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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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Georgia Frigge

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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 BRCA1 promoter variant (rs11655505) and breast cancer riskP. Verderio, S. Pizzamiglio, M. Southey, A. Spurdle, J. Hopper, X. Chen, J. Beesley, R. Schmutzler, C. Engel, B. Burwinkel and 8 other author(s). Journal of medical genetics, 47 (4): 268–270 (2010)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 and 69 other author(s). American journal of human genetics, 81 (6): 1186–1200 (2007)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)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 and 99 other author(s). Human molecular genetics, 20 (23): 4732–4747 (2011)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 and 169 other author(s). Human molecular genetics, 20 (16): 3304–3321 (2011)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 and 63 other author(s). Breast cancer research : BCR, 12 (6): R102 (2010)Genome-wide association study identifies novel breast cancer susceptibility lociD. Easton, K. Pooley, A. Dunning, P. Pharoah, D. Thompson, D. Ballinger, J. Struewing, J. Morrison, H. Field, R. Luben and 92 other author(s). Nature, 447 (7148): 1087--1093 (June 2007)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 "Chenevix-Trench, Georgia"