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Article

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Human molecular genetics - 1 Feb 2008

Kirov George, Gumus Dilihan, Chen Wei, Norton Nadine, Georgieva Lyudmila, Sari Murat, O'Donovan Michael C, Erdogan Fikret, Owen Michael J, Ropers Hans-Hilger, Ullmann Reinhard

Abstract excerpt

Copy number variations (CNVs) account for a substantial proportion of human genomic variation, and have been shown to cause neurodevelopmental disorders. We sought to determine the relevance of CNVs to the aetiology of schizophrenia (SZ). Whole-genome, high-resolution, tiling path BAC array comparative genomic hybridization (array CGH) was employed to test DNA from 93 individuals with DSM-IV SZ. Common DNA copy...

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Source

Identifiers

PMID: 17989066
DOI: 10.1093/hmg/ddm323

Genes

APBA2
NRXN1

Provenance

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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