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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Biol Psychiatry
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2016
Gaiak:
Archival Report
Sarrera elektronikoa: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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