Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder-Reference-Cited by-同舟云学术

Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

Published:2017-02 Issue:2 Volume:7 Page:e1034-e1034
ISSN:2158-3188
Container-title:Translational Psychiatry
language:en
Short-container-title:Transl Psychiatry

Author:

Lescai F^ORCID,Als T D,Li Q^ORCID,Nyegaard M^ORCID,Andorsdottir G,Biskopstø M,Hedemand A,Fiorentino A,O'Brien N,Jarram A,Liang J,Grove J^ORCID,Pallesen J,Eickhardt E^ORCID,Mattheisen M,Bolund L,Demontis D,Wang A G,McQuillin A,Mors O,Wang J,Børglum A D

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://www.nature.com/articles/tp20173.pdf

Reference53 articles.

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3. Cross-Disorder Group of the Psychiatric Genomics Consortium, Smoller JW, Craddock N, Kendler K, Lee PH, Neale BM et al. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Lancet 2013; 381: 1371–1379.

4. Ruderfer DM, Fanous AH, Ripke S, McQuillin A, Amdur RL, et al Schizophrenia Working Group of Psychiatric Genomics Consortium. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Mol Psychiatry 2014; 19: 1017–1024.

5. Nyegaard M, Demontis D, Foldager L, Hedemand A, Flint TJ, Sørensen KM et al. CACNA1C (rs1006737) is associated with schizophrenia. Mol Psychiatry 2010; 15: 119–121.

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