Wang W - Search Results

1

De novo mutations identified by whole-genome sequencing implicate chromatin modifications in obsessive-compulsive disorder.

Lin GN, Song W, Wang W, Wang P, Yu H, Cai W, Jiang X, Huang W, Qian W, Chen Y, Chen M, Yu S, Xu T, Jiao Y, Liu Q, Zhang C, Yi Z, Fan Q, Chen J, Wang Z. Lin GN, et al. Among authors: wang w, wang z, wang p. Sci Adv. 2022 Jan 14;8(2):eabi6180. doi: 10.1126/sciadv.abi6180. Epub 2022 Jan 12. Sci Adv. 2022. PMID: 35020433 Free PMC article.

2

De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application.

Wang W, Corominas R, Lin GN. Wang W, et al. Front Genet. 2019 Apr 3;10:258. doi: 10.3389/fgene.2019.00258. eCollection 2019. Front Genet. 2019. PMID: 31001316 Free PMC article. Review.

3

Use of tobacco in schizophrenia: A double-edged sword.

Fang Y, Wang W, Zhu C, Lin GN, Cheng Y, Zou J, Cui D. Fang Y, et al. Among authors: wang w. Brain Behav. 2019 Nov;9(11):e01433. doi: 10.1002/brb3.1433. Epub 2019 Oct 11. Brain Behav. 2019. PMID: 31605440 Free PMC article.

4

PsyMuKB: An Integrative De Novo Variant Knowledge Base for Developmental Disorders.

Lin GN, Guo S, Tan X, Wang W, Qian W, Song W, Wang J, Yu S, Wang Z, Cui D, Wang H. Lin GN, et al. Among authors: wang h, wang w, wang j, wang z. Genomics Proteomics Bioinformatics. 2019 Aug;17(4):453-464. doi: 10.1016/j.gpb.2019.10.002. Epub 2019 Dec 4. Genomics Proteomics Bioinformatics. 2019. PMID: 31809863 Free PMC article.

5

The interaction of ASAH1 and NGF gene involving in neurotrophin signaling pathway contributes to schizophrenia susceptibility and psychopathology.

Su Y, Yang L, Li Z, Wang W, Xing M, Fang Y, Cheng Y, Lin GN, Cui D. Su Y, et al. Among authors: wang w. Prog Neuropsychopharmacol Biol Psychiatry. 2021 Jan 10;104:110015. doi: 10.1016/j.pnpbp.2020.110015. Epub 2020 Jun 19. Prog Neuropsychopharmacol Biol Psychiatry. 2021. PMID: 32569620

6

Integrative Analysis Identified Key Schizophrenia Risk Factors from an Abnormal Behavior Mouse Gene Set.

Chen M, Wang W, Song W, Qian W, Lin GN. Chen M, et al. Among authors: wang w. Life (Basel). 2021 Feb 23;11(2):172. doi: 10.3390/life11020172. Life (Basel). 2021. PMID: 33672431 Free PMC article.

7

Alternatively Splicing Interactomes Identify Novel Isoform-Specific Partners for NSD2.

Wang W, Chen Y, Zhao J, Chen L, Song W, Li L, Lin GN. Wang W, et al. Front Cell Dev Biol. 2021 Feb 25;9:612019. doi: 10.3389/fcell.2021.612019. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33718354 Free PMC article.

8

Dissection of the Genetic Association between Anorexia Nervosa and Obsessive-Compulsive Disorder at the Network and Cellular Levels.

Song W, Wang W, Yu S, Lin GN. Song W, et al. Among authors: wang w. Genes (Basel). 2021 Mar 27;12(4):491. doi: 10.3390/genes12040491. Genes (Basel). 2021. PMID: 33801746 Free PMC article.

9

Spatiotemporal 7q11.23 protein network analysis implicates the role of DNA repair pathway during human brain development.

Chen L, Wang W, Cai W, Song W, Qian W, Lin GN. Chen L, et al. Among authors: wang w. Sci Rep. 2021 Apr 15;11(1):8246. doi: 10.1038/s41598-021-87632-x. Sci Rep. 2021. PMID: 33859276 Free PMC article.

10

Loss of Setd2 associates with aberrant microRNA expression and contributes to inflammatory bowel disease progression in mice.

Chen Y, Liu M, Wang W, Cai W, Song W, Li L, Lin GN. Chen Y, et al. Among authors: wang w. Genomics. 2021 Jul;113(4):2441-2454. doi: 10.1016/j.ygeno.2021.05.034. Epub 2021 May 28. Genomics. 2021. PMID: 34052319 Free article.

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