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Article

Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data.

BMC genomics - 20 Jul 2012

Marenne Gaëlle, Real Francisco X, Rothman Nathaniel, Rodríguez-Santiago Benjamin, Pérez-Jurado Luis, Kogevinas Manolis, García-Closas Montse, Silverman Debra T, Chanock Stephen J, Génin Emmanuelle, Malats Núria

Abstract excerpt

BACKGROUND: Structural variations such as copy number variants (CNV) influence the expression of different phenotypic traits. Algorithms to identify CNVs through SNP-array platforms are available. The ability to evaluate well-characterized CNVs such as GSTM1 (1p13.3) deletion provides an importan...

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Source

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Identifiers

PMID: 22817656
DOI: 10.1186/1471-2164-13-326
PMCID: PMC3425254

Genes

GSTM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22817656-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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