Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
Author(s) -
Craig C. Teerlink,
Daniel Leongamornlert,
Tokhir Dadaev,
Alun Thomas,
James M. Farnham,
Robert A. Stephenson,
Shaun M. Riska,
Shan K. McDonnell,
Daniel J. Schaid,
William J. Catàlona,
S. Lilly Zheng,
Kathleen A. Cooney,
Anna M. Ray,
Kimberly A. Zuhlke,
Ethan M. Lange,
Graham G. Giles,
Melissa C. Southey,
Liesel M. FitzGerald,
Antje E. Rinckleb,
Manuel Luedeke,
Christiane Maier,
Janet L. Stanford,
Elaine A. Ostrander,
Elina Kaikkonen,
Csilla Sipeky,
Teuvo L.J. Tammela,
Johanna Schleutker,
Kathleen E. Wiley,
Sarah D. Isaacs,
Patrick C. Walsh,
William B. Isaacs,
Jianfeng Xu,
Géraldine CancelTassin,
Olivier Cussenot,
Diptasri Mandal,
Cecelia Laurie,
Cathy C. Laurie,
Stephen N. Thibodeau,
Rosalind A. Eeles,
Zsofia KoteJarai,
Lisa CanAlbright
Publication year - 2016
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/3mny-1202
Subject(s) - haplotype , genetics , genome wide association study , prostate cancer , biology , genome , genetic association , cancer , gene , single nucleotide polymorphism , genotype
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