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cancer breast carrier brca 1 mutation breast cancer risk genetic university study breast cancer research genetics service center department association hospital service analysis institute centre brca 2 carriers grant allele estimate model sample mutation carriers brca 2 brca 1 carriers cancer research american foundation brca 2 mutations evidence genotype medicine family health netherland genet effect result ptrend cancer risk multiplicative model table clinic variant susceptibility per-allele germany onlinefirst consortium cimba 557ser disease ratio antoniou american journal fgfr 2 oncology cancer institute hazard france article haplotype population downloaded copyright italy breast cancer risks cancer center canada polymorphism diagnosis modi fiers breast cancer alleles analyses genotyping netherlands cancer institute
3 Most Recent Publications
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Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers
(Article)
Spurdle, A.B. Marquart, L. Gschwantler-Kaulich, D. Blum, J.L. Tung, N. Weitzel, J.N. Lynch, H. Garber, J. Easton, D.F. Peock, S. Cook, J. Oliver, C. McGuffog, L. Frost, D. Conroy, D. Evans, D.G. Lalloo, F. Eeles, R. Izatt, L. Davidson, R. Chu, C. Eccles, D. Selkirk, C.G. Healey, S. Daly, M. Isaacs, C. Stoppa-Lyonnet, D. Buecher, B. Belotti, M. Mazoyer, S. Barjhoux, L. Verny-Pierre, C. Lassett, C. Dreyfus, H. Sinilnikova, O. Pujol, P. Collonge-Rame, M.-A. Rookus, M.A. Verhoef, S. Kriege, M. Hoogerbrugge, N. Ausems, M.G.E.M. Os, T.A.M. van Wijnen, J.T. Devilee, P. Wan, F. Meijers-Heijboer, H. Blok, M.J. Heikinen, T. Nevanlinna, H. Jakubowska, A. Lubinski, J. Huzarski, T. Byrski, T. Durocher, F. Couch, F.J. Chenevix-Trench, G. Lindor, N.M. Wang, X. Thomassen, M. Domchek, S.M. Nathanson, K.L. Caligo, M.A. Jernström, H. Liljegren, A. Ehrencrona, H. Karlsson, P. Beesley, J. Ganz, P.A. Olopade, O.I. Tomlinson, G. Neuhausen, S.L. Antoniou, A.C. Chenevix-Trench, G. Rebbeck, T.R. Singer, C.F. Dressler, A.-C. |
2011-05-01
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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction
(Article)
Antoniou, A.C. Beesley, J. Isaacs, C. Bonadona, V. Lassett, C. Dreyfus, H. Leroux, D. Hardouin, A. Berthet, P. Faivre, L. Loustalot, C. Noguchi, T. Sobol, H. Ganz, P.A. Rouleau, E. Nogues, C. Frenay, M. Vénat-Bouvet, L. Hopper, J. Daly, M. Terry, M-B. John, E.M. Buys, S.S. Yassin, Y. Tomlinson, G. Miron, A. Goldgar, D. Singer, C.F. Dressler, C. Gschwantler-Kaulich, D. Pfeiler, G. Hansen, T.V.O. Jnson, L. Agnarsson, B.A. Kirchhoff, T. Olopade, O.I. Offit, K. Devlin, V. Dutra-Clarke, A. Piedmonte, M. Rodriguez, G.C. Wakeley, K. Boggess, J.F. Basil, J. Schwartz, P.E. Blank, S.V. Couch, F.J. Toland, A.E. Montagna, M. Casella, C. Imyanitov, E.N. Tihomirova, L. Blanco, I. Lazaro, C. Ramus, S.J. Sucheston, L. Karlan, B.Y. Wang, X. Gross, J. Schmutzler, R.K. Wappenschmidt, B. Engel, C. Meindl, A. Lochmann, M. Arnold, N. Heidemann, S. Varon-Mateeva, R. Niederacher, D. Lindor, N.M. Sutter, C. Deissler, H. Gadzicki, D. Preisler-Adams, S. Kast, K. Schönbuchner, I. Caldes, T. Hoya, M. de La Aittomäki, K. Nevanlinna, H. Pankratz, V.S. Simard, J. Spurdle, A.B. Holland, H. Chenevix-Trench, G. Platte, R. Easton, D.F. Radice, P. Manoukian, S. McGuffog, L. Peissel, B. Zaffaroni, D. Barile, M. Viel, A. Allavena, A. Dall'Olio, V. Peterlongo, P. Szabo, C. Zikan, M. Claes, K. Sinilnikova, O. Poppe, B. Foretova, L. Mai, P.L. Greene, M.H. Rennert, G. Lejbkowicz, F. Glendon, G. Ozcelik, H. Andrulis, I.L. Thomassen, M. Healey, S. Gerdes, A-M. Sunde, L. Cruger, D. Jensen, U.B. Caligo, M.A. Friedman, E. Kaufman, B. Laitman, Y. Milgrom, R. Dubrovsky, M. Neuhausen, S.L. Cohen, S. Borg, A. Jernström, H. Lindblom, A. Rantala, J. Stenmark-Askmalm, M. Melin, B. Nathanson, K.L. Domchek, S.M. Jakubowska, A. Ding, Y.C. Lubinski, J. Huzarski, T. Osorio, A. Lasa, A. Durán, M. Tejada, M.I. Godino, J. Benitez, J. Hamann, U. Kriege, M. Rebbeck, T.R. Hoogerbrugge, N. Luijt, R.B. van der Asperen, C.J. van Devilee, P. Meijers-Heijboer, E.J. Blok, M.J. Aalfs, C. Hogervorst, F.B.L. Rookus, M.A. Cook, J. Weitzel, J. Oliver, C. Frost, D. Conroy, D. Evans, D.G. Lalloo, F. Pichert, G. Davidson, R. Cole, T.J. Paterson, J. Hodgson, S.V. Lynch, H. Morrison, P.J. Porteous, M.E. Walker, L. Kennedy, M.J. Dorkins, H. Peock, S. Godwin, A.K. Stoppa-Lyonnet, D. Pauw, A. de Mazoyer, S. |
2010-12-01
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Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
(Article)
Antoniou, A.C. Spurdle, A.B. Hofmann, W. Sutter, C. Niederacher, D. Deissler, H. Caldes, T. Kämpjärvi, K. Nevanlinna, H. Simard, J. Beesley, J. Chen, X. Sinilnikova, O. Neuhausen, S.L. Rebbeck, T.R. Wagner, T. Lynch, H. Isaacs, C. Weitzel, J. Ganz, P.A. Daly, M. Tomlinson, G. Olopade, O.I. Healey, S. Blum, J.L. Couch, F.J. Peterlongo, P. Manoukian, S. Barile, M. Radice, P. Szabo, C. Pereira, L.H.M. Greene, M.H. Rennert, G. Pooley, K.A. Lejbkowicz, F. Barnett-Griness, O. Andrulis, I.L. Ozcelik, H. Gerdes, A-M. Caligo, M.A. Laitman, Y. Kaufman, B. Milgrom, R. Friedman, E. Schmutzler, R.K. Domchek, S.M. Nathanson, K.L. Osorio, A. Llort, G. Milne, R.L. Benítez, J. Hamann, U. Hogervorst, F.B.L. Manders, P. Ligtenberg, M. Versmold, B. Ouweland, A.M.W. van den Peock, S. Cook, M. Platte, R. Evans, D.G. Eeles, R. Pichert, G. Chu, C. Eccles, D. Davidson, R. Engel, C. Douglas, F. Godwin, A.K. Barjhoux, L. Mazoyer, S. Sobol, H. Bourdon, V. Eisinger, F. Chompret, A. Capoulade, C. Bressac-de Paillerets, B. Meindl, A. Lenoir, G.M. Gauthier-Villars, M. Houdayer, C. Stoppa-Lyonnet, D. Chenevix-Trench, G. Easton, D.F. Arnold, N. |
2008-04-11
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