Xiaoxu Yang

Title(s)Assistant Project Scientist, Neurosciences
SchoolVc-health Sciences-schools
Address9500 Gilman Drive #
La Jolla CA 92093
ORCID ORCID Icon0000-0003-0219-0023 Additional info
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    Collapse Biography 
    Collapse Education and Training
    University of California, San Diego, La Jolla, CA, USAPostdoc08/2023Neurosciences
    Peking University, Beijing, PRCPhD07/2018Bioinformatics
    Beijing Normal University, Beijing, PRCBS07/2013Bioscience
    Collapse Awards and Honors
    NIH/NICHD2023  - 2028Pathway to Independence Award
    Peking University2018  - 2018Outstanding Graduate
    Peking University2013  - 2017The President's Scholarship
    Beijing Normal University2013  - 2013Outstanding Graduate
    Ministry of Education, China2011  - 2011National Scholarship
    Beijing Normal University2010  - 2012First Prize Scholarship

    Collapse Overview 
    Collapse In The News

    Collapse Research 
    Collapse Research Activities and Funding
    Mechanisms controlling HIV latency and pathogenesis in microglia
    NIH/NIMH R21MH134401Aug 14, 2023 - Aug 13, 2025
    Role: Principal Investigator
    Understanding genomic stability betweengenerations by assessing mutational burdens in single sperms
    NIH/NICHD K99HD111686Jul 15, 2023 - Jun 30, 2028
    Role: Principal Investigator

    Collapse ORNG Applications 
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    Collapse Twitter
    Collapse Featured Videos

    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. Mapping recurrent mosaic copy number variation in human neurons. Nat Commun. 2024 May 17; 15(1):4220. Sun C, Kathuria K, Emery SB, Kim B, Burbulis IE, Shin JH, Brain Somatic Mosaicism Network, Weinberger DR, Moran JV, Kidd JM, Mills RE, McConnell MJ. PMID: 38760338.
      View in: PubMed   Mentions:
    2. Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain. Nature. 2024 Apr 10. Chung C, Yang X, Hevner RF, Kennedy K, Vong KI, Liu Y, Patel A, Nedunuri R, Barton ST, Noel G, Barrows C, Stanley V, Mittal S, Breuss MW, Schlachetzki JCM, Kingsmore SF, Gleeson JG. PMID: 38600385.
      View in: PubMed   Mentions:
    3. Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases. Sci Data. 2023 11 20; 10(1):813. Garrison MA, Jang Y, Bae T, Cherskov A, Emery SB, Fasching L, Jones A, Moldovan JB, Molitor C, Pochareddy S, Peters MA, Shin JH, Wang Y, Yang X, Akbarian S, Chess A, Gage FH, Gleeson JG, Kidd JM, McConnell M, Mills RE, Moran JV, Park PJ, Sestan N, Urban AE, Vaccarino FM, Walsh CA, Weinberger DR, Wheelan SJ, Abyzov A, BSMN Consortium. PMID: 37985666; PMCID: PMC10662356.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    4. Post-zygotic brain mosaicism as a result of partial reversion of pre-zygotic aneuploidy. Nat Genet. 2023 Nov; 55(11):1784-1785. Chung C, Yang X, Gleeson JG. PMID: 37872451; PMCID: PMC10842191.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    5. Genomic Mosaicism of the Brain: Origin, Impact, and Utility. Neurosci Bull. 2023 Oct 29. Graham JH, Schlachetzki JCM, Yang X, Breuss MW. PMID: 37898991.
      View in: PubMed   Mentions:    Fields:    
    6. Cell-type-resolved somatic mosaicism reveals clonal dynamics of the human forebrain. bioRxiv. 2023 Oct 26. Chung C, Yang X, Hevner RF, Kennedy K, Vong KI, Liu Y, Patel A, Nedunuri R, Barton ST, Barrows C, Stanley V, Mittal S, Breuss MW, Schlachetzki JCM, Gleeson JG. PMID: 37961480; PMCID: PMC10634852.
      View in: PubMed   Mentions:
    7. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions. Cell Genom. 2023 Aug 09; 3(8):100356. Maury EA, Sherman MA, Genovese G, Gilgenast TG, Kamath T, Burris SJ, Rajarajan P, Flaherty E, Akbarian S, Chess A, McCarroll SA, Loh PR, Phillips-Cremins JE, Brennand KJ, Macosko EZ, Walters JTR, O'Donovan M, Sullivan P, Psychiatric Genomic Consortium Schizophrenia and CNV workgroup, Brain Somatic Mosaicism Network, Sebat J, Lee EA, Walsh CA. PMID: 37601975; PMCID: PMC10435376.
      View in: PubMed   Mentions: 3  
    8. MECP2 germline mosaicism plays an important part in the inheritance of Rett syndrome: a study of MECP2 germline mosaicism in males. BMC Med. 2023 04 20; 21(1):155. Wen Y, Wang J, Zhang Q, Yang X, Wei L, Bao X. PMID: 37081442; PMCID: PMC10120091.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    9. Mapping the Complex Genetic Landscape of Human Neurons. bioRxiv. 2023 Mar 07. Sun C, Kathuria K, Emery SB, Kim B, Burbulis IE, Shin JH, Brain Somatic Mosaicism Network, Weinberger DR, Moran JV, Kidd JM, Mills RE, McConnell MJ. PMID: 36945473; PMCID: PMC10028870.
      View in: PubMed   Mentions:
    10. Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nat Genet. 2023 02; 55(2):209-220. Chung C, Yang X, Bae T, Vong KI, Mittal S, Donkels C, Westley Phillips H, Li Z, Marsh APL, Breuss MW, Ball LL, Garcia CAB, George RD, Gu J, Xu M, Barrows C, James KN, Stanley V, Nidhiry AS, Khoury S, Howe G, Riley E, Xu X, Copeland B, Wang Y, Kim SH, Kang HC, Schulze-Bonhage A, Haas CA, Urbach H, Prinz M, Limbrick DD, Gurnett CA, Smyth MD, Sattar S, Nespeca M, Gonda DD, Imai K, Takahashi Y, Chen HH, Tsai JW, Conti V, Guerrini R, Devinsky O, Silva WA, Machado HR, Mathern GW, Abyzov A, Baldassari S, Baulac S, Focal Cortical Dysplasia Neurogenetics Consortium, Brain Somatic Mosaicism Network, Gleeson JG. PMID: 36635388; PMCID: PMC9961399.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    11. Control-independent mosaic single nucleotide variant detection with DeepMosaic. Nat Biotechnol. 2023 06; 41(6):870-877. Yang X, Xu X, Breuss MW, Antaki D, Ball LL, Chung C, Shen J, Li C, George RD, Wang Y, Bae T, Cheng Y, Abyzov A, Wei L, Alexandrov LB, Sebat JL, NIMH Brain Somatic Mosaicism Network, Gleeson JG. PMID: 36593400; PMCID: PMC10314968.
      View in: PubMed   Mentions: 8     Fields:    
    12. Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencing. J Hum Genet. 2022 Dec 08. Chen J, Chen Y, Yang Y, Niu X, Zhang J, Zeng Q, Liu A, Xu X, Yang X, Li S, Yang X, Wang Y, Zhang Y. PMID: 36482122.
      View in: PubMed   Mentions: 1     Fields:    
    13. RJAfinder: An automated tool for quantification of responding to joint attention behaviors in autism spectrum disorder using eye tracking data. Front Neurosci. 2022; 16:915464. Zhang J, Li Z, Wu Y, Ye AY, Chen L, Yang X, Wu Q, Wei L. PMID: 36466175; PMCID: PMC9714660.
      View in: PubMed   Mentions: 1  
    14. PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency. Front Neurol. 2022; 13:1041509. Chen Y, Yang X, Chen J, Yang X, Yang Y, Liu A, Zhang X, Wu W, Sun D, Yang Z, Jiang Y, Zhang Y. PMID: 36408521; PMCID: PMC9669318.
      View in: PubMed   Mentions:
    15. Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability. Science. 2022 07 29; 377(6605):511-517. Bae T, Fasching L, Wang Y, Shin JH, Suvakov M, Jang Y, Norton S, Dias C, Mariani J, Jourdon A, Wu F, Panda A, Pattni R, Chahine Y, Yeh R, Roberts RC, Huttner A, Kleinman JE, Hyde TM, Straub RE, Walsh CA, Brain Somatic Mosaicism Network§, Urban AE, Leckman JF, Weinberger DR, Vaccarino FM, Abyzov A. PMID: 35901164; PMCID: PMC9420557.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    16. Unbiased mosaic variant assessment in sperm: a cohort study to test predictability of transmission. Elife. 2022 07 05; 11. Breuss MW, Yang X, Stanley V, McEvoy-Venneri J, Xu X, Morales AJ, Gleeson JG. PMID: 35787314; PMCID: PMC9255958.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    17. Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation. Brain. 2022 05 24; 145(4):1551-1563. von Elsner L, Chai G, Schneeberger PE, Harms FL, Casar C, Qi M, Alawi M, Abdel-Salam GMH, Zaki MS, Arndt F, Yang X, Stanley V, Hempel M, Gleeson JG, Kutsche K. PMID: 34694367; PMCID: PMC9128818.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    18. Somatic mosaicism reveals clonal distributions of neocortical development. Nature. 2022 04; 604(7907):689-696. Breuss MW, Yang X, Schlachetzki JCM, Antaki D, Lana AJ, Xu X, Chung C, Chai G, Stanley V, Song Q, Newmeyer TF, Nguyen A, O'Brien S, Hoeksema MA, Cao B, Nott A, McEvoy-Venneri J, Pasillas MP, Barton ST, Copeland BR, Nahas S, Van Der Kraan L, Ding Y, NIMH Brain Somatic Mosaicism Network, Glass CK, Gleeson JG. PMID: 35444276; PMCID: PMC9436791.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    19. A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. N Engl J Med. 2021 09 30; 385(14):1292-1301. Chai G, Szenker-Ravi E, Chung C, Li Z, Wang L, Khatoo M, Marshall T, Jiang N, Yang X, McEvoy-Venneri J, Stanley V, Anzenberg P, Lang N, Wazny V, Yu J, Virshup DM, Nygaard R, Mancia F, Merdzanic R, Toralles MBP, Pitanga PML, Puri RD, Hernan R, Chung WK, Bertoli-Avella AM, Al-Sannaa N, Zaki MS, Willert K, Reversade B, Gleeson JG. PMID: 34587386; PMCID: PMC9017221.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    20. Developmental and temporal characteristics of clonal sperm mosaicism. Cell. 2021 09 02; 184(18):4772-4783.e15. Yang X, Breuss MW, Xu X, Antaki D, James KN, Stanley V, Ball LL, George RD, Wirth SA, Cao B, Nguyen A, McEvoy-Venneri J, Chai G, Nahas S, Van Der Kraan L, Ding Y, Sebat J, Gleeson JG. PMID: 34388390; PMCID: PMC8496133.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    21. Sperm mosaicism: implications for genomic diversity and disease. Trends Genet. 2021 10; 37(10):890-902. Breuss MW, Yang X, Gleeson JG. PMID: 34158173; PMCID: PMC9484299.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    22. Comprehensive identification of somatic nucleotide variants in human brain tissue. Genome Biol. 2021 03 29; 22(1):92. Wang Y, Bae T, Thorpe J, Sherman MA, Jones AG, Cho S, Daily K, Dou Y, Ganz J, Galor A, Lobon I, Pattni R, Rosenbluh C, Tomasi S, Tomasini L, Yang X, Zhou B, Akbarian S, Ball LL, Bizzotto S, Emery SB, Doan R, Fasching L, Jang Y, Juan D, Lizano E, Luquette LJ, Moldovan JB, Narurkar R, Oetjens MT, Rodin RE, Sekar S, Shin JH, Soriano E, Straub RE, Zhou W, Chess A, Gleeson JG, Marquès-Bonet T, Park PJ, Peters MA, Pevsner J, Walsh CA, Weinberger DR, Brain Somatic Mosaicism Network, Vaccarino FM, Moran JV, Urban AE, Kidd JM, Mills RE, Abyzov A. PMID: 33781308; PMCID: PMC8006362.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    23. Landmarks of human embryonic development inscribed in somatic mutations. Science. 2021 03 19; 371(6535):1249-1253. Bizzotto S, Dou Y, Ganz J, Doan RN, Kwon M, Bohrson CL, Kim SN, Bae T, Abyzov A, NIMH Brain Somatic Mosaicism Network, Park PJ, Walsh CA. PMID: 33737485; PMCID: PMC8170505.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansCells
    24. Machine learning reveals bilateral distribution of somatic L1 insertions in human neurons and glia. Nat Neurosci. 2021 02; 24(2):186-196. Zhu X, Zhou B, Pattni R, Gleason K, Tan C, Kalinowski A, Sloan S, Fiston-Lavier AS, Mariani J, Petrov D, Barres BA, Duncan L, Abyzov A, Vogel H, Brain Somatic Mosaicism Network, Moran JV, Vaccarino FM, Tamminga CA, Levinson DF, Urban AE. PMID: 33432196; PMCID: PMC8806165.
      View in: PubMed   Mentions: 15     Fields:    
    25. The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2021 02; 24(2):176-185. Rodin RE, Dou Y, Kwon M, Sherman MA, D'Gama AM, Doan RN, Rento LM, Girskis KM, Bohrson CL, Kim SN, Nadig A, Luquette LJ, Gulhan DC, Brain Somatic Mosaicism Network, Park PJ, Walsh CA. PMID: 33432195; PMCID: PMC7983596.
      View in: PubMed   Mentions: 48     Fields:    Translation:HumansCells
    26. Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly. Neuron. 2021 01 20; 109(2):241-256.e9. Chai G, Webb A, Li C, Antaki D, Lee S, Breuss MW, Lang N, Stanley V, Anzenberg P, Yang X, Marshall T, Gaffney P, Wierenga KJ, Chung BH, Tsang MH, Pais LS, Lovgren AK, VanNoy GE, Rehm HL, Mirzaa G, Leon E, Diaz J, Neumann A, Kalverda AP, Manfield IW, Parry DA, Logan CV, Johnson CA, Bonthron DT, Valleley EMA, Issa MY, Abdel-Ghafar SF, Abdel-Hamid MS, Jennings P, Zaki MS, Sheridan E, Gleeson JG. PMID: 33220177; PMCID: PMC8800389.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimalsCells
    27. A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome. Eur J Hum Genet. 2021 02; 29(2):271-279. Ghosh SG, Scala M, Beetz C, Helman G, Stanley V, Yang X, Breuss MW, Mazaheri N, Selim L, Hadipour F, Pais L, Stutterd CA, Karageorgou V, Begtrup A, Crunk A, Juusola J, Willaert R, Flore LA, Kennelly K, Spencer C, Brown M, Trapane P, Hurst ACE, Lane Rutledge S, Goodloe DH, McDonald MT, Shashi V, Schoch K, Undiagnosed Diseases Network, Tomoum H, Zaitoun R, Hadipour Z, Galehdari H, Pagnamenta AT, Mojarrad M, Sedaghat A, Dias P, Quintas S, Eslahi A, Shariati G, Bauer P, Simons C, Houlden H, Issa MY, Zaki MS, Maroofian R, Gleeson JG. PMID: 32901138; PMCID: PMC7868361.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    28. MosaicBase: A Knowledgebase of Postzygotic Mosaic Variants in Noncancer Disease-related and Healthy Human Individuals. Genomics Proteomics Bioinformatics. 2020 04; 18(2):140-149. Yang X, Yang C, Zheng X, Xiong L, Tao Y, Wang M, Ye AY, Wu Q, Dou Y, Luo J, Wei L, Huang AY. PMID: 32911083; PMCID: PMC7646124.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    29. mTOR pathway somatic variants and the molecular pathogenesis of hemimegalencephaly. Epilepsia Open. 2020 Mar; 5(1):97-106. Garcia CAB, Carvalho SCS, Yang X, Ball LL, George RD, James KN, Stanley V, Breuss MW, Thomé U, Santos MV, Saggioro FP, Neder Serafini L, Silva WA, Gleeson JG, Machado HR. PMID: 32140648; PMCID: PMC7049797.
      View in: PubMed   Mentions: 5     Fields:    
    30. Autism risk in offspring can be assessed through quantification of male sperm mosaicism. Nat Med. 2020 01; 26(1):143-150. Breuss MW, Antaki D, George RD, Kleiber M, James KN, Ball LL, Hong O, Mitra I, Yang X, Wirth SA, Gu J, Garcia CAB, Gujral M, Brandler WM, Musaev D, Nguyen A, McEvoy-Venneri J, Knox R, Sticca E, Botello MCC, Uribe Fenner J, Pérez MC, Arranz M, Moffitt AB, Wang Z, Hervás A, Devinsky O, Gymrek M, Sebat J, Gleeson JG. PMID: 31873310; PMCID: PMC7032648.
      View in: PubMed   Mentions: 48     Fields:    Translation:HumansCells
    31. Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy. Hum Mol Genet. 2019 11 15; 28(22):3755-3765. Pelorosso C, Watrin F, Conti V, Buhler E, Gelot A, Yang X, Mei D, McEvoy-Venneri J, Manent JB, Cetica V, Ball LL, Buccoliero AM, Vinck A, Barba C, Gleeson JG, Guerrini R, Represa A. PMID: 31411685; PMCID: PMC6935386.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansAnimalsCells
    32. Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly. J Med Genet. 2020 04; 57(4):274-282. Ghosh SG, Wang L, Breuss MW, Green JD, Stanley V, Yang X, Ross D, Traynor BJ, Alhashem AM, Azam M, Selim L, Bastaki L, Elbastawisy HI, Temtamy S, Zaki M, Gleeson JG. PMID: 31586943; PMCID: PMC7405652.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    33. An expanded landscape of human long noncoding RNA. Nucleic Acids Res. 2019 09 05; 47(15):7842-7856. Jiang S, Cheng SJ, Ren LC, Wang Q, Kang YJ, Ding Y, Hou M, Yang XX, Lin Y, Liang N, Gao G. PMID: 31350901; PMCID: PMC6735957.
      View in: PubMed   Mentions: 59     Fields:    Translation:Humans
    34. Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals. PLoS Genet. 2019 04; 15(4):e1008043. Zhao B, Wu Q, Ye AY, Guo J, Zheng X, Yang X, Yan L, Liu QR, Hyde TM, Wei L, Huang AY. PMID: 30973874; PMCID: PMC6478352.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    35. ATP1A3 mosaicism in families with alternating hemiplegia of childhood. Clin Genet. 2019 07; 96(1):43-52. Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. PMID: 30891744; PMCID: PMC6850116.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    36. Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort. Genet Med. 2019 06; 21(6):1330-1338. Zhang Q, Yang X, Wang J, Li J, Wu Q, Wen Y, Zhao Y, Zhang X, Yao H, Wu X, Yu S, Wei L, Bao X. PMID: 30405208; PMCID: PMC6752670.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    37. Mosaicism and incomplete penetrance of PCDH19 mutations. J Med Genet. 2019 02; 56(2):81-88. Liu A, Yang X, Yang X, Wu Q, Zhang J, Sun D, Yang Z, Jiang Y, Wu X, Wei L, Zhang Y. PMID: 30287595; PMCID: PMC6581080.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    38. A model for postzygotic mosaicisms quantifies the allele fraction drift, mutation rate, and contribution to de novo mutations. Genome Res. 2018 07; 28(7):943-951. Ye AY, Dou Y, Yang X, Wang S, Huang AY, Wei L. PMID: 29875290; PMCID: PMC6028137.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    39. Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs. PLoS Genet. 2018 05; 14(5):e1007395. Huang AY, Yang X, Wang S, Zheng X, Wu Q, Ye AY, Wei L. PMID: 29763432; PMCID: PMC5969758.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    40. AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. Database (Oxford). 2018 01 01; 2018. Yang C, Li J, Wu Q, Yang X, Huang AY, Zhang J, Ye AY, Dou Y, Yan L, Zhou WZ, Kong L, Wang M, Ai C, Yang D, Wei L. PMID: 30339214; PMCID: PMC6193446.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    41. Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort. Sci Rep. 2017 Nov 15; 7(1):15677. Yang X, Liu A, Xu X, Yang X, Zeng Q, Ye AY, Yu Z, Wang S, Huang AY, Wu X, Wu Q, Wei L, Zhang Y. PMID: 29142202; PMCID: PMC5688122.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    42. [Study on mosaicism of SCN1A gene mutation in parents of children with Dravet syndrome]. Zhonghua Er Ke Za Zhi. 2017 Nov 02; 55(11):818-823. Liu AJ, Yang XX, Xu XJ, Wu QX, Tian XJ, Yang XL, Wu XR, Wei LP, Zhang YH. PMID: 29141311.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    43. MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples. Nucleic Acids Res. 2017 Jun 02; 45(10):e76. Huang AY, Zhang Z, Ye AY, Dou Y, Yan L, Yang X, Zhang Y, Wei L. PMID: 28132024; PMCID: PMC5449543.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    44. Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. Hum Mutat. 2017 08; 38(8):1002-1013. Dou Y, Yang X, Li Z, Wang S, Zhang Z, Ye AY, Yan L, Yang C, Wu Q, Li J, Zhao B, Huang AY, Wei L. PMID: 28503910; PMCID: PMC5518181.
      View in: PubMed   Mentions: 39     Fields:    Translation:Humans
    45. Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq. Nat Commun. 2017 05 22; 8:15335. Wang K, Lai S, Yang X, Zhu T, Lu X, Wu CI, Ruan J. PMID: 28530222; PMCID: PMC5458117.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    46. Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Hum Mutat. 2015 Sep; 36(9):861-72. Xu X, Yang X, Wu Q, Liu A, Yang X, Ye AY, Huang AY, Li J, Wang M, Yu Z, Wang S, Zhang Z, Wu X, Wei L, Zhang Y. PMID: 26096185; PMCID: PMC5034833.
      View in: PubMed   Mentions: 49     Fields:    Translation:Humans
    47. "Bioinformatics: introduction and methods," a bilingual Massive Open Online Course (MOOC) as a new example for global bioinformatics education. PLoS Comput Biol. 2014 Dec; 10(12):e1003955. Ding Y, Wang M, He Y, Ye AY, Yang X, Liu F, Meng Y, Gao G, Wei L. PMID: 25503717; PMCID: PMC4263353.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    48. Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals. Cell Res. 2014 Nov; 24(11):1311-27. Huang AY, Xu X, Ye AY, Wu Q, Yan L, Zhao B, Yang X, He Y, Wang S, Zhang Z, Gu B, Zhao HQ, Wang M, Gao H, Gao G, Zhang Z, Yang X, Wu X, Zhang Y, Wei L. PMID: 25312340; PMCID: PMC4220156.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansCells
    49. Aerospora of an Eragrostis curvula pasture in South Africa. Onderstepoort J Vet Res. 1979 Mar; 46(1):19-25. Van Der Merwe WJ, Eicker A, Marasas WF, Kellerman TS. PMID: 460819.
      View in: PubMed   Mentions: 1     Fields:    Translation:AnimalsCells
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