遗传力
全基因组关联研究
遗传力缺失问题
病因学
遗传关联
共病
双胞胎研究
流行病学
精神科
表型
医学
生物
遗传学
临床心理学
心理学
遗传变异
单核苷酸多态性
内科学
基因型
基因
作者
Verneri Anttila,Brendan Bulik‐Sullivan,Hilary K. Finucane,Raymond K. Walters,José Brás,Laramie E. Duncan,Valentina Escott‐Price,Guido J. Falcone,Padhraig Gormley,Rainer Malik,Nikolaos A. Patsopoulos,Stephan Ripke,Zhi Wei,Dongmei Yu,Phil H. Lee,Patrick Turley,Benjamin Grenier‐Boley,Vincent Chouraki,Yoichiro Kamatani,Claudine Berr
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2018-06-21
卷期号:360 (6395)
被引量:2014
标识
DOI:10.1126/science.aap8757
摘要
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We quantified the genetic sharing of 25 brain disorders from genome-wide association studies of 265,218 patients and 784,643 control participants and assessed their relationship to 17 phenotypes from 1,191,588 individuals. Psychiatric disorders share common variant risk, whereas neurological disorders appear more distinct from one another and from the psychiatric disorders. We also identified significant sharing between disorders and a number of brain phenotypes, including cognitive measures. Further, we conducted simulations to explore how statistical power, diagnostic misclassification, and phenotypic heterogeneity affect genetic correlations. These results highlight the importance of common genetic variation as a risk factor for brain disorders and the value of heritability-based methods in understanding their etiology.
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