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Paper Details

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Hum Genet
31
2016
10q11.23, 11q13, 17q12, 3q26, 6q25.3, 8q24, 8q24.21, CASC19, PRNCR1, Prostate Cancer, SNPs, familial prostate cancer, haplotype, prostate cancer, prostate cancer predisposition locus, rs138042437, rs183373024, rs188140481, single nucleotide polymorphism
Author NameAffiliation
Daniel LeongamornlertInstitute of Cancer Research
Tokhir DadaevInstitute of Cancer Research
Alun ThomasUniversity of Utah School of Medicine
Shannon K McDonnellMayo Clinic
Daniel J SchaidMayo Clinic
Kathleen A CooneyUniversity of Michigan Medical School ann arbor
Kathleen A CooneyUniversity of Michigan Medical School ann arbor
Kathleen A CooneyUniversity of Michigan Medical School ann arbor
Kathleen A CooneyUniversity of Michigan Medical School ann arbor
Ethan M LangeUniversity of North Carolina
Ethan M LangeUniversity of North Carolina
Graham G Giles
Graham G GilesMonash University
Graham G GilesUniversity of Melbourne
Janet L StanfordFred Hutchinson Cancer Research Center (FHCRC)
Janet L StanfordFred Hutchinson Cancer Research Center (FHCRC)
Elaine A OstranderNational Human Genome Research Institute (NHGRI), National Institutes of Health (NIH)
Elaine A OstranderNational Human Genome Research Institute (NHGRI), National Institutes of Health (NIH)
Johanna SchleutkerTurku University Hospital
Johanna SchleutkerTurku University Hospital
William B IsaacsBrady Urological Institute, Johns Hopkins University
Jianfeng XuNorthShore University Health System
Cathy C LaurieUniversity of Washington
Stephen N ThibodeauMayo Clinic
Rosalind A EelesInstitute of Cancer Research
Zsofia Kote-JaraiInstitute of Cancer Research
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