Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ros Eeles"'
Autor:
Fredrick R. Schumacher, Chee Goh, Ros Eeles, Clara Cieza-Borrella, Edward J. Saunders, Zsofia Kote-Jarai, Mahbubl Ahmed
Publikováno v:
Prostate Cancer and Prostatic Diseases
Ahmed, M, Goh, C, Saunders, E, Cieza-Borrella, C, Kote-Jarai, Z, Schumacher, F R, Eeles, R & The PRACTICAL Consortium 2020, ' Germline genetic variation in prostate susceptibility does not predict outcomes in the chemoprevention trials PCPT and SELECT ', Prostate Cancer and Prostatic Diseases, vol. 23, no. 2, pp. 333-342 . https://doi.org/10.1038/s41391-019-0181-y
Ahmed, M, Goh, C, Saunders, E, Cieza-Borrella, C, Kote-Jarai, Z, Schumacher, F R, Eeles, R & The PRACTICAL Consortium 2020, ' Germline genetic variation in prostate susceptibility does not predict outcomes in the chemoprevention trials PCPT and SELECT ', Prostate Cancer and Prostatic Diseases, vol. 23, no. 2, pp. 333-342 . https://doi.org/10.1038/s41391-019-0181-y
Background The development of prostate cancer can be influenced by genetic and environmental factors. Numerous germline SNPs influence prostate cancer susceptibility. The functional pathways in which these SNPs increase prostate cancer susceptibility
Autor:
Daniel R. Barnes, Matti A. Rookus, Lesley McGuffog, Goska Leslie, Thea M. Mooij, Joe Dennis, Nasim Mavaddat, Julian Adlard, Munaza Ahmed, Kristiina Aittomäki, Nadine Andrieu, Irene L. Andrulis, Norbert Arnold, Banu K. Arun, Jacopo Azzollini, Judith Balmaña, Rosa B. Barkardottir, Daniel Barrowdale, Javier Benitez, Pascaline Berthet, Katarzyna Białkowska, Amie M. Blanco, Marinus J. Blok, Bernardo Bonanni, Susanne E. Boonen, Åke Borg, Aniko Bozsik, Angela R. Bradbury, Paul Brennan, Carole Brewer, Joan Brunet, Saundra S. Buys, Trinidad Caldés, Maria A. Caligo, Ian Campbell, Lise Lotte Christensen, Wendy K. Chung, Kathleen B.M. Claes, Chrystelle Colas, Marie-Agnès Collonge-Rame, Capucine Delnatte, Laurence Faivre, Sophie Giraud, Christine Lasset, Véronique Mari, Noura Mebirouk, Emmanuelle Mouret-Fourme, Hélène Schuster, Dominique Stoppa-Lyonnet, Antonis Antoniou, Jackie Cook, Rosemarie Davidson, Douglas Easton, Ros Eeles, D. Gareth Evans, Debra Frost, Helen Hanson, Louise Izatt, Kai-ren Ong, Lucy Side, Aoife O’Shaughnessy-Kirwan, Marc Tischkowitz, Lisa Walker, Mary B. Daly, Miguel de la Hoya, Robin de Putter, Peter Devilee, Orland Diez, Yuan Chun Ding, Susan M. Domchek, Cecilia M. Dorfling, Martine Dumont, Bent Ejlertsen, Christoph Engel, Lenka Foretova, Florentia Fostira, Michael Friedlander, Eitan Friedman, Patricia A. Ganz, Judy Garber, Andrea Gehrig, Anne-Marie Gerdes, Paul Gesta, Gord Glendon, Andrew K. Godwin, David E. Goldgar, Anna González-Neira, Mark H. Greene, Daphne Gschwantler-Kaulich, Eric Hahnen, Ute Hamann, Julia Hentschel, Frans B.L. Hogervorst, Maartje J. Hooning, Judit Horvath, Chunling Hu, Peter J. Hulick, Evgeny N. Imyanitov, Georgia Chenevix-Trench, Kelly-Anne Phillips, Amanda Spurdle, Marinus Blok, Frans Hogervorst, Maartje Hooning, Marco Koudijs, Arjen Mensenkamp, Hanne Meijers-Heijboer, Matti Rookus, Klaartje van Engelen, Catherine Noguès, Claudine Isaacs, Angel Izquierdo, Anna Jakubowska, Paul A. James, Ramunas Janavicius, Esther M. John, Vijai Joseph, Beth Y. Karlan, Karin Kast, Torben A. Kruse, Ava Kwong, Yael Laitman, Conxi Lazaro, Jenny Lester, Fabienne Lesueur, Annelie Liljegren, Jennifer T. Loud, Jan Lubiński, Phuong L. Mai, Siranoush Manoukian, Hanne E.J. Meijers-Heijboer, Alfons Meindl, Arjen R. Mensenkamp, Austin Miller, Marco Montagna, Semanti Mukherjee, Anna Marie Mulligan, Katherine L. Nathanson, Susan L. Neuhausen, Heli Nevanlinna, Dieter Niederacher, Finn Cilius Nielsen, Liene Nikitina-Zake, Edith Olah, Olufunmilayo I. Olopade, Ana Osorio, Claus-Eric Ott, Laura Papi, Sue K. Park, Michael T. Parsons, Inge Sokilde Pedersen, Bernard Peissel, Ana Peixoto, Paolo Peterlongo, Georg Pfeiler, Karolina Prajzendanc, Miquel Angel Pujana, Paolo Radice, Juliane Ramser, Susan J. Ramus, Johanna Rantala, Gad Rennert, Harvey A. Risch, Mark Robson, Karina Rønlund, Ritu Salani, Leigha Senter, Payal D. Shah, Priyanka Sharma, Lucy E. Side, Christian F. Singer, Thomas P. Slavin, Penny Soucy, Melissa C. Southey, Amanda B. Spurdle, Doris Steinemann, Zoe Steinsnyder, Christian Sutter, Yen Yen Tan, Manuel R. Teixeira, Soo Hwang Teo, Darcy L. Thull, Silvia Tognazzo, Amanda E. Toland, Alison H. Trainer, Nadine Tung, Elizabeth J. van Rensburg, Ana Vega, Jeroen Vierstraete, Gabriel Wagner, Shan Wang-Gohrke, Barbara Wappenschmidt, Jeffrey N. Weitzel, Siddhartha Yadav, Xin Yang, Drakoulis Yannoukakos, Dario Zimbalatti, Kenneth Offit, Mads Thomassen, Fergus J. Couch, Rita K. Schmutzler, Jacques Simard, Douglas F. Easton, Antonis C. Antoniou
Publikováno v:
Genetics in Medicine, 22(10), 1653-1666. Lippincott Williams and Wilkins
Genetics in Medicine
Genetics in Medicine, 2020, 22 (10), pp.1653-1666. ⟨10.1038/s41436-020-0862-x⟩
Scientia
Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Delnatte, C, Devilee, P, Horvath, J, Nielsen, F C, Pedersen, I S, GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Barnes, D R, Rookus, M A, Mcguffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-rame, M, Cook, J, Daly, M B, Davidson, R, De La Hoya, M, De Putter, R, Delnatte, C, Devilee, P, Ejlertsen, B, Gerdes, A, Nielsen, F C & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M-A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Delnatte, C, Devilee, P, Diez, O, Ding, Y C & Pedersen, I S 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Genetics in Medicine, 22(10), 1653-1666. Nature Publishing Group
Genetics in Medicine, 22(10), 1653-1666. Lippincott Williams & Wilkins
Genetics in Medicine, 22(10), 1653-1666. SPRINGERNATURE
Genetics in Medicine, Nature Publishing Group, 2020, 22 (10), pp.1653-1666. ⟨10.1038/s41436-020-0862-x⟩
Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L-L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Gerdes, A M, Kruse, T A, Pedersen, I S, Rønlund, K, Thomassen, M, GEMO Study Collaborators, EMBRACE Collaborators, kConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Genetics in Medicine, 22, 1653-1666
GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Dipòsit Digital de la UB
Universidad de Barcelona
GENETICS IN MEDICINE
Genetics in Medicine, 22, 10, pp. 1653-1666
Genetics in Medicine
Genetics in Medicine, 2020, 22 (10), pp.1653-1666. ⟨10.1038/s41436-020-0862-x⟩
Scientia
Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Delnatte, C, Devilee, P, Horvath, J, Nielsen, F C, Pedersen, I S, GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Barnes, D R, Rookus, M A, Mcguffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-rame, M, Cook, J, Daly, M B, Davidson, R, De La Hoya, M, De Putter, R, Delnatte, C, Devilee, P, Ejlertsen, B, Gerdes, A, Nielsen, F C & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M-A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Delnatte, C, Devilee, P, Diez, O, Ding, Y C & Pedersen, I S 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Genetics in Medicine, 22(10), 1653-1666. Nature Publishing Group
Genetics in Medicine, 22(10), 1653-1666. Lippincott Williams & Wilkins
Genetics in Medicine, 22(10), 1653-1666. SPRINGERNATURE
Genetics in Medicine, Nature Publishing Group, 2020, 22 (10), pp.1653-1666. ⟨10.1038/s41436-020-0862-x⟩
Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L-L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Gerdes, A M, Kruse, T A, Pedersen, I S, Rønlund, K, Thomassen, M, GEMO Study Collaborators, EMBRACE Collaborators, kConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Genetics in Medicine, 22, 1653-1666
GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x
Dipòsit Digital de la UB
Universidad de Barcelona
GENETICS IN MEDICINE
Genetics in Medicine, 22, 10, pp. 1653-1666
Contains fulltext : 229292.pdf (Publisher’s version ) (Open Access) PURPOSE: We assessed the associations between population-based polygenic risk scores (PRS) for breast (BC) or epithelial ovarian cancer (EOC) with cancer risks for BRCA1 and BRCA2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3029ddb1c317fd1f62f6f475f3d6664
https://research.vumc.nl/en/publications/df63a109-0100-470b-9379-c44745d8115d
https://research.vumc.nl/en/publications/df63a109-0100-470b-9379-c44745d8115d
Autor:
Anis A. Hamid, Karina Dalsgaard Sørensen, Timothy R. Rebbeck, Mark Pomerantz, Jong Y. Park, Matthew L. Freedman, Sarah C. Markt, Sonja I. Berndt, Ana Vega, Ros Eeles, Kristina M. Jordahl, Christopher Sweeney, Victoria Wang, Daniela Börnigen, Lorelei A. Mucci, Gwo-Shu Mary Lee, Huma Q. Rana, Nawaid Usmani, Milan S. Geybels, Janet L. Stanford, Frank Claessens, Kathryn L. Penney, Curtis Huttenhower, Travis Gerke
Publikováno v:
Prostate, 81(10), 683-693. Wiley
Prostate
Wang, V, Geybels, M S, Jordahl, K M, Gerke, T, Hamid, A, Penney, K L, Markt, S C, Freedman, M, Pomerantz, M, Lee, G-S M, Rana, H, Börnigen, D, Rebbeck, T R, Huttenhower, C, Eeles, R A, Stanford, J L, Consortium, P, Berndt, S I, Claessens, F, Sørensen, K D, Park, J Y, Vega, A, Usmani, N, Mucci, L & Sweeney, C J 2021, ' A polymorphism in the promoter of FRAS1 is a candidate SNP associated with metastatic prostate cancer ', The Prostate, vol. 81, no. 10, pp. 683-693 . https://doi.org/10.1002/pros.24148
Prostate
Wang, V, Geybels, M S, Jordahl, K M, Gerke, T, Hamid, A, Penney, K L, Markt, S C, Freedman, M, Pomerantz, M, Lee, G-S M, Rana, H, Börnigen, D, Rebbeck, T R, Huttenhower, C, Eeles, R A, Stanford, J L, Consortium, P, Berndt, S I, Claessens, F, Sørensen, K D, Park, J Y, Vega, A, Usmani, N, Mucci, L & Sweeney, C J 2021, ' A polymorphism in the promoter of FRAS1 is a candidate SNP associated with metastatic prostate cancer ', The Prostate, vol. 81, no. 10, pp. 683-693 . https://doi.org/10.1002/pros.24148
BACKGROUND: Inflammation and one of its mediators, NF-kappa B (NFκB), have been implicated in prostate cancer carcinogenesis. We assessed whether germline polymorphisms associated with NFκB are associated with the risk of developing lethal disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a6d58fc258d0073462c02aa355e1e00
https://cris.maastrichtuniversity.nl/en/publications/e63af996-9e2e-42d3-9cdc-227c22ce54a6
https://cris.maastrichtuniversity.nl/en/publications/e63af996-9e2e-42d3-9cdc-227c22ce54a6
Autor:
Luigi Mori, Maria Christina Sini, Michela Biancolella, Florentia Fostira, Andreas Hadjisavvas, Susan M. Domchek, Conxi Lázaro, Gabriele Lorenzo Capone, T. L. Chris Chan, Jeffrey N. Weitzel, Mark E. Robson, Diana Eccles, Inge Søkilde Pedersen, Gianluca Tedaldi, Sarah M. Nielsen, Iris L. Romero, Arcangela De Nicolo, Orland Diez, Arjen R. Mensenkamp, Jana Soukupova, Pietro Cavalli, Ros Eeles, Ana Vega, Kathleen Claes, Maria A. Loizidou, David E. Goldgar, Olufunmilayo I. Olopade, Amanda E. Toland, Yvonne Wallis, Mads Thomassen, Setareh Moghadasi, Fergus J. Couch, Mariarosaria Calvello, Judith Balmaña, Encarna B. Gomez-Garcia, Maria Rossing, Claude Houdayer, Erica Vaccari, April Morrow, Thomas Hansen, Maria Grazia Tibiletti, Sophie Krieger, Liliana Varesco, Nadia Naldi, Therese Törngren, Rien Blok, Fahd Al-Mulla, Henriette Roed Nielsen, Angela R. Solano, Amanda B. Spurdle, Akira Hirasawa, Laura Cortesi, Siranoush Manoukian, Maria A. Caligo, Barbara Wappenschmidt, Manuel R. Teixeira, Marianna Puzzo, Miguel de la Hoya, Alvaro N.A. Monteiro, Petra Kleiblova, Anna Efremidis, Edenir Inêz Palmero, Simona De Toffol, Nicholas Pachter, Maria Piane
Publikováno v:
Nielsen, S M, Eccles, D M, Romero, I L, Al-Mulla, F, Balmaña, J, Biancolella, M, Blok, R, Caligo, M A, Calvello, M, Capone, G L, Cavalli, P, Chan, T L C, Claes, K B M, Cortesi, L, Couch, F J, de la Hoya, M, De Toffol, S, Diez, O, Domchek, S M, Eeles, R, Efremidis, A, Fostira, F, Goldgar, D, Hadjisavvas, A, Hansen, T V O, Hirasawa, A, Houdayer, C, Kleiblova, P, Krieger, S, Lázaro, C, Loizidou, M, Manoukian, S, Mensenkamp, A R, Moghadasi, S, Monteiro, A N, Mori, L, Morrow, A, Naldi, N, Nielsen, H R, Olopade, O I, Pachter, N S, Palmero, E I, Pedersen, I S, Piane, M, Puzzo, M, Robson, M, Rossing, M, Sini, M C, Solano, A & Thomassen, M 2018, ' Genetic testing and clinical management practices for variants in non-BRCA1/2 breast (and breast/ovarian) cancer susceptibility genes : An international survey by the Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) clinical working group ', JCO Precision Oncology, vol. 2 . https://doi.org/10.1200/PO.18.00091
Nielsen, S M, Eccles, D M, Romero, I L, Al-Mulla, F, Balmaña, J, Biancolella, M, Blok, R, Caligo, M A, Calvello, M, Capone, G L, Cavalli, P, Chan, T L C, Claes, K B M, Cortesi, L, Couch, F J, de la Hoya, M, De Toffol, S, Diez, O, Domchek, S M, Eeles, R, Efremidis, A, Fostira, F, Goldgar, D, Hadjisavvas, A, Hansen, T V O, Hirasawa, A, Houdayer, C, Kleiblova, P, Krieger, S, Lázaro, C, Loizidou, M, Manoukian, S, Mensenkamp, A R, Moghadasi, S, Monteiro, A N, Mori, L, Morrow, A, Naldi, N, Nielsen, H R, Olopade, O I, Pachter, N S, Palmero, E I, Pedersen, I S, Piane, M, Puzzo, M, Robson, M, Rossing, M, Sini, M C, Solano, A, Soukupova, J, Tedaldi, G, Teixeira, M, Thomassen, M, Tibiletti, M G, Toland, A, Törngren, T, Vaccari, E, Varesco, L, Vega, A, Wallis, Y, Wappenschmidt, B, Weitzel, J, Spurdle, A B, De Nicolo, A & Gómez-García, E B 2018, ' Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes : An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group ', JCO Precision Oncology, vol. 2 . https://doi.org/10.1200/PO.18.00091
JCO Precision Oncology, 2, 1-43. American Society of Clinical Oncology
Journal of clinical oncology 2 (2018). doi:10.1200/PO.18.00091
info:cnr-pdr/source/autori:Nielsen, Sarah M.; Eccles, Diana M.; Romero, Iris L.; Al-Mulla, Fand; Balmana, Judith; Biancolella, Michela; Blok, Rien; Caligo, Maria Adelaide; Calvello, Mariarosaria; Capone, Gabriele Lorenzo; Cavalli, Pietro; Chan, T. L. Chris; Claes, Kathleen B. M.; Cortesi, Laura; Couch, Fergus J.; de la Hoya, Miguel; de Toffol, Simona; Diez, Orland; Domchek, Susan M.; Eeles, Ros; Efremidis, Anna; Fostira, Florentia; Goldgar, David; Hadjisavvas, Andreas; Hansen, Thomas v O.; Hirasawa, Akira; Houdayer, Claude; Kleiblova, Petra; Krieger, Sophie; Lazaro, Conxi; Loizidou, Maria; Manoukian, Siranoush; Mensenkamp, Arjen R.; Moghadasi, Setareh; Monteiro, Alvaro N.; Mori, Luigi; Morrow, April; Naldi, Nadia; Nielsen, Henriette R.; Olopade, Olufunmilayo, I; Pachter, Nicholas S.; Palrnero, Edenir, I; Pedersen, Inge S.; Piane, Maria; Puzzo, Marianna; Robson, Mark; Rossing, Maria; Sini, Maria Christina; Solano, Angela; Soukupova, Jana; Tedaldi, Gianluca; Teixeira, Manuel; Thomassen, Mads; Tibiletti, Maria Grazia; Toland, Amanda; Torngren, Therese; Vaccari, Erica; Varesco, Liliana; Vega, Ana; Wallis, Yvonne; Wappenschmidt, Barbara; Weitzel, Jeffrey; Spurdle, Amanda B.; De Nicolo, Arcangela; Gomez-Garcia, Encarna B./titolo:Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1%2F2 Breast (and Breast%2FOvarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group/doi:10.1200%2FPO.18.00091/rivista:Journal of clinical oncology/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:2
JCO Precision Oncology
Nielsen, S M, Eccles, D M, Romero, I L, Al-Mulla, F, Balmaña, J, Biancolella, M, Blok, R, Caligo, M A, Calvello, M, Capone, G L, Cavalli, P, Chan, T L C, Claes, K B M, Cortesi, L, Couch, F J, de la Hoya, M, De Toffol, S, Diez, O, Domchek, S M, Eeles, R, Efremidis, A, Fostira, F, Goldgar, D, Hadjisavvas, A, Hansen, T V O, Hirasawa, A, Houdayer, C, Kleiblova, P, Krieger, S, Lázaro, C, Loizidou, M, Manoukian, S, Mensenkamp, A R, Moghadasi, S, Monteiro, A N, Mori, L, Morrow, A, Naldi, N, Nielsen, H R, Olopade, O I, Pachter, N S, Palmero, E I, Pedersen, I S, Piane, M, Puzzo, M, Robson, M, Rossing, M, Sini, M C, Solano, A, Soukupova, J, Tedaldi, G, Teixeira, M, Thomassen, M, Tibiletti, M G, Toland, A, Törngren, T, Vaccari, E, Varesco, L, Vega, A, Wallis, Y, Wappenschmidt, B, Weitzel, J, Spurdle, A B, De Nicolo, A & Gómez-García, E B 2018, ' Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes : An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group ', JCO Precision Oncology, vol. 2 . https://doi.org/10.1200/PO.18.00091
JCO Precision Oncology, 2, 1-43. American Society of Clinical Oncology
Journal of clinical oncology 2 (2018). doi:10.1200/PO.18.00091
info:cnr-pdr/source/autori:Nielsen, Sarah M.; Eccles, Diana M.; Romero, Iris L.; Al-Mulla, Fand; Balmana, Judith; Biancolella, Michela; Blok, Rien; Caligo, Maria Adelaide; Calvello, Mariarosaria; Capone, Gabriele Lorenzo; Cavalli, Pietro; Chan, T. L. Chris; Claes, Kathleen B. M.; Cortesi, Laura; Couch, Fergus J.; de la Hoya, Miguel; de Toffol, Simona; Diez, Orland; Domchek, Susan M.; Eeles, Ros; Efremidis, Anna; Fostira, Florentia; Goldgar, David; Hadjisavvas, Andreas; Hansen, Thomas v O.; Hirasawa, Akira; Houdayer, Claude; Kleiblova, Petra; Krieger, Sophie; Lazaro, Conxi; Loizidou, Maria; Manoukian, Siranoush; Mensenkamp, Arjen R.; Moghadasi, Setareh; Monteiro, Alvaro N.; Mori, Luigi; Morrow, April; Naldi, Nadia; Nielsen, Henriette R.; Olopade, Olufunmilayo, I; Pachter, Nicholas S.; Palrnero, Edenir, I; Pedersen, Inge S.; Piane, Maria; Puzzo, Marianna; Robson, Mark; Rossing, Maria; Sini, Maria Christina; Solano, Angela; Soukupova, Jana; Tedaldi, Gianluca; Teixeira, Manuel; Thomassen, Mads; Tibiletti, Maria Grazia; Toland, Amanda; Torngren, Therese; Vaccari, Erica; Varesco, Liliana; Vega, Ana; Wallis, Yvonne; Wappenschmidt, Barbara; Weitzel, Jeffrey; Spurdle, Amanda B.; De Nicolo, Arcangela; Gomez-Garcia, Encarna B./titolo:Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1%2F2 Breast (and Breast%2FOvarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group/doi:10.1200%2FPO.18.00091/rivista:Journal of clinical oncology/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:2
JCO Precision Oncology
Purpose To describe a snapshot of international genetic testing practices, specifically regarding the use of multigene panels, for hereditary breast/ovarian cancers. We conducted a survey through the Evidence-Based Network for the Interpretation of G
Autor:
Olufunmilayo I. Olopade, Darcy L. Thull, Raanan Berger, Mary Beth Terry, Michel Longy, Timothy R. Rebbeck, Gord Glendon, Min Hyuk Lee, Javier Benitez, Mark T. Rogers, Mark H. Greene, Dezheng Huo, Adalgeir Arason, Carole Brewer, Siranoush Manoukian, Jackie Cook, Louise Izatt, Yuan Chun Ding, Dieter Niederacher, Nadine Tung, Sophie Giraud, Henriette Roed Nielsen, Antonis C. Antoniou, Bernhard H. F. Weber, Bruno Buecher, Goska Leslie, Amanda E. Toland, Anna Marie Mulligan, Ane Y. Schmidt, Noralane M. Lindor, Véronique Mari, Tara M. Friebel, Cecilia M. Dorfling, Ugnius Mickys, Lenka Foretova, Andrew K. Godwin, Bernd Dworniczak, Tsun Leung Chan, Monica Barile, Angela R. Solano, Susan J. Ramus, Laurence Faivre, Susan L. Neuhausen, Ana Peixoto, Julio Abugattas, Mattias Van Heetvelde, Jacqueline Eason, Muhammad Usman Rashid, Barbara Pasini, Henrique de Campos Reis Galvão, Heli Nevanlinna, Lucy Side, Nina Peruga, Marco Montagna, Amie Blanco, Alison H. Trainer, Cristina Zanzottera, Arjen R. Mensenkamp, Douglas F. Easton, Inge Søkilde Pedersen, Kenneth Offit, Judy Garber, Sook-Yee Yoon, Uffe Birk Jensen, Irene Konstantopoulou, Barbara Wappenschmidt, Stefanie Engert, Robert L. Nussbaum, Kai-ren Ong, Ros Eeles, Marinus J. Blok, Yael Laitman, Alex Teulé, Marion Gauthier-Villars, Daniel Barrowdale, Mads Thomassen, Torben A Kruse, Hanne Meijers-Heijboer, Abigail Thomas, Susan M. Domchek, Jacques Simard, Jamal Zidan, Paul A. James, Rob B. van der Luijt, Nina Ditsch, Annette Lee, Joseph Vijai, Kathleen R. Blazer, Elizabeth J. van Rensburg, János Papp, Lizet E. van der Kolk, Eitan Friedman, Pascal Pujol, Johanna Rantala, Patricia A. Ganz, Esther M. John, Conxi Lázaro, Jacek Gronwald, Paul Gesta, Jan Hauke, Simona Agata, Leo Auerbach, Paolo Radice, Fabienne Prieur, Beth Y. Karlan, Antoine De Pauw, Paolo Peterlongo, Sandrine M. Caputo, Sue K. Park, Marc Tischkowitz, Jocelyne Chiquette, Karin Kast, Annemieke H. van der Hout, Eric Hahnen, Grzegorz Sukiennicki, Debra Frost, Noura Mebirouk, Angel Izquierdo, Alex Henderson, Carolina Velázquez, Raymonda Varon-Mateeva, J. Margriet Collée, Soo-Hwang Teo, Esther Pohl, Rosa B. Barkardottir, Rita K. Schmutzler, Kim De Leeneer, Andrea Gehrig, D. Gareth Evans, Jeffrey N. Weitzel, Katherine L. Nathanson, Lesley McGuffog, Christoph Engel, Amanda B. Spurdle, Austin Miller, Edith Olah, Hans Ehrencrona, Almuth Caliebe, Zoltan Matrai, Ian G. Campbell, Christina G. Selkirk, Kirsten B. Moysich, Ella Asseryanis, Wendy K. Chung, Michael T. Parsons, Shan Wang-Gohrke, Thomas P. Slavin, Karen H. Lu, Gustavo C. Rodriguez, Julian Adlard, Christian F. Singer, Lesley Andrews, Jacopo Azzollini, Peter J. Hulick, Judith Balmaña, Anne-Marie Gerdes, Frans B. L. Hogervorst, Capucine Delnatte, Miguel de la Hoya, Katarzyna Kaczmarek, Angelica M. Gutierrez-Barrera, Claudine Isaacs, Lisa Walker, Doris Steinemann, Huu Phuc Nguyen, Anna von Wachenfeldt, Saundra S. Buys, Fabienne Lesueur, Kristin K. Zorn, Kerstin Rhiem, Manuel R. Teixeira, Linda Steele, Ava Kwong, Alfons Meindl, Evgeny N. Imyanitov, Giuseppe Giannini, Banu Arun, Vilius Rudaitis, Norbert Arnold, Ellen Honisch, Melissa C. Southey, Ramunas Janavicius, Finn Cilius Nielsen, Jacob Korach, Ana Vega, Nisha Pradhan, David E. Goldgar, Anna Jakubowska, Angela R. Bradbury, Cora M. Aalfs, kConFab Investigators, Lídia Feliubadaló, Annelie Liljegren, Ana Osorio, Sabine Topka, Julia Hentschel, Katie Snape, Fergus J. Couch, Ute Hamann, Anna Öfverholm, Edenir Inêz Palmero, Jacob Musinsky, Adriana Lasa, Silvia Tognazzo, Payal D. Shah, Drakoulis Yannoukakos, Valérie Bonadona, Laura Papi, Georgia Chenevix-Trench, Christi J. van Asperen, Hagay Sobol, Kristiina Aittomäki, Cristina Martínez-Bouzas, Jan Lubinski, Csilla Szabo, Joanne Ngeow, Hebon, Maria A. Caligo, Priyanka Sharma, Anne-Bine Skytte, Christian Sutter, Yen Y. Tan, Trinidad Caldés, Rosemarie Davidson, Jenny Lester, Andreas Berger, Mark E. Robson, Jennifer T. Loud, Cynthia Villarreal-Garza, Eva Machackova, Leigha Senter, Irene L. Andrulis, Sandra Fert Ferrer, Diana Torres, Sung-Won Kim, Karolina Prajzendanc, Christine Lasset, Embrace, Jeffrey M. Fowler, Bernardo Bonanni, Bent Ejlertsen, Liliana Varesco, Orland Diez, Kathleen Claes
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2018, 39 (5), pp.593-620. ⟨10.1002/humu.23406⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Rebbeck, T R, Friebel, T M, Friedman, E, Hamann, U, Huo, D, Kwong, A, Olah, E, Olopade, O I, Solano, A R, Teo, S-H, Thomassen, M, Weitzel, J N, Chan, T L, Couch, F J, Goldgar, D E, Kruse, T A, Palmero, E I, Park, S K, Torres, D, van Rensburg, E J, McGuffog, L, Parsons, M T, Leslie, G, Aalfs, C M, Abugattas, J, Adlard, J, Agata, S, Aittomäki, K, Andrews, L, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Asseryanis, E, Auerbach, L, Azzollini, J, Balmaña, J, Barile, M, Barkardottir, R B, Barrowdale, D, Benitez, J, Berger, A, Berger, R, Blanco, A M, Blazer, K R, Blok, M J, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caldes, T, Caliebe, A, Caligo, M A, Campbell, I, Caputo, S M, Chiquette, J, Chung, W K, Claes, K B M, Collée, J M, Cook, J, Davidson, R, de la Hoya, M, De Leeneer, K, de Pauw, A, Delnatte, C, Diez, O, Ding, Y C, Ditsch, N, Domchek, S M, Dorfling, C M, Velazquez, C, Dworniczak, B, Eason, J, Easton, D F, Eeles, R, Ehrencrona, H, Ejlertsen, B, EMBRACE, Engel, C, Engert, S, Evans, D G, Faivre, L, Feliubadaló, L, Ferrer, S F, Foretova, L, Fowler, J, Frost, D, Galvão, H C R, Ganz, P A, Garber, J, Gauthier-Villars, M, Gehrig, A, GEMO Study Collaborators, Gerdes, A-M, Gesta, P, Giannini, G, Giraud, S, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Gutierrez-Barrera, A, Hahnen, E, Hauke, J, HEBON, Henderson, A, Hentschel, J, Hogervorst, F B L, Honisch, E, Imyanitov, E N, Isaacs, C, Izatt, L, Izquierdo, A, Jakubowska, A, James, P, Janavicius, R, Jensen, U B, John, E M, Vijai, J, Kaczmarek, K, Karlan, B Y, Kast, K, KConFab Investigators, Kim, S-W, Konstantopoulou, I, Korach, J, Laitman, Y, Lasa, A, Lasset, C, Lázaro, C, Lee, A, Lee, M H, Lester, J, Lesueur, F, Liljegren, A, Lindor, N M, Longy, M, Loud, J T, Lu, K H, Lubinski, J, Machackova, E, Manoukian, S, Mari, V, Martínez-Bouzas, C, Matrai, Z, Mebirouk, N, Meijers-Heijboer, H E J, Meindl, A, Mensenkamp, A, Mickys, U, Miller, A, Montagna, M, Moysich, K B, Mulligan, A M, Musinsky, J, Neuhausen, S L, Nevanlinna, H, Ngeow, J, Nguyen, H P, Niederacher, D, Nielsen, H R, Nielsen, F C, Nussbaum, R L, Offit, K, Öfverholm, A, Ong, K-R, Osorio, A, Papi, L, Papp, J, Pasini, B, Pedersen, I S, Peixoto, A, Peruga, N, Peterlongo, P, Pohl, E, Pradhan, N, Prajzendanc, K, Prieur, F, Pujol, P, Radice, P, Ramus, S J, Rantala, J, Rashid, M U, Rhiem, K, Robson, M, Rodriguez, G C, Rogers, M T, Rudaitis, V, Schmidt, A Y, Schmutzler, R K, Senter, L, Shah, P D, Sharma, P, Side, L E, Simard, J, Singer, C F, Skytte, A-B, Slavin, T P, Snape, K, Sobol, H, Southey, M C, Steele, L, Steinemann, D, Sukiennicki, G, Sutter, C, Szabo, C I, Tan, Y Y, Teixeira, M R, Terry, M B, Teulé, A, Thomas, A, Thull, D L, Tischkowitz, M, Tognazzo, S, Toland, A E, Topka, S, Trainer, A H, Tung, N, van Asperen, C J, van der Hout, A H, van der Kolk, L E, van der Luijt, R B, Van Heetvelde, M, Varesco, L, Varon-Mateeva, R, Vega, A, Villarreal-Garza, C, von Wachenfeldt, A, Walker, L, Wang-Gohrke, S, Wappenschmidt, B, Weber, B H F, Yannoukakos, D, Yoon, S-Y, Zanzottera, C, Zidan, J, Zorn, K K, Selkirk, C G H, Hulick, P J, Chenevix-Trench, G, Spurdle, A B, Antoniou, A C & Nathanson, K L 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
Jensen, U B 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. ' . https://doi.org/10.1002/humu.23406
Human Mutation, 39, 5, pp. 593-620
Human Mutation, 39(5), 593-620. Wiley
Human Mutation: Variation, Informatics and Disease, 39(5), 593-620
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Rebbeck, T R, Friebel, T M, Friedman, E, Hamann, U, Huo, D, Kwong, A, Olah, E, Olopade, O I, Solano, A R, Teo, S-H, Thomassen, M, Weitzel, J N, Chan, T L, Couch, F J, Goldgar, D E, Kruse, T A, Palmero, E I, Park, S K, Torres, D, van Rensburg, E J, McGuffog, L, Parsons, M T, Leslie, G, Aalfs, C M, Abugattas, J, Adlard, J, Agata, S, Aittomäki, K, Andrews, L, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Asseryanis, E, Auerbach, L, Azzollini, J, Balmaña, J, Barile, M, Barkardottir, R B, Barrowdale, D, Benitez, J, Berger, A, Berger, R, Blanco, A M, Blazer, K R, Blok, M J, Bonadona, V, Gerdes, A-M, Nielsen, H R, Skytte, A-B & EMBRACE 2018, ' Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Human Mutation, 39, 593-620
Human Mutation, 39(5), 593-620. Wiley-Liss Inc.
Digital.CSIC. Repositorio Institucional del CSIC
EMBRACE, GEMO Study Collaborators, HEBON & KConFab Investigators 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
EMBRACE 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
Human mutation, 39(5), 593-620. Wiley-Liss Inc.
The CIMBA Consortium & Evans, D G 2018, ' Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations ', Human Mutation . https://doi.org/10.1002/humu.23406
Rebbeck, TR; Friebel, TM; Friedman, E; Hamann, U; Huo, D; Kwong, A; et al.(2018). Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. HUMAN MUTATION, 39(5), 593-620. doi: 10.1002/humu.23406. UCLA: Retrieved from: http://www.escholarship.org/uc/item/3q49q09h
Human Mutation, Wiley, 2018, 39 (5), pp.593-620. ⟨10.1002/humu.23406⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Rebbeck, T R, Friebel, T M, Friedman, E, Hamann, U, Huo, D, Kwong, A, Olah, E, Olopade, O I, Solano, A R, Teo, S-H, Thomassen, M, Weitzel, J N, Chan, T L, Couch, F J, Goldgar, D E, Kruse, T A, Palmero, E I, Park, S K, Torres, D, van Rensburg, E J, McGuffog, L, Parsons, M T, Leslie, G, Aalfs, C M, Abugattas, J, Adlard, J, Agata, S, Aittomäki, K, Andrews, L, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Asseryanis, E, Auerbach, L, Azzollini, J, Balmaña, J, Barile, M, Barkardottir, R B, Barrowdale, D, Benitez, J, Berger, A, Berger, R, Blanco, A M, Blazer, K R, Blok, M J, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caldes, T, Caliebe, A, Caligo, M A, Campbell, I, Caputo, S M, Chiquette, J, Chung, W K, Claes, K B M, Collée, J M, Cook, J, Davidson, R, de la Hoya, M, De Leeneer, K, de Pauw, A, Delnatte, C, Diez, O, Ding, Y C, Ditsch, N, Domchek, S M, Dorfling, C M, Velazquez, C, Dworniczak, B, Eason, J, Easton, D F, Eeles, R, Ehrencrona, H, Ejlertsen, B, EMBRACE, Engel, C, Engert, S, Evans, D G, Faivre, L, Feliubadaló, L, Ferrer, S F, Foretova, L, Fowler, J, Frost, D, Galvão, H C R, Ganz, P A, Garber, J, Gauthier-Villars, M, Gehrig, A, GEMO Study Collaborators, Gerdes, A-M, Gesta, P, Giannini, G, Giraud, S, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Gutierrez-Barrera, A, Hahnen, E, Hauke, J, HEBON, Henderson, A, Hentschel, J, Hogervorst, F B L, Honisch, E, Imyanitov, E N, Isaacs, C, Izatt, L, Izquierdo, A, Jakubowska, A, James, P, Janavicius, R, Jensen, U B, John, E M, Vijai, J, Kaczmarek, K, Karlan, B Y, Kast, K, KConFab Investigators, Kim, S-W, Konstantopoulou, I, Korach, J, Laitman, Y, Lasa, A, Lasset, C, Lázaro, C, Lee, A, Lee, M H, Lester, J, Lesueur, F, Liljegren, A, Lindor, N M, Longy, M, Loud, J T, Lu, K H, Lubinski, J, Machackova, E, Manoukian, S, Mari, V, Martínez-Bouzas, C, Matrai, Z, Mebirouk, N, Meijers-Heijboer, H E J, Meindl, A, Mensenkamp, A, Mickys, U, Miller, A, Montagna, M, Moysich, K B, Mulligan, A M, Musinsky, J, Neuhausen, S L, Nevanlinna, H, Ngeow, J, Nguyen, H P, Niederacher, D, Nielsen, H R, Nielsen, F C, Nussbaum, R L, Offit, K, Öfverholm, A, Ong, K-R, Osorio, A, Papi, L, Papp, J, Pasini, B, Pedersen, I S, Peixoto, A, Peruga, N, Peterlongo, P, Pohl, E, Pradhan, N, Prajzendanc, K, Prieur, F, Pujol, P, Radice, P, Ramus, S J, Rantala, J, Rashid, M U, Rhiem, K, Robson, M, Rodriguez, G C, Rogers, M T, Rudaitis, V, Schmidt, A Y, Schmutzler, R K, Senter, L, Shah, P D, Sharma, P, Side, L E, Simard, J, Singer, C F, Skytte, A-B, Slavin, T P, Snape, K, Sobol, H, Southey, M C, Steele, L, Steinemann, D, Sukiennicki, G, Sutter, C, Szabo, C I, Tan, Y Y, Teixeira, M R, Terry, M B, Teulé, A, Thomas, A, Thull, D L, Tischkowitz, M, Tognazzo, S, Toland, A E, Topka, S, Trainer, A H, Tung, N, van Asperen, C J, van der Hout, A H, van der Kolk, L E, van der Luijt, R B, Van Heetvelde, M, Varesco, L, Varon-Mateeva, R, Vega, A, Villarreal-Garza, C, von Wachenfeldt, A, Walker, L, Wang-Gohrke, S, Wappenschmidt, B, Weber, B H F, Yannoukakos, D, Yoon, S-Y, Zanzottera, C, Zidan, J, Zorn, K K, Selkirk, C G H, Hulick, P J, Chenevix-Trench, G, Spurdle, A B, Antoniou, A C & Nathanson, K L 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
Jensen, U B 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. ' . https://doi.org/10.1002/humu.23406
Human Mutation, 39, 5, pp. 593-620
Human Mutation, 39(5), 593-620. Wiley
Human Mutation: Variation, Informatics and Disease, 39(5), 593-620
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Rebbeck, T R, Friebel, T M, Friedman, E, Hamann, U, Huo, D, Kwong, A, Olah, E, Olopade, O I, Solano, A R, Teo, S-H, Thomassen, M, Weitzel, J N, Chan, T L, Couch, F J, Goldgar, D E, Kruse, T A, Palmero, E I, Park, S K, Torres, D, van Rensburg, E J, McGuffog, L, Parsons, M T, Leslie, G, Aalfs, C M, Abugattas, J, Adlard, J, Agata, S, Aittomäki, K, Andrews, L, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Asseryanis, E, Auerbach, L, Azzollini, J, Balmaña, J, Barile, M, Barkardottir, R B, Barrowdale, D, Benitez, J, Berger, A, Berger, R, Blanco, A M, Blazer, K R, Blok, M J, Bonadona, V, Gerdes, A-M, Nielsen, H R, Skytte, A-B & EMBRACE 2018, ' Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Human Mutation, 39, 593-620
Human Mutation, 39(5), 593-620. Wiley-Liss Inc.
Digital.CSIC. Repositorio Institucional del CSIC
EMBRACE, GEMO Study Collaborators, HEBON & KConFab Investigators 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
EMBRACE 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406
Human mutation, 39(5), 593-620. Wiley-Liss Inc.
The CIMBA Consortium & Evans, D G 2018, ' Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations ', Human Mutation . https://doi.org/10.1002/humu.23406
Rebbeck, TR; Friebel, TM; Friedman, E; Hamann, U; Huo, D; Kwong, A; et al.(2018). Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. HUMAN MUTATION, 39(5), 593-620. doi: 10.1002/humu.23406. UCLA: Retrieved from: http://www.escholarship.org/uc/item/3q49q09h
The prevalence and spectrum of germline mutations in BRCA1 and BRCA2 have been reported in single populations, with the majority of reports focused on White in Europe and North America. The Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab526fd54e17412cf2be87645b672d04
https://www.repository.cam.ac.uk/handle/1810/274227
https://www.repository.cam.ac.uk/handle/1810/274227
Autor:
Christian F. Singer, Louise Izatt, Yen Y. Tan, Emmanuelle Mouret-Fourme, Embrace, Genepso, Bcfr, Hebon, kConFab, Marie Navratilova, Lucy Side, Trinidad Caldés, Rosemarie Davidson, Kelly-Anne Phillips, Saundra S. Buys, Dominique Leroux, Mary B. Daly, Melissa C. Southey, Marian J.E. Mourits, Brita Arver, Theo A. M. van Os, Anne-Marie Gerdes, Douglas F. Easton, Marie-José Roos-Blom, Michael Friedlander, Lieske H. Schrijver, David E. Goldgar, Anna Jakubowska, Roger L. Milne, Håkan Olsson, Lisa Walker, Ros Eeles, Flora E. van Leeuwen, Mary Porteous, Sue-Anne McLachlan, Pascaline Berthet, Lenka Foretova, Catherine Noguès, Matti A. Rookus, Debra Frost, Daniel Barrowdale, Esther M. John, Julian Adlard, Encarna B. Gomez Garcia, Nadine Andrieu, Laurence Venat-Bouvet, Anita Bane, John L. Hopper, Mary Beth Terry, Jacques Simard, Ana Osorio, Antonis C. Antoniou, Christoph Engel, Wendy K. Chung, Karin Kast, Ibccs, D. Gareth Evans, Valérie Bonadona, Edith Olah, Steve Ellis, Christi J. van Asperen, T.M. Mooij
Publikováno v:
JNCI cancer spectrum, 2(2). Oxford University Press
JNCI Cancer Spectrum
JNCI Cancer Spectrum, Oxford University Press, 2021, 2 (2), pky023. ⟨10.1093/jncics/pky023⟩
EMBRACE Investigators, GENEPSO, BCFR, HEBON, kConFab, IBCCS, & Evans, D G 2018, ' Oral contraceptive use and breast cancer risk: retrospective and prospective analyses from a BRCA1 and BRCA2 mutation carrier cohort study ', JNCI Cancer spectrum, vol. 2, no. 2 . https://doi.org/10.1093/jncics/pky023
JNCI Cancer Spectrum, 2021, 2 (2), pky023. ⟨10.1093/jncics/pky023⟩
JNCI Cancer Spectrum, 2(2):023. Oxford University Press
JNCI cancer spectrum, 2(2):pky023. Oxford University Press
JNCI Cancer Spectrum
JNCI Cancer Spectrum, Oxford University Press, 2021, 2 (2), pky023. ⟨10.1093/jncics/pky023⟩
EMBRACE Investigators, GENEPSO, BCFR, HEBON, kConFab, IBCCS, & Evans, D G 2018, ' Oral contraceptive use and breast cancer risk: retrospective and prospective analyses from a BRCA1 and BRCA2 mutation carrier cohort study ', JNCI Cancer spectrum, vol. 2, no. 2 . https://doi.org/10.1093/jncics/pky023
JNCI Cancer Spectrum, 2021, 2 (2), pky023. ⟨10.1093/jncics/pky023⟩
JNCI Cancer Spectrum, 2(2):023. Oxford University Press
JNCI cancer spectrum, 2(2):pky023. Oxford University Press
Background For BRCA1 and BRCA2 mutation carriers, the association between oral contraceptive preparation (OCP) use and breast cancer (BC) risk is still unclear. Methods Breast camcer risk associations were estimated from OCP data on 6030 BRCA1 and 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::753be79ab5051dc8af8808db94529a4b
https://pure.amc.nl/en/publications/oral-contraceptive-use-and-breast-cancer-risk(b6082b00-b685-43ee-a278-be969d1f1197).html
https://pure.amc.nl/en/publications/oral-contraceptive-use-and-breast-cancer-risk(b6082b00-b685-43ee-a278-be969d1f1197).html
Autor:
Eitan Friedman, Mattias Van Heetvelde, Jennifer B. Permuth, Joseph Vijai, Patricia A. Ganz, Jennifer A. Doherty, Argyrios Ziogas, Bernard Peissel, Edwin S. Iversen, Angela Brooks-Wilson, Ingo B. Runnebaum, Amanda B. Spurdle, Heli Nevanlinna, Kenneth Offit, Laura Papi, Georgia Chenevix-Trench, Saundra S. Buys, Martin Köbel, Fabienne Lesueur, Elizabeth W. Pugh, Joe Dennis, Sylvie Mazoyer, Diana Eccles, Shirley Hodgson, Jolanta Lissowska, Judy Garber, Pascal Pujol, Kristin K. Zorn, Orland Diez, Marcia Adams, Thomas Conner, Renée T. Fortner, Tjoung-Won Park-Simon, Vanesa García-Barberán, Kerstin Rhiem, Norbert Arnold, Karoline Kuchenbaecker, Susan M. Domchek, María Josefa Mosteiro García, Matthias W. Beckmann, Alex Henderson, Melissa C. Larson, Jane Romm, Anja Rudolph, Steven A. Narod, Mats Jernetz, Jolanta Kupryjanczyk, Natalia Bogdanova, Jacob Musinsky, Helga B. Salvesen, Jonathan Beesley, Paolo Peterlongo, Arif B. Ekici, Clarice R. Weinberg, Marion Piedmonte, Christian F. Singer, Robert L. Nussbaum, Katja K.H. Aben, Michael J. Birrer, Juul T. Wijnen, Elizabeth M. Poole, Phuong L. Mai, David J. Hunter, Tanja Pejovic, Athanassios Vratimos, Barbara Wappenschmidt, Nicolas Wentzensen, Marcus Q. Bernardini, Leigha Senter, Terence Cescon, Daniel W. Cramer, Silvia Tognazzo, Drakoulis Yannoukakos, Jacopo Azzollini, Ignace Vergote, Karen H. Lu, Gustavo C. Rodriguez, Julian Adlard, Tomasz Huzarski, Mark H. Greene, Susan L. Neuhausen, Marina Bermisheva, Alicja Wolk, Paulo C Lyra, Usha Menon, Ralf Bützow, Siddhartha Kar, Manuel R. Teixeira, Conxi Lázaro, Agnieszka Dansonka-Mieszkowska, Aleksandra Gentry-Maharaj, Zsofia K. Stadler, Melissa C. Southey, Ramunas Janavicius, Douglas F. Easton, Digna R. Velez Edwards, Jocelyne Chiquette, Karin Kast, Jonathan Tyrer, Georg Pfeiler, Tara M. Friebel, Bruno Buecher, Goska Leslie, Jackie Cook, Catherine M. Phelan, Steve Ellis, Estrid Høgdall, Beth Y. Karlan, Anthony J. Swerdlow, Sarah E. Ferguson, Rosalind Glasspool, Frans B. L. Hogervorst, Lotte Nedergaard, Britton Trabert, Jack A. Taylor, Irene L. Andrulis, Paolo Radice, Dennis J. Hazelett, Mads Thomassen, Dong Liang, Joseph H. Rothstein, Loren Lipworth, Melissa A. Merritt, Ana Vega, Petra H.M. Peeters, Claus Høgdall, Anna M. Piskorz, Bernardo Bonanni, Janet M. Lee, Malcolm C. Pike, Clemens Liebrich, Zachary C. Fogarty, Bent Ejlertsen, Yuan Chun Ding, Dieter Niederacher, Michael E. Carney, Dominique Stoppa-Lyonnet, Nadine Tung, Curtis Olswold, Ana Osorio, Fiona Bruinsma, Christine Walsh, Fabienne Prieur, Lara E. Sucheston-Campbell, Stephen B. Gruber, Maartje J. Hooning, George Fountzilas, Amanda Black, David E. Goldgar, Anna Jakubowska, Paul D.P. Pharoah, Angela R. Bradbury, Helene Holland, Ruth C. Travis, Susana Banerjee, Penelope M. Webb, Brooke L. Fridley, Clara Bodelon, Mary Anne Rossing, Yen Y. Tan, Rosa B. Barkardottir, Jong Won Lee, Stephen J. Chanock, Bruce Poppe, Sandra Fert Ferrer, Melissa Moffitt, Taymaa May, Gustavo Mendoza-Fandiño, Christopher A. Haiman, Alicia Beeghly-Fadiel, Rebecca Sutphen, Michelle A.T. Hildebrandt, Lambertus A. Kiemeney, Thilo Dörk, Douglas A. Levine, Gerasimos Aravantinos, Celeste Leigh Pearce, Sue K. Park, David Van Den Berg, Louise Izatt, Hannah P. Yang, Graham G. Giles, Linda S. Cook, John R. McLaughlin, Nick Orr, Weiva Sieh, Raymonda Varon-Mateeva, Marco Montagna, Honglin Song, Laura Ottini, Ruea-Yea Huang, Joanna Moes-Sosnowska, Anders Bojesen, David M. O'Malley, Andrew K. Godwin, Lucy Side, Sung-Won Kim, Lukasz Szafron, Christoph Engel, Harvey A. Risch, Alexander Hein, Penny Soucy, Elza Khusnutdinova, Ana Peixoto, Arto Leminen, Cora M. Aalfs, Matthias Dürst, Mary B. Daly, Patricia Rice, Nadeem Siddiqui, Dale P. Sandler, Ava Kwong, Madalene Earp, Marjorie J. Riggan, Inge Søkilde Pedersen, Susanne K. Kjaer, Mercedes Durán, Joellen M. Schildkraut, James D. Brenton, D. Gareth Evans, Liisa M. Pelttari, Kimberly F. Doheny, Karen Hosking, Miquel Angel Pujana, Salina B. Chan, Joan Brunet, Trinidad Caldés, Rosemarie Davidson, Jessica N. McAlpine, Jenny Lester, Niclas Håkansson, Kai-ren Ong, Ros Eeles, Francesmary Modugno, Martin Gore, Loic Le Marchand, Robert A. Vierkant, Wendy K. Chung, Christopher I. Amos, N. Charlotte Onland-Moret, Brita Arver, Marc Tischkowitz, Craig Luccarini, Daniel Barrowdale, Laima Tihomirova, Louise A. Brinton, Fergus J. Couch, Alfons Meindl, Nerea Larrañaga, Cristina Rodríguez-Antona, Alice S. Whittemore, Johanna I. Kiiski, Todd L. Edwards, Eric Hahnen, Grzegorz Sukiennicki, Els Van Nieuwenhuysen, Elizabeth J. van Rensburg, Michael Jones, Åke Borg, Edith Olah, Ute Hamann, Liv Cecilie Vestrheim Thomsen, Xiaoqing Chen, Ganna Chornokur, Minouk J. Schoemaker, Marc T. Goodman, Fanny Dao, Andrea Gehrig, Hagay Sobol, Nhu D. Le, Esther M. John, Adriaan Vanderstichele, Antonia Trichopoulou, Kunle Odunsi, Yukie Bean, David G. Huntsman, Lidia Pezzani, V. Wendy Setiawan, Marinus J. Blok, Yael Laitman, Mary Porteous, Patricia Harrington, Samantha Poblete, Shashikant Lele, Anne M. van Altena, Mingajeva Elvira, Lene Lundvall, Dominique Leroux, Annemarie H. van der Hout, Darya Prokofyeva, Debra Frost, Yoke-Eng Chiew, Gad Rennert, Stacey J. Winham, Muy-Kheng Tea, Kirsten B. Moysich, Angel Izquierdo, Anna H. Wu, Christine Rappaport-Fuerhauser, Peter Hillemanns, Rob B. van der Luijt, Gord Glendon, Jan Lubinński, Csilla Szabo, Gillian Mitchell, Andrea L. Richardson, Mark E. Robson, Roger L. Milne, Thomas Hansen, Francesca Damiola, Tameka Shelford, Natalia Antonenkova, Julie Lecarpentier, Paul A. James, Claudine Isaacs, Gianluca Severi, Maria A. Caligo, Teodora Goranova, Kate Lawrenson, Sandra Orsulic, Priyanka Sharma, Holly R. Harris, Peter A. Fasching, Christian Sutter, Torben A Kruse, Line Bjørge, Lesley McGuffog, Leon F.A.G. Massuger, Lynne R. Wilkens, Reidun K. Kopperud, Jillian Hung, Iain A. McNeish, Hanne Meijers-Heijboer, Uffe Birk Jensen, Diether Lambrechts, Johanna Rantala, Kelly-Anne Phillips, Michelle M.M. Woo, Kathryn L. Terry, Kathleen Claes, Ellen L. Goode, Olufunmilayo I. Olopade, Darcy L. Thull, Ailith Pirie, Sharon E. Johnatty, Soo Hwang Teo, Aimee A D'Aloisio, Evgeny N. Imyanitov, Domenico Palli, Andrew Berchuck, Banu Arun, Florentia Fostira, Jan Hauke, Jenny Chang-Claude, Pamela J. Thompson, Peter J. Hulick, Per Broberg, Arjen R. Mensenkamp, Xifeng Wu, Alicia A. Tone, Jacques Simard, Ursula Eilber, Jacek Gronwald, Kenneth Blankstein, James M. Flanagan, Alvaro N.A. Monteiro, Timea Pocza, Rita K. Schmutzler, Jeffrey N. Weitzel, Simon A. Gayther, William D. Foulkes, Valerie McGuire, Katherine L. Nathanson, Kevin H. Eng, Anna deFazio, Ian G. Campbell, Capucine Delnatte, Shan Wang-Gohrke, Jenna Lilyquist, Matti A. Rookus, Sakaeva Dina Damirovna, Laure Dossus, Simon G. Coetzee, Catherine J. Kennedy, Roberta B. Ness, James Paul, Andrew Lee, Linda E. Kelemen, Judith Balmaña, Anne-Marie Gerdes, Laure Barjhoux, Håkan Olsson, Lisa Walker, Doris Steinemann, Cecilia M. Dorfling, Julie M. Cunningham, Shelley S. Tworoger, Allan Jensen, Thomas A. Sellers, Javier Benitez, Anthony N. Karnezis, Hoda Anton-Culver, Carole Brewer, Siranoush Manoukian, Dorothea Wand, Ed Dicks, Antonis C. Antoniou, Amanda E. Toland, Anna Marie Mulligan, Päivi Kannisto, Rikki Cannioto, Bernd Dworniczak, Susan J. Ramus, Anna V. Tinker
Publikováno v:
Nature Genetics, 49(5), 680-691. Nature Publishing Group
Digital.CSIC. Repositorio Institucional del CSIC
instname
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A R, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmaña, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y T, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Black, A, Blankstein, K, Blok, M J, Pedersen, I S & AOCS study group 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-691 . https://doi.org/10.1038/ng.3826
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Nature Genetics, 49(5), 680. Nature Publishing Group
Recercat. Dipósit de la Recerca de Catalunya
Nature Genetics, 49(5), 680-+. Nature Publishing Group
NATURE GENETICS
Nature Genetics
Nature genetics, 49(5), 680-691. Nature Publishing Group
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmana, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Black, A, Blankstein, K, Blok, M J, Jensen, U B, AOCS Study Grp, EMEMBRACE Study, GEMO Study Collaborators, HEBON Study & OPAL Study Grp 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-+ . https://doi.org/10.1038/ng.3826
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmaña, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Black, A, Blankstein, K, Hooning, M J, Meijers-Heijboer, H, HEBON Study, AOCS study group, EMBRACE Study, OPAL study group, KConFab Investigators & GEMO Study Collaborators 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-691 . https://doi.org/10.1038/ng.3826
Dipòsit Digital de la UB
Universidad de Barcelona
Nature Genetics, Nature Publishing Group, 2017, 49 (5), pp.680-691. ⟨10.1038/ng.3826⟩
Nature Genetics, 49(5), 680
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J & Orr, N 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, pp. 680-691 . https://doi.org/10.1038/ng.3826
Nature Genetics, 49, 5, pp. 680-691
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmaña, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Bojesen, A, Gerdes, A-M, Kruse, T A, Thomassen, M & AOCS study group 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-691 . https://doi.org/10.1038/ng.3826
Nature Genetics, 49, 680-691
Digital.CSIC. Repositorio Institucional del CSIC
instname
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A R, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmaña, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y T, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Black, A, Blankstein, K, Blok, M J, Pedersen, I S & AOCS study group 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-691 . https://doi.org/10.1038/ng.3826
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Nature Genetics, 49(5), 680. Nature Publishing Group
Recercat. Dipósit de la Recerca de Catalunya
Nature Genetics, 49(5), 680-+. Nature Publishing Group
NATURE GENETICS
Nature Genetics
Nature genetics, 49(5), 680-691. Nature Publishing Group
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmana, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Black, A, Blankstein, K, Blok, M J, Jensen, U B, AOCS Study Grp, EMEMBRACE Study, GEMO Study Collaborators, HEBON Study & OPAL Study Grp 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-+ . https://doi.org/10.1038/ng.3826
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmaña, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Black, A, Blankstein, K, Hooning, M J, Meijers-Heijboer, H, HEBON Study, AOCS study group, EMBRACE Study, OPAL study group, KConFab Investigators & GEMO Study Collaborators 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-691 . https://doi.org/10.1038/ng.3826
Dipòsit Digital de la UB
Universidad de Barcelona
Nature Genetics, Nature Publishing Group, 2017, 49 (5), pp.680-691. ⟨10.1038/ng.3826⟩
Nature Genetics, 49(5), 680
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J & Orr, N 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, pp. 680-691 . https://doi.org/10.1038/ng.3826
Nature Genetics, 49, 5, pp. 680-691
Phelan, C M, Kuchenbaecker, K B, Tyrer, J P, Kar, S P, Lawrenson, K, Winham, S J, Dennis, J, Pirie, A, Riggan, M J, Chornokur, G, Earp, M A, Lyra, P C, Lee, J M, Coetzee, S, Beesley, J, McGuffog, L, Soucy, P, Dicks, E, Lee, A, Barrowdale, D, Lecarpentier, J, Leslie, G, Aalfs, C M, Aben, K K H, Adams, M, Adlard, J, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Aravantinos, G, Arnold, N, Arun, B K, Arver, B, Azzollini, J, Balmaña, J, Banerjee, S N, Barjhoux, L, Barkardottir, R B, Bean, Y, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Bernardini, M Q, Birrer, M J, Bjorge, L, Bojesen, A, Gerdes, A-M, Kruse, T A, Thomassen, M & AOCS study group 2017, ' Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer ', Nature Genetics, vol. 49, no. 5, pp. 680-691 . https://doi.org/10.1038/ng.3826
Nature Genetics, 49, 680-691
The OCAC OncoArray genotyping project: et al.
To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), we pooled data from multiple genome-wide genotyping projects totaling 25,509 EOC cases and 40,941 c
To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), we pooled data from multiple genome-wide genotyping projects totaling 25,509 EOC cases and 40,941 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::729fa0fd3d32d2b40319c1007008477b
https://research.vumc.nl/en/publications/c8060098-86c9-4726-9f15-648de0136322
https://research.vumc.nl/en/publications/c8060098-86c9-4726-9f15-648de0136322
Autor:
Kuchenbaecker, Karoline B., Lesley, Mcguffog, Daniel, Barrowdale, Andrew, Lee, Penny, Soucy, Sue, Healey, Joe, Dennis, Michael, Lush, Mark, Robson, Spurdle, Amanda B., Ramus, Susan J., Nasim, Mavaddat, Mary Beth Terry, Neuhausen, Susan L., Ute, Hamann, Melissa, Southey, John, Esther M., Chung, Wendy K., Daly, Mary B., Buys, Saundra S., Goldgar, David E., Dorfling, Cecilia M., van Rensburg, Elizabeth J., Yuan Chun Ding, Bent, Ejlertsen, Anne-Marie, Gerdes, Hansen, Thomas V. O., Susan, Slager, Emily, Hallberg, Javier, Benitez, Ana, Osorio, Nancy, Cohen, William, Lawler, Weitzel, Jeffrey N., Paolo, Peterlongo, Valeria, Pensotti, Riccardo, Dolcetti, Monica, Barile, Bernardo, Bonanni, Jacopo, Azzollini, Siranoush, Manoukian, Bernard, Peissel, Paolo, Radice, Antonella, Savarese, Papi, Laura, Giannini, Giuseppe, Florentia, Fostira, Irene, Konstantopoulou, Julian, Adlard, Carole, Brewer, Jackie, Cook, Rosemarie, Davidson, Diana, Eccles, Ros, Eeles, Steve, Ellis, Embrace, Debra, Frost, Shirley, Hodgson, Louise, Izatt, Fiona, Lalloo, Kai-ren, Ong, Godwin, Andrew K., Norbert, Arnold, Bernd, Dworniczak, Christoph, Engel, Andrea, Gehrig, Eric, Hahnen, Jan, Hauke, Karin, Kast, Alfons, Meindl, Dieter, Niederacher, Rita Katharina Schmutzler, Raymonda, Varon-Mateeva, Shan, Wang-Gohrke, Barbara, Wappenschmidt, Laure, Barjhoux, Marie-Agne`s, Collonge-Rame, Camille, Elan, GEMO Study Collaborators, Lisa, Golmard, Emmanuelle, Barouk-Simonet, Fabienne, Lesueur, Sylvie, Mazoyer, Joanna, Sokolowska, Dominique Stoppa- Lyonnet, Claudine, Isaacs, Claes, Kathleen B. M., Bruce, Poppe, Miguel de la Hoya, Vanesa, Garcia-Barberan, Kristiina, Aittom€aki, Heli, Nevanlinna, Ausems, Margreet G. E. M., de Lange, J. L., Gomez Garcia, Encarna B., Hebon, Hogervorst, Frans B. L., Kets, Carolien M., Meijers-Heijboer, Hanne E. J., Oosterwijk, Jan C., Rookus, Matti A., van Asperen, Christi J., van den Ouweland, Ans M. W., van Doorn, Helena C., van Os, Theo A. M., Ava, Kwong, Edith, Olah, Orland, Diez, Joan, Brunet, Conxi, Lazaro, Alex, Teule´, Jacek, Gronwald, Anna, Jakubowska, Katarzyna, Kaczmarek, Jan, Lubinski, Grzegorz, Sukiennicki, Barkardottir, Rosa B., Jocelyne, Chiquette, Simona, Agata, Marco, Montagna, Teixeira, Manuel R., Kconfab, Investigators, Sue Kyung Park, Curtis, Olswold, Marc, Tischkowitz, Lenka, Foretova, Pragna, Gaddam, Joseph, Vijai, Georg, Pfeiler, Christine, Rappaport-Fuerhauser, Singer, Christian F., Tea, Muy-Kheng M., Greene, Mark H., Loud, Jennifer T., Gad, Rennert, Imyanitov, Evgeny N., Hulick, Peter J., Hays, John L., Marion, Piedmonte, Rodriguez, Gustavo C., Julie, Martyn, Gord, Glendon, Anna Marie Mulligan, Andrulis, Irene L., Amanda Ewart Toland, Uffe Birk Jensen, Kruse, Torben A., Inge Sokilde Pedersen, Mads, Thomassen, Caligo, Maria A., Soo-Hwang, Teo, Raanan, Berger, Eitan, Friedman, Yael, Laitman, Brita, Arver, Ake, Borg, Hans, Ehrencrona, Johanna, Rantala, Olopade, Olufunmilayo I., Ganz, Patricia A., Nussbaum, Robert L., Bradbury, Angela R., Domchek, Susan M., Nathanson, Katherine L., Arun, Banu K., Paul, James, Karlan, Beth Y., Jenny, Lester, Jacques, Simard, Pharoah, Paul D. P., Kenneth, Offit, Couch, Fergus J., Georgia, Chenevix-Trench, Easton, Douglas F., Antoniou, Antonis C.
Publikováno v:
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
JNCI Journal of the National Cancer Institute
JNCI Journal of the National Cancer Institute
Background: Genome-wide association studies (GWAS) have identified 94 common single-nucleotide polymorphisms (SNPs) associated with breast cancer (BC) risk and 18 associated with ovarian cancer (OC) risk. Several of these are also associated with ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4109753b16c39f5db17b458d2200be26
https://biblio.ugent.be/publication/8525301
https://biblio.ugent.be/publication/8525301
Autor:
Craig C. Teerlink, Christiane Maier, Graham G. Giles, Jianfeng Xu, Douglas F. Easton, Kathleen E. Wiley, Christophe Egrot, William J. Catalona, John D. Carpten, Zsofia Kote-Jarai, Stephen N. Thibodeau, Fredrik Wiklund, Kimberly A. Zuhlke, Nicola J. Camp, Guangfu Jin, Tiina Wahlfors, Michelle Guy, Elaine A. Ostrander, Johanna Schleutker, S. Lilly Zheng, Ros Eeles, Teuvo L.J. Tammela, Monica Emanuelsson, Lisa A. Cannon-Albright, Sarah D. Isaacs, John L. Hopper, Walther Vogel, Ethan M. Lange, Patrick C. Walsh, Antje E. Rinckleb, William D. Foulkes, Lingyi Lu, Ingrid Oakley-Girvan, Geraldine Cancel-Tassin, Daniel J. Schaid, Olivier Cussenot, William B. Isaacs, Liesel M. FitzGerald, Alice S. Whittemore, Kathleen A. Cooney, Shannon K. McDonnell, Gianluca Severi, Joan E. Bailey-Wilson, Janet L. Stanford, Chih-Lin Hsieh, Anna M. Ray, Henrik Grönberg
Publikováno v:
Human Genetics. 133:347-356
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 prostate cancer is not well studied. Here, we a
Autor:
Maria A. Caligo, Carol Chu, Xianshu Wang, Senno Verhoef, Joanne L. Blum, Bruno Buecher, Amanda B. Spurdle, Theo A. M. van Os, Per Karlsson, Olga M. Sinilnikova, Sue Healey, Hanne Meijers-Heijboer, Georgia Chenevix-Trench, Marinus J. Blok, Timothy R. Rebbeck, Douglas F. Easton, Mary B. Daly, Annelie Liljegren, Margaret Cook, Christina G. Selkirk, Dominique Stoppa-Lyonnet, Mieke Kriege, Nadine Tung, Muriel Belotti, Susan Peock, Fiona Lalloo, Louise Izatt, Mads Thomassen, Henry T. Lynch, Christian F. Singer, Susan M. Domchek, Margreet G. E. M. Ausems, Tomasz Byrski, Olufunmilayo I. Olopade, Noralane M. Lindor, Claudine Isaacs, Katherine L. Nathanson, Gail E. Tomlinson, Clare Oliver, Hans Ehrencrona, Anna Jakubowska, Francine Durocher, Pascal Pujol, Debra Frost, Tuomas Heikkinen, Christine Lasset, Rosemarie Davidson, Jan Lubinski, Marie Agnés Collonge-Rame, Patricia A. Ganz, Nicoline Hoogerbrugge, Fergus J. Couch, Lesley McGuffog, Matti A. Rookus, Heli Nevanlinna, Helena Jernström, Sylvie Mazoyer, Jonathan Beesley, Judy Garber, Diana Eccles, Don M. Conroy, Xiaoqing Chen, Daphne Gschwantler-Kaulich, Tomasz Huzarski, Carole Verny-Pierre, Antonis C. Antoniou, D. Gareth Evans, Louise Marquart, Juul T. Wijnen, Ros Eeles, Peter Devilee, Laure Barjhoux, Fei Wan, Anne Catharine Dressler, Susan L. Neuhausen, Jeff Weitzel, Hélène Dreyfus
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention, 20, 5, pp. 1032-8
Cancer Epidemiology, Biomarkers and Prevention
Cancer Epidemiology, Biomarkers and Prevention, American Association for Cancer Research, 2011, 20, pp.1032-1038
Spurdle, A B, Marquart, L, McGuffog, L, Healey, S, Sinilnikova, O, Wan, F, Chen, X, Beesley, J, Singer, C F, Dressler, A-C, Gschwantler-Kaulich, D, Blum, J L, Tung, N, Weitzel, J, Lynch, H, Garber, J, Easton, D F, Peock, S, Cook, M, Oliver, C T, Frost, D, Conroy, D, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Chu, C, Eccles, D, Selkirk, C G, Daly, M, Isaacs, C, Stoppa-Lyonnet, D, Sinilnikova, O M, Buecher, B, Belotti, M, Mazoyer, S, Barjhoux, L, Verny-Pierre, C, Lasset, C, Dreyfus, H, Pujol, P, Collonge-Rame, M-A, Rookus, M A, Verhoef, S, Kriege, M, Hoogerbrugge, N, Ausems, M G E M, van Os, T A, Thomassen, M & GEMO Study Collaborators 2011, ' Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers ', Cancer Epidemiology, Biomarkers & Prevention, vol. 20, no. 5, pp. 1032-8 . https://doi.org/10.1158/1055-9965.EPI-10-0909
Spurdle, A B, Marquart, L, McGuffog, L, Healey, S, Sinilnikova, O, Wan, F, Chen, X Q, Beesley, J, Singer, C F, Dressler, A C, Gschwantler-Kaulich, D, Blum, J L, Tung, N, Weitzel, J, Lynch, H, Garber, J, Easton, D F, Peock, S, Cook, M, Oliver, C T, Frost, D, Conroy, D, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Chu, C, Eccles, D, Selkirk, C G, Daly, M, Isaacs, C, Stoppa-Lyonnet, D, Sinilnikova, O M, Buecher, B, Belotti, M, Mazoyer, S, Barjhoux, L, Verny-Pierre, C, Lasset, C, Dreyfus, H, Pujol, P, Collonge-Rame, M A, Rookus, M A, Verhoef, S, Kriege, M, Hoogerbrugge, N, Ausems, M G E M, Os, T A, van Wijnen, J, Devilee, P, Meijers-Heijboer, E J, Blok, M J, Heikkinen, T, Nevanlinna, H, Jakubowska, A, Lubinski, J, Huzarski, T, Byrski, T, Durocher, F, Couch, F J, Lindor, N M, Wang, X S, Thomassen, M, Domchek, S, Nathanson, K, Caligo, M A, Jernstrom, H, Liljegren, A, Ehrencrona, H, For, P K, Ganz, P A, Olopade, O I, Tomlinson, G, Neuhausen, S, Antoniou, A C, Chenevix-Trench, G & Rebbeck, T R 2011, ' Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers ', Cancer Epidemiology Biomarkers and Prevention, vol. 20, no. 5, pp. 1032-1038 . https://doi.org/10.1158/1055-9965.EPI-10-0909
Cancer epidemiology, biomarkers & prevention, 20(5), 1032-1038. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers and Prevention, 20(5), 1032-1038
Cancer Epidemiology, Biomarkers and Prevention, 2011, 20 (5), pp.1032-1038. ⟨10.1158/1055-9965.EPI-10-0909⟩
Cancer Epidemiology Biomarkers and Prevention, 20(5), 1032-1038. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers & Prevention, 20, 1032-8
Cancer Epidemiology Biomarkers & Prevention, 20(5), 1032-1038. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers and Prevention
Cancer Epidemiology, Biomarkers and Prevention, American Association for Cancer Research, 2011, 20, pp.1032-1038
Spurdle, A B, Marquart, L, McGuffog, L, Healey, S, Sinilnikova, O, Wan, F, Chen, X, Beesley, J, Singer, C F, Dressler, A-C, Gschwantler-Kaulich, D, Blum, J L, Tung, N, Weitzel, J, Lynch, H, Garber, J, Easton, D F, Peock, S, Cook, M, Oliver, C T, Frost, D, Conroy, D, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Chu, C, Eccles, D, Selkirk, C G, Daly, M, Isaacs, C, Stoppa-Lyonnet, D, Sinilnikova, O M, Buecher, B, Belotti, M, Mazoyer, S, Barjhoux, L, Verny-Pierre, C, Lasset, C, Dreyfus, H, Pujol, P, Collonge-Rame, M-A, Rookus, M A, Verhoef, S, Kriege, M, Hoogerbrugge, N, Ausems, M G E M, van Os, T A, Thomassen, M & GEMO Study Collaborators 2011, ' Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers ', Cancer Epidemiology, Biomarkers & Prevention, vol. 20, no. 5, pp. 1032-8 . https://doi.org/10.1158/1055-9965.EPI-10-0909
Spurdle, A B, Marquart, L, McGuffog, L, Healey, S, Sinilnikova, O, Wan, F, Chen, X Q, Beesley, J, Singer, C F, Dressler, A C, Gschwantler-Kaulich, D, Blum, J L, Tung, N, Weitzel, J, Lynch, H, Garber, J, Easton, D F, Peock, S, Cook, M, Oliver, C T, Frost, D, Conroy, D, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Chu, C, Eccles, D, Selkirk, C G, Daly, M, Isaacs, C, Stoppa-Lyonnet, D, Sinilnikova, O M, Buecher, B, Belotti, M, Mazoyer, S, Barjhoux, L, Verny-Pierre, C, Lasset, C, Dreyfus, H, Pujol, P, Collonge-Rame, M A, Rookus, M A, Verhoef, S, Kriege, M, Hoogerbrugge, N, Ausems, M G E M, Os, T A, van Wijnen, J, Devilee, P, Meijers-Heijboer, E J, Blok, M J, Heikkinen, T, Nevanlinna, H, Jakubowska, A, Lubinski, J, Huzarski, T, Byrski, T, Durocher, F, Couch, F J, Lindor, N M, Wang, X S, Thomassen, M, Domchek, S, Nathanson, K, Caligo, M A, Jernstrom, H, Liljegren, A, Ehrencrona, H, For, P K, Ganz, P A, Olopade, O I, Tomlinson, G, Neuhausen, S, Antoniou, A C, Chenevix-Trench, G & Rebbeck, T R 2011, ' Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers ', Cancer Epidemiology Biomarkers and Prevention, vol. 20, no. 5, pp. 1032-1038 . https://doi.org/10.1158/1055-9965.EPI-10-0909
Cancer epidemiology, biomarkers & prevention, 20(5), 1032-1038. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers and Prevention, 20(5), 1032-1038
Cancer Epidemiology, Biomarkers and Prevention, 2011, 20 (5), pp.1032-1038. ⟨10.1158/1055-9965.EPI-10-0909⟩
Cancer Epidemiology Biomarkers and Prevention, 20(5), 1032-1038. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers & Prevention, 20, 1032-8
Cancer Epidemiology Biomarkers & Prevention, 20(5), 1032-1038. American Association for Cancer Research Inc.
Background: Inherited BRCA1 and BRCA2 (BRCA1/2) mutations confer elevated breast cancer risk. Knowledge of factors that can improve breast cancer risk assessment in BRCA1/2 mutation carriers may improve personalized cancer prevention strategies. Meth