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(81 - 100 of 132)

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Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
MicroRNA Related Polymorphisms and Breast Cancer Risk
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium
Association between CASP8 -652 6N Del Polymorphism (rs3834129) and Colorectal Cancer Risk: Results from a Multi-Centric Study (vol 9, e85538, 2014)
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
Association between CASP8-652 6N Del Polymorphism (rs3834129) and Colorectal Cancer Risk: Results from a Multi-Centric Study
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility
Genome-wide association studies identify four ER negative-specific breast cancer risk loci

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