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  1. No Access

    Article

    Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

    Previous genome-wide association studies (GWAS) of prostate cancer risk focused on cases unselected for family history and have reported over 100 significant associations. The International Consortium for Pros...

    Craig C. Teerlink, Daniel Leongamornlert, Tokhir Dadaev, Alun Thomas… in Human Genetics (2016)

  2. No Access

    Article

    Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

    Previous GWAS studies have reported significant associations between various common SNPs and prostate cancer risk using cases unselected for family history. How these variants influence risk in familial prosta...

    Craig C. Teerlink, Stephen N. Thibodeau, Shannon K. McDonnell… in Human Genetics (2014)

  3. No Access

    Article

    Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

    Multiple prostate cancer (PCa) risk-related loci have been discovered by genome-wide association studies (GWAS) based on case–control designs. However, GWAS findings may be confounded by population stratificat...

    Guangfu **, Lingyi Lu, Kathleen A. Cooney, Anna M. Ray… in Human Genetics (2012)

  4. No Access

    Article

    Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21

    Christopher Haiman and colleagues report a genome-wide association study for prostate cancer in African-American males drawn from 11 epidemiological studies of prostate cancer, with replication including indiv...

    Christopher A Haiman, Gary K Chen, William J Blot, Sara S Strom… in Nature Genetics (2011)

  5. No Access

    Article

    Hereditary prostate cancer as a feature of Lynch Syndrome

    Lynch Syndrome is an autosomal dominant condition characterized by early onset colorectal cancer (CRC) and is associated with cancers of the gastrointestinal and reproductive tracts. Germline mutations in DNA ...

    Christina M. Bauer, Anna M. Ray, Bronwen A. Halstead-Nussloch… in Familial Cancer (2011)

  6. No Access

    Article

    Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

    Rosalind Eeles and colleagues present a genome-wide association study for prostate cancer. They report seven loci newly associated with prostate cancer susceptibility.

    Rosalind A Eeles, Zsofia Kote-Jarai, Ali Amin Al Olama, Graham G Giles… in Nature Genetics (2009)