Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

Wellcome Trust Case Control Consortium, Detelina Grozeva, George Kirov, Dobril Ivanov, Ian R Jones, Lisa Jones, Elaine K Green, David M St Clair, Allan H Young, Nicol Ferrier, Anne E Farmer, Peter McGuffin, Peter A Holmans, Michael J Owen, Michael C O'Donovan, Nick Craddock

Research output: Contribution to journalArticlepeer-review

Abstract

Recent studies suggest that copy number variation in the human genome is extensive and may play an important role in susceptibility to disease, including neuropsychiatric disorders such as schizophrenia and autism. The possible involvement of copy number variants (CNVs) in bipolar disorder has received little attention to date.
Original languageEnglish
Pages (from-to)318-27
Number of pages10
JournalArchives of General Psychiatry
Volume67
Issue number4
DOIs
Publication statusPublished - 2010

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