Rare Copy Number Variants: A Point of Rarity in Genetic Risk for Bipolar Disorder and Schizophrenia

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 h...

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Veröffentlicht in:	Archives of general psychiatry 2010-04, Vol.67 (4), p.318-327
Hauptverfasser:	Grozeva, Detelina, Kirov, George, Ivanov, Dobril, Jones, Ian R, Jones, Lisa, Green, Elaine K, St Clair, David M, Young, Allan H, Ferrier, Nicol, Farmer, Anne E, McGuffin, Peter, Holmans, Peter A, Owen, Michael J, O’Donovan, Michael C, Craddock, Nick
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult and adolescent clinical studies Biological and medical sciences Bipolar Disorder - genetics Bipolar disorders DNA Copy Number Variations - genetics Genetic Predisposition to Disease - genetics Genome-Wide Association Study Genotype Humans Medical sciences Mood disorders Oligonucleotide Array Sequence Analysis Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Risk Factors Schizophrenia - genetics
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