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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

F. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis, M. Gaudet, E. Dicks, M. Kosel, S. Healey, O. Sinilnikova, A. Lee, F. Bacot, D. Vincent, Hogervorst, Frans B L, S. Peock, D. Stoppa-Lyonnet, A. Jakubowska, P. Radice, R. Schmutzler, S. Domchek, M. Piedmonte, C. Singer, E. Friedman, M. Thomassen, Hansen, Thomas V O, S. Neuhausen, C. Szabo, I. Blanco, M. Greene, B. Karlan, J. Garber, C. Phelan, J. Weitzel, M. Montagna, E. Olah, I. Andrulis, A. Godwin, D. Yannoukakos, D. Goldgar, T. Caldes, H. Nevanlinna, A. Osorio, M. Terry, M. Daly, van Rensburg, Elizabeth J, U. Hamann, S. Ramus, A. Toland, M. Caligo, O. Olopade, N. Tung, K. Claes, M. Beattie, M. Southey, E. Imyanitov, M. Tischkowitz, R. Janavicius, E. John, A. Kwong, O. Diez, J. Balmaña, R. Barkardottir, B. Arun, G. Rennert, S. Teo, P. Ganz, I. Campbell, van der Hout, Annemarie H, van Deurzen, Carolien H M, C. Seynaeve, Gómez Garcia, Encarna B, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, Gille, Johannes J P, Ausems, Margreet G E M, M. Blok, Ligtenberg, Marjolijn J L, M. Rookus, P. Devilee, S. Verhoef, van Os, Theo A M, J. Wijnen, D. Frost, S. Ellis, E. Fineberg, R. Platte, D. Evans, L. Izatt, R. Eeles, J. Adlard, D. Eccles, J. Cook, C. Brewer, F. Douglas, S. Hodgson, P. Morrison, L. Side, A. Donaldson, C. Houghton, M. Rogers, H. Dorkins, J. Eason, H. Gregory, E. McCann, A. Murray, A. Calender, A. Hardouin, P. Berthet, C. Delnatte, C. Nogues, C. Lasset, C. Houdayer, D. Leroux, E. Rouleau, F. Prieur, F. Damiola, H. Sobol, I. Coupier, L. Venat-Bouvet, L. Castera, M. Gauthier-Villars, M. Léoné, P. Pujol, S. Mazoyer, Y. Bignon, E. Złowocka-Perłowska, J. Gronwald, J. Lubinski, K. Durda, K. Jaworska, T. Huzarski, A. Spurdle, A. Viel, B. Peissel, B. Bonanni, G. Melloni, L. Ottini, L. Papi, L. Varesco, M. Tibiletti, P. Peterlongo, S. Volorio, S. Manoukian, V. Pensotti, N. Arnold, C. Engel, H. Deissler, D. Gadzicki, A. Gehrig, K. Kast, K. Rhiem, A. Meindl, D. Niederacher, N. Ditsch, H. Plendl, S. Preisler-Adams, S. Engert, C. Sutter, R. Varon-Mateeva, B. Wappenschmidt, Weber, Bernhard H F, B. Arver, M. Stenmark-Askmalm, N. Loman, R. Rosenquist, Z. Einbeigi, K. Nathanson, T. Rebbeck, S. Blank, D. Cohn, G. Rodriguez, L. Small, M. Friedlander, V. Bae-Jump, A. Fink-Retter, C. Rappaport, D. Gschwantler-Kaulich, G. Pfeiler, M. Tea, N. Lindor, B. Kaufman, S. Shimon Paluch, Y. Laitman, A. Skytte, A. Gerdes, I. Pedersen, S. Moeller, T. Kruse, U. Jensen, J. Vijai, K. Sarrel, M. Robson, N. Kauff, A. Mulligan, G. Glendon, H. Ozcelik, B. Ejlertsen, F. Nielsen, L. Jønson, M. Andersen, Y. Ding, L. Steele, L. Foretova, A. Teulé, C. Lazaro, J. Brunet, M. Pujana, P. Mai, J. Loud, C. Walsh, J. Lester, S. Orsulic, S. Narod, J. Herzog, S. Sand, S. Tognazzo, S. Agata, T. Vaszko, J. Weaver, A. Stavropoulou, S. Buys, A. Romero, de la Hoya, Miguel, K. Aittomäki, T. Muranen, M. Duran, W. Chung, A. Lasa, C. Dorfling, A. Miron, J. Benitez, L. Senter, D. Huo, S. Chan, A. Sokolenko, J. Chiquette, L. Tihomirova, T. Friebel, B. Agnarsson, K. Lu, F. Lejbkowicz, P. James, P. Hall, A. Dunning, D. Tessier, J. Cunningham, S. Slager, C. Wang, S. Hart, K. Stevens, J. Simard, T. Pastinen, V. Pankratz, K. Offit, D. Easton, G. Chenevix-Trench, and A. Antoniou. PLoS genetics, 9 (3): e1003212 (2013)

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Gisela Sobol

Roman Sobol

Nikolaj Sobolev

Horst Soboll

Sibylle Soboll

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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriersD. Cox, J. Simard, D. Sinnett, Y. Hamdi, P. Soucy, M. Ouimet, L. Barjhoux, C. Verny-Pierre, L. McGuffog, S. Healey and 99 other author(s). Human molecular genetics, 20 (23): 4732–4747 (2011)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriersA. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, A. Lee, D. Barrowdale, S. Healey, O. Sinilnikova and 171 other author(s). Breast cancer research : BCR, 14 (1): R33 (2012)Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk predictionA. Antoniou, J. Beesley, L. McGuffog, O. Sinilnikova, S. Healey, S. Neuhausen, Y. Ding, T. Rebbeck, J. Weitzel, H. Lynch and 168 other author(s). Cancer research, 70 (23): 9742–9754 (2010)Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersA. Antoniou, A. Spurdle, O. Sinilnikova, S. Healey, K. Pooley, R. Schmutzler, B. Versmold, C. Engel, A. Meindl, N. Arnold and 76 other author(s). American journal of human genetics, 82 (4): 937–948 (2008)Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskF. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis and 252 other author(s). PLoS genetics, 9 (3): e1003212 (2013)

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Disambiguation of "Sobol, Hagay"

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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Please choose a person to relate this publication to

Gisela Sobol

Roman Sobol

Nikolaj Sobolev

Horst Soboll

Sibylle Soboll

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Sobol, Hagay"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Please choose a person to relate this publication to

Gisela Sobol

Roman Sobol

Nikolaj Sobolev

Horst Soboll

Sibylle Soboll

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk