Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.neubiorev.2011.09.001
DC FieldValue
dc.titleGenome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: What have we learnt?
dc.contributor.authorLee, K.W.
dc.contributor.authorWoon, P.S.
dc.contributor.authorTeo, Y.Y.
dc.contributor.authorSim, K.
dc.date.accessioned2014-11-26T05:05:46Z
dc.date.available2014-11-26T05:05:46Z
dc.date.issued2012-01
dc.identifier.citationLee, 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
dc.identifier.issn01497634
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/109116
dc.description.abstractSchizophrenia (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
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.neubiorev.2011.09.001
dc.sourceScopus
dc.subjectAssociation
dc.subjectBipolar disorder
dc.subjectGenome
dc.subjectSchizophrenia
dc.subjectStructural variations
dc.typeReview
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1016/j.neubiorev.2011.09.001
dc.description.sourcetitleNeuroscience and Biobehavioral Reviews
dc.description.volume36
dc.description.issue1
dc.description.page556-571
dc.description.codenNBRED
dc.identifier.isiut000300458800036
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