4.8 Review

y The genetics of bipolar disorder

期刊

MOLECULAR PSYCHIATRY
卷 25, 期 3, 页码 544-559

出版社

SPRINGERNATURE
DOI: 10.1038/s41380-019-0634-7

关键词

-

资金

  1. Intramural Research Program of the NIMH
  2. NATIONAL INSTITUTE OF MENTAL HEALTH [ZIAMH002810, ZIAMH002843] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Bipolar disorder (BD) is one of the most heritable mental illnesses, but the elucidation of its genetic basis has proven to be a very challenging endeavor. Genome-Wide Association Studies (GWAS) have transformed our understanding of BD, providing the first reproducible evidence of specific genetic markers and a highly polygenic architecture that overlaps with that of schizophrenia, major depression, and other disorders. Individual GWAS markers appear to confer little risk, but common variants together account for about 25% of the heritability of BD. A few higher-risk associations have also been identified, such as a rare copy number variant on chromosome 16p11.2. Large scale next-generation sequencing studies are actively searching for other alleles that confer substantial risk. As our understanding of the genetics of BD improves, there is growing optimism that some clear biological pathways will emerge, providing a basis for future studies aimed at molecular diagnosis and novel therapeutics.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据