Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder

BACKGROUND: Defining the molecular genomic basis of the likelihood of developing depressive disorder is a considerable challenge. We previously associated rare, exonic deletion copy number variants (CNV) with recurrent depressive disorder (RDD). Sex chromosome abnormalities also have been observed t...

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Detalhes bibliográficos
Publicado no:Biol Psychiatry
Main Authors: Rucker, James J.H., Tansey, Katherine E., Rivera, Margarita, Pinto, Dalila, Cohen-Woods, Sarah, Uher, Rudolf, Aitchison, Katherine J., Craddock, Nick, Owen, Michael J., Jones, Lisa, Jones, Ian, Korszun, Ania, Barnes, Michael R., Preisig, Martin, Mors, Ole, Maier, Wolfgang, Rice, John, Rietschel, Marcella, Holsboer, Florian, Farmer, Anne E., Craig, Ian W., Scherer, Stephen W., McGuffin, Peter, Breen, Gerome
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2016
Assuntos:
Archival Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4725574/
https://ncbi.nlm.nih.gov/pubmed/25861698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2015.02.025
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