Genome-wide association studies have found SNPs at 17q22 to be associated with breast cancer risk. To identify potential causal variants related to breast cancer risk, we performed a high resolution fine-mapping analysis that involved genotyping 517 SNPs using a custom Illumina iSelect array (iCOGS) followed by imputation of genotypes for 3,134 SNPs in more than 89,000 participants of European ancestry from the Breast Cancer Association Consortium (BCAC). We identified 28 highly correlated common variants, in a 53 Kb region spanning two introns of the STXBP4 gene, that are strong candidates for driving breast cancer risk (lead SNP rs2787486 (OR = 0.92; CI 0.90-0.94; P = 8.96 × 10(-15))) and are correlated with two previously reported risk-a...
PURPOSE: Cis-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part,...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...
Genome-wide association studies have found SNPs at 17q22 to be associated with breast cancer risk. T...
NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs...
NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs...
Identifying the underlying genetic drivers of the heritability of breast cancer prognosis remains el...
Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with brea...
Publisher's version (útgefin grein).Quantifying the genetic correlation between cancers can provide ...
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathw...
Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial factors...
Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial factors...
open79siFUNDING: This work was supported by the Intramural Research Program of the Division of Canc...
Publisher's version (útgefin grein)Breast cancer is a common disease partially caused by genetic ris...
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathw...
PURPOSE: Cis-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part,...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...
Genome-wide association studies have found SNPs at 17q22 to be associated with breast cancer risk. T...
NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs...
NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs...
Identifying the underlying genetic drivers of the heritability of breast cancer prognosis remains el...
Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with brea...
Publisher's version (útgefin grein).Quantifying the genetic correlation between cancers can provide ...
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathw...
Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial factors...
Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial factors...
open79siFUNDING: This work was supported by the Intramural Research Program of the Division of Canc...
Publisher's version (útgefin grein)Breast cancer is a common disease partially caused by genetic ris...
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathw...
PURPOSE: Cis-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part,...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...