Pages
-
-
Genome-wide association study of germline variants and breast cancer-specific mortality
-
-
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
-
-
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
-
-
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
-
-
Body mass index and breast cancer survival: a Mendelian randomization analysis
-
-
PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1
-
-
Association analysis identifies 65 new breast cancer risk loci
-
-
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
-
-
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
-
-
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
-
-
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
-
-
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
-
-
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
-
-
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
-
-
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
-
-
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
-
-
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
Pages