Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Tayo BO, Sun YV, Gottesman O, Adeyemo A, Johnson AD, Young JH, Rice K, Duan Q, Chen F, Li Y, Tang H, Fornage M, Keene KL, Andrews JS, Smith JA, Faul JD, Guangfa Z, Guo W, Liu Y, Murray SS, Musani SK, Srinivasan S, Velez Edwards DR, Wang H, Becker LC, Bovet P, Bochud M, Broeckel U, Burnier M, Carty C, Chasman DI, Ehret G, Chen WM, Chen G, Chen W, Ding J, Dreisbach AW, Evans MK, Guo X, Garcia ME, Jensen R, Keller MF, Lettre G, Lotay V, Martin LW, Moore JH, Morrison AC, Mosley TH, Ogunniyi A, Palmas W, Papanicolaou G, Penman A, Polak JF, Ridker PM, Salako B, Singleton AB, Shriner D, Taylor KD, Vasan R, Wiggins K, Williams SM, Yanek LR, Zhao W, Zonderman AB, Becker DM, Berenson G, Boerwinkle E, Bottinger E, Cushman M, Eaton C, Nyberg F, Heiss G, Hirschhron JN, Howard VJ, Karczewsk KJ, Lanktree MB, Liu K, Liu Y, Loos R, Margolis K, Snyder M, Psaty BM, Schork NJ, Weir DR, Rotimi CN, Sale MM, Harris T, Kardia SL, Hunt SC, Arnett D, Redline S, Cooper RS, Risch NJ, Rao DC, Rotter JI, Chakravarti A, Reiner AP, Levy D, Keating BJ, Zhu X. PMID: 23972371.
      View in: PubMed   Mentions: 71     Fields:    Translation:Humans
    121. Discovery and validation of blood biomarkers for suicidality. Mol Psychiatry. 2013 Dec; 18(12):1249-64. Le-Niculescu H, Levey DF, Ayalew M, Palmer L, Gavrin LM, Jain N, Winiger E, Bhosrekar S, Shankar G, Radel M, Bellanger E, Duckworth H, Olesek K, Vergo J, Schweitzer R, Yard M, Ballew A, Shekhar A, Sandusky GE, Schork NJ, Kurian SM, Salomon DR, Niculescu AB. PMID: 23958961.
      View in: PubMed   Mentions: 45     Fields:    Translation:Humans
    122. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet. 2013 Sep; 45(9):984-94. Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R, Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA, Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N, Battaglia A, Bauer M, Bayés M, Bellivier F, Bergen SE, Berrettini W, Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH, Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Bruggeman R, Cormican P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM, Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D, Czamara D, Datta S, Dawson G, Day R, De Geus EJ, Degenhardt F, Djurovic S, Donohoe GJ, Doyle AE, Duan J, Dudbridge F, Duketis E, Ebstein RP, Edenberg HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger M, Fombonne E, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer NB, Freitag CM, Friedl M, Frisén L, Gallagher L, Gejman PV, Georgieva L, Gershon ES, Geschwind DH, Giegling I, Gill M, Gordon SD, Gordon-Smith K, Green EK, Greenwood TA, Grice DE, Gross M, Grozeva D, Guan W, Gurling H, De Haan L, Haines JL, Hakonarson H, Hallmayer J, Hamilton SP, Hamshere ML, Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S, Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hoogendijk WJ, Hottenga JJ, Hultman CM, Hus V, Ingason A, Ising M, Jamain S, Jones EG, Jones I, Jones L, Tzeng JY, Kähler AK, Kahn RS, Kandaswamy R, Keller MC, Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Klauck SM, Klei L, Knowles JA, Kohli MA, Koller DL, Konte B, Korszun A, Krabbendam L, Krasucki R, Kuntsi J, Kwan P, Landén M, Långström N, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Ledbetter DH, Lee PH, Lencz T, Lesch KP, Levinson DF, Lewis CM, Li J, Lichtenstein P, Lieberman JA, Lin DY, Linszen DH, Liu C, Lohoff FW, Loo SK, Lord C, Lowe JK, Lucae S, MacIntyre DJ, Madden PA, Maestrini E, Magnusson PK, Mahon PB, Maier W, Malhotra AK, Mane SM, Martin CL, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll SA, McGhee KA, McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McMahon WM, McQuillin A, Medeiros H, Medland SE, Meier S, Melle I, Meng F, Meyer J, Middeldorp CM, Middleton L, Milanova V, Miranda A, Monaco AP, Montgomery GW, Moran JL, Moreno-De-Luca D, Morken G, Morris DW, Morrow EM, Moskvina V, Muglia P, Mühleisen TW, Muir WJ, Müller-Myhsok B, Murtha M, Myers RM, Myin-Germeys I, Neale MC, Nelson SF, Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nöthen MM, Nurnberger JI, Nwulia EA, Nyholt DR, O'Dushlaine C, Oades RD, Olincy A, Oliveira G, Olsen L, Ophoff RA, Osby U, Owen MJ, Palotie A, Parr JR, Paterson AD, Pato CN, Pato MT, Penninx BW, Pergadia ML, Pericak-Vance MA, Pickard BS, Pimm J, Piven J, Posthuma D, Potash JB, Poustka F, Propping P, Puri V, Quested DJ, Quinn EM, Ramos-Quiroga JA, Rasmussen HB, Raychaudhuri S, Rehnström K, Reif A, Ribasés M, Rice JP, Rietschel M, Roeder K, Roeyers H, Rossin L, Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Sanders SJ, Santangelo SL, Sergeant JA, Schachar R, Schalling M, Schatzberg AF, Scheftner WA, Schellenberg GD, Scherer SW, Schork NJ, Schulze TG, Schumacher J, Schwarz M, Scolnick E, Scott LJ, Shi J, Shilling PD, Shyn SI, Silverman JM, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke EJ, St Clair D, State M, Steffens M, Steinhausen HC, Strauss JS, Strohmaier J, Stroup TS, Sutcliffe JS, Szatmari P, Szelinger S, Thirumalai S, Thompson RC, Todorov AA, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Van Os J, Vicente AM, Vieland VJ, Vincent JB, Visscher PM, Walsh CA, Wassink TH, Watson SJ, Weissman MM, Werge T, Wienker TF, Wijsman EM, Willemsen G, Williams N, et al. PMID: 23933821.
      View in: PubMed   Mentions: 599     Fields:    Translation:Humans
    123. Genetic parts to a preventive medicine whole. Genome Med. 2013; 5(6):54. Schork NJ. PMID: 23806045.
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    124. Genomic risk models improve prediction of longitudinal lipid levels in children and young adults. Front Genet. 2013; 4:86. Wineinger NE, Harper A, Libiger O, Srinivasan SR, Chen W, Berenson GS, Schork NJ. PMID: 23734161.
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    125. MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension. Hum Mol Genet. 2013 Sep 15; 22(18):3624-40. Friese RS, Altshuler AE, Zhang K, Miramontes-Gonzalez JP, Hightower CM, Jirout ML, Salem RM, Gayen JR, Mahapatra NR, Biswas N, Cale M, Vaingankar SM, Kim HS, Courel M, Taupenot L, Ziegler MG, Schork NJ, Pravenec M, Mahata SK, Schmid-Schönbein GW, O'Connor DT. PMID: 23674521.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimalsCells
    126. Perceptions of genetic counseling services in direct-to-consumer personal genomic testing. Clin Genet. 2013 Oct; 84(4):335-9. Darst BF, Madlensky L, Schork NJ, Topol EJ, Bloss CS. PMID: 23590221.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    127. Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. Am J Psychiatry. 2013 May; 170(5):521-32. Greenwood TA, Swerdlow NR, Gur RE, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Green MF, Gur RC, Lazzeroni LC, Nuechterlein KH, Olincy A, Radant AD, Ray A, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar CA, Tsuang DW, Tsuang MT, Turetsky BI, Light GA, Braff DL. PMID: 23511790.
      View in: PubMed   Mentions: 49     Fields:    Translation:Humans
    128. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PLoS Genet. 2013 Apr; 9(4):e1003449. Schork AJ, Thompson WK, Pham P, Torkamani A, Roddey JC, Sullivan PF, Kelsoe JR, O'Donovan MC, Furberg H, Schork NJ, Andreassen OA, Dale AM. PMID: 23637621.
      View in: PubMed   Mentions: 107     Fields:    Translation:Humans
    129. Genome-wide association study of age at menarche in African-American women. Hum Mol Genet. 2013 Aug 15; 22(16):3329-46. Demerath EW, Liu CT, Franceschini N, Chen G, Palmer JR, Smith EN, Chen CT, Ambrosone CB, Arnold AM, Bandera EV, Berenson GS, Bernstein L, Britton A, Cappola AR, Carlson CS, Chanock SJ, Chen W, Chen Z, Deming SL, Elks CE, Evans MK, Gajdos Z, Henderson BE, Hu JJ, Ingles S, John EM, Kerr KF, Kolonel LN, Le Marchand L, Lu X, Millikan RC, Musani SK, Nock NL, North K, Nyante S, Press MF, Rodriquez-Gil JL, Ruiz-Narvaez EA, Schork NJ, Srinivasan SR, Woods NF, Zheng W, Ziegler RG, Zonderman A, Heiss G, Gwen Windham B, Wellons M, Murray SS, Nalls M, Pastinen T, Rajkovic A, Hirschhorn J, Adrienne Cupples L, Kooperberg C, Murabito JM, Haiman CA. PMID: 23599027.
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    130. Impact of direct-to-consumer genomic testing at long term follow-up. J Med Genet. 2013 Jun; 50(6):393-400. Bloss CS, Wineinger NE, Darst BF, Schork NJ, Topol EJ. PMID: 23559530.
      View in: PubMed   Mentions: 49     Fields:    Translation:Humans
    131. Complex patterns of genomic admixture within southern Africa. PLoS Genet. 2013; 9(3):e1003309. Petersen DC, Libiger O, Tindall EA, Hardie RA, Hannick LI, Glashoff RH, Mukerji M, Fernandez P, Haacke W, Schork NJ, Hayes VM. PMID: 23516368.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    132. The dental plaque microbiome in health and disease. PLoS One. 2013; 8(3):e58487. Peterson SN, Snesrud E, Liu J, Ong AC, Kilian M, Schork NJ, Bretz W. PMID: 23520516.
      View in: PubMed   Mentions: 41     Fields:    Translation:HumansCTClinical Trials
    133. Patterns of population epigenomic diversity. Nature. 2013 Mar 14; 495(7440):193-8. Schmitz RJ, Schultz MD, Urich MA, Nery JR, Pelizzola M, Libiger O, Alix A, McCosh RB, Chen H, Schork NJ, Ecker JR. PMID: 23467092.
      View in: PubMed   Mentions: 169     Fields:    Translation:AnimalsCells
    134. Characteristics of genomic test consumers who spontaneously share results with their health care provider. Health Commun. 2014; 29(1):105-8. Darst BF, Madlensky L, Schork NJ, Topol EJ, Bloss CS. PMID: 23384116.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    135. A Method for Inferring an Individual's Genetic Ancestry and Degree of Admixture Associated with Six Major Continental Populations. Front Genet. 2012; 3:322. Libiger O, Schork NJ. PMID: 23335941.
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    136. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum Mol Genet. 2013 Apr 15; 22(8):1663-78. Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, Gaunt TR, Gho JM, Gieger C, Gong Y, Isaacs A, Kleber ME, Mateo Leach I, McDonough CW, Meijs MF, Mellander O, Molony CM, Nolte IM, Padmanabhan S, Price TS, Rajagopalan R, Shaffer J, Shah S, Shen H, Soranzo N, van der Most PJ, Van Iperen EP, Van Setten J, Van Setten JA, Vonk JM, Zhang L, Beitelshees AL, Berenson GS, Bhatt DL, Boer JM, Boerwinkle E, Burkley B, Burt A, Chakravarti A, Chen W, Cooper-Dehoff RM, Curtis SP, Dreisbach A, Duggan D, Ehret GB, Fabsitz RR, Fornage M, Fox E, Furlong CE, Gansevoort RT, Hofker MH, Hovingh GK, Kirkland SA, Kottke-Marchant K, Kutlar A, Lacroix AZ, Langaee TY, Li YR, Lin H, Liu K, Maiwald S, Malik R, Murugesan G, Newton-Cheh C, O'Connell JR, Onland-Moret NC, Ouwehand WH, Palmas W, Penninx BW, Pepine CJ, Pettinger M, Polak JF, Ramachandran VS, Ranchalis J, Redline S, Ridker PM, Rose LM, Scharnag H, Schork NJ, Shimbo D, Shuldiner AR, Srinivasan SR, Stolk RP, Taylor HA, Thorand B, Trip MD, van Duijn CM, Verschuren WM, Wijmenga C, Winkelmann BR, Wyatt S, Young JH, Boehm BO, Caulfield MJ, Chasman DI, Davidson KW, Doevendans PA, Fitzgerald GA, Gums JG, Hakonarson H, Hillege HL, Illig T, Jarvik GP, Johnson JA, Kastelein JJ, Koenig W, März W, Mitchell BD, Murray SS, Oldehinkel AJ, Rader DJ, Reilly MP, Reiner AP, Schadt EE, Silverstein RL, Snieder H, Stanton AV, Uitterlinden AG, van der Harst P, van der Schouw YT, Samani NJ, Johnson AD, Munroe PB, de Bakker PI, Zhu X, Levy D, Keating BJ, Asselbergs FW. PMID: 23303523.
      View in: PubMed   Mentions: 55     Fields:    Translation:Humans
    137. The Minnesota Center for Twin and Family Research genome-wide association study. Twin Res Hum Genet. 2012 Dec; 15(6):767-74. Miller MB, Basu S, Cunningham J, Eskin E, Malone SM, Oetting WS, Schork N, Sul JH, Iacono WG, McGue M. PMID: 23363460.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansCTClinical Trials
    138. Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants. Heart Rhythm. 2013 Mar; 10(3):401-8. Deo R, Nalls MA, Avery CL, Smith JG, Evans DS, Keller MF, Butler AM, Buxbaum SG, Li G, Miguel Quibrera P, Smith EN, Tanaka T, Akylbekova EL, Alonso A, Arking DE, Benjamin EJ, Berenson GS, Bis JC, Chen LY, Chen W, Cummings SR, Ellinor PT, Evans MK, Ferrucci L, Fox ER, Heckbert SR, Heiss G, Hsueh WC, Kerr KF, Limacher MC, Liu Y, Lubitz SA, Magnani JW, Mehra R, Marcus GM, Murray SS, Newman AB, Njajou O, North KE, Paltoo DN, Psaty BM, Redline SS, Reiner AP, Robinson JG, Rotter JI, Samdarshi TE, Schnabel RB, Schork NJ, Singleton AB, Siscovick D, Soliman EZ, Sotoodehnia N, Srinivasan SR, Taylor HA, Trevisan M, Zhang Z, Zonderman AB, Newton-Cheh C, Whitsel EA. PMID: 23183192.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    139. Impact of ancestry and common genetic variants on QT interval in African Americans. Circ Cardiovasc Genet. 2012 Dec; 5(6):647-55. Smith JG, Avery CL, Evans DS, Nalls MA, Meng YA, Smith EN, Palmer C, Tanaka T, Mehra R, Butler AM, Young T, Buxbaum SG, Kerr KF, Berenson GS, Schnabel RB, Li G, Ellinor PT, Magnani JW, Chen W, Bis JC, Curb JD, Hsueh WC, Rotter JI, Liu Y, Newman AB, Limacher MC, North KE, Reiner AP, Quibrera PM, Schork NJ, Singleton AB, Psaty BM, Soliman EZ, Solomon AJ, Srinivasan SR, Alonso A, Wallace R, Redline S, Zhang ZM, Post WS, Zonderman AB, Taylor HA, Murray SS, Ferrucci L, Arking DE, Evans MK, Fox ER, Sotoodehnia N, Heckbert SR, Whitsel EA, Newton-Cheh C. PMID: 23166209.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    140. Long-term influence of normal variation in neonatal characteristics on human brain development. Proc Natl Acad Sci U S A. 2012 Dec 04; 109(49):20089-94. Walhovd KB, Fjell AM, Brown TT, Kuperman JM, Chung Y, Hagler DJ, Roddey JC, Erhart M, McCabe C, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst TM, Frazier J, Gruen JR, Kaufmann WE, Murray SS, van Zijl P, Mostofsky S, Dale AM. PMID: 23169628.
      View in: PubMed   Mentions: 49     Fields:    Translation:Humans
    141. Interaction between serotonin transporter and dopamine D2/D3 receptor radioligand measures is associated with harm avoidant symptoms in anorexia and bulimia nervosa. Psychiatry Res. 2013 Feb 28; 211(2):160-8. Bailer UF, Frank GK, Price JC, Meltzer CC, Becker C, Mathis CA, Wagner A, Barbarich-Marsteller NC, Bloss CS, Putnam K, Schork NJ, Gamst A, Kaye WH. PMID: 23154100.
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    142. Multimodal imaging of the self-regulating developing brain. Proc Natl Acad Sci U S A. 2012 Nov 27; 109(48):19620-5. Fjell AM, Walhovd KB, Brown TT, Kuperman JM, Chung Y, Hagler DJ, Venkatraman V, Roddey JC, Erhart M, McCabe C, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Darst BF, Schork NJ, Casey BJ, Chang L, Ernst TM, Gruen JR, Kaufmann WE, Kenet T, Frazier J, Murray SS, Sowell ER, van Zijl P, Mostofsky S, Jernigan TL, Dale AM. PMID: 23150548.
      View in: PubMed   Mentions: 72     Fields:    Translation:Humans
    143. Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. Circ Cardiovasc Genet. 2012 Dec; 5(6):639-46. Butler AM, Yin X, Evans DS, Nalls MA, Smith EN, Tanaka T, Li G, Buxbaum SG, Whitsel EA, Alonso A, Arking DE, Benjamin EJ, Berenson GS, Bis JC, Chen W, Deo R, Ellinor PT, Heckbert SR, Heiss G, Hsueh WC, Keating BJ, Kerr KF, Li Y, Limacher MC, Liu Y, Lubitz SA, Marciante KD, Mehra R, Meng YA, Newman AB, Newton-Cheh C, North KE, Palmer CD, Psaty BM, Quibrera PM, Redline S, Reiner AP, Rotter JI, Schnabel RB, Schork NJ, Singleton AB, Smith JG, Soliman EZ, Srinivasan SR, Zhang ZM, Zonderman AB, Ferrucci L, Murray SS, Evans MK, Sotoodehnia N, Magnani JW, Avery CL. PMID: 23139255.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    144. Clinical implications of human population differences in genome-wide rates of functional genotypes. Front Genet. 2012; 3:211. Torkamani A, Pham P, Libiger O, Bansal V, Zhang G, Scott-Van Zeeland AA, Tewhey R, Topol EJ, Schork NJ. PMID: 23125845.
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    145. Genotype prediction of adult type 2 diabetes from adolescence in a multiracial population. Pediatrics. 2012 Nov; 130(5):e1235-42. Vassy JL, Dasmahapatra P, Meigs JB, Schork NJ, Magnussen CG, Chen W, Raitakari OT, Pencina MJ, Jamal SM, Berenson GS, Goodman E. PMID: 23071215.
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    146. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am J Hum Genet. 2012 Nov 02; 91(5):823-38. Asselbergs FW, Guo Y, van Iperen EP, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J, Baumert J, Beitelshees AL, Bhangale TR, Chen YD, Gaunt TR, Gong Y, Hopewell JC, Johnson T, Kleber ME, Langaee TY, Li M, Li YR, Liu K, McDonough CW, Meijs MF, Middelberg RP, Musunuru K, Nelson CP, O'Connell JR, Padmanabhan S, Pankow JS, Pankratz N, Rafelt S, Rajagopalan R, Romaine SP, Schork NJ, Shaffer J, Shen H, Smith EN, Tischfield SE, van der Most PJ, van Vliet-Ostaptchouk JV, Verweij N, Volcik KA, Zhang L, Bailey KR, Bailey KM, Bauer F, Boer JM, Braund PS, Burt A, Burton PR, Buxbaum SG, Chen W, Cooper-Dehoff RM, Cupples LA, deJong JS, Delles C, Duggan D, Fornage M, Furlong CE, Glazer N, Gums JG, Hastie C, Holmes MV, Illig T, Kirkland SA, Kivimaki M, Klein R, Klein BE, Kooperberg C, Kottke-Marchant K, Kumari M, LaCroix AZ, Mallela L, Murugesan G, Ordovas J, Ouwehand WH, Post WS, Saxena R, Scharnagl H, Schreiner PJ, Shah T, Shields DC, Shimbo D, Srinivasan SR, Stolk RP, Swerdlow DI, Taylor HA, Topol EJ, Toskala E, van Pelt JL, van Setten J, Yusuf S, Whittaker JC, Zwinderman AH, Anand SS, Balmforth AJ, Berenson GS, Bezzina CR, Boehm BO, Boerwinkle E, Casas JP, Caulfield MJ, Clarke R, Connell JM, Cruickshanks KJ, Davidson KW, Day IN, de Bakker PI, Doevendans PA, Dominiczak AF, Hall AS, Hartman CA, Hengstenberg C, Hillege HL, Hofker MH, Humphries SE, Jarvik GP, Johnson JA, Kaess BM, Kathiresan S, Koenig W, Lawlor DA, März W, Melander O, Mitchell BD, Montgomery GW, Munroe PB, Murray SS, Newhouse SJ, Onland-Moret NC, Poulter N, Psaty B, Redline S, Rich SS, Rotter JI, Schunkert H, Sever P, Shuldiner AR, Silverstein RL, Stanton A, Thorand B, Trip MD, Tsai MY, van der Harst P, van der Schoot E, van der Schouw YT, Verschuren WM, Watkins H, Wilde AA, Wolffenbuttel BH, Whitfield JB, Hovingh GK, Ballantyne CM, Wijmenga C, Reilly MP, Martin NG, Wilson JG, Rader DJ, Samani NJ, Reiner AP, Hegele RA, Kastelein JJ, Hingorani AD, Talmud PJ, Hakonarson H, Elbers CC, Keating BJ, Drenos F. PMID: 23063622.
      View in: PubMed   Mentions: 88     Fields:    Translation:Humans
    147. Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin. Am J Med Genet B Neuropsychiatr Genet. 2012 Dec; 159B(8):941-50. Nissen S, Liang S, Shehktman T, Kelsoe JR, Greenwood TA, Nievergelt CM, McKinney R, Shilling PD, Smith EN, Schork NJ, Bloss CS, Nurnberger JI, Edenberg HJ, Foroud T, Koller DL, Gershon ES, Liu C, Badner JA, Scheftner WA, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon FJ, Berrettini WH, Potash JB, Zandi PP, Mahon PB, McInnis MG, Zöllner S, Zhang P, Craig DW, Szelinger S, Barrett TB, Schulze TG. PMID: 23038240.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    148. Noncoding transcription within the Igh distal V(H) region at PAIR elements affects the 3D structure of the Igh locus in pro-B cells. Proc Natl Acad Sci U S A. 2012 Oct 16; 109(42):17004-9. Verma-Gaur J, Torkamani A, Schaffer L, Head SR, Schork NJ, Feeney AJ. PMID: 23027941.
      View in: PubMed   Mentions: 38     Fields:    Translation:Cells
    149. Statistical properties of multivariate distance matrix regression for high-dimensional data analysis. Front Genet. 2012; 3:190. Zapala MA, Schork NJ. PMID: 23060897.
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    150. Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses. J Am Coll Cardiol. 2012 Oct 23; 60(17):1678-89. Zhang K, Rao F, Miramontes-Gonzalez JP, Hightower CM, Vaught B, Chen Y, Greenwood TA, Schork AJ, Wang L, Mahata M, Stridsberg M, Khandrika S, Biswas N, Fung MM, Waalen J, Middelberg RP, Heath AC, Montgomery GW, Martin NG, Whitfield JB, Baker DG, Schork NJ, Nievergelt CM, O'Connor DT. PMID: 23021333.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    151. Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. Transl Psychiatry. 2012 Sep 25; 2:e165. Meier S, Mattheisen M, Vassos E, Strohmaier J, Treutlein J, Josef F, Breuer R, Degenhardt F, Mühleisen TW, Müller-Myhsok B, Steffens M, Schmael C, McMahon FJ, Nöthen MM, Cichon S, Schulze TG, Rietschel M, Kelsoe JR, Greenwood TA, Nievergelt CM, Barrett TB, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, Nurnberger J, Edenberg HJ, Foroud T, Koller DL, Gershon ES, Liu CY, Badner JA, Scheftner W, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon F, Chen DT, Schulze TG, Berrettini W, Potash JB, Zandi PP, Mahon PB, McInnis M, Craig D, Szelinger S. PMID: 23010768.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    152. Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300. BMC Genomics. 2012 Sep 25; 13:508. Tewhey R, Cannavino CR, Leake JA, Bansal V, Topol EJ, Torkamani A, Bradley JS, Schork NJ. PMID: 23009684.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    153. Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Hum Mol Genet. 2012 Dec 15; 21(24):5385-94. Mangino M, Hwang SJ, Spector TD, Hunt SC, Kimura M, Fitzpatrick AL, Christiansen L, Petersen I, Elbers CC, Harris T, Chen W, Srinivasan SR, Kark JD, Benetos A, El Shamieh S, Visvikis-Siest S, Christensen K, Berenson GS, Valdes AM, Viñuela A, Garcia M, Arnett DK, Broeckel U, Province MA, Pankow JS, Kammerer C, Liu Y, Nalls M, Tishkoff S, Thomas F, Ziv E, Psaty BM, Bis JC, Rotter JI, Taylor KD, Smith E, Schork NJ, Levy D, Aviv A. PMID: 23001564.
      View in: PubMed   Mentions: 73     Fields:    Translation:HumansCells
    154. Genotypic and phenotypic evaluation of the evolution of high-level daptomycin nonsusceptibility in vancomycin-resistant Enterococcus faecium. Antimicrob Agents Chemother. 2012 Nov; 56(11):6051-3. Humphries RM, Kelesidis T, Tewhey R, Rose WE, Schork N, Nizet V, Sakoulas G. PMID: 22948885.
      View in: PubMed   Mentions: 25     Fields:    Translation:Cells
    155. Assessing group differences in biodiversity by simultaneously testing a user-defined selection of diversity indices. Mol Ecol Resour. 2012 Nov; 12(6):1068-78. Pallmann P, Schaarschmidt F, Hothorn LA, Fischer C, Nacke H, Priesnitz KU, Schork NJ. PMID: 22934781.
      View in: PubMed   Mentions: 6     Fields:    
    156. Blood-based gene expression signatures of infants and toddlers with autism. J Am Acad Child Adolesc Psychiatry. 2012 Sep; 51(9):934-44.e2. Glatt SJ, Tsuang MT, Winn M, Chandler SD, Collins M, Lopez L, Weinfeld M, Carter C, Schork N, Pierce K, Courchesne E. PMID: 22917206.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    157. Influences of FTO gene on onset age of adult overweight. Hum Genet. 2012 Dec; 131(12):1851-9. Mei H, Chen W, Mills K, He J, Srinivasan SR, Schork N, Murray S, Berenson GS. PMID: 22842737.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    158. Whole genome sequencing analysis of Plasmodium vivax using whole genome capture. BMC Genomics. 2012 Jun 21; 13:262. Bright AT, Tewhey R, Abeles S, Chuquiyauri R, Llanos-Cuentas A, Ferreira MU, Schork NJ, Vinetz JM, Winzeler EA. PMID: 22721170.
      View in: PubMed   Mentions: 16     Fields:    Translation:AnimalsCells
    159. Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease. Mol Psychiatry. 2013 May; 18(5):568-75. Vélez JI, Chandrasekharappa SC, Henao E, Martinez AF, Harper U, Jones M, Solomon BD, Lopez L, Garcia G, Aguirre-Acevedo DC, Acosta-Baena N, Correa JC, Lopera-Gómez CM, Jaramillo-Elorza MC, Rivera D, Kosik KS, Schork NJ, Swanson JM, Lopera F, Arcos-Burgos M. PMID: 22710270.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    160. Influence of genetic polymorphisms on the effect of high- and standard-dose clopidogrel after percutaneous coronary intervention: the GIFT (Genotype Information and Functional Testing) study. J Am Coll Cardiol. 2012 May 29; 59(22):1928-37. Price MJ, Murray SS, Angiolillo DJ, Lillie E, Smith EN, Tisch RL, Schork NJ, Teirstein PS, Topol EJ. PMID: 22624833.
      View in: PubMed   Mentions: 37     Fields:    Translation:HumansCells
    161. Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. Mol Psychiatry. 2012 Sep; 17(9):887-905. Ayalew M, Le-Niculescu H, Levey DF, Jain N, Changala B, Patel SD, Winiger E, Breier A, Shekhar A, Amdur R, Koller D, Nurnberger JI, Corvin A, Geyer M, Tsuang MT, Salomon D, Schork NJ, Fanous AH, O'Donovan MC, Niculescu AB. PMID: 22584867.
      View in: PubMed   Mentions: 122     Fields:    Translation:HumansAnimals
    162. Predictors of risk and resilience for posttraumatic stress disorder among ground combat Marines: methods of the Marine Resiliency Study. Prev Chronic Dis. 2012; 9:E97. Baker DG, Nash WP, Litz BT, Geyer MA, Risbrough VB, Nievergelt CM, O'Connor DT, Larson GE, Schork NJ, Vasterling JJ, Hammer PS, Webb-Murphy JA. PMID: 22575082.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    163. Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. PLoS Genet. 2012; 8(3):e1002592. Chow ML, Pramparo T, Winn ME, Barnes CC, Li HR, Weiss L, Fan JB, Murray S, April C, Belinson H, Fu XD, Wynshaw-Boris A, Schork NJ, Courchesne E. PMID: 22457638.
      View in: PubMed   Mentions: 62     Fields:    Translation:HumansCells
    164. Characterization of circulating endothelial cells in acute myocardial infarction. Sci Transl Med. 2012 Mar 21; 4(126):126ra33. Damani S, Bacconi A, Libiger O, Chourasia AH, Serry R, Gollapudi R, Goldberg R, Rapeport K, Haaser S, Topol S, Knowlton S, Bethel K, Kuhn P, Wood M, Carragher B, Schork NJ, Jiang J, Rao C, Connelly M, Fowler VM, Topol EJ. PMID: 22440735.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    165. Cohort Profile: the international childhood cardiovascular cohort (i3C) consortium. Int J Epidemiol. 2013 Feb; 42(1):86-96. Dwyer T, Sun C, Magnussen CG, Raitakari OT, Schork NJ, Venn A, Burns TL, Juonala M, Steinberger J, Sinaiko AR, Prineas RJ, Davis PH, Woo JG, Morrison JA, Daniels SR, Chen W, Srinivasan SR, Viikari JS, Berenson GS. PMID: 22434861.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    166. Preprocessing and Quality Control Strategies for Illumina DASL Assay-Based Brain Gene Expression Studies with Semi-Degraded Samples. Front Genet. 2012; 3:11. Chow ML, Winn ME, Li HR, April C, Wynshaw-Boris A, Fan JB, Fu XD, Courchesne E, Schork NJ. PMID: 22375143.
      View in: PubMed   Mentions:
    167. Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. Proc Natl Acad Sci U S A. 2012 Mar 06; 109(10):3985-90. Bakken TE, Roddey JC, Djurovic S, Akshoomoff N, Amaral DG, Bloss CS, Casey BJ, Chang L, Ernst TM, Gruen JR, Jernigan TL, Kaufmann WE, Kenet T, Kennedy DN, Kuperman JM, Murray SS, Sowell ER, Rimol LM, Mattingsdal M, Melle I, Agartz I, Andreassen OA, Schork NJ, Dale AM, Weiner M, Aisen P, Petersen R, Jack CR, Jagust W, Trojanowki JQ, Toga AW, Beckett L, Green RC, Saykin AJ, Morris J, Liu E, Montine T, Gamst A, Thomas RG, Donohue M, Walter S, Gessert D, Sather T, Harvey D, Kornak J, Dale A, Bernstein M, Felmlee J, Fox N, Thompson P, Schuff N, Alexander G, DeCarli C, Bandy D, Koeppe RA, Foster N, Reiman EM, Chen K, Mathis C, Cairns NJ, Taylor-Reinwald L, Trojanowki JQ, Shaw L, Lee VM, Korecka M, Crawford K, Neu S, Foroud TM, Potkin S, Shen L, Kachaturian Z, Frank R, Snyder PJ, Molchan S, Kaye J, Quinn J, Lind B, Dolen S, Schneider LS, Pawluczyk S, Spann BM, Brewer J, Vanderswag H, Heidebrink JL, Lord JL, Johnson K, Doody RS, Villanueva-Meyer J, Chowdhury M, Stern Y, Honig LS, Bell KL, Morris JC, Ances B, Carroll M, Leon S, Mintun MA, Schneider S, Marson D, Griffith R, Clark D, Grossman H, Mitsis E, Romirowsky A, deToledo-Morrell L, Shah RC, Duara R, Varon D, Roberts P, Albert M, Onyike C, Kielb S, Rusinek H, de Leon MJ, Glodzik L, De Santi S, Doraiswamy PM, Petrella JR, Coleman RE, Arnold SE, Karlawish JH, Wolk D, Smith CD, Jicha G, Hardy P, Lopez OL, Oakley M, Simpson DM, Porsteinsson AP, Goldstein BS, Martin K, Makino KM, Ismail MS, Brand C, Mulnard RA, Thai G, Mc-Adams-Ortiz C, Womack K, Mathews D, Quiceno M, Diaz-Arrastia R, King R, Weiner M, Martin-Cook K, DeVous M, Levey AI, Lah JJ, Cellar JS, Burns JM, Anderson HS, Swerdlow RH, Apostolova L, Lu PH, Bartzokis G, Silverman DH, Graff-Radford NR, Parfitt F, Johnson H, Farlow MR, Hake AM, Matthews BR, Herring S, van Dyck CH, Carson RE, MacAvoy MG, Chertkow H, Bergman H, Hosein C, Black S, Stefanovic B, Caldwell C, Hsiung R, Feldman H, Mudge B, Assaly M, Kertesz A, Rogers J, Trost D, Bernick C, Munic D, Kerwin D, Mesulam MM, Lipowski K, Wu CK, Johnson N, Sadowsky C, Martinez W, Villena T, Turner RS, Johnson K, Reynolds B, Sperling RA, Johnson KA, Marshall G, Frey M, Yesavage J, Taylor JL, Lane B, Rosen A, Tinklenberg J, Sabbagh M, Belden C, Jacobson S, Kowall N, Killiany R, Budson AE, Norbash A, Johnson PL, Obisesan TO, Wolday S, Bwayo SK, Lerner A, Hudson L, Ogrocki P, Fletcher E, Carmichael O, Olichney J, Kittur S, Borrie M, Lee TY, Bartha R, Johnson S, Asthana S, Carlsson CM, Potkin SG, Preda A, Nguyen D, Tariot P, Fleisher A, Reeder S, Bates V, Capote H, Rainka M, Scharre DW, Kataki M, Zimmerman EA, Celmins D, Brown AD, Pearlson GD, Blank K, Anderson K, Santulli RB, Schwartz ES, Sink KM, Williamson JD, Garg P, Watkins F, Ott BR, Querfurth H, Tremont G, Salloway S, Malloy P, Correia S, Rosen HJ, Miller BL, Mintzer J, Longmire CF, Spicer K, Finger E, Rachinsky I, Drost D, Jernigan T, McCabe C, Grant E, Ernst T, Kuperman J, Chung Y, Murray S, Bloss C, Darst B, Pritchett L, Saito A, Amaral D, DiNino M, Eyngorina B, Sowell E, Houston S, Soderberg L, Kaufmann W, van Zijl P, Rizzo-Busack H, Javid M, Mehta N, Ruberry E, Powers A, Rosen B, Gebhard N, Manigan H, Frazier J, Kennedy D, Yakutis L, Hill M, Gruen J, Bosson-Heenan J, Carlson H. PMID: 22343285.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimals
    168. Longitudinal replication studies of GWAS risk SNPs influencing body mass index over the course of childhood and adulthood. PLoS One. 2012; 7(2):e31470. Mei H, Chen W, Jiang F, He J, Srinivasan S, Smith EN, Schork N, Murray S, Berenson GS. PMID: 22355368.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    169. Skewed primary Ig? repertoire and V-J joining in C57BL/6 mice: implications for recombination accessibility and receptor editing. J Immunol. 2012 Mar 01; 188(5):2305-15. Aoki-Ota M, Torkamani A, Ota T, Schork N, Nemazee D. PMID: 22287713.
      View in: PubMed   Mentions: 28     Fields:    Translation:AnimalsCells
    170. Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--a meta-analysis of three independent studies. PLoS One. 2012; 7(1):e28931. Hernesniemi JA, Seppälä I, Lyytikäinen LP, Mononen N, Oksala N, Hutri-Kähönen N, Juonala M, Taittonen L, Smith EN, Schork NJ, Chen W, Srinivasan SR, Berenson GS, Murray SS, Laitinen T, Jula A, Kettunen J, Ripatti S, Laaksonen R, Viikari J, Kähönen M, Raitakari OT, Lehtimäki T. PMID: 22295058.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    171. Whole genome sequences of a male and female supercentenarian, ages greater than 114?years. Front Genet. 2011; 2:90. Sebastiani P, Riva A, Montano M, Pham P, Torkamani A, Scherba E, Benson G, Milton JN, Baldwin CT, Andersen S, Schork NJ, Steinberg MH, Perls TT. PMID: 22303384.
      View in: PubMed   Mentions:
    172. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Mol Psychiatry. 2013 Mar; 18(3):340-6. Gamazon ER, Badner JA, Cheng L, Zhang C, Zhang D, Cox NJ, Gershon ES, Kelsoe JR, Greenwood TA, Nievergelt CM, Chen C, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, Nurnberger JI, Edenberg HJ, Foroud T, Koller DL, Scheftner WA, Coryell W, Rice J, Lawson WB, Nwulia EA, Hipolito M, Byerley W, McMahon FJ, Schulze TG, Berrettini WH, Potash JB, Zandi PP, Mahon PB, McInnis MG, Zöllner S, Zhang P, Craig DW, Szelinger S, Barrett TB, Liu C. PMID: 22212596.
      View in: PubMed   Mentions: 81     Fields:    Translation:HumansCells
    173. Strategies and methods to study sex differences in cardiovascular structure and function: a guide for basic scientists. Biol Sex Differ. 2011 Dec 12; 2:14. Miller VM, Kaplan JR, Schork NJ, Ouyang P, Berga SL, Wenger NK, Shaw LJ, Webb RC, Mallampalli M, Steiner M, Taylor DA, Merz CN, Reckelhoff JF. PMID: 22152231.
      View in: PubMed   Mentions: 13     Fields:    
    174. An assessment of the individual and collective effects of variants on height using twins and a developmentally informative study design. PLoS Genet. 2011 Dec; 7(12):e1002413. Vrieze SI, McGue M, Miller MB, Legrand LN, Schork NJ, Iacono WG. PMID: 22174699.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    175. Environmental and genetic contributions to indicators of oral malodor in twins. Twin Res Hum Genet. 2011 Dec; 14(6):568-72. Bretz WA, Biesbrock A, Corby PM, Corby AL, Bretz WG, Wessel J, Schork NJ. PMID: 22506313.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    176. Association of direct-to-consumer genome-wide disease risk estimates and self-reported disease. Genet Epidemiol. 2012 Jan; 36(1):66-70. Bloss CS, Topol EJ, Schork NJ. PMID: 22127769.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    177. Genomic information as a behavioral health intervention: can it work? Per Med. 2011 Nov; 8(6):659-667. Bloss CS, Madlensky L, Schork NJ, Topol EJ. PMID: 22199991.
      View in: PubMed   Mentions: 13     Fields:    
    178. Genetic variants and blood pressure in a population-based cohort: the Cardiovascular Risk in Young Finns study. Hypertension. 2011 Dec; 58(6):1079-85. Oikonen M, Tikkanen E, Juhola J, Tuovinen T, Seppälä I, Juonala M, Taittonen L, Mikkilä V, Kähönen M, Ripatti S, Viikari J, Lehtimäki T, Havulinna AS, Kee F, Newton-Cheh C, Peltonen L, Schork NJ, Murray SS, Berenson GS, Chen W, Srinivasan SR, Salomaa V, Raitakari OT. PMID: 22025373.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    179. Transgenerational epigenetic instability is a source of novel methylation variants. Science. 2011 Oct 21; 334(6054):369-73. Schmitz RJ, Schultz MD, Lewsey MG, O'Malley RC, Urich MA, Libiger O, Schork NJ, Ecker JR. PMID: 21921155.
      View in: PubMed   Mentions: 196     Fields:    Translation:AnimalsCells
    180. Genome-wide expression assay comparison across frozen and fixed postmortem brain tissue samples. BMC Genomics. 2011 Sep 10; 12:449. Chow ML, Li HR, Winn ME, April C, Barnes CC, Wynshaw-Boris A, Fan JB, Fu XD, Courchesne E, Schork NJ. PMID: 21906392.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    181. A geographic cline of skull and brain morphology among individuals of European Ancestry. Hum Hered. 2011; 72(1):35-44. Bakken TE, Dale AM, Schork NJ. PMID: 21849792.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    182. Gene expression profiling of human whole blood samples with the Illumina WG-DASL assay. BMC Genomics. 2011 Aug 15; 12:412. Winn ME, Shaw M, April C, Klotzle B, Fan JB, Murray SS, Schork NJ. PMID: 21843359.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    183. Direct-to-consumer personalized genomic testing. Hum Mol Genet. 2011 Oct 15; 20(R2):R132-41. Bloss CS, Darst BF, Topol EJ, Schork NJ. PMID: 21828075.
      View in: PubMed   Mentions: 36     Fields:    Translation:Humans
    184. Background gene expression networks significantly enhance drug response prediction by transcriptional profiling. Pharmacogenomics J. 2012 Oct; 12(5):446-52. Torkamani A, Schork NJ. PMID: 21826086.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    185. Annotating individual human genomes. Genomics. 2011 Oct; 98(4):233-41. Torkamani A, Scott-Van Zeeland AA, Topol EJ, Schork NJ. PMID: 21839162.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    186. Dental caries pathogenicity: a genomic and metagenomic perspective. Int Dent J. 2011 Aug; 61 Suppl 1:11-22. Peterson SN, Snesrud E, Schork NJ, Bretz WA. PMID: 21726221.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansAnimalsCells
    187. Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia. Arch Gen Psychiatry. 2011 Aug; 68(8):781-90. Bakken TE, Bloss CS, Roddey JC, Joyner AH, Rimol LM, Djurovic S, Melle I, Sundet K, Agartz I, Andreassen OA, Dale AM, Schork NJ. PMID: 21810643.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    188. Association of candidate genes with phenotypic traits relevant to anorexia nervosa. Eur Eat Disord Rev. 2011 Nov-Dec; 19(6):487-93. Root TL, Szatkiewicz JP, Jonassaint CR, Thornton LM, Pinheiro AP, Strober M, Bloss C, Berrettini W, Schork NJ, Kaye WH, Bergen AW, Magistretti P, Brandt H, Crawford S, Crow S, Fichter MM, Goldman D, Halmi KA, Johnson C, Kaplan AS, Keel PK, Klump KL, La Via M, Mitchell JE, Rotondo A, Treasure J, Woodside DB, Bulik CM. PMID: 21780254.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    189. Genetic association of recovery from eating disorders: the role of GABA receptor SNPs. Neuropsychopharmacology. 2011 Oct; 36(11):2222-32. Bloss CS, Berrettini W, Bergen AW, Magistretti P, Duvvuri V, Strober M, Brandt H, Crawford S, Crow S, Fichter MM, Halmi KA, Johnson C, Kaplan AS, Keel P, Klump KL, Mitchell J, Treasure J, Woodside DB, Marzola E, Schork NJ, Kaye WH. PMID: 21750581.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    190. Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. PLoS Genet. 2011 Jun; 7(6):e1002134. Smith EN, Koller DL, Panganiban C, Szelinger S, Zhang P, Badner JA, Barrett TB, Berrettini WH, Bloss CS, Byerley W, Coryell W, Edenberg HJ, Foroud T, Gershon ES, Greenwood TA, Guo Y, Hipolito M, Keating BJ, Lawson WB, Liu C, Mahon PB, McInnis MG, McMahon FJ, McKinney R, Murray SS, Nievergelt CM, Nurnberger JI, Nwulia EA, Potash JB, Rice J, Schulze TG, Scheftner WA, Shilling PD, Zandi PP, Zöllner S, Craig DW, Schork NJ, Kelsoe JR. PMID: 21738484.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    191. Identification of polymorphisms associated with hypertriglyceridemia and prolonged survival induced by bexarotene in treating non-small cell lung cancer. Anticancer Res. 2011 Jun; 31(6):2303-11. Luo W, Schork NJ, Marschke KB, Ng SC, Hermann TW, Zhang J, Sanders JM, Tooker P, Malo N, Zapala MA, Dziewanowska ZE, Negro-Vilar A, Meglasson MD. PMID: 21737656.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    192. Methylenetetrahydrofolate reductase (MTHFR) polymorphism A1298C (Glu429Ala) predicts decline in renal function over time in the African-American Study of Kidney Disease and Hypertension (AASK) Trial and Veterans Affairs Hypertension Cohort (VAHC). Nephrol Dial Transplant. 2012 Jan; 27(1):197-205. Fung MM, Salem RM, Lipkowitz MS, Bhatnagar V, Pandey B, Schork NJ, O'Connor DT. PMID: 21613384.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    193. Convergent functional genomics of anxiety disorders: translational identification of genes, biomarkers, pathways and mechanisms. Transl Psychiatry. 2011 May 24; 1:e9. Le-Niculescu H, Balaraman Y, Patel SD, Ayalew M, Gupta J, Kuczenski R, Shekhar A, Schork N, Geyer MA, Niculescu AB. PMID: 22832404.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansAnimalsCells
    194. CCCTC-binding factor (CTCF) and cohesin influence the genomic architecture of the Igh locus and antisense transcription in pro-B cells. Proc Natl Acad Sci U S A. 2011 Jun 07; 108(23):9566-71. Degner SC, Verma-Gaur J, Wong TP, Bossen C, Iverson GM, Torkamani A, Vettermann C, Lin YC, Ju Z, Schulz D, Murre CS, Birshtein BK, Schork NJ, Schlissel MS, Riblet R, Murre C, Feeney AJ. PMID: 21606361.
      View in: PubMed   Mentions: 99     Fields:    Translation:AnimalsCells
    195. Analysis of 94 candidate genes and 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. Am J Psychiatry. 2011 Sep; 168(9):930-46. Greenwood TA, Lazzeroni LC, Murray SS, Cadenhead KS, Calkins ME, Dobie DJ, Green MF, Gur RE, Gur RC, Hardiman G, Kelsoe JR, Leonard S, Light GA, Nuechterlein KH, Olincy A, Radant AD, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Freedman R, Braff DL. PMID: 21498463.
      View in: PubMed   Mentions: 108     Fields:    Translation:Humans
    196. Efficient and cost effective population resequencing by pooling and in-solution hybridization. PLoS One. 2011 Mar 30; 6(3):e18353. Bansal V, Tewhey R, Leproust EM, Schork NJ. PMID: 21479135.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    197. Ectopic B-cell clusters that infiltrate transplanted human kidneys are clonal. Proc Natl Acad Sci U S A. 2011 Apr 05; 108(14):5560-5. Cheng J, Torkamani A, Grover RK, Jones TM, Ruiz DI, Schork NJ, Quigley MM, Hall FW, Salomon DR, Lerner RA. PMID: 21415369.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
    198. Standard- vs high-dose clopidogrel based on platelet function testing after percutaneous coronary intervention: the GRAVITAS randomized trial. JAMA. 2011 Mar 16; 305(11):1097-105. Price MJ, Berger PB, Teirstein PS, Tanguay JF, Angiolillo DJ, Spriggs D, Puri S, Robbins M, Garratt KN, Bertrand OF, Stillabower ME, Stillablower ME, Aragon JR, Kandzari DE, Stinis CT, Lee MS, Manoukian SV, Cannon CP, Schork NJ, Topol EJ. PMID: 21406646.
      View in: PubMed   Mentions: 212     Fields:    Translation:Humans
    199. Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects. PLoS Genet. 2011 Mar; 7(3):e1001331. Pramparo T, Libiger O, Jain S, Li H, Youn YH, Hirotsune S, Schork NJ, Wynshaw-Boris A. PMID: 21423666.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimalsCells
    200. The n-of-1 clinical trial: the ultimate strategy for individualizing medicine? Per Med. 2011 Mar; 8(2):161-173. Lillie EO, Patay B, Diamant J, Issell B, Topol EJ, Schork NJ. PMID: 21695041.
      View in: PubMed   Mentions: 103     Fields:    
    201. Grand challenges in statistical genetics/genomics methodology. Front Genet. 2011; 2:5. Tiwari HK, Schork NJ. PMID: 22303304.
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    202. The importance of phase information for human genomics. Nat Rev Genet. 2011 03; 12(3):215-23. Tewhey R, Bansal V, Torkamani A, Topol EJ, Schork NJ. PMID: 21301473.
      View in: PubMed   Mentions: 70     Fields:    Translation:Humans
    203. Group and site differences on the California Verbal Learning Test in persons with schizophrenia and their first-degree relatives: findings from the Consortium on the Genetics of Schizophrenia (COGS). Schizophr Res. 2011 May; 128(1-3):102-10. Stone WS, Giuliano AJ, Tsuang MT, Braff DL, Cadenhead KS, Calkins ME, Dobie DJ, Faraone SV, Freedman R, Green MF, Greenwood TA, Gur RE, Gur RC, Light GA, Mintz J, Nuechterlein KH, Olincy A, Radant AD, Roe AH, Schork NJ, Siever LJ, Silverman JM, Swerdlow NR, Thomas AR, Tsuang DW, Turetsky BI, Seidman LJ. PMID: 21288694.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    204. Digital medicine and the Scripps Translational Science Institute. Clin Transl Sci. 2011 Feb; 4(1):8-9. Topol EJ, Schork NJ, Smith JM. PMID: 21348949.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    205. Effect of direct-to-consumer genomewide profiling to assess disease risk. N Engl J Med. 2011 Feb 10; 364(6):524-34. Bloss CS, Schork NJ, Topol EJ. PMID: 21226570.
      View in: PubMed   Mentions: 196     Fields:    Translation:Humans
    206. An application and empirical comparison of statistical analysis methods for associating rare variants to a complex phenotype. Pac Symp Biocomput. 2011; 76-87. Bansal V, Libiger O, Torkamani A, Schork NJ. PMID: 21121035.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    207. Catapulting clopidogrel pharmacogenomics forward. Nat Med. 2011 Jan; 17(1):40-1. Topol EJ, Schork NJ. PMID: 21217678.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    208. The next phase in human genetics. Nat Biotechnol. 2011 Jan; 29(1):38-9. Bansal V, Tewhey R, Topol EJ, Schork NJ. PMID: 21221098.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    209. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. Am J Hum Genet. 2011 Jan 07; 88(1):6-18. Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, Pankratz N, Pankow JS, Shah S, Taylor K, Barnard J, Peters BJ, Maloney CM, Lobmeyer MT, Stanton A, Zafarmand MH, Romaine SP, Mehta A, van Iperen EP, Gong Y, Price TS, Smith EN, Kim CE, Li YR, Asselbergs FW, Atwood LD, Bailey KM, Bhatt D, Bauer F, Behr ER, Bhangale T, Boer JM, Boehm BO, Bradfield JP, Brown M, Braund PS, Burton PR, Carty C, Chandrupatla HR, Chen W, Connell J, Dalgeorgou C, Boer Ad, Drenos F, Elbers CC, Fang JC, Fox CS, Frackelton EC, Fuchs B, Furlong CE, Gibson Q, Gieger C, Goel A, Grobbee DE, Hastie C, Howard PJ, Huang GH, Johnson WC, Li Q, Kleber ME, Klein BE, Klein R, Kooperberg C, Ky B, Lacroix A, Lanken P, Lathrop M, Li M, Marshall V, Melander O, Mentch FD, Meyer NJ, Monda KL, Montpetit A, Murugesan G, Nakayama K, Nondahl D, Onipinla A, Rafelt S, Newhouse SJ, Otieno FG, Patel SR, Putt ME, Rodriguez S, Safa RN, Sawyer DB, Schreiner PJ, Simpson C, Sivapalaratnam S, Srinivasan SR, Suver C, Swergold G, Sweitzer NK, Thomas KA, Thorand B, Timpson NJ, Tischfield S, Tobin M, Tomaszewski M, Tomaszweski M, Verschuren WM, Wallace C, Winkelmann B, Zhang H, Zheng D, Zhang L, Zmuda JM, Clarke R, Balmforth AJ, Danesh J, Day IN, Schork NJ, de Bakker PI, Delles C, Duggan D, Hingorani AD, Hirschhorn JN, Hofker MH, Humphries SE, Kivimaki M, Lawlor DA, Kottke-Marchant K, Mega JL, Mitchell BD, Morrow DA, Palmen J, Redline S, Shields DC, Shuldiner AR, Sleiman PM, Smith GD, Farrall M, Jamshidi Y, Christiani DC, Casas JP, Hall AS, Doevendans PA, Christie JD, Berenson GS, Murray SS, Illig T, Dorn GW, Cappola TP, Boerwinkle E, Sever P, Rader DJ, Reilly MP, Caulfield M, Talmud PJ, Topol E, Engert JC, Wang K, Dominiczak A, Hamsten A, Curtis SP, Silverstein RL, Lange LA, Sabatine MS, Trip M, Saleheen D, Peden JF, Cruickshanks KJ, März W, O'Connell JR, Klungel OH, Wijmenga C, Maitland-van der Zee AH, Schadt EE, Johnson JA, Jarvik GP, Papanicolaou GJ, Grant SF, Munroe PB, North KE, Samani NJ, Koenig W, Gaunt TR, Anand SS, van der Schouw YT, Soranzo N, Fitzgerald GA, Reiner A, Hegele RA, Hakonarson H, Keating BJ. PMID: 21194676.
      View in: PubMed   Mentions: 52     Fields:    Translation:Humans
    210. Genomics for disease treatment and prevention. Psychiatr Clin North Am. 2011 Mar; 34(1):147-66. Bloss CS, Jeste DV, Schork NJ. PMID: 21333845.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansPHPublic Health
    211. The VA Hypertension Primary Care Longitudinal Cohort: Electronic medical records in the post-genomic era. Health Informatics J. 2010 Dec; 16(4):274-86. Salem RM, Pandey B, Richard E, Fung MM, Garcia EP, Brophy VH, Schork NJ, O'Connor DT, Bhatnagar V. PMID: 21216807.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    212. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet. 2010 Dec; 42(12):1077-85. Elks CE, Perry JR, Sulem P, Chasman DI, Franceschini N, He C, Lunetta KL, Visser JA, Byrne EM, Cousminer DL, Gudbjartsson DF, Esko T, Feenstra B, Hottenga JJ, Koller DL, Kutalik Z, Lin P, Mangino M, Marongiu M, McArdle PF, Smith AV, Stolk L, van Wingerden SH, Zhao JH, Albrecht E, Corre T, Ingelsson E, Hayward C, Magnusson PK, Smith EN, Ulivi S, Warrington NM, Zgaga L, Alavere H, Amin N, Aspelund T, Bandinelli S, Barroso I, Berenson GS, Bergmann S, Blackburn H, Boerwinkle E, Buring JE, Busonero F, Campbell H, Chanock SJ, Chen W, Cornelis MC, Couper D, Coviello AD, d'Adamo P, de Faire U, de Geus EJ, Deloukas P, Döring A, Smith GD, Easton DF, Eiriksdottir G, Emilsson V, Eriksson J, Ferrucci L, Folsom AR, Foroud T, Garcia M, Gasparini P, Geller F, Gieger C, Gudnason V, Hall P, Hankinson SE, Ferreli L, Heath AC, Hernandez DG, Hofman A, Hu FB, Illig T, Järvelin MR, Johnson AD, Karasik D, Khaw KT, Kiel DP, Kilpeläinen TO, Kolcic I, Kraft P, Launer LJ, Laven JS, Li S, Liu J, Levy D, Martin NG, McArdle WL, Melbye M, Mooser V, Murray JC, Murray SS, Nalls MA, Navarro P, Nelis M, Ness AR, Northstone K, Oostra BA, Peacock M, Palmer LJ, Palotie A, Paré G, Parker AN, Pedersen NL, Peltonen L, Pennell CE, Pharoah P, Polasek O, Plump AS, Pouta A, Porcu E, Rafnar T, Rice JP, Ring SM, Rivadeneira F, Rudan I, Sala C, Salomaa V, Sanna S, Schlessinger D, Schork NJ, Scuteri A, Segrè AV, Shuldiner AR, Soranzo N, Sovio U, Srinivasan SR, Strachan DP, Tammesoo ML, Tikkanen E, Toniolo D, Tsui K, Tryggvadottir L, Tyrer J, Uda M, van Dam RM, van Meurs JB, Vollenweider P, Waeber G, Wareham NJ, Waterworth DM, Weedon MN, Wichmann HE, Willemsen G, Wilson JF, Wright AF, Young L, Zhai G, Zhuang WV, Bierut LJ, Boomsma DI, Boyd HA, Crisponi L, Demerath EW, van Duijn CM, Econs MJ, Harris TB, Hunter DJ, Loos RJ, Metspalu A, Montgomery GW, Ridker PM, Spector TD, Streeten EA, Stefansson K, Thorsteinsdottir U, Uitterlinden AG, Widen E, Murabito JM, Ong KK, Murray A. PMID: 21102462.
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    213. Altered DNA methylation in leukocytes with trisomy 21. PLoS Genet. 2010 Nov 18; 6(11):e1001212. Kerkel K, Schupf N, Hatta K, Pang D, Salas M, Kratz A, Minden M, Murty V, Zigman WB, Mayeux RP, Jenkins EC, Torkamani A, Schork NJ, Silverman W, Croy BA, Tycko B. PMID: 21124956.
      View in: PubMed   Mentions: 37     Fields:    Translation:HumansCells
    214. A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. Mol Psychiatry. 2011 Sep; 16(9):949-59. Wang K, Zhang H, Bloss CS, Duvvuri V, Kaye W, Schork NJ, Berrettini W, Hakonarson H. PMID: 21079607.
      View in: PubMed   Mentions: 64     Fields:    Translation:Humans
    215. In silico QTL mapping of basal liver iron levels in inbred mouse strains. Physiol Genomics. 2011 Feb 11; 43(3):136-47. McLachlan S, Lee SM, Steele TM, Hawthorne PL, Zapala MA, Eskin E, Schork NJ, Anderson GJ, Vulpe CD. PMID: 21062905.
      View in: PubMed   Mentions: 10     Fields:    Translation:Animals
    216. A covering method for detecting genetic associations between rare variants and common phenotypes. PLoS Comput Biol. 2010 Oct 14; 6(10):e1000954. Bhatia G, Bansal V, Harismendy O, Schork NJ, Topol EJ, Frazer K, Bafna V. PMID: 20976246.
      View in: PubMed   Mentions: 47     Fields:    
    217. Statistical analysis strategies for association studies involving rare variants. Nat Rev Genet. 2010 Nov; 11(11):773-85. Bansal V, Libiger O, Torkamani A, Schork NJ. PMID: 20940738.
      View in: PubMed   Mentions: 221     Fields:    Translation:Humans
    218. Multicenter validation of the diagnostic accuracy of a blood-based gene expression test for assessing obstructive coronary artery disease in nondiabetic patients. Ann Intern Med. 2010 Oct 05; 153(7):425-34. Rosenberg S, Elashoff MR, Beineke P, Daniels SE, Wingrove JA, Tingley WG, Sager PT, Sehnert AJ, Yau M, Kraus WE, Newby LK, Schwartz RS, Voros S, Ellis SG, Tahirkheli N, Waksman R, McPherson J, Lansky A, Winn ME, Schork NJ, Topol EJ. PMID: 20921541.
      View in: PubMed   Mentions: 61     Fields:    Translation:HumansCTClinical Trials
    219. 5-HT1A receptor binding is increased after recovery from bulimia nervosa compared to control women and is associated with behavioral inhibition in both groups. Int J Eat Disord. 2011 Sep; 44(6):477-87. Bailer UF, Bloss CS, Frank GK, Price JC, Meltzer CC, Mathis CA, Geyer MA, Wagner A, Becker CR, Schork NJ, Kaye WH. PMID: 20872754.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    220. Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. PLoS Genet. 2010 Sep 09; 6(9):e1001094. Smith EN, Chen W, Kähönen M, Kettunen J, Lehtimäki T, Peltonen L, Raitakari OT, Salem RM, Schork NJ, Shaw M, Srinivasan SR, Topol EJ, Viikari JS, Berenson GS, Murray SS. PMID: 20838585.
      View in: PubMed   Mentions: 61     Fields:    Translation:Humans
    221. FTO influences on longitudinal BMI over childhood and adulthood and modulation on relationship between birth weight and longitudinal BMI. Hum Genet. 2010 Dec; 128(6):589-96. Mei H, Chen W, Srinivasan SR, Jiang F, Schork N, Murray S, Smith E, So JD, Berenson GS. PMID: 20811910.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    222. Consumer perceptions of direct-to-consumer personalized genomic risk assessments. Genet Med. 2010 Sep; 12(9):556-66. Bloss CS, Ornowski L, Silver E, Cargill M, Vanier V, Schork NJ, Topol EJ. PMID: 20717041.
      View in: PubMed   Mentions: 57     Fields:    Translation:Humans
    223. Contemporary human genetic strategies in aging research. Ageing Res Rev. 2011 Apr; 10(2):191-200. Bloss CS, Pawlikowska L, Schork NJ. PMID: 20709627.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    224. Association study of 182 candidate genes in anorexia nervosa. Am J Med Genet B Neuropsychiatr Genet. 2010 Jul; 153B(5):1070-80. Pinheiro AP, Bulik CM, Thornton LM, Sullivan PF, Root TL, Bloss CS, Berrettini WH, Schork NJ, Kaye WH, Bergen AW, Magistretti P, Brandt H, Crawford S, Crow S, Fichter MM, Goldman D, Halmi KA, Johnson C, Kaplan AS, Keel PK, Klump KL, La Via M, Mitchell JE, Strober M, Rotondo A, Treasure J, Woodside DB. PMID: 20468064.
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    225. Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort. Neurobiol Aging. 2010 Aug; 31(8):1355-63. Lakatos A, Derbeneva O, Younes D, Keator D, Bakken T, Lvova M, Brandon M, Guffanti G, Reglodi D, Saykin A, Weiner M, Macciardi F, Schork N, Wallace DC, Potkin SG. PMID: 20538375.
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    226. Mindscape: a convergent perspective on life, mind, consciousness and happiness. J Affect Disord. 2010 Jun; 123(1-3):1-8. Niculescu AB, Schork NJ, Salomon DR. PMID: 19595463.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansAnimals
    227. Progression of chronic kidney disease: Adrenergic genetic influence on glomerular filtration rate decline in hypertensive nephrosclerosis. Am J Nephrol. 2010; 32(1):23-30. Chen Y, Lipkowitz MS, Salem RM, Fung MM, Bhatnagar V, Mahata M, Nievergelt CM, Rao F, Mahata SK, Schork NJ, Hicks PJ, Bowden DW, Freedman BI, Brophy VH, O'Connor DT. PMID: 20484896.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    228. The effects of globin on microarray-based gene expression analysis of mouse blood. Mamm Genome. 2010 Jun; 21(5-6):268-75. Winn ME, Zapala MA, Hovatta I, Risbrough VB, Lillie E, Schork NJ. PMID: 20473674.
      View in: PubMed   Mentions: 4     Fields:    Translation:Animals
    229. Human behavioral informatics in genetic studies of neuropsychiatric disease: multivariate profile-based analysis. Brain Res Bull. 2010 Sep 30; 83(3-4):177-88. Bloss CS, Schiabor KM, Schork NJ. PMID: 20433907.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    230. Curve-based multivariate distance matrix regression analysis: application to genetic association analyses involving repeated measures. Physiol Genomics. 2010 Jul 07; 42(2):236-47. Salem RM, O'Connor DT, Schork NJ. PMID: 20423962.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    231. Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. Proc Natl Acad Sci U S A. 2010 May 18; 107(20):9293-8. Levy D, Neuhausen SL, Hunt SC, Kimura M, Hwang SJ, Chen W, Bis JC, Fitzpatrick AL, Smith E, Johnson AD, Gardner JP, Srinivasan SR, Schork N, Rotter JI, Herbig U, Psaty BM, Sastrasinh M, Murray SS, Vasan RS, Province MA, Glazer NL, Lu X, Cao X, Kronmal R, Mangino M, Soranzo N, Spector TD, Berenson GS, Aviv A. PMID: 20421499.
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    232. Inhibition of the P50 cerebral evoked response to repeated auditory stimuli: results from the Consortium on Genetics of Schizophrenia. Schizophr Res. 2010 Jun; 119(1-3):175-82. Olincy A, Braff DL, Adler LE, Cadenhead KS, Calkins ME, Dobie DJ, Green MF, Greenwood TA, Gur RE, Gur RC, Light GA, Mintz J, Nuechterlein KH, Radant AD, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Wagner BD, Freedman R. PMID: 20382002.
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    233. Genetic regulation of catecholamine synthesis, storage and secretion in the spontaneously hypertensive rat. Hum Mol Genet. 2010 Jul 01; 19(13):2567-80. Jirout ML, Friese RS, Mahapatra NR, Mahata M, Taupenot L, Mahata SK, Kren V, Zídek V, Fischer J, Maatz H, Ziegler MG, Pravenec M, Hubner N, Aitman TJ, Schork NJ, O'Connor DT. PMID: 20378607.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
    234. Antisaccade performance in schizophrenia patients, their first-degree biological relatives, and community comparison subjects: data from the COGS study. Psychophysiology. 2010 Sep; 47(5):846-56. Radant AD, Dobie DJ, Calkins ME, Olincy A, Braff DL, Cadenhead KS, Freedman R, Green MF, Greenwood TA, Gur RE, Gur RC, Light GA, Meichle SP, Millard SP, Mintz J, Nuechterlein KH, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang MT, Turetsky BI, Tsuang DW. PMID: 20374545.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    235. Extremes of unexplained variation as a phenotype: an efficient approach for genome-wide association studies of cardiovascular disease. Circ Cardiovasc Genet. 2010 Apr; 3(2):215-21. Lanktree MB, Hegele RA, Schork NJ, Spence JD. PMID: 20407100.
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    236. Longitudinal magnetic resonance imaging study of cortical development through early childhood in autism. J Neurosci. 2010 Mar 24; 30(12):4419-27. Schumann CM, Bloss CS, Barnes CC, Wideman GM, Carper RA, Akshoomoff N, Pierce K, Hagler D, Schork N, Lord C, Courchesne E. PMID: 20335478.
      View in: PubMed   Mentions: 173     Fields:    Translation:Humans
    237. Coexpression network analysis of neural tissue reveals perturbations in developmental processes in schizophrenia. Genome Res. 2010 Apr; 20(4):403-12. Torkamani A, Dean B, Schork NJ, Thomas EA. PMID: 20197298.
      View in: PubMed   Mentions: 59     Fields:    Translation:Humans
    238. Genotype-based risk and pharmacogenetic sampling in clinical trials. J Biopharm Stat. 2010 Mar; 20(2):315-33. Schork NJ, Topol EJ. PMID: 20309761.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    239. Accurate detection and genotyping of SNPs utilizing population sequencing data. Genome Res. 2010 Apr; 20(4):537-45. Bansal V, Harismendy O, Tewhey R, Murray SS, Schork NJ, Topol EJ, Frazer KA. PMID: 20150320.
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    240. Suggestive evidence for linkage of ADHD features in bipolar disorder to chromosome 10p14. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 05; 153B(1):260-8. Joo EJ, Greenwood TA, Schork N, McKinney RA, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Kelsoe JR. PMID: 19603423.
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    241. Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure. J Hypertens. 2010 Jan; 28(1):76-86. Chen Y, Wen G, Rao F, Zhang K, Wang L, Rodriguez-Flores JL, Sanchez AP, Mahata M, Taupenot L, Sun P, Mahata SK, Tayo B, Schork NJ, Ziegler MG, Hamilton BA, O'Connor DT. PMID: 20009769.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    242. Kinase mutations in human disease: interpreting genotype-phenotype relationships. Nat Rev Genet. 2010 Jan; 11(1):60-74. Lahiry P, Torkamani A, Schork NJ, Hegele RA. PMID: 20019687.
      View in: PubMed   Mentions: 89     Fields:    Translation:HumansAnimals
    243. Sex-dependent association of common variants of microcephaly genes with brain structure. Proc Natl Acad Sci U S A. 2010 Jan 05; 107(1):384-8. Rimol LM, Agartz I, Djurovic S, Brown AA, Roddey JC, Kähler AK, Mattingsdal M, Athanasiu L, Joyner AH, Schork NJ, Halgren E, Sundet K, Melle I, Dale AM, Andreassen OA. PMID: 20080800.
      View in: PubMed   Mentions: 53     Fields:    Translation:HumansAnimals
    244. Identification of blood biomarkers for psychosis using convergent functional genomics. Mol Psychiatry. 2011 Jan; 16(1):37-58. Kurian SM, Le-Niculescu H, Patel SD, Bertram D, Davis J, Dike C, Yehyawi N, Lysaker P, Dustin J, Caligiuri M, Lohr J, Lahiri DK, Nurnberger JI, Faraone SV, Geyer MA, Tsuang MT, Schork NJ, Salomon DR, Niculescu AB. PMID: 19935739.
      View in: PubMed   Mentions: 61     Fields:    Translation:Humans
    245. Not so lost in the genetic crowd. Nat Genet. 2009 Nov; 41(11):1163-4. Schork NJ, Bansal V. PMID: 19862007.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    246. Sequence and structure signatures of cancer mutation hotspots in protein kinases. PLoS One. 2009 Oct 16; 4(10):e7485. Dixit A, Yi L, Gowthaman R, Torkamani A, Schork NJ, Verkhivker GM. PMID: 19834613.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    247. Adrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis. Nephrol Dial Transplant. 2009 Dec; 24(12):3677-86. Fung MM, Chen Y, Lipkowitz MS, Salem RM, Bhatnagar V, Mahata M, Nievergelt CM, Rao F, Mahata SK, Schork NJ, Brophy VH, O'Connor DT. PMID: 19745105.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    248. A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations. Proc Natl Acad Sci U S A. 2009 Sep 08; 106(36):15483-8. Joyner AH, J CR, Bloss CS, Bakken TE, Rimol LM, Melle I, Agartz I, Djurovic S, Topol EJ, Schork NJ, Andreassen OA, Dale AM. PMID: 19717458.
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    249. Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs. J Pharmacol Exp Ther. 2009 Nov; 331(2):419-28. Rana BK, Wessel J, Mahboubi V, Rao F, Haeller J, Gayen JR, Eskin E, Valle AM, Das M, Mahata SK, Taupenot L, Stridsberg M, Talley TT, Ziegler MG, Smith DW, Schork NJ, O'Connor DT, Taylor P. PMID: 19671882.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    250. Comparison of genetic distance measures using human SNP genotype data. Hum Biol. 2009 Aug; 81(4):389-406. Libiger O, Nievergelt CM, Schork NJ. PMID: 20067366.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    251. Identification of rare cancer driver mutations by network reconstruction. Genome Res. 2009 Sep; 19(9):1570-8. Torkamani A, Schork NJ. PMID: 19574499.
      View in: PubMed   Mentions: 49     Fields:    Translation:HumansCells
    252. Prestige centrality-based functional outlier detection in gene expression analysis. Bioinformatics. 2009 Sep 01; 25(17):2222-8. Torkamani A, Schork NJ. PMID: 19549629.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    253. Genome-wide association study of bipolar disorder in European American and African American individuals. Mol Psychiatry. 2009 Aug; 14(8):755-63. Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W, Byerley W, Coryell W, Craig D, Edenberg HJ, Eskin E, Foroud T, Gershon E, Greenwood TA, Hipolito M, Koller DL, Lawson WB, Liu C, Lohoff F, McInnis MG, McMahon FJ, Mirel DB, Murray SS, Nievergelt C, Nurnberger J, Nwulia EA, Paschall J, Potash JB, Rice J, Schulze TG, Scheftner W, Panganiban C, Zaitlen N, Zandi PP, Zöllner S, Schork NJ, Kelsoe JR. PMID: 19488044.
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    254. Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity. Aging Cell. 2009 Aug; 8(4):460-72. Pawlikowska L, Hu D, Huntsman S, Sung A, Chu C, Chen J, Joyner AH, Schork NJ, Hsueh WC, Reiner AP, Psaty BM, Atzmon G, Barzilai N, Cummings SR, Browner WS, Kwok PY, Ziv E. PMID: 19489743.
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    255. Common vs. rare allele hypotheses for complex diseases. Curr Opin Genet Dev. 2009 Jun; 19(3):212-9. Schork NJ, Murray SS, Frazer KA, Topol EJ. PMID: 19481926.
      View in: PubMed   Mentions: 241     Fields:    Translation:HumansCells
    256. Human genetic variation and its contribution to complex traits. Nat Rev Genet. 2009 Apr; 10(4):241-51. Frazer KA, Murray SS, Schork NJ, Topol EJ. PMID: 19293820.
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    257. Evaluation of next generation sequencing platforms for population targeted sequencing studies. Genome Biol. 2009; 10(3):R32. Harismendy O, Ng PC, Strausberg RL, Wang X, Stockwell TB, Beeson KY, Schork NJ, Murray SS, Topol EJ, Levy S, Frazer KA. PMID: 19327155.
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    258. Convergent functional genomics of genome-wide association data for bipolar disorder: comprehensive identification of candidate genes, pathways and mechanisms. Am J Med Genet B Neuropsychiatr Genet. 2009 Mar 05; 150B(2):155-81. Le-Niculescu H, Patel SD, Bhat M, Kuczenski R, Faraone SV, Tsuang MT, McMahon FJ, Schork NJ, Nurnberger JI, Niculescu AB. PMID: 19025758.
      View in: PubMed   Mentions: 76     Fields:    Translation:HumansAnimalsCells
    259. Computational modeling of structurally conserved cancer mutations in the RET and MET kinases: the impact on protein structure, dynamics, and stability. Biophys J. 2009 Feb; 96(3):858-74. Dixit A, Torkamani A, Schork NJ, Verkhivker G. PMID: 19186126.
      View in: PubMed   Mentions: 19     Fields:    Translation:Cells
    260. Autonomic function in hypertension; role of genetic variation at the catecholamine storage vesicle protein chromogranin B. Circ Cardiovasc Genet. 2009 Feb; 2(1):46-56. Zhang K, Rao F, Rana BK, Gayen JR, Calegari F, King A, Rosa P, Huttner WB, Stridsberg M, Mahata M, Vaingankar S, Mahboubi V, Salem RM, Rodriguez-Flores JL, Fung MM, Smith DW, Schork NJ, Ziegler MG, Taupenot L, Mahata SK, O'Connor DT. PMID: 20011129.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    261. Heritability of nonalcoholic fatty liver disease. Gastroenterology. 2009 May; 136(5):1585-92. Schwimmer JB, Celedon MA, Lavine JE, Salem R, Campbell N, Schork NJ, Shiehmorteza M, Yokoo T, Chavez A, Middleton MS, Sirlin CB. PMID: 19208353.
      View in: PubMed   Mentions: 94     Fields:    Translation:Humans
    262. Pathway and network analysis with high-density allelic association data. Methods Mol Biol. 2009; 563:289-301. Torkamani A, Schork NJ. PMID: 19597792.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    263. The relative importance of genetics and environment on mammographic density. Cancer Epidemiol Biomarkers Prev. 2009 Jan; 18(1):102-12. Ursin G, Lillie EO, Lee E, Cockburn M, Schork NJ, Cozen W, Parisky YR, Hamilton AS, Astrahan MA, Mack T. PMID: 19124487.
      View in: PubMed   Mentions: 31     Fields:    Translation:Humans
    264. G-protein-coupled receptor kinase 4 polymorphisms and blood pressure response to metoprolol among African Americans: sex-specificity and interactions. Am J Hypertens. 2009 Mar; 22(3):332-8. Bhatnagar V, O'Connor DT, Brophy VH, Schork NJ, Richard E, Salem RM, Nievergelt CM, Bakris GL, Middleton JP, Norris KC, Wright J, Hiremath L, Contreras G, Appel LJ, Lipkowitz MS. PMID: 19119263.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    265. Singleton deletions throughout the genome increase risk of bipolar disorder. Mol Psychiatry. 2009 Apr; 14(4):376-80. Zhang D, Cheng L, Qian Y, Alliey-Rodriguez N, Kelsoe JR, Greenwood T, Nievergelt C, Barrett TB, McKinney R, Schork N, Smith EN, Bloss C, Nurnberger J, Edenberg HJ, Foroud T, Sheftner W, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon F, Schulze TG, Berrettini W, Potash JB, Belmonte PL, Zandi PP, McInnis MG, Zöllner S, Craig D, Szelinger S, Koller D, Christian SL, Liu C, Gershon ES. PMID: 19114987.
      View in: PubMed   Mentions: 60     Fields:    Translation:Humans
    266. Cancer driver mutations in protein kinase genes. Cancer Lett. 2009 Aug 28; 281(2):117-27. Torkamani A, Verkhivker G, Schork NJ. PMID: 19081671.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansAnimals
    267. Adrenergic polymorphism and the human stress response. Ann N Y Acad Sci. 2008 Dec; 1148:282-96. Rao F, Zhang L, Wessel J, Zhang K, Wen G, Kennedy BP, Rana BK, Das M, Rodriguez-Flores JL, Smith DW, Cadman PE, Salem RM, Mahata SK, Schork NJ, Taupenot L, Ziegler MG, O'Connor DT. PMID: 19120120.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    268. Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion. J Am Coll Cardiol. 2008 Oct 28; 52(18):1468-81. Chen Y, Rao F, Rodriguez-Flores JL, Mahata M, Fung MM, Stridsberg M, Vaingankar SM, Wen G, Salem RM, Das M, Cockburn MG, Schork NJ, Ziegler MG, Hamilton BA, Mahata SK, Taupenot L, O'Connor DT. PMID: 19017515.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    269. Promoter polymorphisms in ACE (angiotensin I-converting enzyme) associated with clinical outcomes in hypertension. Clin Pharmacol Ther. 2009 Jan; 85(1):36-44. Johnson AD, Gong Y, Wang D, Langaee TY, Shin J, Cooper-Dehoff RM, Schork NJ, Binkley P, Pepine CJ, Johnson JA, Sadee W. PMID: 18946466.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    270. Mechanisms underlying hypoxia tolerance in Drosophila melanogaster: hairy as a metabolic switch. PLoS Genet. 2008 Oct; 4(10):e1000221. Zhou D, Xue J, Lai JC, Schork NJ, White KP, Haddad GG. PMID: 18927626.
      View in: PubMed   Mentions: 51     Fields:    Translation:AnimalsCells
    271. Pathway analysis of seven common diseases assessed by genome-wide association. Genomics. 2008 Nov; 92(5):265-72. Torkamani A, Topol EJ, Schork NJ. PMID: 18722519.
      View in: PubMed   Mentions: 168     Fields:    Translation:Humans
    272. Evidence for a heritable unidimensional symptom factor underlying obsessionality. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 05; 147B(6):676-85. Mathews CA, Greenwood T, Wessel J, Azzam A, Garrido H, Chavira DA, Chandavarkar U, Bagnarello M, Stein M, Schork NJ. PMID: 18163383.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    273. Identification of ALK as a major familial neuroblastoma predisposition gene. Nature. 2008 Oct 16; 455(7215):930-5. Mossé YP, Laudenslager M, Longo L, Cole KA, Wood A, Attiyeh EF, Laquaglia MJ, Sennett R, Lynch JE, Perri P, Laureys G, Speleman F, Kim C, Hou C, Hakonarson H, Torkamani A, Schork NJ, Brodeur GM, Tonini GP, Rappaport E, Devoto M, Maris JM. PMID: 18724359.
      View in: PubMed   Mentions: 350     Fields:    Translation:HumansCells
    274. Abnormal auditory N100 amplitude: a heritable endophenotype in first-degree relatives of schizophrenia probands. Biol Psychiatry. 2008 Dec 15; 64(12):1051-9. Turetsky BI, Greenwood TA, Olincy A, Radant AD, Braff DL, Cadenhead KS, Dobie DJ, Freedman R, Green MF, Gur RE, Gur RC, Light GA, Mintz J, Nuechterlein KH, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Calkins ME. PMID: 18701089.
      View in: PubMed   Mentions: 45     Fields:    Translation:Humans
    275. beta-adrenergic receptor gene polymorphisms and beta-blocker treatment outcomes in hypertension. Clin Pharmacol Ther. 2008 Dec; 84(6):715-21. Pacanowski MA, Gong Y, Cooper-Dehoff RM, Schork NJ, Shriver MD, Langaee TY, Pepine CJ, Johnson JA. PMID: 18615004.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    276. Congenital disease SNPs target lineage specific structural elements in protein kinases. Proc Natl Acad Sci U S A. 2008 Jul 01; 105(26):9011-6. Torkamani A, Kannan N, Taylor SS, Schork NJ. PMID: 18579784.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansCells
    277. Alpha-adducin polymorphism associated with increased risk of adverse cardiovascular outcomes: results from GENEtic Substudy of the INternational VErapamil SR-trandolapril STudy (INVEST-GENES). Am Heart J. 2008 Aug; 156(2):397-404. Gerhard T, Gong Y, Beitelshees AL, Mao X, Lobmeyer MT, Cooper-DeHoff RM, Langaee TY, Schork NJ, Shriver MD, Pepine CJ, Johnson JA. PMID: 18657677.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    278. Predicting functional regulatory polymorphisms. Bioinformatics. 2008 Aug 15; 24(16):1787-92. Torkamani A, Schork NJ. PMID: 18562267.
      View in: PubMed   Mentions: 8     Fields:    Translation:Cells
    279. Identification of EpCAM as the gene for congenital tufting enteropathy. Gastroenterology. 2008 Aug; 135(2):429-37. Sivagnanam M, Mueller JL, Lee H, Chen Z, Nelson SF, Turner D, Zlotkin SH, Pencharz PB, Ngan BY, Libiger O, Schork NJ, Lavine JE, Taylor S, Newbury RO, Kolodner RD, Hoffman HM. PMID: 18572020.
      View in: PubMed   Mentions: 46     Fields:    Translation:HumansCells
    280. Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure. Kidney Int. 2008 Jul; 74(1):115-25. Chen Y, Rao F, Rodriguez-Flores JL, Mahapatra NR, Mahata M, Wen G, Salem RM, Shih PA, Das M, Schork NJ, Ziegler MG, Hamilton BA, Mahata SK, O'Connor DT. PMID: 18432188.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    281. Verbal working memory impairments in individuals with schizophrenia and their first-degree relatives: findings from the Consortium on the Genetics of Schizophrenia. Schizophr Res. 2008 Aug; 103(1-3):218-28. Horan WP, Braff DL, Nuechterlein KH, Sugar CA, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Greenwood TA, Gur RE, Gur RC, Light GA, Mintz J, Olincy A, Radant AD, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Green MF. PMID: 18406578.
      View in: PubMed   Mentions: 42     Fields:    Translation:Humans
    282. Suggestive linkage of a chromosomal locus on 18p11 to cyclothymic temperament in bipolar disorder families. Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 05; 147(3):326-32. Evans LM, Akiskal HS, Greenwood TA, Nievergelt CM, Keck PE, McElroy SL, Sadovnick AD, Remick RA, Schork NJ, Kelsoe JR. PMID: 18081158.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    283. Prediction of cancer driver mutations in protein kinases. Cancer Res. 2008 Mar 15; 68(6):1675-82. Torkamani A, Schork NJ. PMID: 18339846.
      View in: PubMed   Mentions: 49     Fields:    Translation:HumansCells
    284. Inheritance of occlusal topography: a twin study. Eur Arch Paediatr Dent. 2008 Mar; 9(1):19-24. Su CY, Corby PM, Elliot MA, Studen-Pavlovich DA, Ranalli DN, Rosa B, Wessel J, Schork NJ, Hart TC, Bretz WA. PMID: 18328234.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    285. Accommodating linkage disequilibrium in genetic-association analyses via ridge regression. Am J Hum Genet. 2008 Feb; 82(2):375-85. Malo N, Libiger O, Schork NJ. PMID: 18252218.
      View in: PubMed   Mentions: 67     Fields:    
    286. Advances in endophenotyping schizophrenia. World Psychiatry. 2008 Feb; 7(1):11-8. Braff DL, Greenwood TA, Swerdlow NR, Light GA, Schork NJ. PMID: 18458787.
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    287. Chromogranin A polymorphisms are associated with hypertensive renal disease. J Am Soc Nephrol. 2008 Mar; 19(3):600-14. Salem RM, Cadman PE, Chen Y, Rao F, Wen G, Hamilton BA, Rana BK, Smith DW, Stridsberg M, Ward HJ, Mahata M, Mahata SK, Bowden DW, Hicks PJ, Freedman BI, Schork NJ, O'Connor DT. PMID: 18235090.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    288. Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans. Circulation. 2008 Jan 29; 117(4):517-25. Fung MM, Nguyen C, Mehtani P, Salem RM, Perez B, Thomas B, Das M, Schork NJ, Mahata SK, Ziegler MG, O'Connor DT. PMID: 18180394.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    289. DNA sequence-based phenotypic association analysis. Adv Genet. 2008; 60:195-217. Schork NJ, Wessel J, Malo N. PMID: 18358322.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansAnimals
    290. Methods for handling multiple testing. Adv Genet. 2008; 60:293-308. Rice TK, Schork NJ, Rao DC. PMID: 18358325.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    291. Gene expression in mouse brain following chronic hypoxia: role of sarcospan in glial cell death. Physiol Genomics. 2008 Feb 19; 32(3):370-9. Zhou D, Wang J, Zapala MA, Xue J, Schork NJ, Haddad GG. PMID: 18056785.
      View in: PubMed   Mentions: 23     Fields:    Translation:AnimalsCells
    292. Further evidence for association of GRK3 to bipolar disorder suggests a second disease mutation. Psychiatr Genet. 2007 Dec; 17(6):315-22. Barrett TB, Emberton JE, Nievergelt CM, Liang SG, Hauger RL, Eskin E, Schork NJ, Kelsoe JR. PMID: 18075471.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    293. Heritability of oral microbial species in caries-active and caries-free twins. Twin Res Hum Genet. 2007 Dec; 10(6):821-8. Corby PM, Bretz WA, Hart TC, Schork NJ, Wessel J, Lyons-Weiler J, Paster BJ. PMID: 18179393.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    294. Powerful designs for genetic association studies that consider twins and sibling pairs with discordant genotypes. Genet Epidemiol. 2007 Nov; 31(7):789-96. Wessel J, Schork AJ, Tiwari HK, Schork NJ. PMID: 17549743.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    295. Initial heritability analyses of endophenotypic measures for schizophrenia: the consortium on the genetics of schizophrenia. Arch Gen Psychiatry. 2007 Nov; 64(11):1242-50. Greenwood TA, Braff DL, Light GA, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Green MF, Gur RE, Gur RC, Mintz J, Nuechterlein KH, Olincy A, Radant AD, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Schork NJ. PMID: 17984393.
      View in: PubMed   Mentions: 152     Fields:    Translation:Humans
    296. Angiotensin-converting enzyme gene polymorphism predicts the time-course of blood pressure response to angiotensin converting enzyme inhibition in the AASK trial. J Hypertens. 2007 Oct; 25(10):2082-92. Bhatnagar V, O'Connor DT, Schork NJ, Salem RM, Nievergelt CM, Rana BK, Smith DW, Bakris GL, Middleton JP, Norris KC, Wright JT, Cheek D, Hiremath L, Contreras G, Appel LJ, Lipkowitz MS. PMID: 17885551.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    297. Accurate prediction of deleterious protein kinase polymorphisms. Bioinformatics. 2007 Nov 01; 23(21):2918-25. Torkamani A, Schork NJ. PMID: 17855419.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimalsCells
    298. Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk. J Clin Invest. 2007 Sep; 117(9):2658-71. Zhang L, Rao F, Zhang K, Khandrika S, Das M, Vaingankar SM, Bao X, Rana BK, Smith DW, Wessel J, Salem RM, Rodriguez-Flores JL, Mahata SK, Schork NJ, Ziegler MG, O'Connor DT. PMID: 17717598.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansAnimals
    299. KCNMB1 genotype influences response to verapamil SR and adverse outcomes in the INternational VErapamil SR/Trandolapril STudy (INVEST). Pharmacogenet Genomics. 2007 Sep; 17(9):719-29. Beitelshees AL, Gong Y, Wang D, Schork NJ, Cooper-Dehoff RM, Langaee TY, Shriver MD, Sadee W, Knot HJ, Pepine CJ, Johnson JA. PMID: 17700361.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCellsCTClinical Trials
    300. Biogenesis of the secretory granule: chromogranin A coiled-coil structure results in unusual physical properties and suggests a mechanism for granule core condensation. Biochemistry. 2007 Sep 25; 46(38):10999-1012. Mosley CA, Taupenot L, Biswas N, Taulane JP, Olson NH, Vaingankar SM, Wen G, Schork NJ, Ziegler MG, Mahata SK, O'Connor DT. PMID: 17718510.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    301. A simulation-based analysis of chromosome segment sharing among a group of arbitrarily related individuals. Eur J Hum Genet. 2007 Dec; 15(12):1260-8. Libiger O, Schork NJ. PMID: 17700628.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    302. Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo. Circulation. 2007 Aug 28; 116(9):993-1006. Rao F, Zhang L, Wessel J, Zhang K, Wen G, Kennedy BP, Rana BK, Das M, Rodriguez-Flores JL, Smith DW, Cadman PE, Salem RM, Mahata SK, Schork NJ, Taupenot L, Ziegler MG, O'Connor DT. PMID: 17698732.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansCells
    303. Laminin-alpha4 and integrin-linked kinase mutations cause human cardiomyopathy via simultaneous defects in cardiomyocytes and endothelial cells. Circulation. 2007 Jul 31; 116(5):515-25. Knöll R, Postel R, Wang J, Krätzner R, Hennecke G, Vacaru AM, Vakeel P, Schubert C, Murthy K, Rana BK, Kube D, Knöll G, Schäfer K, Hayashi T, Holm T, Kimura A, Schork N, Toliat MR, Nürnberg P, Schultheiss HP, Schaper W, Schaper J, Bos E, Den Hertog J, van Eeden FJ, Peters PJ, Hasenfuss G, Chien KR, Bakkers J. PMID: 17646580.
      View in: PubMed   Mentions: 70     Fields:    Translation:HumansAnimalsCells
    304. Detecting genetic variation in microarray expression data. Genome Res. 2007 Aug; 17(8):1228-35. Greenhall JA, Zapala MA, Cáceres M, Libiger O, Barlow C, Schork NJ, Lockhart DJ. PMID: 17609390.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimals
    305. An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension. Hum Mol Genet. 2007 Jul 15; 16(14):1752-64. Wen G, Wessel J, Zhou W, Ehret GB, Rao F, Stridsberg M, Mahata SK, Gent PM, Das M, Cooper RS, Chakravarti A, Zhou H, Schork NJ, O'connor DT, Hamilton BA. PMID: 17584765.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    306. Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family. Genomics. 2007 Jul; 90(1):49-58. Torkamani A, Schork NJ. PMID: 17498919.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    307. Accommodating pathway information in expression quantitative trait locus analysis. Genomics. 2007 Jul; 90(1):132-42. Wessel J, Zapala MA, Schork NJ. PMID: 17493783.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    308. Endophenotyping schizophrenia. Am J Psychiatry. 2007 May; 164(5):705-7. Braff D, Schork NJ, Gottesman II. PMID: 17475726.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    309. Gene-by-environment (serotonin transporter and childhood maltreatment) interaction for anxiety sensitivity, an intermediate phenotype for anxiety disorders. Neuropsychopharmacology. 2008 Jan; 33(2):312-9. Stein MB, Schork NJ, Gelernter J. PMID: 17460615.
      View in: PubMed   Mentions: 65     Fields:    Translation:Humans
    310. Heredity of endothelin secretion: human twin studies reveal the influence of polymorphism at the chromogranin A locus, a novel determinant of endothelial function. Circulation. 2007 May 01; 115(17):2282-91. Lillie EO, Mahata M, Khandrika S, Rao F, Bundey RA, Wen G, Chen Y, Taupenot L, Smith DW, Mahata SK, Ziegler MG, Cockburn M, Schork NJ, O'Connor DT. PMID: 17438153.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    311. Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension. Circulation. 2007 May 01; 115(17):2271-81. Rao F, Wen G, Gayen JR, Das M, Vaingankar SM, Rana BK, Mahata M, Kennedy BP, Salem RM, Stridsberg M, Abel K, Smith DW, Eskin E, Schork NJ, Hamilton BA, Ziegler MG, Mahata SK, O'Connor DT. PMID: 17438154.
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    312. Single nucleotide polymorphism discovery and haplotype analysis of Ca2+-dependent K+ channel beta-1 subunit. Pharmacogenet Genomics. 2007 Apr; 17(4):267-75. Gong Y, Beitelshees AL, Wessel J, Langaee TY, Schork NJ, Johnson JA. PMID: 17496725.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    313. Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program. Genet Epidemiol. 2007 Apr; 31(3):195-210. Greenwood TA, Libiger O, Kardia S, Hanis C, Morrison AC, Gu CC, Rice T, Miller M, Turner ST, Myers RH, Grove J, Hsiao CF, Weder AB, Schork NJ. PMID: 17266112.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    314. An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP). Hum Genet. 2007 Jun; 121(5):577-90. Gu CC, Hunt SC, Kardia S, Turner ST, Chakravarti A, Schork N, Olshen R, Curb D, Jaquish C, Boerwinkle E, Rao DC. PMID: 17372766.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    315. Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism. Hypertension. 2007 May; 49(5):1015-31. Rao F, Wessel J, Wen G, Zhang L, Rana BK, Kennedy BP, Greenwood TA, Salem RM, Chen Y, Khandrika S, Hamilton BA, Smith DW, Holstein-Rathlou NH, Ziegler MG, Schork NJ, O'Connor DT. PMID: 17353515.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    316. Multi-site studies of acoustic startle and prepulse inhibition in humans: initial experience and methodological considerations based on studies by the Consortium on the Genetics of Schizophrenia. Schizophr Res. 2007 May; 92(1-3):237-51. Swerdlow NR, Sprock J, Light GA, Cadenhead K, Calkins ME, Dobie DJ, Freedman R, Green MF, Greenwood TA, Gur RE, Mintz J, Olincy A, Nuechterlein KH, Radant AD, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Tsuang DW, Tsuang MT, Turetsky BI, Braff DL. PMID: 17346930.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    317. Heritability and clinical features of multigenerational families with obsessive-compulsive disorder and hoarding. Am J Med Genet B Neuropsychiatr Genet. 2007 Mar 05; 144B(2):174-82. Mathews CA, Nievergelt CM, Azzam A, Garrido H, Chavira DA, Wessel J, Bagnarello M, Reus VI, Schork NJ. PMID: 17290446.
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    318. Generalized analysis of molecular variance. PLoS Genet. 2007 Apr 06; 3(4):e51. Nievergelt CM, Libiger O, Schork NJ. PMID: 17411342.
      View in: PubMed   Mentions: 38     Fields:    Translation:HumansCells
    319. C-reactive protein, an 'intermediate phenotype' for inflammation: human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/beta-adrenergic pathway loci. J Hypertens. 2007 Feb; 25(2):329-43. Wessel J, Moratorio G, Rao F, Mahata M, Zhang L, Greene W, Rana BK, Kennedy BP, Khandrika S, Huang P, Lillie EO, Shih PA, Smith DW, Wen G, Hamilton BA, Ziegler MG, Witztum JL, Schork NJ, Schmid-Schönbein GW, O'Connor DT. PMID: 17211240.
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    320. Successful aging: from phenotype to genotype. Biol Psychiatry. 2007 Aug 15; 62(4):282-93. Glatt SJ, Chayavichitsilp P, Depp C, Schork NJ, Jeste DV. PMID: 17210144.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    321. DNA variation and brain region-specific expression profiles exhibit different relationships between inbred mouse strains: implications for eQTL mapping studies. Genome Biol. 2007; 8(2):R25. Hovatta I, Zapala MA, Broide RS, Schadt EE, Libiger O, Schork NJ, Lockhart DJ, Barlow C. PMID: 17324278.
      View in: PubMed   Mentions: 36     Fields:    Translation:Animals
    322. Multiple ADH genes modulate risk for drug dependence in both African- and European-Americans. Hum Mol Genet. 2007 Feb 15; 16(4):380-90. Luo X, Kranzler HR, Zuo L, Wang S, Schork NJ, Gelernter J. PMID: 17185388.
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    323. Population-based sample reveals gene-gender interactions in blood pressure in White Americans. Hypertension. 2007 Jan; 49(1):96-106. Rana BK, Insel PA, Payne SH, Abel K, Beutler E, Ziegler MG, Schork NJ, O'Connor DT. PMID: 17159089.
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    324. Multivariate regression analysis of distance matrices for testing associations between gene expression patterns and related variables. Proc Natl Acad Sci U S A. 2006 Dec 19; 103(51):19430-5. Zapala MA, Schork NJ. PMID: 17146048.
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    325. Deconstructing schizophrenia: an overview of the use of endophenotypes in order to understand a complex disorder. Schizophr Bull. 2007 Jan; 33(1):21-32. Braff DL, Freedman R, Schork NJ, Gottesman II. PMID: 17088422.
      View in: PubMed   Mentions: 127     Fields:    Translation:Humans
    326. Statistical genetics concepts and approaches in schizophrenia and related neuropsychiatric research. Schizophr Bull. 2007 Jan; 33(1):95-104. Schork NJ, Greenwood TA, Braff DL. PMID: 17035359.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    327. The Consortium on the Genetics of Endophenotypes in Schizophrenia: model recruitment, assessment, and endophenotyping methods for a multisite collaboration. Schizophr Bull. 2007 Jan; 33(1):33-48. Calkins ME, Dobie DJ, Cadenhead KS, Olincy A, Freedman R, Green MF, Greenwood TA, Gur RE, Gur RC, Light GA, Mintz J, Nuechterlein KH, Radant AD, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Braff DL. PMID: 17035358.
      View in: PubMed   Mentions: 65     Fields:    Translation:Humans
    328. Successful multi-site measurement of antisaccade performance deficits in schizophrenia. Schizophr Res. 2007 Jan; 89(1-3):320-9. Radant AD, Dobie DJ, Calkins ME, Olincy A, Braff DL, Cadenhead KS, Freedman R, Green MF, Greenwood TA, Gur RE, Light GA, Meichle SP, Mintz J, Nuechterlein KH, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang MT, Turetsky BI, Tsuang DW. PMID: 17023145.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    329. Generalized genomic distance-based regression methodology for multilocus association analysis. Am J Hum Genet. 2006 Nov; 79(5):792-806. Wessel J, Schork NJ. PMID: 17033957.
      View in: PubMed   Mentions: 89     Fields:    Translation:Humans
    330. PhenoChipping of psychotic disorders: a novel approach for deconstructing and quantitating psychiatric phenotypes. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 05; 141B(6):653-62. Niculescu AB, Lulow LL, Ogden CA, Le-Niculescu H, Salomon DR, Schork NJ, Caligiuri MP, Lohr JB. PMID: 16838358.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    331. Heritability estimates for dental caries and sucrose sweetness preference. Arch Oral Biol. 2006 Dec; 51(12):1156-60. Bretz WA, Corby PM, Melo MR, Coelho MQ, Costa SM, Robinson M, Schork NJ, Drewnowski A, Hart TC. PMID: 16934741.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    332. Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans. Hum Genet. 2006 Jul; 119(6):624-33. Tang H, Jorgenson E, Gadde M, Kardia SL, Rao DC, Zhu X, Schork NJ, Hanis CL, Risch N. PMID: 16738946.
      View in: PubMed   Mentions: 47     Fields:    Translation:Humans
    333. Tic symptom profiles in subjects with Tourette Syndrome from two genetically isolated populations. Biol Psychiatry. 2007 Feb 01; 61(3):292-300. Mathews CA, Jang KL, Herrera LD, Lowe TL, Budman CL, Erenberg G, Naarden A, Bruun RD, Schork NJ, Freimer NB, Reus VI. PMID: 16581034.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    334. Diplotype trend regression analysis of the ADH gene cluster and the ALDH2 gene: multiple significant associations with alcohol dependence. Am J Hum Genet. 2006 Jun; 78(6):973-87. Luo X, Kranzler HR, Zuo L, Wang S, Schork NJ, Gelernter J. PMID: 16685648.
      View in: PubMed   Mentions: 61     Fields:    Translation:Humans
    335. Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder. Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 05; 141B(3):234-41. Nievergelt CM, Kripke DF, Barrett TB, Burg E, Remick RA, Sadovnick AD, McElroy SL, Keck PE, Schork NJ, Kelsoe JR. PMID: 16528748.
      View in: PubMed   Mentions: 96     Fields:    Translation:HumansCells
    336. Rho kinase polymorphism influences blood pressure and systemic vascular resistance in human twins: role of heredity. Hypertension. 2006 May; 47(5):937-47. Seasholtz TM, Wessel J, Rao F, Rana BK, Khandrika S, Kennedy BP, Lillie EO, Ziegler MG, Smith DW, Schork NJ, Brown JH, O'Connor DT. PMID: 16585408.
      View in: PubMed   Mentions: 37     Fields:    Translation:HumansCells
    337. The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program. Eur J Hum Genet. 2006 Apr; 14(4):469-77. Chang YP, Kim JD, Schwander K, Rao DC, Miller MB, Weder AB, Cooper RS, Schork NJ, Province MA, Morrison AC, Kardia SL, Quertermous T, Chakravarti A. PMID: 16493446.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    338. Pleiotropic effects of novel trans-acting loci influencing human sympathochromaffin secretion. Physiol Genomics. 2006 May 16; 25(3):470-9. Greenwood TA, Rao F, Stridsberg M, Mahapatra NR, Mahata M, Lillie EO, Mahata SK, Taupenot L, Schork NJ, O'Connor DT. PMID: 16554546.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansAnimalsCells
    339. Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples. Mol Psychiatry. 2006 Feb; 11(2):125-33, 115. Greenwood TA, Schork NJ, Eskin E, Kelsoe JR. PMID: 16261167.
      View in: PubMed   Mentions: 53     Fields:    Translation:HumansCellsCTClinical Trials
    340. Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism. BMC Genet. 2005 Dec 30; 6 Suppl 1:S35. Libiger O, Schork NJ. PMID: 16451645.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    341. COMT polymorphisms and anxiety-related personality traits. Neuropsychopharmacology. 2005 Nov; 30(11):2092-102. Stein MB, Fallin MD, Schork NJ, Gelernter J. PMID: 15956988.
      View in: PubMed   Mentions: 44     Fields:    Translation:Humans
    342. Longitudinal analysis of heritability for dental caries traits. J Dent Res. 2005 Nov; 84(11):1047-51. Bretz WA, Corby PM, Schork NJ, Robinson MT, Coelho M, Costa S, Melo Filho MR, Weyant RJ, Hart TC. PMID: 16246939.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansPHPublic Health
    343. Histopathology of pediatric nonalcoholic fatty liver disease. Hepatology. 2005 Sep; 42(3):641-9. Schwimmer JB, Behling C, Newbury R, Deutsch R, Nievergelt C, Schork NJ, Lavine JE. PMID: 16116629.
      View in: PubMed   Mentions: 170     Fields:    Translation:Humans
    344. Assessment of multiple displacement amplification for polymorphism discovery and haplotype determination at a highly polymorphic locus, MC1R. Hum Mutat. 2005 Aug; 26(2):145-52. Murthy KK, Mahboubi VS, Santiago A, Barragan MT, Knöll R, Schultheiss HP, O'Connor DT, Schork NJ, Rana BK. PMID: 15957185.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    345. Interactive effects of common beta2-adrenoceptor haplotypes and age on susceptibility to hypertension and receptor function. Hypertension. 2005 Aug; 46(2):301-7. Bao X, Mills PJ, Rana BK, Dimsdale JE, Schork NJ, Smith DW, Rao F, Milic M, O'Connor DT, Ziegler MG. PMID: 16027244.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    346. Genetic variation at the human alpha2B-adrenergic receptor locus: role in blood pressure variation and yohimbine response. Hypertension. 2005 Jun; 45(6):1207-13. Etzel JP, Rana BK, Wen G, Parmer RJ, Schork NJ, O'Connor DT, Insel PA. PMID: 15920038.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    347. Human response to alpha2-adrenergic agonist stimulation studied in an isolated vascular bed in vivo: Biphasic influence of dose, age, gender, and receptor genotype. Clin Pharmacol Ther. 2005 May; 77(5):388-403. King D, Etzel JP, Chopra S, Smith J, Cadman PE, Rao F, Funk SD, Rana BK, Schork NJ, Insel PA, O'Connor DT. PMID: 15900285.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    348. Common genetic mechanisms of blood pressure elevation in two independent rodent models of human essential hypertension. Am J Hypertens. 2005 May; 18(5 Pt 1):633-52. Friese RS, Mahboubi P, Mahapatra NR, Mahata SK, Schork NJ, Schmid-Schönbein GW, O'Connor DT. PMID: 15882546.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimals
    349. Dental caries and microbial acid production in twins. Caries Res. 2005 May-Jun; 39(3):168-72. Bretz WA, Corby PM, Hart TC, Costa S, Coelho MQ, Weyant RJ, Robinson M, Schork NJ. PMID: 15914976.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    350. Genome-wide linkage scans for fasting glucose, insulin, and insulin resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: evidence of linkages to chromosome 7q36 and 19q13 from meta-analysis. Diabetes. 2005 Mar; 54(3):909-14. An P, Freedman BI, Hanis CL, Chen YD, Weder AB, Schork NJ, Boerwinkle E, Province MA, Hsiung CA, Wu X, Quertermous T, Rao DC. PMID: 15734873.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
    351. A comprehensive literature review of haplotyping software and methods for use with unrelated individuals. Hum Genomics. 2005 Mar; 2(1):39-66. Salem RM, Wessel J, Schork NJ. PMID: 15814067.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    352. Admixture mapping as a gene discovery approach for complex human traits and diseases. Curr Hypertens Rep. 2005 Feb; 7(1):31-7. Nievergelt CM, Schork NJ. PMID: 15683584.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    353. Population structure, admixture, and aging-related phenotypes in African American adults: the Cardiovascular Health Study. Am J Hum Genet. 2005 Mar; 76(3):463-77. Reiner AP, Ziv E, Lind DL, Nievergelt CM, Schork NJ, Cummings SR, Phong A, Burchard EG, Harris TB, Psaty BM, Kwok PY. PMID: 15660291.
      View in: PubMed   Mentions: 76     Fields:    Translation:Humans
    354. Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease. Hum Mol Genet. 2005 Feb 15; 14(4):543-53. Soares ML, Coelho T, Sousa A, Batalov S, Conceição I, Sales-Luís ML, Ritchie MD, Williams SM, Nievergelt CM, Schork NJ, Saraiva MJ, Buxbaum JN. PMID: 15649951.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    355. A genomewide scan of male sexual orientation. Hum Genet. 2005 Mar; 116(4):272-8. Mustanski BS, Dupree MG, Nievergelt CM, Bocklandt S, Schork NJ, Hamer DH. PMID: 15645181.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    356. Ethnicity and human genetic linkage maps. Am J Hum Genet. 2005 Feb; 76(2):276-90. Jorgenson E, Tang H, Gadde M, Province M, Leppert M, Kardia S, Schork N, Cooper R, Rao DC, Boerwinkle E, Risch N. PMID: 15627237.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansCells
    357. Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. Am J Hum Genet. 2005 Feb; 76(2):268-75. Tang H, Quertermous T, Rodriguez B, Kardia SL, Zhu X, Brown A, Pankow JS, Province MA, Hunt SC, Boerwinkle E, Schork NJ, Risch NJ. PMID: 15625622.
      View in: PubMed   Mentions: 160     Fields:    Translation:HumansCells
    358. Candidate genes, pathways and mechanisms for bipolar (manic-depressive) and related disorders: an expanded convergent functional genomics approach. Mol Psychiatry. 2004 Nov; 9(11):1007-29. Ogden CA, Rich ME, Schork NJ, Paulus MP, Geyer MA, Lohr JB, Kuczenski R, Niculescu AB. PMID: 15314610.
      View in: PubMed   Mentions: 74     Fields:    Translation:HumansAnimals
    359. Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins. Physiol Genomics. 2004 Nov 17; 19(3):277-91. Zhang L, Rao F, Wessel J, Kennedy BP, Rana BK, Taupenot L, Lillie EO, Cockburn M, Schork NJ, Ziegler MG, O'Connor DT. PMID: 15367723.
      View in: PubMed   Mentions: 38     Fields:    Translation:HumansCells
    360. A polymorphism of the beta1-adrenergic receptor is associated with low extraversion. Biol Psychiatry. 2004 Aug 15; 56(4):217-24. Stein MB, Schork NJ, Gelernter J. PMID: 15312808.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    361. Human sympathetic activation by alpha2-adrenergic blockade with yohimbine: Bimodal, epistatic influence of cytochrome P450-mediated drug metabolism. Clin Pharmacol Ther. 2004 Aug; 76(2):139-53. Le Corre P, Parmer RJ, Kailasam MT, Kennedy BP, Skaar TP, Ho H, Leverge R, Smith DW, Ziegler MG, Insel PA, Schork NJ, Flockhart DA, O'connor DT. PMID: 15289791.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    362. Human haplotype block sizes are negatively correlated with recombination rates. Genome Res. 2004 Jul; 14(7):1358-61. Greenwood TA, Rana BK, Schork NJ. PMID: 15231751.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    363. Genome-wide linkage analysis of chromogranin B expression in the CEPH pedigrees: implications for exocytotic sympathochromaffin secretion in humans. Physiol Genomics. 2004 Jun 17; 18(1):119-27. Greenwood TA, Cadman PE, Stridsberg M, Nguyen S, Taupenot L, Schork NJ, O'Connor DT. PMID: 15138309.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimalsCells
    364. Neuroendocrine transcriptome in genetic hypertension: multiple changes in diverse adrenal physiological systems. Hypertension. 2004 Jun; 43(6):1301-11. Fries RS, Mahboubi P, Mahapatra NR, Mahata SK, Schork NJ, Schmid-Schoenbein GW, O'Connor DT. PMID: 15166183.
      View in: PubMed   Mentions: 16     Fields:    Translation:AnimalsCells
    365. Large-scale integration of human genetic and physical maps. Genome Res. 2004 Jun; 14(6):1199-205. Nievergelt CM, Smith DW, Kohlenberg JB, Schork NJ. PMID: 15140834.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    366. Inherent bias toward the null hypothesis in conventional multipoint nonparametric linkage analysis. Am J Hum Genet. 2004 Feb; 74(2):306-16. Schork NJ, Greenwood TA. PMID: 14732904.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    367. Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology. Am J Hum Genet. 2004 Feb; 74(2):197-207. Wen G, Mahata SK, Cadman P, Mahata M, Ghosh S, Mahapatra NR, Rao F, Stridsberg M, Smith DW, Mahboubi P, Schork NJ, O'Connor DT, Hamilton BA. PMID: 14740315.
      View in: PubMed   Mentions: 43     Fields:    Translation:HumansAnimalsCells
    368. Identifying genes and genetic variation underlying human diseases and complex phenotypes via recombination mapping. J Physiol. 2004 Jan 01; 554(Pt 1):40-5. Broeckel U, Schork NJ. PMID: 14678489.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    369. Identification of quantitative trait Loci for anxiety and locomotion phenotypes in rat recombinant inbred strains. Behav Genet. 2004 Jan; 34(1):93-103. Conti LH, Jirout M, Breen L, Vanella JJ, Schork NJ, Printz MP. PMID: 14739700.
      View in: PubMed   Mentions: 12     Fields:    Translation:Animals
    370. RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathways. Neuron. 2003 Dec 18; 40(6):1119-31. Gold DA, Baek SH, Schork NJ, Rose DW, Larsen DD, Sachs BD, Rosenfeld MG, Hamilton BA. PMID: 14687547.
      View in: PubMed   Mentions: 56     Fields:    Translation:AnimalsCells
    371. Evidence of a contribution of genetic factors to dental caries risk. J Evid Based Dent Pract. 2003 Dec; 3(4):185-189. Bretz WA, Corby P, Schork N, Hart TC. PMID: 22287938.
      View in: PubMed   Mentions: 2     Fields:    
    372. A new framework marker-based linkage map and SDPs for the rat HXB/BXH strain set. Mamm Genome. 2003 Aug; 14(8):537-46. Jirout M, Krenová D, Kren V, Breen L, Pravenec M, Schork NJ, Printz MP. PMID: 12925886.
      View in: PubMed   Mentions: 3     Fields:    Translation:AnimalsCells
    373. Distribution analysis of nonsynonymous polymorphisms within the G-protein-coupled receptor gene family. Genomics. 2003 Mar; 81(3):245-8. Lee A, Rana BK, Schiffer HH, Schork NJ, Brann MR, Insel PA, Weiner DM. PMID: 12659808.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    374. A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans. Am J Hypertens. 2003 Feb; 16(2):151-3. Thiel BA, Chakravarti A, Cooper RS, Luke A, Lewis S, Lynn A, Tiwari H, Schork NJ, Weder AB. PMID: 12559684.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    375. The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell. 2002 Dec 27; 111(7):943-55. Knöll R, Hoshijima M, Hoffman HM, Person V, Lorenzen-Schmidt I, Bang ML, Hayashi T, Shiga N, Yasukawa H, Schaper W, McKenna W, Yokoyama M, Schork NJ, Omens JH, McCulloch AD, Kimura A, Gregorio CC, Poller W, Schaper J, Schultheiss HP, Chien KR. PMID: 12507422.
      View in: PubMed   Mentions: 231     Fields:    Translation:HumansAnimalsCells
    376. Genomic association/linkage of sodium lithium countertransport in CEPH pedigrees. Hypertension. 2002 Nov; 40(5):619-28. Schork NJ, Gardner JP, Zhang L, Fallin D, Thiel B, Jakubowski H, Aviv A. PMID: 12411453.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    377. Identification of hypertension-related QTLs in African American sib pairs. Hypertension. 2002 Nov; 40(5):634-9. Kotchen TA, Broeckel U, Grim CE, Hamet P, Jacob H, Kaldunski ML, Kotchen JM, Schork NJ, Tonellato PJ, Cowley AW. PMID: 12411455.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    378. Gene mapping via the ancestral recombination graph. Theor Popul Biol. 2002 Sep; 62(2):215-29. Larribe F, Lessard S, Schork NJ. PMID: 12167358.
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    379. Power calculations for genetic association studies using estimated probability distributions. Am J Hum Genet. 2002 Jun; 70(6):1480-9. Schork NJ. PMID: 11992254.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    380. Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations. Am J Hum Genet. 2002 May; 70(5):1172-82. Hall MA, Norman PJ, Thiel B, Tiwari H, Peiffer A, Vaughan RW, Prescott S, Leppert M, Schork NJ, Lanchbury JS. PMID: 11951176.
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    381. Evaluation of linkage disequilibrium between chromosome 22q11 single nucleotide polymorphisms in a large outbred population. Am J Med Genet. 2002 Mar 08; 114(2):205-13. Shaw SH, Hutchison D, Saiz R, Abel K, DeLisi LE, Schork NJ, Sherrington R. PMID: 11857583.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    382. Segregation analysis of blood pressure and body mass index in a rural US community. Hum Biol. 2002 Feb; 74(1):11-23. Nath SK, Chakravarti A, Chen CH, Cooper R, Weder A, Schork NJ. PMID: 11931572.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    383. A genetic determinant that specifically regulates the frequency of hematopoietic stem cells. J Immunol. 2002 Jan 15; 168(2):635-42. Morrison SJ, Qian D, Jerabek L, Thiel BA, Park IK, Ford PS, Kiel MJ, Schork NJ, Weissman IL, Clarke MF. PMID: 11777956.
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    384. A genomic-systems biology map for cardiovascular function. Science. 2001 Nov 23; 294(5547):1723-6. Stoll M, Cowley AW, Tonellato PJ, Greene AS, Kaldunski ML, Roman RJ, Dumas P, Schork NJ, Wang Z, Jacob HJ. PMID: 11721057.
      View in: PubMed   Mentions: 53     Fields:    Translation:HumansAnimalsCells
    385. Two-trait-locus linkage analyses of asthma susceptibility. Genet Epidemiol. 2001; 21 Suppl 1:S278-83. Nath SK, Chen CH, Schork NJ. PMID: 11793682.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    386. The future of genetic case-control studies. Adv Genet. 2001; 42:191-212. Schork NJ, Fallin D, Thiel B, Xu X, Broeckel U, Jacob HJ, Cohen D. PMID: 11037322.
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    387. Genome partitioning and whole-genome analysis. Adv Genet. 2001; 42:299-322. Schork NJ. PMID: 11037329.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimals
    388. Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease. Genome Res. 2001 Jan; 11(1):143-51. Fallin D, Cohen A, Essioux L, Chumakov I, Blumenfeld M, Cohen D, Schork NJ. PMID: 11156623.
      View in: PubMed   Mentions: 104     Fields:    Translation:Humans
    389. A common promoter variant of the leptin gene is associated with changes in the relationship between serum leptin and fat mass in obese girls. Diabetes. 2000 Dec; 49(12):2196-200. Le Stunff C, Le Bihan C, Schork NJ, Bougnères P. PMID: 11118025.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    390. The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesity. Nat Genet. 2000 Dec; 26(4):444-6. Le Stunff C, Fallin D, Schork NJ, Bougnères P. PMID: 11101842.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    391. Quantitative trait loci mapping for cholesterol gallstones in AKR/J and C57L/J strains of mice. Physiol Genomics. 2000 Nov 09; 4(1):59-65. Paigen B, Schork NJ, Svenson KL, Cheah YC, Mu JL, Lammert F, Wang DQ, Bouchard G, Carey MC. PMID: 11074014.
      View in: PubMed   Mentions: 20     Fields:    Translation:Animals
    392. Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects. Am J Hum Genet. 2000 Nov; 67(5):1208-18. Schork NJ, Nath SK, Fallin D, Chakravarti A. PMID: 11032785.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    393. Single nucleotide polymorphisms and the future of genetic epidemiology. Clin Genet. 2000 Oct; 58(4):250-64. Schork NJ, Fallin D, Lanchbury JS. PMID: 11076050.
      View in: PubMed   Mentions: 64     Fields:    Translation:Humans
    394. Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data. Am J Hum Genet. 2000 Oct; 67(4):947-59. Fallin D, Schork NJ. PMID: 10954684.
      View in: PubMed   Mentions: 123     Fields:    Translation:Humans
    395. Telomere length inversely correlates with pulse pressure and is highly familial. Hypertension. 2000 Aug; 36(2):195-200. Jeanclos E, Schork NJ, Kyvik KO, Kimura M, Skurnick JH, Aviv A. PMID: 10948077.
      View in: PubMed   Mentions: 101     Fields:    Translation:HumansCells
    396. Lack of association between a biallelic polymorphism in the adducin gene and blood pressure in whites and African Americans. Am J Hypertens. 2000 Jun; 13(6 Pt 1):693-8. Schork NJ, Chakravarti A, Thiel B, Fornage M, Jacob HJ, Cai R, Rotimi CN, Cooper RS, Weder AB. PMID: 10912755.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    397. Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C. Am J Hum Genet. 2000 Jun; 66(6):1833-44. Nair RP, Stuart P, Henseler T, Jenisch S, Chia NV, Westphal E, Schork NJ, Kim J, Lim HW, Christophers E, Voorhees JJ, Elder JT. PMID: 10801386.
      View in: PubMed   Mentions: 59     Fields:    Translation:HumansCells
    398. Peaks and troughs in linkage mapping for the rheumatic diseases. Rheumatology (Oxford). 2000 May; 39(5):453-6. Lanchbury JS, Schork NJ. PMID: 10852972.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    399. Genetically defined risk of salt sensitivity in an intercross of Brown Norway and Dahl S rats. Physiol Genomics. 2000 Apr 27; 2(3):107-15. Cowley AW, Stoll M, Greene AS, Kaldunski ML, Roman RJ, Tonellato PJ, Schork NJ, Dumas P, Jacob HJ. PMID: 11015589.
      View in: PubMed   Mentions: 16     Fields:    Translation:Animals
    400. Synergistic effect of alpha-adducin and ACE genes causes blood pressure changes with body sodium and volume expansion. Kidney Int. 2000 Mar; 57(3):1083-90. Barlassina C, Schork NJ, Manunta P, Citterio L, Sciarrone M, Lanella G, Bianchi G, Cusi D. PMID: 10720960.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    401. Twins. Novel uses to study complex traits and genetic diseases. Trends Genet. 2000 Mar; 16(3):131-4. MacGregor AJ, Snieder H, Schork NJ, Spector TD. PMID: 10689354.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    402. Xenobiotics, dietary interventions, and genetically mediated therapies. Curr Hypertens Rep. 2000 Feb; 2(1):11-2. Schork NJ. PMID: 10981121.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    403. Mapping of a blood pressure quantitative trait locus to chromosome 15q in a Chinese population. Hum Mol Genet. 1999 Dec; 8(13):2551-5. Xu X, Yang J, Rogus J, Chen C, Schork N, Xu X. PMID: 10556304.
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    404. Mapping loci for pentylenetetrazol-induced seizure susceptibility in mice. J Neurosci. 1999 Aug 15; 19(16):6733-9. Ferraro TN, Golden GT, Smith GG, St Jean P, Schork NJ, Mulholland N, Ballas C, Schill J, Buono RJ, Berrettini WH. PMID: 10436030.
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    405. Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. Am J Hum Genet. 1999 Aug; 65(2):531-44. Allison DB, Neale MC, Zannolli R, Schork NJ, Amos CI, Blangero J. PMID: 10417295.
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    406. Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment. Nat Genet. 1999 Jun; 22(2):168-70. Drazen JM, Yandava CN, Dubé L, Szczerback N, Hippensteel R, Pillari A, Israel E, Schork N, Silverman ES, Katz DA, Drajesk J. PMID: 10369259.
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    407. An extreme-sib-pair genome scan for genes regulating blood pressure. Am J Hum Genet. 1999 Jun; 64(6):1694-701. Xu X, Rogus JJ, Terwedow HA, Yang J, Wang Z, Chen C, Niu T, Wang B, Xu H, Weiss S, Schork NJ, Fang Z. PMID: 10330357.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    408. Blood pressure and the T174M and M235T polymorphisms of the angiotensinogen gene. Ann Epidemiol. 1999 May; 9(4):245-53. Niu T, Chen C, Yang J, Wang B, Wang Z, Schork N, Fang Z, Xu X. PMID: 10332930.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    409. A genome-wide scan for loci linked to forearm bone mineral density. Hum Genet. 1999 Mar; 104(3):226-33. Niu T, Chen C, Cordell H, Yang J, Wang B, Wang Z, Fang Z, Schork NJ, Rosen CJ, Xu X. PMID: 10323246.
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    410. Review of "angiotensin genotype, sodium reduction, weight loss, and prevention of hypertension: trials of hypertension prevention, phase II". Curr Hypertens Rep. 1999 Feb-Mar; 1(1):13-4. Schork NJ. PMID: 10981037.
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    411. Telemetry for cardiovascular monitoring in a pharmacological study: new approaches to data analysis. Hypertension. 1999 Jan; 33(1 Pt 2):248-55. Anderson NH, Devlin AM, Graham D, Morton JJ, Hamilton CA, Reid JL, Schork NJ, Dominiczak AF. PMID: 9931112.
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    412. A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. Proc Natl Acad Sci U S A. 1998 Dec 22; 95(26):15531-6. Ginns EI, St Jean P, Philibert RA, Galdzicka M, Damschroder-Williams P, Thiel B, Long RT, Ingraham LJ, Dalwaldi H, Murray MA, Ehlert M, Paul S, Remortel BG, Patel AP, Anderson MC, Shaio C, Lau E, Dymarskaia I, Martin BM, Stubblefield B, Falls KM, Carulli JP, Keith TP, Fann CS, Lacy LG, Allen CR, Hostetter AM, Elston RC, Schork NJ, Egeland JA, Paul SM. PMID: 9861003.
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    413. Genetic regulation of commitment to interleukin 4 production by a CD4(+) T cell-intrinsic mechanism. J Exp Med. 1998 Dec 21; 188(12):2289-99. Bix M, Wang ZE, Thiel B, Schork NJ, Locksley RM. PMID: 9858515.
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    414. The Polycomb-group gene eed is required for normal morphogenetic movements during gastrulation in the mouse embryo. Development. 1998 Nov; 125(22):4495-506. Faust C, Lawson KA, Schork NJ, Thiel B, Magnuson T. PMID: 9778508.
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    415. Multiple phenotype modeling in gene-mapping studies of quantitative traits: power advantages. Am J Hum Genet. 1998 Oct; 63(4):1190-201. Allison DB, Thiel B, St Jean P, Elston RC, Infante MC, Schork NJ. PMID: 9758596.
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    416. The alpha1 Na,K-ATPase gene is a susceptibility hypertension gene in the Dahl salt-sensitiveHSD rat. J Clin Invest. 1998 Sep 15; 102(6):1102-11. Herrera VL, Xie HX, Lopez LV, Schork NJ, Ruiz-Opazo N. PMID: 9739044.
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    417. Linkage analysis, kinship, and the short-term evolution of chromosomes. J Exp Zool. 1998 Sep-Oct 1; 282(1-2):133-49. Schork NJ, Thiel B, St Jean P. PMID: 9723171.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    418. Issues and strategies in the genetic analysis of alcoholism and related addictive behaviors. Alcohol. 1998 Jul; 16(1):71-83. Schork NJ, Schork CM. PMID: 9650638.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    419. The future of genetic epidemiology. Trends Genet. 1998 Jul; 14(7):266-72. Schork NJ, Cardon LR, Xu X. PMID: 9676528.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    420. Extreme selection strategies in gene mapping studies of oligogenic quantitative traits do not always increase power. Hum Hered. 1998 Mar-Apr; 48(2):97-107. Allison DB, Heo M, Schork NJ, Wong SL, Elston RC. PMID: 9526169.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    421. Genetics of complex disease: approaches, problems, and solutions. Am J Respir Crit Care Med. 1997 Oct; 156(4 Pt 2):S103-9. Schork NJ. PMID: 9351588.
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    422. Selected methodological issues in meiotic mapping of obesity genes in humans: issues of power and efficiency. Behav Genet. 1997 Jul; 27(4):401-21. Allison DB, Schork NJ. PMID: 9519565.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    423. Serial backcross mapping of multiple loci associated with resistance to Leishmania major in mice. Immunity. 1997 May; 6(5):551-7. Beebe AM, Mauze S, Schork NJ, Coffman RL. PMID: 9175833.
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    424. Linking genes and environmental exposure: why China presents special opportunities. Cancer Causes Control. 1997 May; 8(3):518-23. Xu X, Schork NJ. PMID: 9498909.
      View in: PubMed   Mentions:    Fields:    Translation:HumansPHPublic Health
    425. Mapping murine loci for seizure response to kainic acid. Mamm Genome. 1997 Mar; 8(3):200-8. Ferraro TN, Golden GT, Smith GG, Schork NJ, St Jean P, Ballas C, Choi H, Berrettini WH. PMID: 9069121.
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    426. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15. Am J Med Genet. 1997 Feb 11; 68(4):433-40. Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwartz S. PMID: 9021017.
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    427. Ventilation and metabolism among rat strains. J Appl Physiol (1985). 1997 Jan; 82(1):317-23. Strohl KP, Thomas AJ, St Jean P, Schlenker EH, Koletsky RJ, Schork NJ. PMID: 9029232.
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    428. Genetically complex cardiovascular traits. Origins, problems, and potential solutions. Hypertension. 1997 Jan; 29(1 Pt 2):145-9. Schork NJ. PMID: 9039094.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    429. High correlation but lack of agreement between direct high-performance gel chromatography analysis and conventional indirect methods for determining lipoprotein cholesterol. Clin Chem. 1996 Dec; 42(12):1996-2001. Krause BR, Schork NJ, Kieft KA, Smith MP, Maciejko JJ. PMID: 8969639.
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    430. Who's afraid of epistasis? Nat Genet. 1996 Dec; 14(4):371-3. Frankel WN, Schork NJ. PMID: 8944011.
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    431. Extensions to quantitative trait locus mapping in experimental organisms. Hypertension. 1996 Dec; 28(6):1104-11. Schork NJ, Nath SP, Lindpaintner K, Jacob HJ. PMID: 8952606.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimals
    432. Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal. Nat Genet. 1996 Oct; 14(2):206-9. Eicher EM, Washburn LL, Schork NJ, Lee BK, Shown EP, Xu X, Dredge RD, Pringle MJ, Page DC. PMID: 8841197.
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    433. Origins of heterogeneous ovarian carcinomas. A molecular cytogenetic analysis of histologically benign, low malignant potential, and fully malignant components. Am J Pathol. 1996 Aug; 149(2):511-20. Wolf NG, Abdul-Karim FW, Schork NJ, Schwartz S. PMID: 8701990.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    434. Mixture distributions in human genetics research. Stat Methods Med Res. 1996 Jun; 5(2):155-78. Schork NJ, Allison DB, Thiel B. PMID: 8817796.
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    435. Genetic dissection of complex traits. Nat Genet. 1996 Apr; 12(4):355-6; author reply 357-8. Witte JS, Elston RC, Schork NJ. PMID: 8630483.
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    436. Psychological factors affecting self-excoriative behavior in women with mild-to-moderate facial acne vulgaris. Psychosomatics. 1996 Mar-Apr; 37(2):127-30. Gupta MA, Gupta AK, Schork NJ. PMID: 8742540.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    437. Genetic analysis of NIDDM. The study of quantitative traits. Diabetes. 1996 Jan; 45(1):1-14. Ghosh S, Schork NJ. PMID: 8522051.
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    438. The use of genetic information in large-scale clinical trials: applications to Alzheimer research. Alzheimer Dis Assoc Disord. 1996; 10 Suppl 1:22-6. Schork NJ, Weder AB. PMID: 8876785.
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    439. A curly-tail modifier locus, mct1, on mouse chromosome 17. Genomics. 1995 Oct 10; 29(3):719-24. Letts VA, Schork NJ, Copp AJ, Bernfield M, Frankel WN. PMID: 8575765.
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    440. Blood pressure in genetically hypertensive rats. Influence of the Y chromosome. Hypertension. 1995 Sep; 26(3):452-9. Davidson AO, Schork N, Jaques BC, Kelman AW, Sutcliffe RG, Reid JL, Dominiczak AF. PMID: 7649581.
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    441. A biometrical genome search in rats reveals the multigenic basis of blood pressure variation. Genome Res. 1995 Sep; 5(2):164-72. Schork NJ, Krieger JE, Trolliet MR, Franchini KG, Koike G, Krieger EM, Lander ES, Dzau VJ, Jacob HJ. PMID: 9132270.
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    442. The genetics of hypertension. Curr Opin Genet Dev. 1995 Jun; 5(3):362-70. Thibonnier M, Schork NJ. PMID: 7549432.
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    443. Perceived touch deprivation and body image: some observations among eating disordered and non-clinical subjects. J Psychosom Res. 1995 May; 39(4):459-64. Gupta MA, Gupta AK, Schork NJ, Watteel GN. PMID: 7562675.
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    444. Touch deprivation has an adverse effect on body image: some preliminary observations. Int J Eat Disord. 1995 Mar; 17(2):185-9. Gupta MA, Schork NJ. PMID: 7757100.
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    445. Psychosomatic study of self-excoriative behavior among male acne patients: preliminary observations. Int J Dermatol. 1994 Dec; 33(12):846-8. Gupta MA, Gupta AK, Schork NJ. PMID: 7883406.
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    446. Genetic dissection of complex traits. Science. 1994 Sep 30; 265(5181):2037-48. Lander ES, Schork NJ. PMID: 8091226.
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    447. Sampling guidelines for testing secondary attack rates associated with short-latency infectious diseases. Stat Med. 1994 Aug 15; 13(15):1563-73. Schork NJ. PMID: 7973234.
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    448. Adaptation, allometry, and hypertension. Hypertension. 1994 Aug; 24(2):145-56. Weder AB, Schork NJ. PMID: 8039837.
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    449. Sex-specific determinants of increased left ventricular mass in the Tecumseh Blood Pressure Study. Circulation. 1994 Aug; 90(2):928-36. Marcus R, Krause L, Weder AB, Dominguez-Meja A, Schork NJ, Julius S. PMID: 8044964.
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    450. Psychosocial correlates of the treatment of photodamaged skin with topical retinoic acid: a prospective controlled study. J Am Acad Dermatol. 1994 Jun; 30(6):969-72. Gupta MA, Schork NJ, Ellis CN. PMID: 8188889.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCTClinical Trials
    451. Recreational exercise and cardiovascular status in the rural community of Tecumseh, Michigan. Blood Press. 1994 May; 3(3):178-84. Gudbrandsson T, Julius S, Jamerson K, Smith S, Krause L, Schork N. PMID: 8069406.
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    452. Hematocrit levels and physiologic factors in relationship to cardiovascular risk in Tecumseh, Michigan. J Hypertens. 1994 Apr; 12(4):455-62. Smith S, Julius S, Jamerson K, Amerena J, Schork N. PMID: 8064170.
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    453. Relationship of growth and blood pressure in inbred rats. Am J Physiol. 1994 Mar; 266(3 Pt 2):R702-8. Schork NJ, Jokelainen P, Grant EJ, Schork MA, Weder AB. PMID: 8160862.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    454. The contribution of pleiotropy to blood pressure and body-mass index variation: the Gubbio Study. Am J Hum Genet. 1994 Feb; 54(2):361-73. Schork NJ, Weder AB, Trevisan M, Laurenzi M. PMID: 8304351.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    455. Depression modulates pruritus perception: a study of pruritus in psoriasis, atopic dermatitis, and chronic idiopathic urticaria. Psychosom Med. 1994 Jan-Feb; 56(1):36-40. Gupta MA, Gupta AK, Schork NJ, Ellis CN. PMID: 8197313.
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    456. Aging-related concerns and body image: possible future implications for eating disorders. Int J Eat Disord. 1993 Dec; 14(4):481-6. Gupta MA, Schork NJ. PMID: 8293030.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    457. Extended multipoint identity-by-descent analysis of human quantitative traits: efficiency, power, and modeling considerations. Am J Hum Genet. 1993 Dec; 53(6):1306-19. Schork NJ. PMID: 8250047.
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    458. Pedigree models for complex human traits involving the mitochondrial genome. Am J Hum Genet. 1993 Dec; 53(6):1320-37. Schork NJ, Guo SW. PMID: 8250048.
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    459. Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. Am J Hum Genet. 1993 Nov; 53(5):1127-36. Schork NJ, Boehnke M, Terwilliger JD, Ott J. PMID: 8213836.
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    460. Alcohol intake and treatment responsiveness of psoriasis: a prospective study. J Am Acad Dermatol. 1993 May; 28(5 Pt 1):730-2. Gupta MA, Schork NJ, Gupta AK, Ellis CN. PMID: 8496416.
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    461. Analysis of coronary angioplasty practice in the United States with an insurance-claims data base. Circulation. 1993 May; 87(5):1489-97. Topol EJ, Ellis SG, Cosgrove DM, Bates ER, Muller DW, Schork NJ, Schork MA, Loop FD. PMID: 8141866.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    462. Suicidal ideation in psoriasis. Int J Dermatol. 1993 Mar; 32(3):188-90. Gupta MA, Schork NJ, Gupta AK, Kirkby S, Ellis CN. PMID: 8444530.
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    463. Stature, drive for thinness and body dissatisfaction: a study of males and females from a non clinical sample. Can J Psychiatry. 1993 Feb; 38(1):59-61. Gupta MA, Schork NJ, Dhaliwal JS. PMID: 8448724.
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    464. Effects of fluoxetine on the oral environment of bulimics. Oral Microbiol Immunol. 1993 Feb; 8(1):62-4. Bretz WA, Krahn DD, Drury M, Schork N, Loesche WJ. PMID: 8510986.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCellsCTClinical Trials
    465. The relative efficiency and power of small-pedigree studies of the heritability of a quantitative trait. Hum Hered. 1993 Jan-Feb; 43(1):1-11. Schork NJ, Schork MA. PMID: 8514319.
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    466. The use of a rapid enzymatic assay in the field for the detection of infections associated with adult periodontitis. J Public Health Dent. 1993; 53(4):235-40. Bretz WA, Eklund SA, Radicchi R, Schork MA, Schork N, Schottenfeld D, Lopatin DE, Loesche WJ. PMID: 8258786.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCellsPHPublic Health
    467. Effect of home blood pressure and gender on estimates of the familial aggregation of blood pressure. The Tecumseh Blood Pressure Study. Hypertension. 1992 Sep; 20(3):314-8. Jamerson KA, Schork N, Julius S. PMID: 1516950.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    468. Correlates of the estimated arterial compliance in the population of Tecumseh, Michigan. Blood Press. 1992 May; 1(1):27-34. Gudbrandsson T, Julius S, Krause L, Jamerson K, Randall OS, Schork N, Weder A. PMID: 1345140.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans