Genome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: What have we learnt?

Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.neubiorev.2011.09.001

Title:	Genome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: What have we learnt?
Authors:	Lee, K.W. Woon, P.S. Teo, Y.Y. Sim, K.
Keywords:	Association Bipolar disorder Genome Schizophrenia Structural variations
Issue Date:	Jan-2012
Citation:	Lee, K.W., Woon, P.S., Teo, Y.Y., Sim, K. (2012-01). Genome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: What have we learnt?. Neuroscience and Biobehavioral Reviews 36 (1) : 556-571. ScholarBank@NUS Repository. https://doi.org/10.1016/j.neubiorev.2011.09.001
Abstract:	Schizophrenia (SZ) and bipolar disorder (BPD) have high heritabilities and are clinically and genetically complex. Genome wide association studies (GWAS) and studies of copy number variations (CNV) in SZ and BPD have allowed probing of their underlying genetic risks. In this systematic review, we assess extant genetic signals from published GWAS and CNV studies of SZ and BPD up till March 2011. Risk genes associated with SZ at genome wide significance level (p value
Source Title:	Neuroscience and Biobehavioral Reviews
URI:	http://scholarbank.nus.edu.sg/handle/10635/109116
ISSN:	01497634
DOI:	10.1016/j.neubiorev.2011.09.001
Appears in Collections:	Staff Publications

There are no files associated with this item.

Check