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Article

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

Biological psychiatry - 1 Oct 2011

Buizer-Voskamp Jacobine E, Muntjewerff Jan-Willem, Strengman Eric, Sabatti Chiara, Stefansson Hreinn, Vorstman Jacob A S, Ophoff Roel A

Abstract excerpt

BACKGROUND: Since 2008, multiple studies have reported on copy number variations (CNVs) in schizophrenia. However, many regions are unique events with minimal overlap between studies. This makes it difficult to gain a comprehensive overview of all CNVs involved in the etiology of schizophrenia. We performed a systematic CNV study on the basis of a homogeneous genome-wide dataset aiming at all CNVs ≥ 50 kilobase...

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Identifiers

PMID: 21489405
DOI: 10.1016/j.biopsych.2011.02.015
PMCID: PMC3137747

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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