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Sparse whole-genome sequencing identifies two loci for major depressive disorder
Cai, N; Bigdeli, TB; Kretzschmar, W; Li, YH; Liang, JQ; Song, L; Hu, JC; Li, QB; Jin, W; Hu, ZF
刊名NATURE
2015-07-30
卷号523期号:7562页码:588
ISSN号0028-0836
DOI10.1038/nature14659
文献子类Article
英文摘要Major depressive disorder (MDD), one of the most frequently encountered forms ofmental illness and a leading cause of disability worldwide(1), poses a major challenge to genetic analysis. To date, no robustly replicated genetic loci have been identified(2), despite analysis of more than 9,000 cases(3). Here, using low-coverage whole-genome sequencing of 5,303 Chinese women with recurrent MDD selected to reduce phenotypic heterogeneity, and 5,337 controls screened to exclude MDD, we identified, and subsequently replicated in an independent sample, two loci contributing to risk of MDD on chromosome 10: one near the SIRT1 gene (P = 2.53 x 10(-10)), the other in an intron of the LHPP gene (P = 6.45 x10(-12)). Analysis of 4,509 cases with a severe subtype of MDD, melancholia, yielded an increased genetic signal at the SIRT1 locus. We attribute our success to the recruitment of relatively homogeneous cases with severe illness.
学科主题Science & Technology - Other Topics
出版地LONDON
资助项目国家自然科学基金项目 ; 国家重点基础研究发展计划以及国家重大科学研究计划(973计划) ; 美国国立卫生研究院项目 ; 英国惠康基金会项目
项目编号Wellcome Trust [WT090532/Z/09/Z, WT083573/Z/07/Z, WT089269/Z/09/Z, WT097307] ; NIH [MH-100549] ; Brain and Behavior Research Foundation ; Agency of Science, Technology and Research (A*STAR) Graduate Academy ; ERC [617306] ; 973 Program [2013CB531301] ; NSFC [31430048, 31222031]
语种英语
WOS记录号WOS:000358655200044
资助机构NSFC ; MOST ; NIH ; Wellcome Trust
内容类型期刊论文
源URL[http://ir.lzu.edu.cn/handle/262010/179379]  
专题第二临床医学院_期刊论文
通讯作者Cai, N (reprint author), Univ Oxford, Wellcome Trust Ctr Human Genet, Roosevelt Dr, Oxford OX3 7BN, England.
推荐引用方式
GB/T 7714
Cai, N,Bigdeli, TB,Kretzschmar, W,et al. Sparse whole-genome sequencing identifies two loci for major depressive disorder[J]. NATURE,2015,523(7562):588.
APA Cai, N.,Bigdeli, TB.,Kretzschmar, W.,Li, YH.,Liang, JQ.,...&Cai, N .(2015).Sparse whole-genome sequencing identifies two loci for major depressive disorder.NATURE,523(7562),588.
MLA Cai, N,et al."Sparse whole-genome sequencing identifies two loci for major depressive disorder".NATURE 523.7562(2015):588.
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