Zobrazeno 1 - 10
of 307
pro vyhledávání: '"D J Schaid"'
Autor:
Keith W. Muir, Amanda B. Spurdle, Anders M. Dale, J K Parsons, Ian G. Mills, D J Schaid, Rosalind A. Eeles, Wojciech Kluzniak, Jenny L Donovan, Andrzej M. Kierzek, C. Slavov, Csilla Sipeky, P Pharoah, Henrik Grönberg, Chun Chieh Fan, Jyotsna Batra, B.G. Nordestgaard, Emma L Turner, F. Wiklund, Jong Y. Park, Johanna Schleutker, Manuel Luedeke, Eleanor I Walsh, Tyler M. Seibert, Zsofia Kote-Jarai, Manuel R. Teixeira, Tammela Tlj., T A Sellers, Freddie C. Hamdy, W. Vogel, Judith A. Clements, Cezary Cybulski, Shannon K. McDonnell, Richard M. Martin, Kathleen Herkommer, Lin H-Y., Olama Aaa., Bernd Holleczek, Huynh-Le M-P., Nora Pashayan, Timothy J. Key, H Brenner, Lisa A. Cannon-Albright, Hardev Pandha, Ruth C. Travis, Dominika Wokołorczyk, Adam S. Kibel, Markus Aly, Doug Easton, Paula Paulo, Ole A. Andreassen, David E. Neal, J A Lane, S. N. Thibodeau, Khaw K-T., Roshan Karunamuni, Ben Schöttker, Vanio Mitev, Sara Benlloch Garcia, Radka Kaneva, Sofia Maia, Christiane Maier, Agnieszka Michael
BackgroundGenetic risk stratification may inform decisions of whether—and when—a man should undergo prostate cancer (PCa) screening. We previously validated a polygenic hazard score (PHS), a weighted sum of 54 single-nucleotide polymorphism genot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4185dbfa6c0a316f465fe6175dce9f9e
https://doi.org/10.1101/619718
https://doi.org/10.1101/619718
Autor:
Robert J. Hamilton, Douglas F. Easton, Suzanne K. Chambers, Edward Giovannucci, Henrik Grönberg, Artitaya Lophatananon, Niclas Håkansson, Sue A. Ingles, Markus Aly, Antonio Gómez-Caamaño, B. E. Henderson, Samantha E.T. Larkin, Manuel Luedeke, Fredrick R. Schumacher, Zan Sun, Karina Dalsgaard Sørensen, Jasmine Lim, Marija Gamulin, Lu Y-J., Meir J. Stampfer, Shannon K. McDonnell, Maria Elena Martinez, Harry Ostrer, Piet Ost, Michael Borre, Monique J. Roobol, F Canzian, D J Schaid, Lin H-Y., Rasmus Bisbjerg, Judith A. Clements, Ezequiel Anokian, Martin Andreas Røder, Ed Saunders, Agnieszka Michael, G Jenster, Bernd Holleczek, Guomin Wang, Jakub Lubiński, Jeri Kim, Genetic Associations, Rosalind A. Eeles, Yves Akoli Koudou, Gemma Castaño-Vinyals, Jing Ma, Leire Moya, Sonja I. Berndt, Thérèse Truong, Maren Weischer, Robert Szulkin, T. Van Den Broeck, Davor Lessel, Børge G. Nordestgaard, Chee Goh, Torben F. Ørntoft, Manolis Kogevinas, Catherine M. Tangen, Gerald L. Andriole, Robert N. Hoover, Ana Vega, Stephanie J. Weinstein, West Cml., Tomislav Kuliš, Neil Fleshner, Graham G. Giles, Barry S. Rosenstein, Z Cui, Marta Cardoso, Tokhir Dadaev, Jenny L Donovan, David E. Neal, Richard M. Martin, Tyrer Jp, Thomas J. Schnoeller, Sandeep Singhal, Clara Cieza-Borrella, Ian M. Thompson, Lisa A. Cannon-Albright, Jong Y. Park, Johanna Schleutker, Brian D. Carter, Esther M. John, Christiane Maier, Matthew Parliament, Antonio Finelli, Mark N. Brook, Gail P. Risbridger, Xin Guo, Lisa G. Horvath, Daniel W. Lin, Mariana C. Stern, Tobias Nordström, Demetrius Albanes, Melissa C. Southey, Zhang H-W., Liesel M. FitzGerald, Christopher I. Amos, Freddie C. Hamdy, P Pharoah, Wayne D. Tilley, Susan M. Gapstur, Teo S-H., Claire Aukim-Hastie, Christopher J. Logothetis, Elio Riboli, Bettina F. Drake, Csilla Sipeky, Alicja Wolk, Cezary Cybulski, Joe Dennis, Olama Aaa., Hermann Brenner, Lorelei A. Mucci, Yuan Chun Ding, L E Beane Freeman, Stella Koutros, G De Meerleer, A. Siddiq, Lisa F. Newcomb, Mitchell J. Machiela, Munaza Ahmed, Jyotsna Batra, Susan L. Neuhausen, Christopher A. Haiman, Stephen J. Chanock, T A Sellers, Florence Menegaux, David V. Conti, Lovise Maehle, O. Cussenot, Neil G. Burnet, Nora Pashayan, Timothy J. Key, P Iversen, Hardev Pandha, Katarina Cuk, David J. Hunter, Khaw K-T., Janet L. Stanford, Loic Le Marchand, Javier Llorca, Steven Joniau, Elaine A. Ostrander, Sarah L. Kerns, van Schaik Rhn., Adam S. Kibel, Robert J. MacInnis, Tammela Tlj., Sune F. Nielsen, Constance Turman, Peter Kraft, Laurence N. Kolonel, Nawaid Usmani, K. De Ruyck, Sara Benlloch, C. Slavov, Azad Hassan Abdul Razack, Milan S. Geybels, Jianfeng Xu, Phyllis J. Goodman, Martin Eklund, Alison M. Dunning, Radka Kaneva, Paul A. Townsend, Kenneth Muir, Manuel R. Teixeira, Sara Lindström, Geraldine Cancel-Tassin, Mechanisms in Oncology, Anssi Auvinen, Victoria L. Stevens, Laura Fachal, Stephen N. Thibodeau, Linda Steele, Manuela Gago-Dominguez, Frank Claessens, Kathryn L. Penney, Fredrik Wiklund, Eli Marie Grindedal, Xin Sheng, Ruth C. Travis, Zsofia Kote-Jarai, Dominika Wokołorczyk, D. Leongamornlert, Paula Paulo, Xueying Mao, Vanio Mitev, Jose Esteban Castelao, Ninghan Feng
Publikováno v:
Nature genetics. 51(2)
Genome-wide association studies (GWAS) and fine-mapping efforts to date have identified more than 100 prostate cancer (PrCa)-susceptibility loci. We meta-analyzed genotype data from a custom high-density array of 46,939 PrCa cases and 27,910 controls
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a590be3ec99e0303f8949b1732215c43
https://pubmed.ncbi.nlm.nih.gov/29892016
https://pubmed.ncbi.nlm.nih.gov/29892016
Autor:
Cezary Cybulski, Rosalind A. Eeles, Douglas F. Easton, Robert Szulkin, Nora Pashayan, Timothy J. Key, B. E. Henderson, G.G. Giles, Hardev Pandha, Jenny L Donovan, Zsofia Kote-Jarai, Henrik Grönberg, Jong Y. Park, Johanna Schleutker, Kenneth Muir, Melissa C. Southey, Fredrick R. Schumacher, Manuel Luedeke, Markus Aly, David E. Neal, Paul D.P. Pharoah, Ruth C. Travis, Børge G. Nordestgaard, Jyotsna Batra, D J Schaid, Fredrik Wiklund, Judith A. Clements, Amanda B. Spurdle, Katja Butterbach, Lisa A. Cannon-Albright, Janet L. Stanford, Kathleen Herkommer, Adam S. Kibel, W. Vogel, Wojciech Kluźniak, Vanio Mitev, Paula Paulo, Liesel M. FitzGerald, Hermann Brenner, T A Sellers, Shannon K. McDonnell, Tammela Tlj., Lin H-Y., Freddie C. Hamdy, Ali Amin Al Olama, Jan Lubinski, Manuel R. Teixeira, C. Slavov, S. N. Thibodeau, Tom Whitington, C. Stegmaier, Andrzej M. Kierzek, Agnieszka Michael, Christiane Maier, Christopher A. Haiman, Sofia Maia, Khaw K-T., Tiina Wahlfors, Martin Eklund, Radka Kaneva, Sara Benlloch
Publikováno v:
The Prostate. 75:1467-1474
BACKGROUND: Polygenic risk scores comprising established susceptibility variants have shown to be informative classifiers for several complex diseases including prostate cancer. For prostate cancer it is unknown if inclusion of genetic markers that h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3bdc3ed21f90505214d096575c0de5c
https://doi.org/10.1002/pros.23037
https://doi.org/10.1002/pros.23037
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Autor:
Artitaya Lophatananon, W. Ryan Diver, Stig E. Bojesen, Roman Corral, Fredrick R. Schumacher, Stephen J. Chanock, Shannon K. McDonnell, Graham G. Giles, Craig C. Teerlink, Douglas F. Easton, Cezary Cybulski, Brian E. Henderson, Judith A. Clements, Ali Amin Al Olama, Francois Bacot, David P. Dearnaley, Elio Riboli, Peter Klarskov, Daniel Vincent, Rosemary A. Wilkinson, Danielle M. Karyadi, Michelle Guy, Vincent Khoo, Christopher A. Haiman, Afshan Siddiq, M. Andreas Røder, Amit Joshi, Jong Y. Park, Walther Vogel, Henrik Grönberg, Angela Cox, Rudolf Kaaks, Nora Pashayan, Timothy J. Key, C. R. J. Woodhouse, Jarmo Virtamo, Meredith Yeager, Malgorzata Tymrakiewicz, Sune F. Nielsen, Richard B. Hayes, Johanna Schleutker, Gianluca Severi, Robert Huddart, Wei Zheng, Thomas A. Sellers, Melanie Maranian, Shahana Ahmed, David E. Neal, Daniel Leongamornlert, Zsofia Kote-Jarai, Tiina Wahlfors, Loic Le Marchand, Kay-Tee Khaw, Tokhir Dadaev, Lisa A. Cannon-Albright, Janet L. Stanford, William J. Blot, Andy C. H. Lee, Freddie C. Hamdy, Siqun L. Zheng, Rosalind A. Eeles, Alison M. Dunning, Mariana C. Stern, Melissa C. Southey, Don M. Conroy, Kenneth Muir, Ahva Shahabi, Alan Horwich, Gerald L. Andriole, Antje E. Rinckleb, Srilakshmi Srinivasan, Tim Dudderidge, Joe Dennis, Radka Kaneva, Vanio Mitev, Angela Morgan, Sue A. Ingles, Adam S. Kibel, Markus Aly, Koveela Govindasami, Maya Ghoussaini, Jenny L Donovan, Manuel R. Teixeira, Emma J. Sawyer, Sara Lindström, Jiangfeng Xu, Maren Weischer, Ed Dicks, Jyotsna Batra, S Jugurnauth-Little, Hui-Yi Lin, Suzanne Kolb, Lisa B. Signorello, Dallas R. English, Antonis C. Antoniou, Federico Canzian, Anssi Auvinen, Mia M. Gaudet, Paula Paulo, Paul D.P. Pharoah, Heiko Müller, Qiuyin Cai, Børge G. Nordestgaard, Esther M. John, Sonja I. Berndt, D J Schaid, Daniele Campa, Chris Ogden, Colin Cooper, Craig Luccarini, Jan Lubinski, Elaine A. Ostrander, Ruth C. Travis, Dominika Wokołorczyk, John L. Hopper, Sofia Maia, Sara Benlloch, Chris Parker, Erika M. Kwon, Nicholas van As, Caroline Baynes, C. Slavov, Teuvo L.J. Tammela, Ethan M. Lange, Daniel C. Tessier, David J. Hunter, Dietrich Rothenbacher, Robert A. Stephenson, Liesel M. FitzGerald, Christiane Maier, Hermann Brenner, Kathleen A. Cooney, Graham A. Colditz, Felicity Lose, Edward J. Saunders, Demetrius Albanes, Stephen N. Thibodeau, Fredrik Wiklund, Amanda B. Spurdle, Jan Adolfsson, Susan M. Gapstur, Peter Kraft, Bettina F. Drake, Alan Thompson
Publikováno v:
Nature Genetics
Nature Genetics; Vol 45
Nature Genetics; Vol 45
Prostate cancer is the most frequently diagnosed cancer in males in developed countries. To identify common prostate cancer susceptibility alleles, we genotyped 211,155 SNPs on a custom Illumina array (iCOGS) in blood DNA from 25,074 prostate cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dc5d5f82460009b403d064c3a16e687
https://doi.org/10.1038/ng.2560
https://doi.org/10.1038/ng.2560
Autor:
Shao, Mengting1 (AUTHOR), Tian, Min1 (AUTHOR), Chen, Kaiyang1 (AUTHOR), Jiang, Hangjin2 (AUTHOR), Zhang, Shuting1 (AUTHOR), Li, Zhenghui1 (AUTHOR), Shen, Yan1 (AUTHOR), Chen, Feng1 (AUTHOR), Shen, Baixin3 (AUTHOR), Cao, Chen1,3 (AUTHOR) caochen@njmu.edu.cn, Gu, Ning1,4 (AUTHOR) guning@nju.edu.cn
Publikováno v:
Advanced Science. 9/25/2024, Vol. 11 Issue 36, p1-14. 14p.
Autor:
D. J Schaid
Publikováno v:
AACR Education book. 2008:465-469
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f4a2dbc054ec4817c750a7312927c0d
https://doi.org/10.1158/aacr.edb-08-8071
https://doi.org/10.1158/aacr.edb-08-8071
Autor:
Scott T. Weiss, D. J. Schaid, Stephen L. Lake, Nan M. Laird, Helen N. Lyon, Kelan G. Tantisira, Edwin K. Silverman
Publikováno v:
Human heredity, 55(1), 56-65. KARGER
In the study of complex traits, the utility of linkage analysis and single marker association tests can be limited for researchers attempting to elucidate the complex interplay between a gene and environmental covariates. For these purposes, tests of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a605b4db773e4368e5c12154de61474d
https://research.rug.nl/en/publications/22a7537c-4ea4-4f4b-801f-854b46e1a9d6
https://research.rug.nl/en/publications/22a7537c-4ea4-4f4b-801f-854b46e1a9d6
Autor:
D J, Brandhagen, V F, Fairbanks, W P, Baldus, C I, Smith, K E, Kruckeberg, D J, Schaid, S N, Thibodeau
Publikováno v:
American Journal of Gastroenterology. 95:2910-2914
The HFE gene contains two mutant alleles; C282Y and H63D. The C282Y mutation occurs in 55-100% of patients with hereditary hemochromatosis. The aim of our study was to re-examine the frequencies of the C282Y and H63D mutations in patients with mild a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9095c810ec3f1ffd0fed97ca9a060ddd
https://doi.org/10.1111/j.1572-0241.2000.03203.x
https://doi.org/10.1111/j.1572-0241.2000.03203.x
Autor:
Shannon K. McDonnell, D J Schaid, S N Thibodeau, F J Couch, D I Schwartz, J A Carney, Mark R. Pittelkow, Lawrence J. Burgart, Lisa A. Boardman, David A. Ahlquist, Lynn C. Hartmann
Publikováno v:
Medicine. 79:293-298
Most reports describe an increased risk of malignancy in Peutz-Jeghers syndrome (PJS). We identified individuals with PJS-like pigmentation but no polyposis, designated as isolated mucocutaneous melanotic pigmentation (IMMP), and 1) characterized the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de4e2e545c8dfa79e15d368a4aed30f
https://doi.org/10.1097/00005792-200009000-00002
https://doi.org/10.1097/00005792-200009000-00002
Autor:
Don M. Conroy, David E. Neal, Jong Y. Park, Johanna Schleutker, Gerald L. Andriole, Amanda B. Spurdle, Peter Kraft, Alison M. Dunning, Esther M. John, Angela Morgan, Kenneth Muir, Douglas F. Easton, Fredrick R. Schumacher, Susan M. Gapstur, Rosalind A. Eeles, Stig E. Bojesen, Zsofia Kote-Jarai, Paul D.P. Pharoah, Francois Bacot, Jan Lubinski, Janet L. Stanford, Hermann Brenner, Cezary Cybulski, Caroline Baynes, Judith A. Clements, Jenny L Donovan, Ruth C. Travis, Edward J. Saunders, Kay-Tee Khaw, Silvia Halim, Demetrius Albanes, Stephen J. Chanock, Malgorzata Tymrakiewicz, Manuel R. Teixeira, D J Schaid, Sara Lindström, Loic Le Marchand, Sarah Jugurn-Little, Stephen N. Thibodeau, Fredrik Wiklund, Lisa A. Cannon-Albright, Maren Weischer, David J. Hunter, Graham G. Giles, Brian E. Henderson, Rosemary A. Wilkinson, Lisa B. Signorello, Michelle Guy, Craig Luccarini, Daniel Leongamornlert, Elio Riboli, Henrik Grönberg, Timothy J. Key, Christiane Maier, Joe Dennis, Walther Vogel, Ali Amin Al Olama, Helen Ross-Adams, Sonja I. Berndt, Ed Dicks, Sara Benlloch, Daniel Vincent, Freddie C. Hamdy, Sue A. Ingles, D. Campa, Rudolf Kaaks, Adam S. Kibel, Gianluca Severi, Daniel C. Tessier, Tokhir Dadaev, Christopher A. Haiman, Richard B. Hayes, Radka Kaneva, Koveela Govindasami, Emma J. Sawyer, Jyotsna Batra, Roslin Russel, Elaine A. Ostrander, Federico Canzian
Publikováno v:
Europe PubMed Central
Human Molecular Genetics
Human Molecular Genetics; Vol 22
Human Molecular Genetics
Human Molecular Genetics; Vol 22
Associations between single nucleotide polymorphisms (snps) at 5p15 and multiple cancer types have been reported. we have previously shown evidence for a strong association between prostate cancer (prca) risk and rs2242652 at 5p15, intronic in the te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74b7a48bf9ebefe593d39a863f2dd871
http://hdl.handle.net/11568/458483
http://hdl.handle.net/11568/458483