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cancer breast study mutation carrier university breast cancer risk genetic breast cancer association department brca 1 center research tumor institute analysis hospital genetics service centre stage allele receptor table sample oncology women mutation carriers case patients service medicine tumor subtypes subtype health factor genotype estimate patient control genet brca 2 mutations family ratio variant germany cancer risk stage 1 netherland model epidemiology susceptibility genome-wide association study population analyses diagnosis status estrogen risk factors france 1.00 article per-allele foundation italy america ptrend disease subject brca 1 carriers brca 2 individual brca 2 carriers downloaded grant case –case analyses hazard genotyping genotyped 1/her antoniou
5 Most Recent Publications
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Associations of breast cancer risk factors with tumor subtypes: A pooled analysis from the breast cancer association consortium studies
(Article)
Yang, X.R. Chang-Claude, J. Fasching, P.A. Shen, C.-Y. Hsiung, C.-N. Wu, P.E. Yu, J.-C. Chen, S.-T. Hsu, G.-C. Haiman, C.A. Henderson, B.E. Le Marchand, L. Kolonel, L.N. Hein, R. Lindblom, A. Margolin, S. Jakubowska, A. Lubinski, J. Huzarski, T. Byrski, T. Górski, B. Gronwald, J. Hooning, M. Hollestelle, A. Spurdle, A.B. Ouweland, A.M.W. van den Jager, A. Kriege, M. Tilanus-Linthorst, M.M.A. Collee, J.M. Wang-Gohrke, S. Pylkäs, K. Jukkola-Vuorinen, A. Mononen, K. Grip, M. Blows, F. Hirvikoski, P. Winqvist, R. Mannermaa, A. Kosma, V.M. Kauppinen, J. Kataja, V. Auvinen, P. Soini, Y. Sironen, R. Bojesen, S.E. Driver, K. Dynnes Ørsted, D. Kaur-Knudsen, D. Flyger, H. Nordestgaard, B.G. Holland, H. Chenevix-Trench, G. Manoukian, S. Barile, M. Radice, P. Hankinson, S.E. Flesch-Janys, D. Hunter, D. Tamimi, R. Sangrajrang, S. Brennan, P. McKay, J. Odefrey, F. Gaborieau, V. Devilee, P. Huijts, P. Tollenaar, R. Heinz, J. Seynaeve, C.M. Dite, G.S. Apicella, C. Hopper, J. Hammet, F. Tsimiklis, H. Smith, L. Southey, M.C. Easton, D.F. Pharoah, P. Sinn, P. Sherman, M. García-Closas, M. Vrieling, A. Heikinen, T. Goode, E.L. Aittomäki, K. Heikkilä, P. Blomqvist, C. Lissowska, J. Peplonska, B. Chanock, S.J. Figueroa, J. Brinton, L.A. Hall, A.S. Czene, k. Couch, F.J. Humphreys, M.K. Darabi, H. Liu, J. Veer, L.J. van 't Leeuwen, F.E. van Andrulis, I.L. Glendon, G. Knight, J.A. Mulligan, A.M. O'Malley, F.P. Nevanlinna, H. Weerasooriya, N. John, E.M. Beckmann, M.W. Hartmann, A. Weihbrecht, S.B. Wachter, D.L. Jud, S.M. Loehberg, C.R. Baglietto, L. English, D.R. Milne, R.L. Giles, G.G. McLean, C.A. Severi, G. Lambrechts, D. Vandorpe, T. Weltens, C. Paridaens, R. Smeets, A. Neven, P. Wildiers, H. Gaudet, M.M. Wang, X. Olson, J.E. Cafourek, V. Fredericksen, Z. Kosel, M. Vachon, C. Cramp, H.E. Connley, D. Cross, S.S. Balasubramanian, S. Schmidt, M.K. Reed, M.W.R. Dörk, T. Bremer, M. Meyer, A. Karstens, J.H. Ay, A. Park-Simon, T.-W. Hillemanns, P. Arias Pérez, J.I. Rodríguez, P.M. Broeks, A. Zamora, P. Benitez, J. Ko, Y.D. Fischer, H.-P. Hamann, U. Pesch, B. Brüning, T. Justenhoven, C. Brauch, H. Eccles, D. Cox, A. Tapper, W. Gerty, S.M. Sawyer, E.J. Tomlinson, I.P. Jones, A. Kerin, M. Miller, N. McInerney, N. Anton-Culver, H. Ziogas, A. |
2011-02-02
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Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
(Article)
Ramus, S.J. kartsonaki, C. Wang, X. Collonge-Rame, M.-A. Vénat-Bouvet, L. Fert-Ferrer, S. Miron, A. Buys, S.S. Hopper, J. Daly, M. John, E.M. Terry, M-B. Goldgar, D. Fredericksen, Z. Hansen, T.V.O. Jønson, L. Ejlertsen, B. Agnarsson, B.A. Offit, K. Kirchhoff, T. Vijai, J. Dutra-Clarke, A. Przybylo, J.A. Montagna, M. Peterlongo, P. Casella, C. Imyanitov, E.N. Janavicius, R. Blanco, I. Lazaro, C. Moysich, K.B. Karlan, B.Y. Gross, J. Beattie, M.S. Schmutzler, R.K. Manoukian, S. Wappenschmidt, B. Meindl, A. Ruehl, I. Fiebig, B. Sutter, C. Arnold, N. Deissler, H. Varon-Mateeva, R. Kast, K. Niederacher, D. Peissel, B. Gadzicki, D. Caldes, T. Hoya, M. de La Nevanlinna, H. Aittomäki, K. Simard, J. Soucy, P. Spurdle, A.B. Holland, H. Easton, D.F. Zaffaroni, D. Antoniou, A.C. Asperen, C.J. van Roversi, G. Barile, M. Viel, A. Allavena, A. Gayther, S.A. Ottini, L. Papi, L. Gismondi, V. Capra, F. Radice, P. Greene, M.H. Mai, P.L. Andrulis, I.L. Glendon, G. Ozcelik, H. Pharoah, P.D.P. Thomassen, M. Gerdes, A-M. Kruse, T.A. Cruger, D. Jensen, U.B. Caligo, M.A. Olsson, H. Kristoffersson, U. Lindblom, A. Arver, B. Sinilnikova, O. Karlsson, P. Stenmark-Askmalm, M. Borg, A. Neuhausen, S.L. Ding, Y.C. Nathanson, K.L. Domchek, S.M. Jakubowska, A. Lubinski, J. Huzarski, T. Beesley, J. Byrski, T. Gronwald, J. Górski, B. Cybulski, C. Dbniak, T. Osorio, A. Durán, M. Tejada, M.-I. Benitez, J. Hamann, U. Chenevix-Trench, G. Rookus, M.A. Verhoef, S. Tilanus-Linthorst, M.A. Vreeswijk, M.P. Bodmer, D. Ausems, M.G.E.M. Os, T.A.M. van Blok, M.J. Meijers-Heijboer, H. Peock, S. McGuffog, L. Cook, J. Oliver, C. Frost, D. Dunning, A.M. Evans, D.G. Eeles, R. Pichert, G. Cole, T.J. Hodgson, S.V. Brewer, C. Healey, S. Morrison, P.J. Porteous, M.E. Kennedy, M.J. Rogers, M.T. Side, L. Donaldson, A. Gregory, H. Godwin, A.K. Stoppa-Lyonnet, D. Moncoutier, V. Couch, F.J. Castera, L. Mazoyer, S. Barjhoux, L. Bonadona, V. Leroux, D. Faivre, L. Lidereau, R. Nogues, C. Bignon, Y.-J. Prieur, F. |
2011-01-19
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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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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 population
(Article)
Antoniou, A.C. Wang, X. Ghoussaini, M. Caldes, T. Hoya, M. de La Singer, C.F. Fink-Retter, A. Greene, M.H. Mai, P.L. Loud, J.T. Guidugli, L. Lindor, N.M. Hansen, T.V.O. Barrowdale, D. Nielsen, F.C. Blanco, I. Lazaro, C. Garber, J. Ramus, S.J. Gayther, S.A. Phelan, C. Narod, S. Szabo, C. Benitez, J. Peock, S. Osorio, A. Nevanlinna, H. Heikkinen, T. Caligo, M.A. Beattie, M.S. Hamman, U. Godwin, A.K. Montagna, M. Casella, C. Neuhausen, S.L. Cook, M. Karlan, B.Y. Tung, N. Toland, A.E. Weitzel, J. Olopade, P. Simard, J. Soucy, P. Rubinstein, W.S. Arason, A. Rennert, G. Oliver, C. Martin, N.G. Montgomery, G.W. Chang-Claude, J. Flesch-Janys, D. Brauch, H. Severi, G. Baglietto, L. Cox, A. Cross, S.S. Miron, P. Frost, D. Gerty, S.M. Tapper, W. Yannoukakos, D. Fountzilas, G. Fasching, P.A. Beckmann, M.W. Dos Santos Silva, I. Peto, J. Lambrechts, D. Paridaens, R. Eccles, D. Rüdiger, T. Försti, A. Winqvist, R. Pylkäs, K. Diasio, R.B. Lee, A.M. Eckel-Passow, J. Vachon, C. Blows, F. Driver, K. Evans, D.G. Dunning, A.M. Pharaoh, P.D.P. Offit, K. Pankratz, V.S. Hakonarson, H. Chenevix-Trench, G. Easton, D.F. Couch, F.J. Eeles, R. Izatt, L. Fredericksen, Z. Chu, C. Douglas, F. Paterson, J. Stoppa-Lyonnet, D. Houdayer, C. Mazoyer, S. Giraud, S. Lassett, C. Remenieras, A. Caron, O. McGuffog, L. Hardouin, A. Berthet, P. Hogervorst, F.B.L. Rookus, M.A. Jager, A. Ouweland, A.M.W. van den Hoogerbrugge, N. Luijt, R.B. van der Meijers-Heijboer, H. G'mez García, E.B. Tarrell, R. Devilee, P. Vreeswijk, M.P. Lubinski, J. Jakubowska, A. Gronwald, J. Huzarski, T. Byrski, T. G'rski, B. Cybulski, C. Spurdle, A.B. Sinilnikova, O. Holland, H. Goldgar, D. John, E.M. Hopper, J. Southey, M.C. Buys, S.S. Daly, M.B. Terry, M-B. Schmutzler, R.K. Wappenschmidt, B. Healey, S. Engel, C. Meindl, A. Preisler-Adams, S. Arnold, N. Niederacher, D. Sutter, C. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Blum, J.L. Morrison, J. Piedmonte, M. Rodriguez, G.C. Wakeley, K. Boggess, J.F. Basil, J. Blank, S.V. Friedman, E. Kaufman, B. Laitman, Y. Milgrom, R. kartsonaki, C. Andrulis, I.L. Glendon, G. Ozcelik, H. Kirchhoff, T. Vijai, J. Gaudet, M.M. Altshuler, D. Guiducci, C. Loman, N. Harbst, K. Lesnick, T. Rantala, J. Ehrencona, H. Gerdes, A-M. Thomassen, M. Sunde, L. Peterlongo, P. Manoukian, S. Bonanni, B. Viel, A. Radice, P. |
2010-10-01
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Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
(Article)
Gaudet, M.M. Kirchhoff, T. Morrison, J. Godwin, A.K. Schmutzler, R.K. Wappenschmidt, B. Engert, S. Arnold, N. Gadzicki, D. Dean, M. Gold, B. Klein, R.J. Couch, F.J. Healey, S. Chenevix-Trench, G. Easton, D.F. Daly, M. Antoniou, A.C. Altshuler, D. Offit, K. Sinilnikova, O. Stoppa-Lyonnet, D. Mazoyer, S. Gauthier-Villars, M. Sobol, H. Longy, M. Frenay, M. Hogervorst, F.B.L. Green, T. Rookus, M.A. Collée, J.M. Hoogerbrugge, N. Roozendaal, K.E. van Piedemonte, M. Rubinstein, W.S. Nerenstone, S. Le, L. van Blank, S.V. Caldes, T. Vijai, J. Hoya, M. de La Nevanlinna, H. Aittomäki, K. Lazaro, C. Blanco, I. Arason, A. Johannsson, O.T. Barkardottir, R.B. Devilee, P. Olopade, O.I. Korn, J.M. Neuhausen, S.L. Wang, X. Fredericksen, Z. Peterlongo, P. Manoukian, S. Barile, M. Viel, A. Radice, P. Phelan, C. Narod, S. Guiducci, C. Rennert, G. Lejbkowicz, F. Flugelman, A. Andrulis, I.L. Glendon, G. Ozcelik, H. Toland, A.E. Montagna, M. D'Andrea, E. Friedman, E. Segrè, A.V. Laitman, Y. Borg, A. Beattie, M.S. Ramus, S.J. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Spurdle, A.B. Chen, X. Holland, H. McGee, K. John, E.M. Hopper, J. Buys, S.S. Daly, M.B. Southey, M.C. Terry, M-B. Tung, N. Hansen, T.V.O. Nielsen, F.C. Greene, M.H. McGuffog, L. Mai, P.L. Osorio, A. Duran, M. Andres, R. Benítez, J. Weitzel, J. Garber, J. Hamann, U. Peock, S. Cook, M. kartsonaki, C. Oliver, C. Frost, D. Platte, R. Evans, D.G. Lalloo, F. Eeles, R. Izatt, L. Walker, L. Eason, J. Barwell, J. |
2010-10-01
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