A rare missense variant in RCL1 segregates with depression in extended families-Reference-Cited by-同舟云学术

A rare missense variant in RCL1 segregates with depression in extended families

Published:2017-03-21 Issue:5 Volume:23 Page:1120-1126
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Amin N,de Vrij F M S,Baghdadi M,Brouwer R W W,van Rooij J G J,Jovanova O,Uitterlinden A G,Hofman A,Janssen H L A,Darwish Murad S,Kraaij R,Stedehouder J,van den Hout M C G N,Kros J M,van IJcken W F J,Tiemeier H,Kushner S A,van Duijn C M

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology

Link

http://www.nature.com/articles/mp201749.pdf

Reference49 articles.

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4. Jacobi F, Wittchen HU, Holting C, Hofler M, Pfister H, Muller N et al. Prevalence, co-morbidity and correlates of mental disorders in the general population: results from the German Health Interview and Examination Survey (GHS). Psychol Med 2004; 34: 597–611.

5. CONVERGE Consortium. Sparse whole-genome sequencing identifies two loci for major depressive disorder. Nature 2015; 523: 588–591.

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