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Identification of rare and common variants in BNIP3L: a schizophrenia susceptibility gene.

Human genomics - 11 May 2020

Zhou Juan, Ma Chuanchuan, Wang Ke, Li Xiuli, Jian Xuemin, Zhang Han, Yuan Jianmin, Yin Jiajun, Chen Jianhua, Shi Yongyong

Abstract excerpt

BACKGROUND: Schizophrenia is a chronic and severe mental disorder, and it has been predicted to be highly polygenic. Common SNPs located in or near BNIP3L were found to be genome-wide significantly associated with schizophrenia in recent genome-wide association studies. The purpose of our study is to investigate potential causal variants in BNIP3L gene. RESULTS: We performed targeted sequencing for all exons and...

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Identifiers

PMID: 32393399
DOI: 10.1186/s40246-020-00266-4
PMCID: PMC7212671

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