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Article

Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?

Neuro endocrinology letters - 1 Jan 2012

Hosak Ladislav, Silhan Petr, Hosakova Jirina

Abstract excerpt

OBJECTIVES: The term "copy number variation/variant" (CNV) denotes a DNA sequence with a magnitude of 1 kb at least which is differently represented among individuals based on its deletion or duplication. Since 2008, multiple studies have reported copy number variations in schizophrenia, and they seem to fill in a gap in our knowledge on the genetic background of schizophrenia. The aim of this review is to sum up...

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PMID: 22592199

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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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