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Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

A. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, E. Cattaneo, M. Barile, V. Pensotti, B. Pasini, R. Dolcetti, G. Giannini, A. Putignano, L. Varesco, P. Radice, P. Mai, M. Greene, I. Andrulis, G. Glendon, H. Ozcelik, M. Thomassen, A. Gerdes, T. Kruse, U. Birk Jensen, D. Crüger, M. Caligo, Y. Laitman, R. Milgrom, B. Kaufman, S. Paluch-Shimon, E. Friedman, N. Loman, K. Harbst, A. Lindblom, B. Arver, H. Ehrencrona, B. Melin, K. Nathanson, S. Domchek, T. Rebbeck, A. Jakubowska, J. Lubinski, J. Gronwald, T. Huzarski, T. Byrski, C. Cybulski, B. Gorski, A. Osorio, Ramón y Cajal, Teresa, F. Fostira, R. Andrés, J. Benitez, U. Hamann, F. Hogervorst, M. Rookus, M. Hooning, M. Nelen, van der Luijt, Rob B, van Os, Theo A M, van Asperen, Christi J, P. Devilee, Meijers-Heijboer, Hanne E J, Gómez Garcia, Encarna B, S. Peock, M. Cook, D. Frost, R. Platte, J. Leyland, D. Evans, F. Lalloo, R. Eeles, L. Izatt, J. Adlard, R. Davidson, D. Eccles, K. Ong, J. Cook, F. Douglas, J. Paterson, M. Kennedy, Z. Miedzybrodzka, A. Godwin, D. Stoppa-Lyonnet, B. Buecher, M. Belotti, C. Tirapo, S. Mazoyer, L. Barjhoux, C. Lasset, D. Leroux, L. Faivre, M. Bronner, F. Prieur, C. Nogues, E. Rouleau, P. Pujol, I. Coupier, M. Frénay, J. Hopper, M. Daly, M. Terry, E. John, S. Buys, Y. Yassin, A. Miron, D. Goldgar, C. Singer, M. Tea, G. Pfeiler, A. Dressler, Hansen, Thomas V O, L. Jønson, B. Ejlertsen, R. Barkardottir, T. Kirchhoff, K. Offit, M. Piedmonte, G. Rodriguez, L. Small, J. Boggess, S. Blank, J. Basil, M. Azodi, A. Toland, M. Montagna, S. Tognazzo, S. Agata, E. Imyanitov, R. Janavicius, C. Lazaro, I. Blanco, Pharoah, Paul D P, L. Sucheston, B. Karlan, C. Walsh, E. Olah, A. Bozsik, S. Teo, J. Seldon, M. Beattie, van Rensburg, Elizabeth J, M. Sluiter, O. Diez, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, I. Ruehl, R. Varon-Mateeva, K. Kast, H. Deissler, D. Niederacher, N. Arnold, D. Gadzicki, I. Schönbuchner, T. Caldes, de la Hoya, Miguel, H. Nevanlinna, K. Aittomäki, M. Dumont, J. Chiquette, M. Tischkowitz, X. Chen, J. Beesley, A. Spurdle, S. Neuhausen, Y. Chun Ding, Z. Fredericksen, X. Wang, V. Pankratz, F. Couch, J. Simard, D. Easton, и G. Chenevix-Trench. Human molecular genetics, 20 (16): 3304–3321 (2011)

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Другие публикации лиц с тем же именем

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 и 169 other автор(ы). Human molecular genetics, 20 (16): 3304–3321 (2011)A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activityL. Guidugli, V. Pankratz, N. Singh, J. Thompson, C. Erding, C. Engel, R. Schmutzler, S. Domchek, K. Nathanson, P. Radice и 5 other автор(ы). Cancer research, 73 (1): 265–275 (2013)Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancersJ. French, M. Ghoussaini, S. Edwards, K. Meyer, K. Michailidou, S. Ahmed, S. Khan, M. Maranian, M. O'Reilly, K. Hillman и 201 other автор(ы). American journal of human genetics, 92 (4): 489–503 (2013)Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriersL. Walker, Z. Fredericksen, X. Wang, R. Tarrell, V. Pankratz, N. Lindor, J. Beesley, S. Healey, X. Chen, D. Stoppa-Lyonnet и 63 other автор(ы). Breast cancer research : BCR, 12 (6): R102 (2010)Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriersD. Cox, J. Simard, D. Sinnett, Y. Hamdi, P. Soucy, M. Ouimet, L. Barjhoux, C. Verny-Pierre, L. McGuffog, S. Healey и 99 other автор(ы). Human molecular genetics, 20 (23): 4732–4747 (2011)Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancerS. Bojesen, K. Pooley, S. Johnatty, J. Beesley, K. Michailidou, J. Tyrer, S. Edwards, H. Pickett, H. Shen, C. Smart и 427 other автор(ы). Nature genetics, 45 (4): 371-84, 384e1-2 (2013)Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)N. Mavaddat, D. Barrowdale, I. Andrulis, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, A. Spurdle, M. Robson, M. Sherman и 123 other автор(ы). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (1): 134–147 (2012)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 и 180 other автор(ы). 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)No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort studyT. Rebbeck, A. Antoniou, T. Llopis, H. Nevanlinna, K. Aittomäki, J. Simard, A. Spurdle, F. Couch, Pereira, Lutecia H Mateus, M. Greene и 34 other автор(ы). Breast cancer research and treatment, 115 (1): 185–192 (2009)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)

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