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Article

Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients.

Journal of psychiatric research - 1 Oct 2010

Saus Ester, Brunet Anna, Armengol Lluís, Alonso Pino, Crespo José M, Fernández-Aranda Fernando, Guitart Miriam, Martín-Santos Rocío, Menchón José Manuel, Navinés Ricard, Soria Virginia, Torrens Marta, Urretavizcaya Mikel, Vallès Vicenç, Gratacòs Mònica, Estivill Xavier

Abstract excerpt

BACKGROUND: Copy number variations (CNV) have become an important source of human genome variability noteworthy to consider when studying genetic susceptibility to complex diseases. As recent studies have found evidences for the potential involvement of CNVs in psychiatric disorders, we have stud...

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Identifiers

PMID: 20398908
DOI: 10.1016/j.jpsychires.2010.03.007

Genes

COMT
GRM7
SSTR5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20398908-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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