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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Archival Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725574/
https://www.ncbi.nlm.nih.gov/pubmed/25861698
http://dx.doi.org/10.1016/j.biopsych.2015.02.025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725574/
https://www.ncbi.nlm.nih.gov/pubmed/25861698
http://dx.doi.org/10.1016/j.biopsych.2015.02.025

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