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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk (vol 55, pg 1435, 2023)
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
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
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
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
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
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
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
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles
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