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9 Most Recent Publications
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Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
(Article)
Osorio, A. Milne, R.L. Konstantopoulou, I. Hogervorst, F.B.L. Verhoef, S. Dooren, M.F. van Jager, A. Ausems, M.G.E.M. Aalfs, C. Asperen, C.J. van Vreeswijk, M.P. Waisfisz, Q. Pallás-Alonso, C.R. Roozendaal, C.E.P. van Ligtenberg, M. Easton, D.F. Peock, S. Cook, M.S. Oliver, C.T. Frost, D. Curzon, B. Evans, D.G. Lalloo, F. Pita, G. Eeles, R. Izatt, L. Davidson, R. Adlard, J.W. Eccles, D. Ong, K.R. Douglas, F. Downing, S. Brewer, C. Walker, L. Peterlongo, P. Nevanlinna, H. Aittomäki, K. Couch, F.J. Fredericksen, Z. Lindor, N.M. Godwin, A.K. Isaacs, C. Caligo, M.A. Loman, N. Jernström, H. Teulé, A. Barbany-Bustinza, G. Liljegren, A. Ehrencrona, H. Stenmark-Askmalm, M. Feliubadaló, L. Manoukian, S. Peissel, B. Zaffaroni, D. Bonanni, B. Fortuzzi, S. Nathanson, K.L. Johannsson, O.T. Chenevix-Trench, G. Chen, X.C. Beesley, J. Spurdle, A.B. Sinilnikova, O. Healey, S. McGuffog, L. Antoniou, A.C. Brunet, J. Domchek, S.M. Radice, P. Benítez, J. Rebbeck, T.R. Lasa, A. |
2011-05-01
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Exploring the link between MORF4L1 and risk of breast cancer
(Article)
Martrat, G. Maxwell, C.A. Aguilar, H. Torres, D. Caligo, M.A. Godwin, A.K. Imyanitov, E.N. Janavicius, R. Sinilnikova, O. Stoppa-Lyonnet, D. Mazoyer, S. Verny-Pierre, C. Castera, L. Fernández-Rodríguez, J. Pauw, A. de Bignon, Y. Uhrhammer, N. Peyrat, J.-P. Vennin, P. Ferrer, S.F. Collonge-Rame, M.-A. Mortemousque, I. McGuffog, L. Chenevix-Trench, G. Seal, S. Pereira-Smith, O.M. Antoniou, A.C. Cerón, J. Surrallés, J. Pujana, M.A. Asperen, C.J. van Renwick, A. Rahman, N. Kühl, J. Neveling, K. Schindler, D. Ramírez, M.J. Castellà, M. Tominaga, E. Hernández, G. Easton, D.F. Peock, S. Cook, J. Oliver, C. Frost, D. Platte, R. Evans, D.G. Lalloo, F. Eeles, R. Porta-de-la-Riva, M. Izatt, L. Chu, C. Davidson, R. Ong, K. Douglas, F. Hodgson, S.V. Brewer, C. Morrison, P.J. Porteous, M.E. Peterlongo, P. Bonifaci, N. Manoukian, S. Peissel, B. Zaffaroni, D. Roversi, G. Barile, M. Viel, A. Pasini, B. Ottini, L. Putignano, A.L. Savarese, A. Gómez-Baldó, L. Bernard, L. Radice, P. Healey, S. Spurdle, A.B. Chen, X. Beesley, J. Rookus, M.A. Verhoef, S. Tilanus-Linthorst, M.M.A. Vreeswijk, M.P. Bogliolo, M. Bodmer, D. Ausems, M.G.E.M. Os, T.A.M. van Blok, M.J. Meijers-Heijboer, E.J. Hogervorst, F.B.L. Goldgar, D. Buys, S.S. John, E.M. Miron, A. Lázaro, C. Southey, M.C. Daly, M. Harbst, K. Borg, A. Rantala, J. Barbany-Bustinza, G. Ehrencrona, H. Stenmark-Askmalm, M. Kaufman, B. Laitman, Y. Blanco, I. Milgrom, R. Friedman, E. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Johannsson, O.T. Couch, F.J. Wang, X. Fredericksen, Z. Cuadras, D. Brunet, J. Moreno, V. Pientka, F.K. Depping, R. Caldes, T. Osorio, A. Benítez, J. Bueren, J. Heikinen, T. Nevanlinna, H. Hamann, U. |
2011-04-05
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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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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
(Article)
Antoniou, A.C. Sinilnikova, O. Neuhausen, S.L. Gschwantler-Kaulich, D. Staudigl, C. Hansen, T.V.O. Barkardottir, R.B. Kirchhoff, T. Pal, P. Kosarin, K. Offit, K. Piedmonte, M. Rodriguez, G.C. Ding, Y.C. Wakeley, K. Boggess, J.F. Basil, J. Schwartz, P.E. Blank, S.V. Toland, A.E. Montagna, M. Casella, C. Imyanitov, E.N. Allavena, A. Couch, F.J. Schmutzler, R.K. Versmold, B. Engel, C. Meindl, A. Ditsch, N. Arnold, N. Niederacher, D. Deissler, H. Fiebig, B. Suttner, C. Wang, X. Schönbuchner, I. Gadzicki, D. Caldes, T. Hoya, M. de La Pooley, K.A. Easton, D.F. Fredericksen, Z. Peterlongo, P. Peissel, B. Bonanni, B. Viel, A. Bernard, L. McGuffog, L. Radice, P. Szabo, C. Foretova, L. Zikan, M. Claes, K. Greene, M.H. Mai, P.L. Rennert, G. Lejbkowicz, F. Andrulis, I.L. Healey, S. Ozcelik, H. Glendon, G. Gerdes, A-M. Thomassen, M. Sunde, L. Caligo, M.A. Laitman, Y. Kontorovich, T. Cohen, S. Kaufman, B. Nevanlinna, H. Dagan, E. Baruch, R.G. Friedman, E. Harbst, K. Barbany-Bustinza, G. Rantala, J. Ehrencrona, H. Karlsson, P. Domchek, S.M. Nathanson, K.L. Heikinen, T. Osorio, A. Blanco, I. Lasa, A. Benitez, J. Hamann, U. Hogervorst, F.B.L. Rookus, M.A. Collee, J.M. Devilee, P. Ligtenberg, M. Simard, J. Luijt, R.B. van der Aalfs, C. Waisfisz, Q. Wijnen, J.T. Roozendaal, C.E.P. van Peock, S. Cook, J. Frost, D. Oliver, C. Platte, R. Spurdle, A.B. Evans, D.G. Lalloo, F. Eeles, R. Izatt, L. Davidson, R. Chu, C. Eccles, D. Cole, T.J. Hodgson, S.V. Godwin, A.K. Beesley, J. Stoppa-Lyonnet, D. Buecher, B. Léoné, M. Bressac-de Paillerets, B. Remenieras, A. Caron, O. Lenoir, G.M. Sevenet, N. Longy, M. Ferrer, S.F. Chenevix-Trench, G. Prieur, F. Goldgar, D. Miron, A. John, E.M. Buys, S.S. Daly, M. Hopper, J. Terry, M-B. Yassin, Y. Singer, C.F. |
2009-11-16
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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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Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies
(Article)
González-Neira, A. Rosa-Rosa, J.M. Pita, G. Devilee, P. Goldgar, D. Benítez, J. Osorio, A. Gonzalez, E. Southey, M.C. Sinilnikova, O. Lynch, H. Oldenburg, R. Asperen, C.J. van Hoogerbrugge, N. |
2007-08-30
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