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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, and A. Antoniou. Breast cancer research : BCR, 13 (6): R110 (2011)

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Bernardo

Marc Bonanni

Arno Bonanni

Andrea Bonanni

Bernardo Fritzsche

Other publications of authors with the same name

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 and 252 other author(s). 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 and 172 other author(s). Breast cancer research : BCR, 13 (6): R110 (2011)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 and 168 other author(s). Nature genetics, 42 (10): 885–892 (2010)Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, O. Sinilnikova, L. McGuffog, S. Healey, H. Nevanlinna, T. Heikkinen, J. Simard, A. Spurdle, J. Beesley, X. Chen and 127 other author(s). Human molecular genetics, 18 (22): 4442–4456 (2009)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 and 171 other author(s). Breast cancer research : BCR, 14 (1): R33 (2012)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 and 427 other author(s). Nature genetics, 45 (4): 371-84, 384e1-2 (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 and 201 other author(s). American journal of human genetics, 92 (4): 489–503 (2013)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 and 176 other author(s). Human mutation, 33 (4): 690–702 (2012)

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Disambiguation of "Bonanni, Bernardo"