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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Gepubliceerd in:Biol Psychiatry
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Elsevier 2016
Onderwerpen:
Archival Report
Online toegang: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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