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Nicholas Schork

Title(s)Adjunct Professor, Family Medicine and Public Health
SchoolVc-health Sciences-schools
Address9500 Gilman Drive #
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 UH2AG064706Sep 15, 2019 - Aug 31, 2021
    Role: Principal Investigator
    Integrative Resource to Develop Translational Strategies to Promote Longevity
    NIH U24AG051129Sep 15, 2015 - May 31, 2020
    Role: Principal Investigator
    The Bipolar Genome Study
    NIH R01MH094483Jul 1, 2012 - Apr 30, 2016
    Role: Principal Investigator
    Functional genomic tools for in vivo study of P. vivax
    NIH R21AI085374Jun 15, 2010 - Nov 30, 2012
    Role: Principal Investigator
    Biomarkers of Autism at 12 months: From Brain Overgrowth to Genes
    NIH P50MH081755Aug 6, 2007 - Jul 31, 2012
    Role: Co-Investigator
    Longevity Consortium
    NIH U19AG023122Sep 30, 2004 - Oct 31, 2017
    Role: Co-Principal Investigator
    Genomics for Transplantation: Discovery and Biomarkers
    NIH U19AI063603Sep 1, 2004 - Aug 31, 2016
    Role: Co-Investigator
    FAMILY BLOOD PRESSURE PROGRAM
    NIH 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. signatureSearch: environment for gene expression signature searching and functional interpretation. Nucleic Acids Res. 2020 12 02; 48(21):e124. Duan Y, Evans DS, Miller RA, Schork NJ, Cummings SR, Girke T. PMID: 33068417.
      View in: PubMed   Mentions:    Fields:    
    2. Conserved Genomic Terminals of SARS-CoV-2 as Coevolving Functional Elements and Potential Therapeutic Targets. mSphere. 2020 11 25; 5(6). PMID: 33239366.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    3. Impacts of personal DNA ancestry testing. J Community Genet. 2020 Aug 13. Rubanovich CK, Taitingfong R, Triplett C, Libiger O, Schork NJ, Wagner JK, Bloss CS. PMID: 32789669.
      View in: PubMed   Mentions:
    4. A 25-y longitudinal dolphin cohort supports that long-lived individuals in same environment exhibit variation in aging rates. Proc Natl Acad Sci U S A. 2020 08 25; 117(34):20950-20958. Venn-Watson S, Jensen ED, Schork NJ. PMID: 32778591.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    5. Strategies for Testing Intervention Matching Schemes in Cancer. Clin Pharmacol Ther. 2020 Sep; 108(3):542-552. Schork NJ, Goetz LH, Lowey J, Trent J. PMID: 32535886.
      View in: PubMed   Mentions:    Fields:    
    6. Conserved Genomic Terminals of SARS-CoV-2 as Co-evolving Functional Elements and Potential Therapeutic Targets. bioRxiv. 2020 Jul 06. Chan AP, Choi Y, Schork NJ. PMID: 32676601.
      View in: PubMed   Mentions:
    7. 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: 1     Fields:    Translation:HumansAnimalsCells
    8. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addict Biol. 2021 Jan; 26(1):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: 2     Fields:    
    9. 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: 7     Fields:    Translation:HumansAnimals
    10. 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 11 13; 74(Suppl_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: 2     Fields:    Translation:Humans
    11. Genetic Support for Longevity-Enhancing Drug Targets: Issues, Preliminary Data, and Future Directions. J Gerontol A Biol Sci Med Sci. 2019 11 13; 74(Suppl_1):S61-S71. McCorrison J, Girke T, Goetz LH, Miller RA, Schork NJ. PMID: 31724058.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    12. 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: 7     Fields:    
    13. 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.
      View in: PubMed   Mentions:
    14. 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: 46     Fields:    Translation:Humans
    15. 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:
    16. 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
    17. 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:
    18. 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: 103     Fields:    Translation:Humans
    19. 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: 3     Fields:    Translation:Humans
    20. 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: 4     Fields:    Translation:HumansAnimalsCells
    21. 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
    22. Artificial Intelligence and Personalized Medicine. Cancer Treat Res. 2019; 178:265-283. Schork NJ. PMID: 31209850.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    23. 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: 29     Fields:    Translation:AnimalsCells
    24. 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: 1     Fields:    Translation:Humans
    25. 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:
    26. 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: 3     Fields:    Translation:Humans
    27. 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.
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    28. 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.
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    29. 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.
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    30. Genetic risks and clinical rewards. Nat Genet. 2018 09; 50(9):1210-1211. Schork AJ, Schork MA, Schork NJ. PMID: 30158681.
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    31. 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.
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    32. 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.
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    33. Personalized medicine: motivation, challenges, and progress. Fertil Steril. 2018 06; 109(6):952-963. Goetz LH, Schork NJ. PMID: 29935653.
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    34. 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.
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    35. 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.
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    36. The big data revolution and human genetics. Hum Mol Genet. 2018 05 01; 27(R1):R1. Schork NJ. PMID: 29672687.
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    37. Randomized clinical trials and personalized medicine: A commentary on deaton and cartwright. Soc Sci Med. 2018 08; 210:71-73. Schork NJ. PMID: 29786513.
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    38. 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.
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    39. 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.
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    40. 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.
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    41. 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.
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    42. 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.
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    43. 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.
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    44. Precision medicine for suicidality: from universality to subtypes and personalization. Mol Psychiatry. 2017 09; 22(9):1250-1273. PMID: 28809398.
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    45. Integrated Genomic Medicine: A Paradigm for Rare Diseases and Beyond. Adv Genet. 2017; 97:81-113. Schork NJ, Nazor K. PMID: 28838357.
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    46. Single-Subject Studies in Translational Nutrition Research. Annu Rev Nutr. 2017 08 21; 37:395-422. Schork NJ, Goetz LH. PMID: 28715990.
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    47. Nonalcoholic fatty liver disease with cirrhosis increases familial risk for advanced fibrosis. J Clin Invest. 2017 Jun 30; 127(7):2697-2704. PMID: 28628033.
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    48. Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls. BMC Genomics. 2017 06 12; 18(1):458. PMID: 28606096.
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    49. 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.
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    50. 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. PMID: 28467925.
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    51. 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. PMID: 28447399.
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    52. Analysis of variability in high throughput screening data: applications to melanoma cell lines and drug responses. Oncotarget. 2017 Apr 25; 8(17):27786-27799. PMID: 28212541.
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    53. 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.
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    54. Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population. . 2017 Jun; 174(4):435-450. Peng Q, Schork NJ, Wilhelmsen KC, Ehlers CL. PMID: 28436151.
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    55. Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites. Nat Genet. 2017 Apr; 49(4):568-578. PMID: 28263315.
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    56. Genome-wide association study of paliperidone efficacy. Pharmacogenet Genomics. 2017 01; 27(1):7-18. PMID: 27846195.
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    57. 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. PMID: 27897007.
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    58. Identification of novel loci affecting circulating chromogranins and related peptides. Hum Mol Genet. 2017 01 01; 26(1):233-242. PMID: 28011710.
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    59. 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.
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    60. Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population. J Psychiatry Neurosci. 2016 10; 41(6):413-421. PMID: 27091718.
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    61. 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. PMID: 27577874.
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    62. Conservation of Distinct Genetically-Mediated Human Cortical Pattern. PLoS Genet. 2016 07; 12(7):e1006143. PMID: 27459196.
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    63. Shared genetic effects between hepatic steatosis and fibrosis: A prospective twin study. Hepatology. 2016 11; 64(5):1547-1558. PMID: 27315352.
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    64. 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. PMID: 27439388.
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    65. Epigenomic Diversity in a Global Collection of Arabidopsis thaliana Accessions. Cell. 2016 Jul 14; 166(2):492-505. PMID: 27419873.
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    66. 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. PMID: 27402763.
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    67. 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. PMID: 27329760.
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    68. 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. PMID: 27167163.
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    69. Towards understanding and predicting suicidality in women: biomarkers and clinical risk assessment. Mol Psychiatry. 2016 06; 21(6):768-85. PMID: 27046645.
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    70. 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. PMID: 25953057.
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    71. Whole-genome mutational burden analysis of three pluripotency induction methods. Nat Commun. 2016 Feb 19; 7:10536. PMID: 26892726.
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    72. Using single nuclei for RNA-seq to capture the transcriptome of postmortem neurons. Nat Protoc. 2016 Mar; 11(3):499-524. PMID: 26890679.
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    73. 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.
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    74. 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. PMID: 26731281.
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    75. Partial Least Squares Regression Can Aid in Detecting Differential Abundance of Multiple Features in Sets of Metagenomic Samples. Front Genet. 2015; 6:350. PMID: 26734061.
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    76. 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. PMID: 26608796.
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    77. Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies. PLoS One. 2015; 10(10):e0139355. PMID: 26436424.
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    78. Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies. BMC Bioinformatics. 2015 Sep 22; 16:304. PMID: 26395405.
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    79. 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. PMID: 26328603.
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    80. Heritability of Hepatic Fibrosis and Steatosis Based on a Prospective Twin Study. Gastroenterology. 2015 Dec; 149(7):1784-93. PMID: 26299412.
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    81. Understanding and predicting suicidality using a combined genomic and clinical risk assessment approach. Mol Psychiatry. 2015 Nov; 20(11):1266-85. PMID: 26283638.
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    82. Large-scale genomics unveil polygenic architecture of human cortical surface area. Nat Commun. 2015 Jul 20; 6:7549. PMID: 26189703.
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    83. Anxiety is related to indices of cortical maturation in typically developing children and adolescents. Brain Struct Funct. 2016 07; 221(6):3013-25. PMID: 26183468.
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    84. Modeling the 3D geometry of the cortical surface with genetic ancestry. Curr Biol. 2015 Aug 03; 25(15):1988-92. PMID: 26166778.
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    85. 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. PMID: 25933357.
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    86. The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. Neuroimage. 2016 Jan 01; 124(Pt B):1149-1154. PMID: 25937488.
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    87. Personalized medicine: Time for one-person trials. Nature. 2015 Apr 30; 520(7549):609-11. PMID: 25925459.
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    88. Dysregulation of soluble epoxide hydrolase and lipidomic profiles in anorexia nervosa. Mol Psychiatry. 2016 Apr; 21(4):537-46. PMID: 25824304.
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    89. Family income, parental education and brain structure in children and adolescents. Nat Neurosci. 2015 May; 18(5):773-8. PMID: 25821911.
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    90. A genome sequencing program for novel undiagnosed diseases. Genet Med. 2015 Dec; 17(12):995-1001. PMID: 25790160.
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    91. Scripps Genome ADVISER: Annotation and Distributed Variant Interpretation SERver. PLoS One. 2015; 10(2):e0116815. PMID: 25706643.
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    92. 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. PMID: 25730879.
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    93. DCAF4, a novel gene associated with leucocyte telomere length. J Med Genet. 2015 Mar; 52(3):157-62. PMID: 25624462.
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    94. Gene expression analysis of head and neck squamous cell carcinoma survival and recurrence. Oncotarget. 2015 Jan 01; 6(1):547-55. PMID: 25575813.
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    95. Protective variant associated with alcohol dependence in a Mexican American cohort. BMC Med Genet. 2014 Dec 21; 15:136. PMID: 25527893.
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    96. 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. PMID: 25392232.
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    97. 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. PMID: 25456346.
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    98. Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample. . 2014 Dec; 165B(8):673-83. PMID: 25270064.
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    99. Functional expression of dental plaque microbiota. Front Cell Infect Microbiol. 2014; 4:108. PMID: 25177549.
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    100. Characterization of genetic variation in the VGLL4 gene in anorexia nervosa. Psychiatr Genet. 2014 Aug; 24(4):183-4. PMID: 24983835.
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    101. Admixture and clinical phenotypic variation. Hum Hered. 2014; 77(1-4):73-86. PMID: 25060271.
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    102. Influence of individual differences in disease perception on consumer response to direct-to-consumer genomic testing. Clin Genet. 2015 Mar; 87(3):225-32. PMID: 24798746.
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    103. 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. PMID: 24901334.
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    104. Genetic risk prediction and neurobiological understanding of alcoholism. Transl Psychiatry. 2014 May 20; 4:e391. PMID: 24844177.
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    105. Mechanisms of linezolid resistance among coagulase-negative staphylococci determined by whole-genome sequencing. mBio. 2014 May 13; 5(3):e00894-14. PMID: 24915435.
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    106. 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. PMID: 24802266.
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    107. 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. PMID: 24791650.
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    108. Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia. Ann Neurol. 2014 Apr; 75(4):542-9. PMID: 24700542.
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    214. Catapulting clopidogrel pharmacogenomics forward. Nat Med. 2011 Jan; 17(1):40-1. Topol EJ, Schork NJ. PMID: 21217678.
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    215. 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: 53     Fields:    Translation:Humans
    216. 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: 6     Fields:    Translation:HumansPHPublic Health
    217. The VA Hypertension Primary Care Longitudinal Cohort: Electronic medical records in the post-genomic era. Health Informatics J. 2010 Dec; 16(4):274-86. PMID: 21216807.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    218. 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.
      View in: PubMed   Mentions: 194     Fields:    Translation:Humans
    219. 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: 46     Fields:    Translation:HumansCells
    220. 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: 69     Fields:    Translation:Humans
    221. 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
    222. 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: 51     Fields:    
    223. 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: 236     Fields:    Translation:Humans
    224. 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: 64     Fields:    Translation:HumansCTClinical Trials
    225. 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
    226. 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: 66     Fields:    Translation:Humans
    227. 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: 10     Fields:    Translation:Humans
    228. 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: 58     Fields:    Translation:Humans
    229. 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: 10     Fields:    Translation:HumansCells
    230. Association study of 182 candidate genes in anorexia nervosa. . 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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    231. 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.
      View in: PubMed   Mentions: 45     Fields:    Translation:Humans
    232. 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
    233. 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
    234. 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: 5     Fields:    Translation:Animals
    235. 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
    236. 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
    237. 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.
      View in: PubMed   Mentions: 124     Fields:    Translation:HumansCells
    238. 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.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    239. 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
    240. 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: 21     Fields:    Translation:Humans
    241. 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.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    242. 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: 187     Fields:    Translation:Humans
    243. 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: 61     Fields:    Translation:Humans
    244. 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
    245. 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.
      View in: PubMed   Mentions: 55     Fields:    Translation:HumansCells
    246. Suggestive evidence for linkage of ADHD features in bipolar disorder to chromosome 10p14. . 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.
      View in: PubMed   Mentions:
    247. 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: 20     Fields:    Translation:Humans
    248. 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: 105     Fields:    Translation:HumansAnimals
    249. 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
    250. 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: 64     Fields:    Translation:Humans
    251. 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
    252. 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: 34     Fields:    Translation:HumansCells
    253. 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: 7     Fields:    Translation:Humans
    254. 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.
      View in: PubMed   Mentions: 60     Fields:    Translation:Humans
    255. 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
    256. 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: 8     Fields:    Translation:Humans
    257. 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: 51     Fields:    Translation:HumansCells
    258. 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
    259. 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.
      View in: PubMed   Mentions: 162     Fields:    Translation:Humans
    260. 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.
      View in: PubMed   Mentions: 154     Fields:    Translation:HumansCells
    261. 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: 258     Fields:    Translation:HumansCells
    262. 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.
      View in: PubMed   Mentions: 381     Fields:    Translation:HumansCells
    263. 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.
      View in: PubMed   Mentions: 249     Fields:    Translation:HumansCells
    264. Convergent functional genomics of genome-wide association data for bipolar disorder: comprehensive identification of candidate genes, pathways and mechanisms. . 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.
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    265. 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
    266. 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
    267. 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: 111     Fields:    Translation:Humans
    268. 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
    269. 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: 34     Fields:    Translation:Humans
    270. 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
    271. 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.
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    272. Cancer driver mutations in protein kinase genes. Cancer Lett. 2009 Aug 28; 281(2):117-27. Torkamani A, Verkhivker G, Schork NJ. PMID: 19081671.
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    273. 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.
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    274. 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.
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    275. 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.
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    276. 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.
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    277. 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.
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    278. Evidence for a heritable unidimensional symptom factor underlying obsessionality. . 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.
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    279. 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.
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    280. 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.
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    281. 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.
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    282. 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.
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    283. 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.
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    284. Predicting functional regulatory polymorphisms. Bioinformatics. 2008 Aug 15; 24(16):1787-92. Torkamani A, Schork NJ. PMID: 18562267.
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    285. 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.
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    286. 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.
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    287. 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.
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    288. Suggestive linkage of a chromosomal locus on 18p11 to cyclothymic temperament in bipolar disorder families. . 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.
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    289. Prediction of cancer driver mutations in protein kinases. Cancer Res. 2008 Mar 15; 68(6):1675-82. Torkamani A, Schork NJ. PMID: 18339846.
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    290. 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.
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    291. 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.
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    292. 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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    293. 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.
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    294. 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.
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    295. DNA sequence-based phenotypic association analysis. Adv Genet. 2008; 60:195-217. Schork NJ, Wessel J, Malo N. PMID: 18358322.
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    296. Methods for handling multiple testing. Adv Genet. 2008; 60:293-308. Rice TK, Schork NJ, Rao DC. PMID: 18358325.
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    297. 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.
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    298. 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.
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    299. 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.
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    300. 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.
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    301. 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.
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    302. 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.
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    303. Accurate prediction of deleterious protein kinase polymorphisms. Bioinformatics. 2007 Nov 01; 23(21):2918-25. Torkamani A, Schork NJ. PMID: 17855419.
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    304. 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.
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    305. 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.
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    306. 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.
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    307. 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.
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    308. 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.
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    309. 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.
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    310. 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.
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    311. 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.
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    312. Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family. Genomics. 2007 Jul; 90(1):49-58. Torkamani A, Schork NJ. PMID: 17498919.
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    313. Accommodating pathway information in expression quantitative trait locus analysis. Genomics. 2007 Jul; 90(1):132-42. Wessel J, Zapala MA, Schork NJ. PMID: 17493783.
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    314. Endophenotyping schizophrenia. Am J Psychiatry. 2007 May; 164(5):705-7. Braff D, Schork NJ, Gottesman II. PMID: 17475726.
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    315. 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.
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    316. 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.
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    317. 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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    318. 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.
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    319. 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.
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    320. 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.
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    321. 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.
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    322. 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.
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    323. Heritability and clinical features of multigenerational families with obsessive-compulsive disorder and hoarding. . 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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    324. Generalized analysis of molecular variance. PLoS Genet. 2007 Apr 06; 3(4):e51. Nievergelt CM, Libiger O, Schork NJ. PMID: 17411342.
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    325. 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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    326. 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.
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    327. 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.
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    328. 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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    329. 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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    330. 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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    331. 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.
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    332. 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.
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    333. 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.
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    334. 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.
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    335. 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.
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    336. PhenoChipping of psychotic disorders: a novel approach for deconstructing and quantitating psychiatric phenotypes. . 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.
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    337. 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.
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    338. 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: 50     Fields:    Translation:Humans
    339. 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: 63     Fields:    Translation:Humans
    340. 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
    341. Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder. . 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:
    342. 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: 38     Fields:    Translation:HumansCells
    343. 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
    344. 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
    345. 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
    346. 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
    347. 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: 32     Fields:    Translation:HumansPHPublic Health
    348. 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: 46     Fields:    Translation:Humans
    349. 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: 187     Fields:    Translation:Humans
    350. 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
    351. 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
    352. 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
    353. 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: 18     Fields:    Translation:Humans
    354. 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: 9     Fields:    Translation:Humans
    355. 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: 18     Fields:    Translation:HumansAnimals
    356. 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
    357. 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: 27     Fields:    Translation:HumansCells
    358. 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
    359. 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: 77     Fields:    Translation:Humans
    360. 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: 31     Fields:    Translation:Humans
    361. 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: 24     Fields:    Translation:HumansCells
    362. 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: 32     Fields:    Translation:HumansCells
    363. 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: 172     Fields:    Translation:HumansCells
    364. 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: 79     Fields:    Translation:HumansAnimals
    365. 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: 39     Fields:    Translation:HumansCells
    366. 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
    367. 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: 12     Fields:    Translation:Humans
    368. 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
    369. 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
    370. 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: 17     Fields:    Translation:AnimalsCells
    371. 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
    372. 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: 12     Fields:    Translation:HumansCells
    373. 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
    374. 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
    375. 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: 13     Fields:    Translation:Animals
    376. 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: 59     Fields:    Translation:AnimalsCells
    377. Evidence of a contribution of genetic factors to dental caries risk. J Evid Based Dent Pract. 2003 Dec; 3(4):185-189. PMID: 22287938.
      View in: PubMed   Mentions: 3     Fields:    
    378. 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
    379. 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
    380. 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
    381. 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: 250     Fields:    Translation:HumansAnimalsCells
    382. 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
    383. 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
    384. 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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    385. 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: 18     Fields:    Translation:Humans
    386. 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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    387. 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
    388. 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
    389. 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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    390. 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.
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    391. Two-trait-locus linkage analyses of asthma susceptibility. Genet Epidemiol. 2001; 21 Suppl 1:S278-83. Nath SK, Chen CH, Schork NJ. PMID: 11793682.
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    392. 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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    393. Genome partitioning and whole-genome analysis. Adv Genet. 2001; 42:299-322. Schork NJ. PMID: 11037329.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimals
    394. 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.
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    395. 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.
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    396. 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: 23     Fields:    Translation:HumansCells
    397. 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
    398. 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: 38     Fields:    Translation:Humans
    399. 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.
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    400. 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.
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    401. 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: 110     Fields:    Translation:HumansCells
    402. 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
    403. 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.
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    404. 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
    405. 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: 17     Fields:    Translation:Animals
    406. 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: 12     Fields:    Translation:Humans
    407. 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: 30     Fields:    Translation:Humans
    408. 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
    409. 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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    410. 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.
      View in: PubMed   Mentions: 56     Fields:    Translation:Animals
    411. 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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    412. 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.
      View in: PubMed   Mentions: 106     Fields:    Translation:HumansCellsCTClinical Trials
    413. 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.
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    414. 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
    415. 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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    416. 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.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    417. 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.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    418. 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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    419. 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.
      View in: PubMed   Mentions: 35     Fields:    Translation:AnimalsCells
    420. 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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    421. 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.
      View in: PubMed   Mentions: 65     Fields:    Translation:Humans
    422. 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.
      View in: PubMed   Mentions: 12     Fields:    Translation:Animals
    423. 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
    424. 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
    425. 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
    426. 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: 22     Fields:    Translation:Humans
    427. 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.
      View in: PubMed   Mentions: 43     Fields:    Translation:Humans
    428. 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
    429. 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.
      View in: PubMed   Mentions: 26     Fields:    Translation:Animals
    430. 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
    431. 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.
      View in: PubMed   Mentions: 23     Fields:    Translation:Animals
    432. 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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    433. 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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    434. 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: 5     Fields:    Translation:Humans
    435. Who's afraid of epistasis? Nat Genet. 1996 Dec; 14(4):371-3. Frankel WN, Schork NJ. PMID: 8944011.
      View in: PubMed   Mentions: 81     Fields:    Translation:Animals
    436. 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
    437. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    438. 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.
      View in: PubMed   Mentions: 30     Fields:    Translation:AnimalsCells
    439. 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
    440. Mixture distributions in human genetics research. Stat Methods Med Res. 1996 Jun; 5(2):155-78. Schork NJ, Allison DB, Thiel B. PMID: 8817796.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    441. 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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    442. 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
    443. Genetic analysis of NIDDM. The study of quantitative traits. Diabetes. 1996 Jan; 45(1):1-14. Ghosh S, Schork NJ. PMID: 8522051.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    444. 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.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    445. 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.
      View in: PubMed   Mentions: 10     Fields:    Translation:Animals
    446. 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.
      View in: PubMed   Mentions: 20     Fields:    Translation:Animals
    447. 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.
      View in: PubMed   Mentions: 18     Fields:    Translation:AnimalsCells
    448. The genetics of hypertension. Curr Opin Genet Dev. 1995 Jun; 5(3):362-70. Thibonnier M, Schork NJ. PMID: 7549432.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimals
    449. 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.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    450. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    451. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    452. Genetic dissection of complex traits. Science. 1994 Sep 30; 265(5181):2037-48. Lander ES, Schork NJ. PMID: 8091226.
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    453. 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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    454. Adaptation, allometry, and hypertension. Hypertension. 1994 Aug; 24(2):145-56. Weder AB, Schork NJ. PMID: 8039837.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimals
    455. 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.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    456. 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
    457. 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.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    458. 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.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    459. 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
    460. 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
    461. 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.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    462. 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.
      View in: PubMed   Mentions: 41     Fields:    Translation:Humans
    463. 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.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    464. 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
    465. 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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    466. 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.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    467. 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: 18     Fields:    Translation:Humans
    468. 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.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    469. 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.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    470. 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
    471. 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.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    472. 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
    473. 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
    474. 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
    475. White coat hypertension: a follow-up. Clin Exp Hypertens A. 1992; 14(1-2):45-53. Julius S, Jamerson K, Gudbrandsson T, Schork N. PMID: 1541046.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    476. Extended pedigree patterned covariance matrix mixed models for quantitative phenotype analysis. Genet Epidemiol. 1992; 9(2):73-86. Schork NJ. PMID: 1639246.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    477. Detection of genetic heterogeneity for complex quantitative phenotypes. Genet Epidemiol. 1992; 9(3):207-23. Schork NJ. PMID: 1521782.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    478. Linkage of MN locus and erythrocyte lithium-sodium countertransport in Tecumseh, Michigan. Hypertension. 1991 Jun; 17(6 Pt 2):977-81. Weder AB, Schork NJ, Julius S. PMID: 2045179.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    479. Red blood cell lithium-sodium countertransport in the tecumseh blood pressure study. Hypertension. 1991 May; 17(5):652-60. Weder AB, Schork NJ, Krause L, Julius S. PMID: 2022408.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    480. Treatment of mildly to moderately photoaged skin with topical tretinoin has a favorable psychosocial effect: a prospective study. J Am Acad Dermatol. 1991 May; 24(5 Pt 1):780-1. Gupta MA, Goldfarb MT, Schork NJ, Weiss JS, Gupta AK, Ellis CN, Voorhees JJ. PMID: 1869652.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCTClinical Trials
    481. Independence of pressure reactivity from pressure levels in Tecumseh, Michigan. Hypertension. 1991 Apr; 17(4 Suppl):III12-21. Julius S, Jones K, Schork N, Johnson E, Krause L, Nazzaro P, Zemva A. PMID: 2013488.
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    482. Efficient computation of patterned covariance matrix mixed models in quantitative segregation analysis. Genet Epidemiol. 1991; 8(1):29-46. Schork N. PMID: 2060770.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    483. Hyperkinetic borderline hypertension in Tecumseh, Michigan. J Hypertens. 1991 Jan; 9(1):77-84. Julius S, Krause L, Schork NJ, Mejia AD, Jones KA, van de Ven C, Johnson EH, Sekkarie MA, Kjeldsen SE, Petrin J. PMID: 1848264.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansPHPublic Health
    484. Psychiatric aspects of the treatment of mild to moderate facial acne. Some preliminary observations. Int J Dermatol. 1990 Dec; 29(10):719-21. Gupta MA, Gupta AK, Schork NJ, Ellis CN, Voorhees JJ. PMID: 2148562.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    485. "White coat" versus "sustained" borderline hypertension in Tecumseh, Michigan. Hypertension. 1990 Dec; 16(6):617-23. Julius S, Mejia A, Jones K, Krause L, Schork N, van de Ven C, Johnson E, Petrin J, Sekkarie MA, Kjeldsen SE. PMID: 2246029.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    486. The aging face: a psychocutaneous perspective. J Dermatol Surg Oncol. 1990 Oct; 16(10):902-4. Gupta MA, Gupta AK, Schork NJ, Ellis CN, Voorhees JJ. PMID: 2229631.
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    487. The association of borderline hypertension with target organ changes and higher coronary risk. Tecumseh Blood Pressure study. JAMA. 1990 Jul 18; 264(3):354-8. Julius S, Jamerson K, Mejia A, Krause L, Schork N, Jones K. PMID: 2362331.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    488. The Tecumseh Blood Pressure Study. Normative data on blood pressure self-determination. Arch Intern Med. 1990 Jun; 150(6):1209-13. Mejia AD, Julius S, Jones KA, Schork NJ, Kneisley J. PMID: 2353854.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    489. Disease entities, mixed multi-normal distributions, and the role of the hyperkinetic state in the pathogenesis of hypertension. Stat Med. 1990 Mar; 9(3):301-14. Schork NJ, Weder AB, Schork MA, Bassett DR, Julius S. PMID: 2343223.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    490. Artefacts in measurement of blood pressure and lack of target organ involvement in the assessment of patients with treatment-resistant hypertension. Ann Intern Med. 1990 Feb 15; 112(4):270-7. Mejia AD, Egan BM, Schork NJ, Zweifler AJ. PMID: 2297205.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    491. Histograms: multimodal or poorly constructed? Am J Hum Genet. 1990 Feb; 46(2):396-7. Schork NJ, Schork MA. PMID: 2301406.
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    492. Predictors of blood pressure and hypertension in Tecumseh, Michigan. Clin Exp Hypertens A. 1990; 12(5):693-708. Kneisley J, Schork N, Julius S. PMID: 2208743.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    493. On the asymmetry of biological frequency distributions. Genet Epidemiol. 1990; 7(6):427-46. Schork NJ, Weder AB, Schork MA. PMID: 2292368.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    494. Testing separate families of segregation hypotheses: bootstrap methods. Am J Hum Genet. 1989 Nov; 45(5):803-13. Schork N, Schork MA. PMID: 2816944.
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    495. Arterial plasma norepinephrine correlates to blood pressure in middle-aged men with sustained essential hypertension. Am Heart J. 1989 Oct; 118(4):775-81. Kjeldsen SE, Schork NJ, Leren P, Eide IK. PMID: 2801485.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans