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Article

Effect of ATM, CHEK2 and ERBB2 TAGSNPs and haplotypes on endometrial cancer risk.

Human molecular genetics - 15 Jan 2007

Einarsdóttir Kristjana, Humphreys Keith, Bonnard Carine, Li Yuqing, Li Yi, Chia Kee Seng, Liu Edison T, Hall Per, Liu Jianjun, Wedrén Sara

Abstract excerpt

Family history of endometrial cancer increases the risk of developing the disease, but it is still largely unknown which germ-line genetic factors are involved in the aetiology of endometrial cancer. In a Swedish population-based case-control study including 705 cases and 1565 controls, we examined common variation in the ATM, CHEK2 and ERBB2 genes in relation to endometrial cancer risk overall, restricted to...

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Source

Identifiers

PMID: 17164260
DOI: 10.1093/hmg/ddl451

Genes

CHEK2
ATM
ERBB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Effect of ATM, CHEK2 and ERBB2 TAGSNPs and haplotypes on endometrial cancer risk.PMID 17164260Read ↗

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Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer.Semantic proximity Read ↗

Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.Semantic proximity Read ↗

CHEK2, MGMT, SULT1E1 and SULT1A1 polymorphisms and endometrial cancer risk.Semantic proximity Read ↗

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Rare coding variants in DNA damage repair genes associated with timing of natural menopauseSemantic proximity Read ↗

Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility.Semantic proximity Read ↗

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