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- Journal Article
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- open access
Fine-scale mapping at 9p22.2 identifies candidate causal variants that modify ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
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- Journal Article
- A1
- open access
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
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- Journal Article
- A1
- open access
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
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- Journal Article
- A1
- open access
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
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Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
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Identification of six new susceptibility loci for invasive epithelial ovarian cancer
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- Journal Article
- A1
- open access
Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
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Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)
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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers