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Article

Breast cancer susceptibility: current knowledge and implications for genetic counselling.

European journal of human genetics : EJHG - 1 Jun 2009

Ripperger Tim, Gadzicki Dorothea, Meindl Alfons, Schlegelberger Brigitte

Abstract excerpt

Breast cancer is the most common malignancy in women in the Western world. Except for the high breast cancer risk in BRCA1 and BRCA2 mutation carriers as well as the risk for breast cancer in certain rare syndromes caused by mutations in TP53, STK11, PTEN, CDH1, NF1 or NBN, familial clustering of...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 19092773
DOI: 10.1038/ejhg.2008.212
PMCID: PMC2947107

Genes

BRCA1
BRCA2
ATM
BRIP1
CDH1
CHEK2
FGFR2
LSP1
NBN
PALB2
PTEN
RAD50
STK11
TGFB1
TOX3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19092773-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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