Jiang Y - Search Results

1

Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.

Li K, Fang Z, Zhao G, Li B, Chen C, Xia L, Wang L, Luo T, Wang X, Wang Z, Zhang Y, Jiang Y, Pan Q, Hu Z, Guo H, Tang B, Liu C, Sun Z, Xia K, Li J. Li K, et al. Among authors: jiang y. J Autism Dev Disord. 2022 Mar;52(3):1299-1313. doi: 10.1007/s10803-021-05031-7. Epub 2021 May 10. J Autism Dev Disord. 2022. PMID: 33970367 Free PMC article.

2

mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.

Li J, Jiang Y, Wang T, Chen H, Xie Q, Shao Q, Ran X, Xia K, Sun ZS, Wu J. Li J, et al. Among authors: jiang y. J Med Genet. 2015 Apr;52(4):275-81. doi: 10.1136/jmedgenet-2014-102656. Epub 2015 Jan 16. J Med Genet. 2015. PMID: 25596308

3

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.

Li J, Cai T, Jiang Y, Chen H, He X, Chen C, Li X, Shao Q, Ran X, Li Z, Xia K, Liu C, Sun ZS, Wu J. Li J, et al. Among authors: jiang y. Mol Psychiatry. 2016 Feb;21(2):290-7. doi: 10.1038/mp.2015.40. Epub 2015 Apr 7. Mol Psychiatry. 2016. PMID: 25849321 Free PMC article.

4

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.

Li J, Cai T, Jiang Y, Chen H, He X, Chen C, Li X, Shao Q, Ran X, Li Z, Xia K, Liu C, Sun ZS, Wu J. Li J, et al. Among authors: jiang y. Mol Psychiatry. 2016 Feb;21(2):298. doi: 10.1038/mp.2015.58. Epub 2015 May 5. Mol Psychiatry. 2016. PMID: 25939403 No abstract available.

5

mirDNMR: a gene-centered database of background de novo mutation rates in human.

Jiang Y, Li Z, Liu Z, Chen D, Wu W, Du Y, Ji L, Jin ZB, Li W, Wu J. Jiang Y, et al. Nucleic Acids Res. 2017 Jan 4;45(D1):D796-D803. doi: 10.1093/nar/gkw1044. Epub 2016 Oct 30. Nucleic Acids Res. 2017. PMID: 27799474 Free PMC article.

6

VarCards: an integrated genetic and clinical database for coding variants in the human genome.

Li J, Shi L, Zhang K, Zhang Y, Hu S, Zhao T, Teng H, Li X, Jiang Y, Ji L, Sun Z. Li J, et al. Among authors: jiang y. Nucleic Acids Res. 2018 Jan 4;46(D1):D1039-D1048. doi: 10.1093/nar/gkx1039. Nucleic Acids Res. 2018. PMID: 29112736 Free PMC article.

7

A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.

Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, Wu J, Xia K, Noonan JP, Sun ZS, He X. Liu Y, et al. Among authors: jiang y. Am J Hum Genet. 2018 Jun 7;102(6):1031-1047. doi: 10.1016/j.ajhg.2018.03.023. Epub 2018 May 10. Am J Hum Genet. 2018. PMID: 29754769 Free PMC article.

8

BrainEXP: a database featuring with spatiotemporal expression variations and co-expression organizations in human brains.

Jiao C, Yan P, Xia C, Shen Z, Tan Z, Tan Y, Wang K, Jiang Y, Huang L, Dai R, Wei Y, Xia Y, Meng Q, Ouyang Y, Yi L, Duan F, Dai J, Zhao S, Liu C, Chen C. Jiao C, et al. Among authors: jiang y. Bioinformatics. 2019 Jan 1;35(1):172-174. doi: 10.1093/bioinformatics/bty576. Bioinformatics. 2019. PMID: 29985970 Free PMC article.

9

Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.

Wu J, Yu P, Jin X, Xu X, Li J, Li Z, Wang M, Wang T, Wu X, Jiang Y, Cai W, Mei J, Min Q, Xu Q, Zhou B, Guo H, Wang P, Zhou W, Hu Z, Li Y, Cai T, Wang Y, Xia K, Jiang YH, Sun ZS. Wu J, et al. Among authors: jiang yh, jiang y. J Genet Genomics. 2018 Oct 20;45(10):527-538. doi: 10.1016/j.jgg.2018.09.002. Epub 2018 Oct 21. J Genet Genomics. 2018. PMID: 30392784

10

The transcription factor POU3F2 regulates a gene coexpression network in brain tissue from patients with psychiatric disorders.

Chen C, Meng Q, Xia Y, Ding C, Wang L, Dai R, Cheng L, Gunaratne P, Gibbs RA, Min S, Coarfa C, Reid JG, Zhang C, Jiao C, Jiang Y, Giase G, Thomas A, Fitzgerald D, Brunetti T, Shieh A, Xia C, Wang Y, Wang Y, Badner JA, Gershon ES, White KP, Liu C. Chen C, et al. Among authors: jiang y. Sci Transl Med. 2018 Dec 19;10(472):eaat8178. doi: 10.1126/scitranslmed.aat8178. Epub 2018 Dec 13. Sci Transl Med. 2018. PMID: 30545964 Free PMC article.

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