Genome wide association studies (GWAS) and large scale replication studies have identified common variants in 79 loci associated with breast cancer, explaining ~14% of the familial risk of the disease. To identify new susceptibility loci, we performed a meta-analysis of 11 GWAS comprising of 15,748 breast cancer cases and 18,084 controls, and 46,785 cases and 42,892 controls from 41 studies genotyped on a 200K custom array (iCOGS). Analyses were restricted to women of European ancestry. Genotypes for more than 11M SNPs were generated by imputation using the 1000 Genomes Project reference panel. We identified 15 novel loci associated with breast cancer at P<5×10−8. Combining association analysis with ChIP-Seq data in mammary cell lines and C...
INTRODUCTION: Previous studies have identified common germline variants nominally associated with b...
Breast cancer susceptibility variants frequently show heterogeneity in associations by tumor subtype...
Atrial fibrillation (AF) affects more than 33 million individuals worldwide1 and has a complex herit...
Genome wide association studies (GWAS) and large scale replication studies have identified common va...
Breast cancer is the most common cancer among women. Common variants at 27 loci have been identified...
Genome-wide association studies have identified breast cancer risk variants in over 150 genomic regi...
Genome-wide association studies (GWAS) have identified 12 epithelial ovarian cancer (EOC) susceptibi...
Breast cancer is the most common cancer among women. To date, 22 common breast cancer susceptibility...
The breast cancer risk variants identified in genome-wide association studies explain only a small f...
Genome-wide association studies (GWAS) have identified >250 loci for body mass index (BMI), impli...
We analyzed 3,872 common genetic variants across the ESR1 locus (encoding estrogen receptor α) in 11...
Mammographic density reflects the amount of stromal and epithelial tissues in relation to adipose ti...
Breast cancer risk is influenced by rare coding variants in susceptibility genes, such as BRCA1, and...
INTRODUCTION: Previous studies have identified common germline variants nominally associated with br...
Germline BRCA1 mutations predispose to breast cancer. To identify genetic modifiers of this risk, we...
INTRODUCTION: Previous studies have identified common germline variants nominally associated with b...
Breast cancer susceptibility variants frequently show heterogeneity in associations by tumor subtype...
Atrial fibrillation (AF) affects more than 33 million individuals worldwide1 and has a complex herit...
Genome wide association studies (GWAS) and large scale replication studies have identified common va...
Breast cancer is the most common cancer among women. Common variants at 27 loci have been identified...
Genome-wide association studies have identified breast cancer risk variants in over 150 genomic regi...
Genome-wide association studies (GWAS) have identified 12 epithelial ovarian cancer (EOC) susceptibi...
Breast cancer is the most common cancer among women. To date, 22 common breast cancer susceptibility...
The breast cancer risk variants identified in genome-wide association studies explain only a small f...
Genome-wide association studies (GWAS) have identified >250 loci for body mass index (BMI), impli...
We analyzed 3,872 common genetic variants across the ESR1 locus (encoding estrogen receptor α) in 11...
Mammographic density reflects the amount of stromal and epithelial tissues in relation to adipose ti...
Breast cancer risk is influenced by rare coding variants in susceptibility genes, such as BRCA1, and...
INTRODUCTION: Previous studies have identified common germline variants nominally associated with br...
Germline BRCA1 mutations predispose to breast cancer. To identify genetic modifiers of this risk, we...
INTRODUCTION: Previous studies have identified common germline variants nominally associated with b...
Breast cancer susceptibility variants frequently show heterogeneity in associations by tumor subtype...
Atrial fibrillation (AF) affects more than 33 million individuals worldwide1 and has a complex herit...