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Xiaoxu Yang

Title(s)Postdoctoral Scholar, Neurosciences
SchoolHealth Sciences
Emailxiy010@ucsd.edu
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    Collapse Biography 
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    Peking University, ChinaPhD07/2018Bioinformatics
    Beijing Normal University, ChinaBS07/2013Bioscience
    Beijing Normal University, China-07/2009Information Science and Technologies

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    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.
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    1. 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. Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly. J Med Genet. 2019 Oct 05. PMID: 31586943.
      View in: PubMed
    2. 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. Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy. Hum Mol Genet. 2019 Aug 14. PMID: 31411685.
      View in: PubMed
    3. Jiang S, Cheng SJ, Ren LC, Wang Q, Kang YJ, Ding Y, Hou M, Yang XX, Lin Y, Liang N, Gao G. An expanded landscape of human long noncoding RNA. Nucleic Acids Res. 2019 Jul 27. PMID: 31350901.
      View in: PubMed
    4. Zhao B, Wu Q, Ye AY, Guo J, Zheng X, Yang X, Yan L, Liu QR, Hyde TM, Wei L, Huang AY. Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals. PLoS Genet. 2019 04; 15(4):e1008043. PMID: 30973874.
      View in: PubMed
    5. 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. ATP1A3 mosaicism in families with alternating hemiplegia of childhood. Clin Genet. 2019 Mar 19. PMID: 30891744.
      View in: PubMed
    6. 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. Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort. Genet Med. 2018 Nov 08. PMID: 30405208.
      View in: PubMed
    7. Liu A, Yang X, Yang X, Wu Q, Zhang J, Sun D, Yang Z, Jiang Y, Wu X, Wei L, Zhang Y. Mosaicism and incomplete penetrance of PCDH19 mutations. J Med Genet. 2019 Feb; 56(2):81-88. PMID: 30287595.
      View in: PubMed
    8. Ye AY, Dou Y, Yang X, Wang S, Huang AY, Wei L. 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. PMID: 29875290.
      View in: PubMed
    9. Huang AY, Yang X, Wang S, Zheng X, Wu Q, Ye AY, Wei L. 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. PMID: 29763432.
      View in: PubMed
    10. 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. AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. Database (Oxford). 2018 01 01; 2018. PMID: 30339214.
      View in: PubMed
    11. 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. Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort. Sci Rep. 2017 Nov 15; 7(1):15677. PMID: 29142202.
      View in: PubMed
    12. Liu AJ, Yang XX, Xu XJ, Wu QX, Tian XJ, Yang XL, Wu XR, Wei LP, Zhang YH. [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. PMID: 29141311.
      View in: PubMed
    13. Huang AY, Zhang Z, Ye AY, Dou Y, Yan L, Yang X, Zhang Y, Wei L. 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. PMID: 28132024.
      View in: PubMed
    14. 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. 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. PMID: 28503910.
      View in: PubMed
    15. Wang K, Lai S, Yang X, Zhu T, Lu X, Wu CI, Ruan J. Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq. Nat Commun. 2017 05 22; 8:15335. PMID: 28530222.
      View in: PubMed
    16. 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. 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. PMID: 26096185.
      View in: PubMed
    17. Ding Y, Wang M, He Y, Ye AY, Yang X, Liu F, Meng Y, Gao G, Wei L. "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. PMID: 25503717.
      View in: PubMed
    18. 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. Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals. Cell Res. 2014 Nov; 24(11):1311-27. PMID: 25312340.
      View in: PubMed
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