Genome Wide Association Analysis of Copy Number Variation in Recurrent Depressive Disorder

Large, rare copy number variants (CNV) have been implicated in a variety of psychiatric disorders, but the role of CNVs in recurrent depression is unclear. We performed a genome-wide analysis of large, rare CNVs in 3,106 cases of recurrent depression, 459 controls screened for lifetime-absence of ps...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Rucker, James J.H., Breen, Gerome, Pinto, Dalila, Pedroso, Inti, Lewis, Cathryn M., Cohen-Woods, Sarah, Uher, Rudolf, Schosser, Alexandra, Rivera, Margarita, Aitchison, Katherine J., Craddock, Nick, Owen, Michael J., Jones, Lisa, Jones, Ian, Korszun, Ania, Muglia, Pierandrea, Barnes, Michael R., Preisig, Martin, Mors, Ole, Gill, Mike, Maier, Wolfgang, Rice, John, Rietschel, Marcella, Holsboer, Florian, Farmer, Anne E., Craig, Ian W., Scherer, Stephen W., McGuffin, Peter
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2011
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3939438/
https://ncbi.nlm.nih.gov/pubmed/22042228
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2011.144
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