[PMID 20585626
] Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia breast cancer consortium
The adjusted odds ratio for breast cancer risk was 1.25 (CI: 1.20?1.31) per rs4784227(T) allele (p = 3.2×10e?25) in the pooled analysis of of over 10,000 samples from all Asian samples, and 1.19 (CI: 1.09-1.31, p = 1.3x10e-4) among European Americans (2,797 cases and 2,662 controls).
[PMID 21445572] Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies
[PMID 22452962] A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
[PMID 23001124] Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression.
[PMID 25995231] ABC: A tool to identify SNVs causing allele-specific transcription factor binding from ChIP-Seq experiments
[PMID 31338012] Association of rs4784227-CASC16 (LOC643714 locus) and rs4782447-ACSF3 polymorphisms and their association with breast cancer risk among Iranian population.
[PMID 31655495] Association of polymorphisms in LOC105377871 and CASC16 with Breast Cancer in the Northwest Chinese Han Population.
] Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia breast cancer consortium
