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cancer breast genetic mutation university breast cancer risk carrier brca 1 study center haplotype genetics service department breast cancer association stage research centre hospital analysis institute sample allele service population region genet stage 1 brca 2 mutations women individual medicine control variant ashkenazi table chromosome receptor health brca 2 netherland america brca 2 carriers oncology brca 1 carriers genotyped state frequency number cancer research foundation genome genotype epidemiology disease effect italy estrogen haplotype structure genotyping 1.00 family 557ser genome-wide selection nature score breast cancer cases brca 2 region model grant susceptibility genotype data author jewish founder stage 2 samples genome-wide association study mutation carriers rs 8170
4 Most Recent Publications
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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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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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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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