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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Article
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados