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Xiaoxu Yang

TitlePostdoctoral Scholar
InstitutionUniversity of California San Diego
DepartmentNeurosciences
Address9500 Gilman Drive #0752
La Jolla CA 92093
Emailxiy010@ucsd.edu
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    Collapse Biography 
    Collapse Education and Training
    Peking University, ChinaPhD07/2018Bioinformatics
    Beijing Normal University, ChinaBS07/2013Bioscience

    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.
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    1. 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
    2. 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. 2018 Oct 04. PMID: 30287595.
      View in: PubMed
    3. 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
    4. 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
    5. 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 Jan 01; 2018. PMID: 30339214.
      View in: PubMed
    6. 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
    7. 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
    8. 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
    9. 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
    10. 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 May 22; 8:15335. PMID: 28530222.
      View in: PubMed
    11. 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
    12. 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
    13. 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