Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

doi:10.1002/ajmg.b.32088

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Article

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Oct 2012

Van Den Bossche Maarten J, Johnstone Mandy, Strazisar Mojca, Pickard Benjamin S, Goossens Dirk, Lenaerts An-Sofie, De Zutter Sonia, Nordin Annelie, Norrback Karl-Fredrik, Mendlewicz Julien, Souery Daniel, De Rijk Peter, Sabbe Bernard G, Adolfsson Rolf, Blackwood Douglas, Del-Favero Jurgen

Abstract excerpt

From a number of genome-wide association studies it was shown that de novo and/or rare copy number variants (CNVs) are found at an increased frequency in neuropsychiatric diseases. In this study we examined the prevalence of CNVs in six genomic regions (1q21.1, 2p16.3, 3q29, 15q11.2, 15q13.3, and 16p11.2) previously implicated in neuropsychiatric diseases. Hereto, a cohort of four neuropsychiatric disorders...

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PMID: 22911887
DOI: 10.1002/ajmg.b.32088

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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