Segregation analyses aim to detect genetic factors that have a major effect on an individual’s risk of disease and to describe them in terms of mode of inheritance, age-specific cumulative risk (penetrance), and allele frequency. We conducted single- and two-locus segregation analyses of data from 1,476 men with prostate cancer diagnosed at age <70 years and ascertained through population registries in Melbourne, Sydney, and Perth, Australia, and from their brothers, fathers, and both maternal and paternal lineal uncles. Estimation and model selection were based on asymptotic likelihood theory and were performed through use of the software MENDEL. All two-locus models gave better fits than did single-locus models, even if lineal uncles were...
Background: Genome-wide association studies have identified multiple genetic variants associated wit...
Item does not contain fulltextBreast cancer and prostate cancer are the most commonly occurring canc...
BACKGROUND: Genome-wide association studies have identified multiple genetic variants associated wit...
Segregation analyses aim to detect genetic factors that have a major effect on an individual’s risk ...
Familial aggregation of prostate cancer is likely to be due to multiple susceptibility loci, perhaps...
SummaryA family-history cancer survey was conducted on 5,486 men who underwent a radical prostatecto...
Prostate cancer is the most frequently diagnosed non-cutaneous cancer in Australia and the second la...
Objectives. To confirm, in a study of a large, independent cohort of families with prostate cancer, ...
OBJECTIVES: To confirm, in a study of a large, independent cohort of families with prostate cancer, ...
Among United States men, prostate cancer is the most commonly diagnosed cancer, and the second most ...
BACKGROUND: Genome-wide association studies have identified multiple genetic variants associated wit...
BACKGROUND: One of the goals of personalized medicine is to generate individual risk profiles that c...
A 10-cM genomewide scan of 94 families with hereditary prostate cancer, including 432 affected men, ...
A previous linkage study provided evidence for a prostate cancer–susceptibility locus at 1q24-25. Su...
Evidence of the existence of major prostate cancer (PC)–susceptibility genes has been provided by mu...
Background: Genome-wide association studies have identified multiple genetic variants associated wit...
Item does not contain fulltextBreast cancer and prostate cancer are the most commonly occurring canc...
BACKGROUND: Genome-wide association studies have identified multiple genetic variants associated wit...
Segregation analyses aim to detect genetic factors that have a major effect on an individual’s risk ...
Familial aggregation of prostate cancer is likely to be due to multiple susceptibility loci, perhaps...
SummaryA family-history cancer survey was conducted on 5,486 men who underwent a radical prostatecto...
Prostate cancer is the most frequently diagnosed non-cutaneous cancer in Australia and the second la...
Objectives. To confirm, in a study of a large, independent cohort of families with prostate cancer, ...
OBJECTIVES: To confirm, in a study of a large, independent cohort of families with prostate cancer, ...
Among United States men, prostate cancer is the most commonly diagnosed cancer, and the second most ...
BACKGROUND: Genome-wide association studies have identified multiple genetic variants associated wit...
BACKGROUND: One of the goals of personalized medicine is to generate individual risk profiles that c...
A 10-cM genomewide scan of 94 families with hereditary prostate cancer, including 432 affected men, ...
A previous linkage study provided evidence for a prostate cancer–susceptibility locus at 1q24-25. Su...
Evidence of the existence of major prostate cancer (PC)–susceptibility genes has been provided by mu...
Background: Genome-wide association studies have identified multiple genetic variants associated wit...
Item does not contain fulltextBreast cancer and prostate cancer are the most commonly occurring canc...
BACKGROUND: Genome-wide association studies have identified multiple genetic variants associated wit...