Li Z - Search Results

1

Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders.

Zhang Y, Wang R, Liu Z, Jiang S, Du L, Qiu K, Li F, Wang Q, Jin J, Chen X, Li Z, Wu J, Zhang N. Zhang Y, et al. Among authors: li f, li z. Am J Med Genet B Neuropsychiatr Genet. 2021 Jan;186(1):3-15. doi: 10.1002/ajmg.b.32821. Epub 2020 Sep 15. Am J Med Genet B Neuropsychiatr Genet. 2021. PMID: 32929885

2

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: li z, li x. 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.

3

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. Hum Mutat. 2017 Jan;38(1):25-33. doi: 10.1002/humu.23125. Epub 2016 Oct 13. Hum Mutat. 2017. PMID: 27676360

4

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. Among authors: li z, li w. 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.

5

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.

Jin ZB, Wu J, Huang XF, Feng CY, Cai XB, Mao JY, Xiang L, Wu KC, Xiao X, Kloss BA, Li Z, Liu Z, Huang S, Shen M, Cheng FF, Cheng XW, Zheng ZL, Chen X, Zhuang W, Zhang Q, Young TL, Xie T, Lu F, Qu J. Jin ZB, et al. Among authors: li z. Proc Natl Acad Sci U S A. 2017 Apr 18;114(16):4219-4224. doi: 10.1073/pnas.1615970114. Epub 2017 Apr 3. Proc Natl Acad Sci U S A. 2017. PMID: 28373534 Free PMC article.

6

Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing.

Liu Z, Li Z, Zhi X, Du Y, Lin Z, Wu J. Liu Z, et al. Among authors: li z. Mol Neurobiol. 2018 Mar;55(3):2483-2493. doi: 10.1007/s12035-017-0483-9. Epub 2017 Apr 6. Mol Neurobiol. 2018. PMID: 28386848

7

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: li z. 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.

8

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: li z, li j. 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.

9

Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain Development.

Liu Z, Zhang N, Zhang Y, Du Y, Zhang T, Li Z, Wu J, Wang X. Liu Z, et al. Among authors: li z. Front Genet. 2018 Sep 18;9:349. doi: 10.3389/fgene.2018.00349. eCollection 2018. Front Genet. 2018. PMID: 30279698 Free PMC article.

10

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: li y, li j, li z. 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

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