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- 2016
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Mark
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
(
- Contribution to journal › Article
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No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
(
- Contribution to journal › Article
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Mark
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
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- Contribution to journal › Article
- 2015
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Mark
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
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- Contribution to journal › Article
- 2014
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Mark
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.
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- Contribution to journal › Article
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Mark
Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
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- Contribution to journal › Article
- 2013
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Mark
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
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- Contribution to journal › Letter
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Mark
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
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- Contribution to journal › Article
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Mark
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
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- Contribution to journal › Article
- 2011
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Mark
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
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- Contribution to journal › Article
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Mark
Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
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- Contribution to journal › Article