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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, Dennis, Joe, Tyrer, Jonathan P, McGuffog, Lesley, Adank, Muriel A, Ahearn, Thomas, Arun, Banu K, Baynes, Caroline, Białkowska, Katarzyna, Bojesen, Stig E, Brauch, Hiltrud, Burwinkel, Barbara, Buys, Saundra S, Caldés, Trinidad, Campa, Daniele, Chanock, Stephen J, EMBRACE Collaborators, Conroy, Don M, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Eliassen, A Heather, Evans, D Gareth, Fostira, Florentia, Gago-Dominguez, Manuela, Gapstur, Susan M, Garcia-Barberan, Vanesa, García-Closas, Montserrat, Gaudet, Mia M, Gayther, Simon A, Gehrig, Andrea, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, González-Neira, Anna, Greene, Mark H, Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A, Hamann, Ute, Harrington, Patricia A, He, Wei, Hollestelle, Antoinette, Horcasitas, Darling J, Hulick, Peter J, Hunter, David J, ABCTB Investigators, Jager, Agnes, James, Paul A, Jensen, Uffe Birk, Kaaks, Rudolf, Kiiski, Johanna I, Kosma, Veli-Matti, Kurian, Allison W, Laitman, Yael, Lambrechts, Diether, Le Marchand, Loic, Lester, Jenny, Lindstrom, Tricia, Luccarini, Craig, Mannermaa, Arto, Manoukian, Siranoush, Martens, John WM, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nielsen, Finn C, O'Brien, Katie M, Olopade, Olufunmilayo I, Olson, Janet E, Ottini, Laura, Park-Simon, Tjoung-Won, Parsons, Michael T, Pedersen, Inge Sokilde, Poppe, Bruce, Presneau, Nadege, Punie, Kevin, Radice, Paolo, Rennert, Gad, Robson, Mark, Saloustros, Emmanouil, Scheuner, Maren T, Scott, Christopher, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Thull, Darcy L, Tischkowitz, Marc, Vijai, Joseph, Wang, Qin, Wappenschmidt, Barbara, Yannoukakos, Drakoulis, Ziogas, Argyrios, Offit, Kenneth, Simard, Jacques, Easton, Douglas F, Antoniou, Antonis C

    Veröffentlicht in Nature communications

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