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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

A. Mulligan, F. Couch, D. Barrowdale, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, M. Robson, M. Sherman, A. Spurdle, B. Wappenschmidt, A. Lee, L. McGuffog, S. Healey, O. Sinilnikova, R. Janavicius, T. Hansen, F. Nielsen, B. Ejlertsen, A. Osorio, I. Muñoz-Repeto, M. Durán, J. Godino, M. Pertesi, J. Benítez, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, E. Cattaneo, B. Bonanni, A. Viel, B. Pasini, L. Papi, L. Ottini, A. Savarese, L. Bernard, P. Radice, U. Hamann, M. Verheus, Meijers-Heijboer, Hanne E J, J. Wijnen, Gómez García, Encarna B, M. Nelen, C. Kets, C. Seynaeve, Tilanus-Linthorst, Madeleine M A, van der Luijt, Rob B, T. van Os, M. Rookus, D. Frost, J. Jones, D. Evans, F. Lalloo, R. Eeles, L. Izatt, J. Adlard, R. Davidson, J. Cook, A. Donaldson, H. Dorkins, H. Gregory, J. Eason, C. Houghton, J. Barwell, L. Side, E. McCann, A. Murray, S. Peock, A. Godwin, R. Schmutzler, K. Rhiem, C. Engel, A. Meindl, I. Ruehl, N. Arnold, D. Niederacher, C. Sutter, H. Deissler, D. Gadzicki, K. Kast, S. Preisler-Adams, R. Varon-Mateeva, I. Schoenbuchner, B. Fiebig, W. Heinritz, D. Schäfer, H. Gevensleben, V. Caux-Moncoutier, M. Fassy-Colcombet, F. Cornelis, S. Mazoyer, M. Léoné, N. Boutry-Kryza, A. Hardouin, P. Berthet, D. Muller, J. Fricker, I. Mortemousque, P. Pujol, I. Coupier, M. Lebrun, C. Kientz, M. Longy, N. Sevenet, D. Stoppa-Lyonnet, C. Isaacs, T. Caldes, de la Hoya, Miguel, T. Heikkinen, K. Aittomäki, I. Blanco, C. Lazaro, R. Barkardottir, P. Soucy, M. Dumont, J. Simard, M. Montagna, S. Tognazzo, E. D'Andrea, S. Fox, M. Yan, T. Rebbeck, O. Olopade, J. Weitzel, H. Lynch, P. Ganz, G. Tomlinson, X. Wang, Z. Fredericksen, V. Pankratz, N. Lindor, C. Szabo, K. Offit, R. Sakr, M. Gaudet, J. Bhatia, N. Kauff, C. Singer, M. Tea, D. Gschwantler-Kaulich, A. Fink-Retter, P. Mai, M. Greene, E. Imyanitov, F. O'Malley, H. Ozcelik, G. Glendon, A. Toland, A. Gerdes, M. Thomassen, T. Kruse, U. Jensen, A. Skytte, M. Caligo, M. Soller, K. Henriksson, v. Wachenfeldt, B. Arver, M. Stenmark-Askmalm, P. Karlsson, Y. Ding, S. Neuhausen, M. Beattie, Pharoah, Paul D P, K. Moysich, K. Nathanson, B. Karlan, J. Gross, E. John, M. Daly, S. Buys, M. Southey, J. Hopper, M. Terry, W. Chung, A. Miron, D. Goldgar, G. Chenevix-Trench, D. Easton, I. Andrulis, и A. Antoniou. Breast cancer research : BCR, 13 (6): R110 (2011)

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Другие публикации лиц с тем же именем

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk predictionA. Antoniou, J. Beesley, L. McGuffog, O. Sinilnikova, S. Healey, S. Neuhausen, Y. Ding, T. Rebbeck, J. Weitzel, H. Lynch и 168 other автор(ы). Cancer research, 70 (23): 9742–9754 (2010)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)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 breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2A. Mulligan, F. Couch, D. Barrowdale, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, M. Robson, M. Sherman, A. Spurdle и 172 other автор(ы). Breast cancer research : BCR, 13 (6): R110 (2011)RAD51 135G--C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studiesA. Antoniou, O. Sinilnikova, J. Simard, M. Léoné, M. Dumont, S. Neuhausen, J. Struewing, D. Stoppa-Lyonnet, L. Barjhoux, D. Hughes и 69 other автор(ы). American journal of human genetics, 81 (6): 1186–1200 (2007)

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