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Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

F. Couch, M. Gaudet, A. Antoniou, S. Ramus, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, X. Wang, T. Kirchhoff, L. McGuffog, D. Barrowdale, A. Lee, S. Healey, O. Sinilnikova, I. Andrulis, H. Ozcelik, A. Mulligan, M. Thomassen, A. Gerdes, U. Jensen, A. Skytte, T. Kruse, M. Caligo, A. Wachenfeldt, G. Barbany-Bustinza, N. Loman, M. Soller, H. Ehrencrona, P. Karlsson, K. Nathanson, T. Rebbeck, S. Domchek, A. Jakubowska, J. Lubinski, K. Jaworska, K. Durda, E. Zlowocka, T. Huzarski, T. Byrski, J. Gronwald, C. Cybulski, B. Górski, A. Osorio, M. Durán, M. Tejada, J. Benitez, U. Hamann, Hogervorst, Frans B L, van Os, Theo A, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, J. Wijnen, M. Blok, M. Kets, M. Hooning, R. Oldenburg, Ausems, Margreet G E M, S. Peock, D. Frost, S. Ellis, R. Platte, E. Fineberg, D. Evans, C. Jacobs, R. Eeles, J. Adlard, R. Davidson, D. Eccles, T. Cole, J. Cook, J. Paterson, C. Brewer, F. Douglas, S. Hodgson, P. Morrison, L. Walker, M. Porteous, M. Kennedy, L. Side, B. Bove, A. Godwin, D. Stoppa-Lyonnet, M. Fassy-Colcombet, L. Castera, F. Cornelis, S. Mazoyer, M. Léoné, N. Boutry-Kryza, B. Bressac-de Paillerets, O. Caron, P. Pujol, I. Coupier, C. Delnatte, L. Akloul, H. Lynch, C. Snyder, S. Buys, M. Daly, M. Terry, W. Chung, E. John, A. Miron, M. Southey, J. Hopper, D. Goldgar, C. Singer, C. Rappaport, M. Tea, A. Fink-Retter, Hansen, Thomas V O, F. Nielsen, A. Arason, J. Vijai, S. Shah, K. Sarrel, M. Robson, M. Piedmonte, K. Phillips, J. Basil, W. Rubinstein, J. Boggess, K. Wakeley, A. Ewart-Toland, M. Montagna, S. Agata, E. Imyanitov, C. Isaacs, R. Janavicius, C. Lazaro, I. Blanco, L. Feliubadalo, J. Brunet, S. Gayther, Pharoah, Paul P D, K. Odunsi, B. Karlan, C. Walsh, E. Olah, S. Teo, P. Ganz, M. Beattie, van Rensburg, Elizabeth J, C. Dorfling, O. Diez, A. Kwong, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, N. Ditsch, N. Arnold, S. Heidemann, D. Niederacher, S. Preisler-Adams, D. Gadzicki, R. Varon-Mateeva, H. Deissler, A. Gehrig, C. Sutter, K. Kast, B. Fiebig, W. Heinritz, T. Caldes, de la Hoya, Miguel, T. Muranen, H. Nevanlinna, M. Tischkowitz, A. Spurdle, S. Neuhausen, Y. Ding, N. Lindor, Z. Fredericksen, V. Pankratz, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, M. Barile, L. Bernard, A. Viel, G. Giannini, L. Varesco, P. Radice, M. Greene, P. Mai, D. Easton, G. Chenevix-Trench, K. Offit, und J. Simard. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (4): 645–657 (2012)

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J Leo van Hemmen

Peter J van Zijl

W L J van Vuuren

Elizabeth Wainwright

Elizabeth Mukidjam

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BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer riskA. Spurdle, P. Whiley, B. Thompson, B. Feng, S. Healey, M. Brown, C. Pettigrew, van Asperen, Christi J, Ausems, Margreet G E M, A. Kattentidt-Mouravieva und 23 andere Autor(en). Journal of medical genetics, 49 (8): 525–532 (2012)Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriersS. Ramus, A. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, O. Sinilnikova, S. Healey, D. Barrowdale und 176 andere Autor(en). Human mutation, 33 (4): 690–702 (2012)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 und 252 andere Autor(en). PLoS genetics, 9 (3): e1003212 (2013)Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel und 169 andere Autor(en). Human molecular genetics, 20 (16): 3304–3321 (2011)Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriersF. Couch, M. Gaudet, A. Antoniou, S. Ramus, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, X. Wang, T. Kirchhoff und 180 andere Autor(en). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (4): 645–657 (2012)

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Disambiguierung von "van Rensburg, Elizabeth J,"