Yang X - Search Results

1

Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases.

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. Garrison MA, et al. Among authors: yang x. Sci Data. 2023 Nov 20;10(1):813. doi: 10.1038/s41597-023-02645-7. Sci Data. 2023. PMID: 37985666 Free PMC article.

2

MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples.

Huang AY, Zhang Z, Ye AY, Dou Y, Yan L, Yang X, Zhang Y, Wei L. Huang AY, et al. Among authors: yang x. Nucleic Acids Res. 2017 Jun 2;45(10):e76. doi: 10.1093/nar/gkx024. Nucleic Acids Res. 2017. PMID: 28132024 Free PMC article.

3

Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations.

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. Dou Y, et al. Among authors: yang c, yang x. Hum Mutat. 2017 Aug;38(8):1002-1013. doi: 10.1002/humu.23255. Epub 2017 May 30. Hum Mutat. 2017. PMID: 28503910 Free PMC article.

4

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort.

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. Yang X, et al. Sci Rep. 2017 Nov 15;7(1):15677. doi: 10.1038/s41598-017-15814-7. Sci Rep. 2017. PMID: 29142202 Free PMC article.

5

Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs.

Huang AY, Yang X, Wang S, Zheng X, Wu Q, Ye AY, Wei L. Huang AY, et al. Among authors: yang x. PLoS Genet. 2018 May 15;14(5):e1007395. doi: 10.1371/journal.pgen.1007395. eCollection 2018 May. PLoS Genet. 2018. PMID: 29763432 Free PMC article.

6

A model for postzygotic mosaicisms quantifies the allele fraction drift, mutation rate, and contribution to de novo mutations.

Ye AY, Dou Y, Yang X, Wang S, Huang AY, Wei L. Ye AY, et al. Among authors: yang x. Genome Res. 2018 Jul;28(7):943-951. doi: 10.1101/gr.230003.117. Epub 2018 Jun 6. Genome Res. 2018. PMID: 29875290 Free PMC article.

7

AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder.

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. Yang C, et al. Among authors: yang d, yang x. Database (Oxford). 2018 Jan 1;2018:bay106. doi: 10.1093/database/bay106. Database (Oxford). 2018. PMID: 30339214 Free PMC article.

8

Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals.

Zhao B, Wu Q, Ye AY, Guo J, Zheng X, Yang X, Yan L, Liu QR, Hyde TM, Wei L, Huang AY. Zhao B, et al. Among authors: yang x. PLoS Genet. 2019 Apr 11;15(4):e1008043. doi: 10.1371/journal.pgen.1008043. eCollection 2019 Apr. PLoS Genet. 2019. PMID: 30973874 Free PMC article.

9

Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy.

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. Pelorosso C, et al. Among authors: yang x. Hum Mol Genet. 2019 Nov 15;28(22):3755-3765. doi: 10.1093/hmg/ddz194. Hum Mol Genet. 2019. PMID: 31411685 Free PMC article.

10

Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly.

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. Ghosh SG, et al. Among authors: yang x. J Med Genet. 2020 Apr;57(4):274-282. doi: 10.1136/jmedgenet-2019-106409. Epub 2019 Oct 5. J Med Genet. 2020. PMID: 31586943 Free PMC article.

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