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

Abstract

CONTEXT 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. OBJECTIVES To… (More)
DOI: 10.1001/archgenpsychiatry.2010.25

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Cite this paper

@article{Grozeva2010RareCN, title={Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.}, author={Detelina Grozeva and George Kirov and Dobril K. Ivanov and Ian Jones and Lisa Jones and Elaine K Green and David St Clair and Allan Hunter Young and Nicol I Ferrier and Anne Farmer and Peter McGuffin and Peter Holmans and Michael J. Owen and Michael C. O'Donovan and Nick J. Craddock}, journal={Archives of general psychiatry}, year={2010}, volume={67 4}, pages={318-27} }