Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms-Reference-Cited by-同舟云学术

Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms

Published:2016-07-19 Issue:4 Volume:22 Page:537-543
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Amin N,Jovanova O,Adams H H H,Dehghan A,Kavousi M,Vernooij M W,Peeters R P,de Vrij F M S,van der Lee S J,van Rooij J G J,van Leeuwen E M,Chaker L,Demirkan A,Hofman A,Brouwer R W W,Kraaij R,Willems van Dijk K,Hankemeier T,van Ijcken W F J,Uitterlinden A G,Niessen W J,Franco O H,Kushner S A,Ikram M A,Tiemeier H^ORCID,van Duijn C M

Publisher

Springer Science and Business Media LLC

Subject

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

Link

https://www.nature.com/articles/mp2016101.pdf

Reference73 articles.

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3. Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Ripke S, Wray NR, Lewis CM, Hamilton SP, Weissman MM et al. A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry 2013; 18: 497–511.

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

5. Sullivan PF . Genetics of disease: associations with depression. Nature 2015; 523: 539–540.

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