Jiang Y - Search Results

1

[Whole-genome sequencing and its application in the research and diagnoses of genetic diseases].

Shao Q, Jiang Y, Wu J. Shao Q, et al. Among authors: jiang y. Yi Chuan. 2014 Nov;36(11):1087-98. Yi Chuan. 2014. PMID: 25567867 Review. Chinese.

2

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

3

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

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):290-7. doi: 10.1038/mp.2015.40. Epub 2015 Apr 7. Mol Psychiatry. 2016. PMID: 25849321 Free PMC article.

5

Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.

Jin ZB, Li Z, Liu Z, Jiang Y, Cai XB, Wu J. Jin ZB, et al. Among authors: jiang y. Biol Rev Camb Philos Soc. 2018 May;93(2):1014-1031. doi: 10.1111/brv.12383. Epub 2017 Nov 20. Biol Rev Camb Philos Soc. 2018. PMID: 29154454 Review.

6

swDMR: A Sliding Window Approach to Identify Differentially Methylated Regions Based on Whole Genome Bisulfite Sequencing.

Wang Z, Li X, Jiang Y, Shao Q, Liu Q, Chen B, Huang D. Wang Z, et al. Among authors: jiang y. PLoS One. 2015 Jul 15;10(7):e0132866. doi: 10.1371/journal.pone.0132866. eCollection 2015. PLoS One. 2015. PMID: 26176536 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

mirVAFC: A Web Server for Prioritizations of Pathogenic Sequence Variants from Exome Sequencing Data via Classifications.

Li Z, Liu Z, Jiang Y, Chen D, Ran X, Sun ZS, Wu J. Li Z, et al. Among authors: jiang y. Hum Mutat. 2017 Jan;38(1):25-33. doi: 10.1002/humu.23125. Epub 2016 Oct 13. Hum Mutat. 2017. PMID: 27676360

9

Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.

Du Y, Li Z, Liu Z, Zhang N, Wang R, Li F, Zhang T, Jiang Y, Zhi X, Wang Z, Wu J. Du Y, et al. Among authors: jiang y. Genet Med. 2020 Jan;22(1):170-180. doi: 10.1038/s41436-019-0610-2. Epub 2019 Jul 23. Genet Med. 2020. PMID: 31332282 Free article.

10

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.

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