A Frameshift Variant in the CHST9 Gene Identified by Family-Based Whole Genome Sequencing Is Associated with Schizophrenia in Chinese Population-Reference-Cited by-同舟云学术

A Frameshift Variant in the CHST9 Gene Identified by Family-Based Whole Genome Sequencing Is Associated with Schizophrenia in Chinese Population

Published:2019-09-03 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Chen Jingchun,Wu Jain-Shing,Mize Travis,Moreno Marvi,Hamid Mahtab,Servin Francisco,Bashy Bita,Zhao Zhongming,Jia Peilin,Tsuang Ming T.,Kendler Kenneth S.,Xiong Momiao,Chen Xiangning

Funder

U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences

U.S. Department of Health & Human Services | NIH | U.S. National Library of Medicine

U.S. Department of Health & Human Services | NIH | National Institute of Mental Health

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-019-49052-w.pdf

Reference48 articles.

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2. Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511, 421–427 (2014).

3. Polushina, T. et al. Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Transl Psychiatry 7 (2017).

4. Bureau, A. et al. Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics 30, 2189–2196 (2014).

5. Sakai, M. et al. Assessment of copy number variations in the brain genome of schizophrenia patients. Mol Cytogenet 8, 46 (2015).

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