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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

F. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis, M. Gaudet, E. Dicks, M. Kosel, S. Healey, O. Sinilnikova, A. Lee, F. Bacot, D. Vincent, Hogervorst, Frans B L, S. Peock, D. Stoppa-Lyonnet, A. Jakubowska, P. Radice, R. Schmutzler, S. Domchek, M. Piedmonte, C. Singer, E. Friedman, M. Thomassen, Hansen, Thomas V O, S. Neuhausen, C. Szabo, I. Blanco, M. Greene, B. Karlan, J. Garber, C. Phelan, J. Weitzel, M. Montagna, E. Olah, I. Andrulis, A. Godwin, D. Yannoukakos, D. Goldgar, T. Caldes, H. Nevanlinna, A. Osorio, M. Terry, M. Daly, van Rensburg, Elizabeth J, U. Hamann, S. Ramus, A. Toland, M. Caligo, O. Olopade, N. Tung, K. Claes, M. Beattie, M. Southey, E. Imyanitov, M. Tischkowitz, R. Janavicius, E. John, A. Kwong, O. Diez, J. Balmaña, R. Barkardottir, B. Arun, G. Rennert, S. Teo, P. Ganz, I. Campbell, van der Hout, Annemarie H, van Deurzen, Carolien H M, C. Seynaeve, Gómez Garcia, Encarna B, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, Gille, Johannes J P, Ausems, Margreet G E M, M. Blok, Ligtenberg, Marjolijn J L, M. Rookus, P. Devilee, S. Verhoef, van Os, Theo A M, J. Wijnen, D. Frost, S. Ellis, E. Fineberg, R. Platte, D. Evans, L. Izatt, R. Eeles, J. Adlard, D. Eccles, J. Cook, C. Brewer, F. Douglas, S. Hodgson, P. Morrison, L. Side, A. Donaldson, C. Houghton, M. Rogers, H. Dorkins, J. Eason, H. Gregory, E. McCann, A. Murray, A. Calender, A. Hardouin, P. Berthet, C. Delnatte, C. Nogues, C. Lasset, C. Houdayer, D. Leroux, E. Rouleau, F. Prieur, F. Damiola, H. Sobol, I. Coupier, L. Venat-Bouvet, L. Castera, M. Gauthier-Villars, M. Léoné, P. Pujol, S. Mazoyer, Y. Bignon, E. Złowocka-Perłowska, J. Gronwald, J. Lubinski, K. Durda, K. Jaworska, T. Huzarski, A. Spurdle, A. Viel, B. Peissel, B. Bonanni, G. Melloni, L. Ottini, L. Papi, L. Varesco, M. Tibiletti, P. Peterlongo, S. Volorio, S. Manoukian, V. Pensotti, N. Arnold, C. Engel, H. Deissler, D. Gadzicki, A. Gehrig, K. Kast, K. Rhiem, A. Meindl, D. Niederacher, N. Ditsch, H. Plendl, S. Preisler-Adams, S. Engert, C. Sutter, R. Varon-Mateeva, B. Wappenschmidt, Weber, Bernhard H F, B. Arver, M. Stenmark-Askmalm, N. Loman, R. Rosenquist, Z. Einbeigi, K. Nathanson, T. Rebbeck, S. Blank, D. Cohn, G. Rodriguez, L. Small, M. Friedlander, V. Bae-Jump, A. Fink-Retter, C. Rappaport, D. Gschwantler-Kaulich, G. Pfeiler, M. Tea, N. Lindor, B. Kaufman, S. Shimon Paluch, Y. Laitman, A. Skytte, A. Gerdes, I. Pedersen, S. Moeller, T. Kruse, U. Jensen, J. Vijai, K. Sarrel, M. Robson, N. Kauff, A. Mulligan, G. Glendon, H. Ozcelik, B. Ejlertsen, F. Nielsen, L. Jønson, M. Andersen, Y. Ding, L. Steele, L. Foretova, A. Teulé, C. Lazaro, J. Brunet, M. Pujana, P. Mai, J. Loud, C. Walsh, J. Lester, S. Orsulic, S. Narod, J. Herzog, S. Sand, S. Tognazzo, S. Agata, T. Vaszko, J. Weaver, A. Stavropoulou, S. Buys, A. Romero, de la Hoya, Miguel, K. Aittomäki, T. Muranen, M. Duran, W. Chung, A. Lasa, C. Dorfling, A. Miron, J. Benitez, L. Senter, D. Huo, S. Chan, A. Sokolenko, J. Chiquette, L. Tihomirova, T. Friebel, B. Agnarsson, K. Lu, F. Lejbkowicz, P. James, P. Hall, A. Dunning, D. Tessier, J. Cunningham, S. Slager, C. Wang, S. Hart, K. Stevens, J. Simard, T. Pastinen, V. Pankratz, K. Offit, D. Easton, G. Chenevix-Trench, и A. Antoniou. PLoS genetics, 9 (3): e1003212 (2013)

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Другие публикации лиц с тем же именем

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersA. Antoniou, A. Spurdle, O. Sinilnikova, S. Healey, K. Pooley, R. Schmutzler, B. Versmold, C. Engel, A. Meindl, N. Arnold и 76 other автор(ы). American journal of human genetics, 82 (4): 937–948 (2008)Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskF. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis и 252 other автор(ы). PLoS genetics, 9 (3): e1003212 (2013)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriersA. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, A. Lee, D. Barrowdale, S. Healey, O. Sinilnikova и 171 other автор(ы). Breast cancer research : BCR, 14 (1): R33 (2012)A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general populationA. Antoniou, X. Wang, Z. Fredericksen, L. McGuffog, R. Tarrell, O. Sinilnikova, S. Healey, J. Morrison, C. Kartsonaki, T. Lesnick и 168 other автор(ы). Nature genetics, 42 (10): 885–892 (2010)Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriersX. Wang, V. Pankratz, Z. Fredericksen, R. Tarrell, M. Karaus, L. McGuffog, Pharaoh, Paul D P, Ponder, Bruce A J, A. Dunning, S. Peock и 34 other автор(ы). Human molecular genetics, 19 (14): 2886–2897 (2010)

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