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Article

Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: a meta-analysis.

Clinical genetics - 1 Jan 2014

Tun N M, Villani G, Ong K, Yoe L, Bo Z M

Abstract excerpt

Testing for BRCA1 mutation has important clinical implications such as identifying risk of second primary cancers and risk of cancer in the family. This study seeks to quantify the risk of having BRCA1 mutation in female breast cancer patients with triple-negative phenotype compared with those with other phenotypes. We undertook a search of MEDLINE and EMBASE databases for relevant studies through 10 May 2013....

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Share to Genes, BRCA1
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24000781
DOI: 10.1111/cge.12270

Genes

BRCA1

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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