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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939438/
https://www.ncbi.nlm.nih.gov/pubmed/22042228
http://dx.doi.org/10.1038/mp.2011.144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939438/
https://www.ncbi.nlm.nih.gov/pubmed/22042228
http://dx.doi.org/10.1038/mp.2011.144

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