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Article

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.

Schizophrenia research - 1 Mar 2012

Grozeva Detelina, Conrad Donald F, Barnes Chris P, Hurles Matthew, Owen Michael J, O'Donovan Michael C, Craddock Nick, Kirov George

Abstract excerpt

BACKGROUND: Several large, rare chromosomal copy number variants (CNVs) have recently been shown to increase risk for schizophrenia and other neuropsychiatric disorders including autism, ADHD, learning difficulties and epilepsy. AIMS: We wanted to examine the frequencies of these schizophrenia-associated variants in a large sample of individuals with non-psychiatric illnesses to better understand the robustness...

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Source

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Identifiers

PMID: 22130109
DOI: 10.1016/j.schres.2011.11.004
PMCID: PMC3315675

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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