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Xiaoxu Yang

Title(s)Postdoctoral Scholar, Neurosciences
SchoolHealth Sciences
Address9500 Gilman Drive #0752
La Jolla CA 92093
Emailxiy010@ucsd.edu
ORCID ORCID Icon0000-0003-0219-0023 Additional info
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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. 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. 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.
      View in: PubMed   Mentions:
    2. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    3. 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.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    4. Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly. J Med Genet. 2020 Apr; 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.
      View in: PubMed   Mentions:    Fields:    
    5. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    6. 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.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    7. 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.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    8. 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.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    9. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    10. 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.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    11. 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.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    12. 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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    13. 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.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    14. [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
    15. 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.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    16. 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.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    17. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    18. 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.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    19. "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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    20. 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.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
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