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cancer haplotype brca 1 university genetic genetics service mutation center breast research study service region centre breast cancer risk hospital department population carrier women genet institute analysis ashkenazi chromosome frequency cancer research brca 2 breast cancer foundation haplotype structure association 557ser allele selection sample grant health medicine brca 2 carriers founder structure genome netherland variation effect cohort brca 2 mutations family bard 1 individual block variant program brca 2 region bottleneck core haplotype cancer institute biomarker trust drift share brca 2-tccgaaga allele simulation article network genomic cys 557ser epidemiol author recombination modi fiers onlinefirst delag italy linkage disequilibrium aj chromosomes ashkenazi jews r 01-ca population bottleneck
2 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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