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10 Most Recent Publications
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Optimal age to start preventive measures in women with BRCA1/2 mutations or high familial breast cancer risk
(Article)
Tilanus-Linthorst, M.M.A. Roozenbeek, B. Eeles, R. Oosterwijk, J.C. Leach, M.O. Steyerberg, E.W. Evans, D.G. Thompson, D. Kaas, R. Manders, P. Asperen, C.J. van Adank, M.A. Hooning, M. Kwan Lim, G.E. |
2013-07-01
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Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: An analysis from the CAPP2 randomised controlled trial
(Article)
Burn, J. Gerdes, A-M. Bisgaard, M.-L. Dunlop, M.G. Ho, J.W.C. Hodgson, S.V. Lindblom, A. Lubinski, J. Morrison, P.J. Murday, V. Ramesar, R. Side, L. Macrae, F.A. Scott, R.J. Thomas, H.J.W. Vasen, H.F. Barker, G. Crawford, G. Elliott, F. Movahedi, M. Pylvanainen, K. Wijnen, J.T. Fodde, R. Mecklin, J.-P. Lynch, H. Mathers, J.C. Bishop, D.T. Moeslein, G. Olschwang, S. Eccles, D. Evans, D.G. Maher, E.R. Bertario, L. |
2011-12-17
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Familial breast cancer: Is it time to move from a reactive to a proactive role?
(Article)
Harris, H. Nippert, I. Julian-Reynier, C. Schmidtke, J. Asperen, C.J. van Gadzicki, D. Tibben, A. Evans, D.G. |
2011-09-01
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Genetic testing for familial/hereditary breast cancer - Comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
(Article)
Gadzicki, D. Evans, D.G. Harris, H. Julian-Reynier, C. Nippert, I. Schmidtke, J. Tibben, A. Asperen, C.J. van Schlegelberger, B. |
2011-06-01
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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
(Article)
Im, K.M. Kirchhoff, T. Guiducci, C. Vénat-Bouvet, L. Stoppa-Lyonnet, D. Chenevix-Trench, G. Easton, D.F. Klein, R.J. Friedman, E. Dean, M. Clark, A.G. Altshuler, D. Antoniou, A.C. Crenshaw, A. Couch, F.J. Offit, K. Gold, B. McGuffog, L. kartsonaki, C. Morrison, J. Healey, S. Sinilnikova, O. Mai, P.L. Greene, M.H. Piedmonte, M. Wang, X. Rubinstein, W.S. Hogervorst, F.B.L. Rookus, M.A. Collée, J.M. Hoogerbrugge, N. Asperen, C.J. van Meijers-Heijboer, H. Roozendaal, C.E. van Caldes, T. Perez-Segura, P. Green, T. Jakubowska, A. Lubinski, J. Huzarski, T. Blecharz, P. Nevanlinna, H. Aittomäki, K. Lazaro, C. Blanco, I. Barkardottir, R.B. Montagna, M. Chow, C.Y. D'Andrea, E. Devilee, P. Olopade, O.I. Neuhausen, S.L. Peissel, B. Bonanni, B. Peterlongo, P. Singer, C.F. Rennert, G. Lejbkowicz, F. Vijai, J. Andrulis, I.L. Glendon, G. Ozcelik, H. Toland, A.E. Caligo, M.A. Beattie, M.S. Chan, S. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Korn, J.M. Phelan, C. Narod, S. John, E.M. Hopper, J. Buys, S.S. Daly, M. Southey, M.C. Terry, M-B. Tung, N. Hansen, T.V.O. Gaudet, M.M. Osorio, A. Benitez, J. Durán, M. Weitzel, J.N. Garber, J. Hamann, U. Peock, S. Cook, J. Oliver, C. Frost, D. Fredericksen, Z. Platte, R. Evans, D.G. Eeles, R. Izatt, L. Paterson, J. Brewer, C. Hodgson, S.V. Porteous, M.E. Walker, L. Rogers, M.T. Shane Pankratz, V. Side, L. Godwin, A.K. Schmutzler, R.K. Wappenschmidt, B. Laitman, Y. Meindl, A. Deissler, H. Varon-Mateeva, R. Preisler-Adams, S. Kast, K. |
2011-05-20
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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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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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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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The MDM2 Promoter SNP285C/309G Haplotype Diminishes Sp1 Transcription Factor Binding and Reduces Risk for Breast and Ovarian Cancer in Caucasians
(Article)
Knappskog, S. Bjørnslett, M. Alhopuro, P. Arola, J. Tollenaar, R.A.E.M. Asperen, C.J. van Seynaeve, C.M. Staalesen, V. Chrisanthar, R. Løkkevik, E. Salvesen, H.B. Evans, D.G. Myklebust, L.M. Newman, W.G. Lin, D. Aaltonen, L.A. Børresen-Dale, A.L. Tell, G.S. Stoltenberg, C. Romundstad, P. Hveem, K. Lillehaug, J.R. Vatten, L. Huijts, P. Devilee, P. Dørum, A. Lønning, P.E. Vreeswijk, M.P. Edvardsen, H. Guo, Y. Zhang, X-A. Yang, H.M. Ylisaukko-oja, S.K. |
2011-02-15
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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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