Genome-wide association studies (GWASs) have identified low-penetrance common variants (i.e., single nucleotide polymorphisms, SNPs) associated with breast cancer susceptibility. Although GWASs are primarily focused on single-locus effects, gene-gene interactions (i.e., epistasis) are also assumed to contribute to the genetic risks for complex diseases including breast cancer. While it has been hypothesized that moderately ranked (P value based) weak single-locus effects in GWASs could potentially harbor valuable information for evaluating epistasis, we lack systematic efforts to investigate SNPs showing consistent associations with weak statistical significance across independent discovery and replication stages. The objectives of this stu...
Background: Recently, several genome-wide association studies have identified various genetic suscep...
Background Recently, several genome-wide association studies have identified various genetic suscept...
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to ...
Genome-wide association studies (GWASs) have identified low-penetrance common variants (i.e., single...
Abstract Background Breast cancer predisposition gene...
A large genotyping project within the Breast Cancer Association Consortium (BCAC) recently identifie...
Part of the substantial unexplained familial aggregation of breast cancer may be due to interactions...
Part of the substantial unexplained familial aggregation of breast cancer may be due to interactions...
Background: Previous gene-environment interaction studies of breast cancer risk have provided sparse...
Part of the substantial unexplained familial aggregation of breast cancer may be due to interactions...
A large genotyping project within the Breast Cancer Association Consortium (BCAC) recently identifie...
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to ...
Background: Recently, several genome-wide association studies have identified various genetic suscep...
Candidate variant association studies have been largely unsuccessful in identifying common breast ca...
Recent studies have identified single nucleotide polymorphisms (SNPs) that significantly modify brea...
Background: Recently, several genome-wide association studies have identified various genetic suscep...
Background Recently, several genome-wide association studies have identified various genetic suscept...
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to ...
Genome-wide association studies (GWASs) have identified low-penetrance common variants (i.e., single...
Abstract Background Breast cancer predisposition gene...
A large genotyping project within the Breast Cancer Association Consortium (BCAC) recently identifie...
Part of the substantial unexplained familial aggregation of breast cancer may be due to interactions...
Part of the substantial unexplained familial aggregation of breast cancer may be due to interactions...
Background: Previous gene-environment interaction studies of breast cancer risk have provided sparse...
Part of the substantial unexplained familial aggregation of breast cancer may be due to interactions...
A large genotyping project within the Breast Cancer Association Consortium (BCAC) recently identifie...
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to ...
Background: Recently, several genome-wide association studies have identified various genetic suscep...
Candidate variant association studies have been largely unsuccessful in identifying common breast ca...
Recent studies have identified single nucleotide polymorphisms (SNPs) that significantly modify brea...
Background: Recently, several genome-wide association studies have identified various genetic suscep...
Background Recently, several genome-wide association studies have identified various genetic suscept...
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to ...