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Article

Failure to confirm CNVs as of aetiological significance in twin pairs discordant for schizophrenia.

Twin research and human genetics : the official journal of the International Society for Twin Studies - 1 Oct 2010

Ono Shinji, Imamura Akira, Tasaki Shinya, Kurotaki Naohiro, Ozawa Hiroki, Yoshiura Koh-ichiro, Okazaki Yuji

Abstract excerpt

Copy number variations (CNVs) are common structural variations in the human genome that strongly affect genomic diversity and can play a role in the development of several diseases, including neurodevelopmental disorders. Recent reports indicate that monozygotic twins can show differential CNV profiles. We searched CNVs in monozygotic twins discordant for schizophrenia to identify susceptible loci for...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 20874467
DOI: 10.1375/twin.13.5.455

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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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