Prostate cancer is the most common non-skin cancer and the second leading cause of cancer related mortality for men in the United States. There is strong empirical and epidemiological evidence supporting a stronger role of genetics in early-onset prostate cancer. We performed a genome-wide association scan for early-onset prostate cancer. Novel aspects of this study include the focus on early-onset disease (defined as men with prostate cancer diagnosed before age 56 years) and use of publically available control genotype data from previous genome-wide association studies. We found genome-wide significant (p<5×10−8) evidence for variants at 8q24 and 11p15 and strong supportive evidence for a number of previously reported loci. We found littl...
Prostate cancer (PrCa) is the most common non-skin cancer diagnosed among males in developed countri...
BACKGROUND: No single-nucleotide polymorphisms (SNPs) specific for aggressive prostate cancer have b...
Prostate cancer is a polygenic disease with a large heritable component. A number of common, low-pen...
Prostate cancer is the most common non-skin cancer and the second leading cause of cancer related mo...
Prostate cancer is the most common cancer in men in Europe and the United States. The genetic herita...
We assessed the evidence for association between 23 recently reported prostate cancer (PCa) variants...
Prostate cancer (PCa) affects more than 190,000 men each year with ~10% of men diagnosed at ≤ 55 yea...
Prostate cancer is the most common cancer in men in Europe and the United States. The genetic herita...
Genome-wide association study–identified prostate cancer risk variants explain only a relatively sma...
Background: Several prostate cancer genome-wide association studies (GWAS) have identified risk-asso...
Background: Of the 200,000 U.S. men annually diagnosed with prostate cancer, approximately 20 % to 3...
Prostate cancer linkage studies have been used to localize rare and presumably highly penetrant canc...
Prostate cancer is a highly heritable disease with large disparities in incidence rates across ances...
Introduction Prostate cancer (PrCa) is the commonest non-cutaneous cancer in men in the UK. Epidemio...
Genome-wide association studies (GWAS) have identified multiple common genetic variants associated ...
Prostate cancer (PrCa) is the most common non-skin cancer diagnosed among males in developed countri...
BACKGROUND: No single-nucleotide polymorphisms (SNPs) specific for aggressive prostate cancer have b...
Prostate cancer is a polygenic disease with a large heritable component. A number of common, low-pen...
Prostate cancer is the most common non-skin cancer and the second leading cause of cancer related mo...
Prostate cancer is the most common cancer in men in Europe and the United States. The genetic herita...
We assessed the evidence for association between 23 recently reported prostate cancer (PCa) variants...
Prostate cancer (PCa) affects more than 190,000 men each year with ~10% of men diagnosed at ≤ 55 yea...
Prostate cancer is the most common cancer in men in Europe and the United States. The genetic herita...
Genome-wide association study–identified prostate cancer risk variants explain only a relatively sma...
Background: Several prostate cancer genome-wide association studies (GWAS) have identified risk-asso...
Background: Of the 200,000 U.S. men annually diagnosed with prostate cancer, approximately 20 % to 3...
Prostate cancer linkage studies have been used to localize rare and presumably highly penetrant canc...
Prostate cancer is a highly heritable disease with large disparities in incidence rates across ances...
Introduction Prostate cancer (PrCa) is the commonest non-cutaneous cancer in men in the UK. Epidemio...
Genome-wide association studies (GWAS) have identified multiple common genetic variants associated ...
Prostate cancer (PrCa) is the most common non-skin cancer diagnosed among males in developed countri...
BACKGROUND: No single-nucleotide polymorphisms (SNPs) specific for aggressive prostate cancer have b...
Prostate cancer is a polygenic disease with a large heritable component. A number of common, low-pen...