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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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Heribert Franssen

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Udo Franssen

Другие публикации лиц с тем же именем

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 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)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 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)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)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)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)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)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)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)

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