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Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
Identification of Novel Genetic Markers of Breast Cancer Survival
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer
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
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
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
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1

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