Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating...
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
About this item
Full title
Author / Creator
International Consortium for Prostate Cancer Genetics , The PRACTICAL consortium , PRACTICAL consortium , Teerlink, Craig C. , Leongamornlert, Daniel , Dadaev, Tokhir , Thomas, Alun , Farnham, James , Stephenson, Robert A. , Riska, Shaun , McDonnell, Shannon K. , Schaid, Daniel J. , Catalona, William J. , Zheng, S. Lilly , Cooney, Kathleen A. , Ray, Anna M. , Zuhlke, Kimberly A. , Lange, Ethan M. , Giles, Graham G. , Southey, Melissa C. , Fitzgerald, Liesel M. , Rinckleb, Antje , Luedeke, Manuel , Maier, Christiane , Stanford, Janet L. , Ostrander, Elaine A. , Kaikkonen, Elina M. , Sipeky, Csilla , Tammela, Teuvo , Schleutker, Johanna , Wiley, Kathleen E. , Isaacs, Sarah D. , Walsh, Patrick C. , Isaacs, William B. , Xu, Jianfeng , Cancel-Tassin, Geraldine , Cussenot, Olivier , Mandal, Diptasri , Laurie, Cecelia , Laurie, Cathy , Thibodeau, Stephen N. , Eeles, Rosalind A. , Kote-Jarai, Zsofia and Cannon-Albright, Lisa
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Subjects
More information
Scope and Contents
Contents
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 Prostate Cancer Genetics (ICPCG) has now performed a GWAS of 2511 (unrelated) familial prostate cancer cases and 1382 unaffected controls from 12...
Alternative Titles
Full title
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
Authors, Artists and Contributors
Author / Creator
The PRACTICAL consortium
PRACTICAL consortium
Teerlink, Craig C.
Leongamornlert, Daniel
Dadaev, Tokhir
Thomas, Alun
Farnham, James
Stephenson, Robert A.
Riska, Shaun
McDonnell, Shannon K.
Schaid, Daniel J.
Catalona, William J.
Zheng, S. Lilly
Cooney, Kathleen A.
Ray, Anna M.
Zuhlke, Kimberly A.
Lange, Ethan M.
Giles, Graham G.
Southey, Melissa C.
Fitzgerald, Liesel M.
Rinckleb, Antje
Luedeke, Manuel
Maier, Christiane
Stanford, Janet L.
Ostrander, Elaine A.
Kaikkonen, Elina M.
Sipeky, Csilla
Tammela, Teuvo
Schleutker, Johanna
Wiley, Kathleen E.
Isaacs, Sarah D.
Walsh, Patrick C.
Isaacs, William B.
Xu, Jianfeng
Cancel-Tassin, Geraldine
Cussenot, Olivier
Mandal, Diptasri
Laurie, Cecelia
Laurie, Cathy
Thibodeau, Stephen N.
Eeles, Rosalind A.
Kote-Jarai, Zsofia
Cannon-Albright, Lisa
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5020907
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5020907
Other Identifiers
ISSN
0340-6717
E-ISSN
1432-1203
DOI
10.1007/s00439-016-1690-6
