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scopus: 35488383300

Oliver, C.

(Clare Oliver)


cancer breast mutation carrier brca 1 breast cancer risk university study genetic breast cancer department research center association genetics service institute centre hospital analysis service brca 2 carriers allele genet sample table oncology netherland haplotype model medicine brca 2 brca 2 mutations stage brca 1 carriers mutation carriers foundation population estimate figure grant rhamm result family health genotype control variant women susceptibility italy france aurka disease region protein individual cancer risk effect depletion polarization evidence stage 1 america expression ptrend netherlands cancer institute germany downloaded genome-wide association study antoniou ratio consortium mrg 15 genotyping modifier 1.00 state modi fiers cancer research hr estimates




10 Most Recent Publications

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer (Article)
Maxwell, C.A. Benitez, J. Mohan, P. Buys, S.S. John, E.M. Miron, A. Southey, M.C. Daly, M. Schmutzler, R.K. Wappenschmidt, B. Meindl, A. Arnold, N. Deissler, H. Català, I. Varon-Mateeva, R. Sutter, C. Niederacher, D. Imyamitov, E. Sinilnikova, O. Stoppa-Lyonne, D. Mazoyer, S. Verny-Pierre, C. Castera, L. Pauw, A. de Petit, A. Bignon, Y.-J. Uhrhammer, N. Peyrat, J.-P. Vennin, P. Ferrer, S.F. Collonge-Rame, M.-A. Mortemousque, I. Spurdle, A.B. Beesley, J. Healey, S. Aguilar, H. Barcellos-Hoff, M.H. Vidal, M. Gruber, S.B. Lazaro, C. Capellá, G. McGuffog, L. Nathanson, K.L. Antoniou, A.C. Chenevix-Trench, G. Fleisch, M.C. Villanueva, A. Moreno, V. Pujana, M.A. Aytes, A. Serra-Musach, J. Rennert, G. Lejbkowicz, F. Peterlongo, P. Gómez-Baldó, L. Manoukian, S. Peissel, B. Ripamonti, C.B. Bonanni, B. Viel, A. Allavena, A. Bernard, L. Radice, P. Friedman, E. Kaufman, B. Osorio, A. Laitman, Y. Dubrovsky, M. Milgrom, R. Jakubowska, A. Cybulski, C. Górski, B. Jaworska, K. Durda, K. Sukiennicki, G. Lubinski, J. Bonifaci, N. Shugart, Y.Y. Domchek, S.M. Letrero, R. Weber, B.L. Hogervorst, F.B.L. Rookus, M.A. Collée, J.M. Devilee, P. Ligtenberg, M. Luijt, R.B. van der Fernández-Ramires, R. Aalfs, C. Waisfisz, Q. Wijnen, J.T. Roozendaal, C.E.P. van Easton, D.F. Peock, S. Cook, J. Oliver, C. Frost, D. Harrington, P. Costes, S.V. Lalloo, F. Eeles, R. Izatt, L. Chu, C. Eccles, D. Douglas, F. Brewer, C. Nevanlinna, H. Heikinen, T. Couch, F.J. Guinó, E. Lindor, N.M. Wang, X. Godwin, A.K. Caligo, M.A. Lombardi, G. Loman, N. Karlsson, P. Ehrencrona, H. Wachenfeldt, A. von Barkardottir, R.B. Chen, H. Hamann, U. Rashid, M.U. Lasa, A. Caldes, T. Andres, R. Schmitt, M. Assmann, V. Stevens, K. Offit, K. Curado, J. Evans, G.J.R. Tilgner, H. Guigó, R. Aiza, G. Brunet, J. Castellsagué, J. Martrat, G. Urruticoechea, A. Blanco, I. Tihomirova, L. Goldgar, D.
2011-11-01
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
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
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
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
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
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers (Article)
Walker, L. Fredericksen, Z. Tirapo, C. Giraud, S. Mazoyer, S. Muller, D.W. Fricker, J.P. Delnatte, C.D. Schmutzler, R.K. Wappenschmidt, B. Engel, C. Schönbuchner, I. Wang, X. Deissler, H. Meindl, A. Hogervorst, F.B.L. Verheus, M. Hooning, M. Ouweland, A.M.W. van den Nelen, M.R. Ausems, M.G.E.M. Aalfs, C. Asperen, C.J. van Tarrell, R. Devilee, P. Gerrits, M.M. Waisfisz, Q. Szabo, C. Easton, D.F. Peock, S. Cook, M. Oliver, C. Frost, D. Harrington, P. Pankratz, V.S. Evans, D.G. Lalloo, F. Eeles, R. Izatt, L. Chu, C. Davidson, R. Eccles, D. Ong, K.R. Cook, J. Rebbeck, T.R. Lindor, N.M. Nathanson, K.L. Domchek, S.M. Singer, C.F. Gschwantler-Kaulich, D. Dressler, C. Pfeiler, G. Godwin, A.K. Heikinen, T. Nevanlinna, H. Agnarsson, B.A. Beesley, J. Caligo, M.A. Olsson, H. Kristoffersson, U. Liljegren, A. Arver, B. Karlsson, P. Melin, B. Sinilnikova, O. McGuffog, L. Antoniou, A.C. Healey, S. Chenevix-Trench, G. Spurdle, A.B. Couch, F.J. Chen, X. Stoppa-Lyonnet, D.
2010-11-29
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
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
Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers (Article)
Wang, X. Pankratz, V.S. Cook, M. Oliver, C. Frost, D. Sinilnikova, O. Stoppa-Lyonnet, D. Mazoyer, S. Houdayer, C. Hogervorst, F.B.L. Hooning, M. Ligtenberg, M. Fredericksen, Z. Spurdle, A.B. Chenevix-Trench, G. Schmutzler, R.K. Wappenschmidt, B. Engel, C. Meindl, A. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Singer, C.F. Tarrell, R. Gschwantler-Kaulich, D. Dressler, C. Fink, A. Szabo, C. Zikan, M. Foretova, L. Claes, K. Thomas, G. Hoover, R.N. Hunter, D.J. Karaus, M. Chanock, S.J. Easton, D.F. Antoniou, A.C. Couch, F.J. McGuffog, L. Pharaoh, P.D.P. Ponder, B.A.J. Dunning, A.M. Peock, S.
2010-04-01
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