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

Juan ZhouChuanchuan MaKe WangXiuli LiXuemin JianHan ZhangJianmin YuanJiajun YinJianhua ChenYongyong Shi
Published in: Human genomics (2020)
Our findings provided further evidence that BNIP3L gene is a susceptibility gene of schizophrenia and revealed functional and potential causal mutations in BNIP3L. However, more functional validations are suggested to better understand the role of BNIP3L in the etiology of schizophrenia.
Keyphrases
  • bipolar disorder
  • copy number
  • genome wide
  • genome wide identification
  • single cell
  • risk assessment
  • dna methylation
  • human health