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Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

F. Couch, M. Gaudet, A. Antoniou, S. Ramus, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, X. Wang, T. Kirchhoff, L. McGuffog, D. Barrowdale, A. Lee, S. Healey, O. Sinilnikova, I. Andrulis, H. Ozcelik, A. Mulligan, M. Thomassen, A. Gerdes, U. Jensen, A. Skytte, T. Kruse, M. Caligo, A. Wachenfeldt, G. Barbany-Bustinza, N. Loman, M. Soller, H. Ehrencrona, P. Karlsson, K. Nathanson, T. Rebbeck, S. Domchek, A. Jakubowska, J. Lubinski, K. Jaworska, K. Durda, E. Zlowocka, T. Huzarski, T. Byrski, J. Gronwald, C. Cybulski, B. Górski, A. Osorio, M. Durán, M. Tejada, J. Benitez, U. Hamann, Hogervorst, Frans B L, van Os, Theo A, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, J. Wijnen, M. Blok, M. Kets, M. Hooning, R. Oldenburg, Ausems, Margreet G E M, S. Peock, D. Frost, S. Ellis, R. Platte, E. Fineberg, D. Evans, C. Jacobs, R. Eeles, J. Adlard, R. Davidson, D. Eccles, T. Cole, J. Cook, J. Paterson, C. Brewer, F. Douglas, S. Hodgson, P. Morrison, L. Walker, M. Porteous, M. Kennedy, L. Side, B. Bove, A. Godwin, D. Stoppa-Lyonnet, M. Fassy-Colcombet, L. Castera, F. Cornelis, S. Mazoyer, M. Léoné, N. Boutry-Kryza, B. Bressac-de Paillerets, O. Caron, P. Pujol, I. Coupier, C. Delnatte, L. Akloul, H. Lynch, C. Snyder, S. Buys, M. Daly, M. Terry, W. Chung, E. John, A. Miron, M. Southey, J. Hopper, D. Goldgar, C. Singer, C. Rappaport, M. Tea, A. Fink-Retter, Hansen, Thomas V O, F. Nielsen, A. Arason, J. Vijai, S. Shah, K. Sarrel, M. Robson, M. Piedmonte, K. Phillips, J. Basil, W. Rubinstein, J. Boggess, K. Wakeley, A. Ewart-Toland, M. Montagna, S. Agata, E. Imyanitov, C. Isaacs, R. Janavicius, C. Lazaro, I. Blanco, L. Feliubadalo, J. Brunet, S. Gayther, Pharoah, Paul P D, K. Odunsi, B. Karlan, C. Walsh, E. Olah, S. Teo, P. Ganz, M. Beattie, van Rensburg, Elizabeth J, C. Dorfling, O. Diez, A. Kwong, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, N. Ditsch, N. Arnold, S. Heidemann, D. Niederacher, S. Preisler-Adams, D. Gadzicki, R. Varon-Mateeva, H. Deissler, A. Gehrig, C. Sutter, K. Kast, B. Fiebig, W. Heinritz, T. Caldes, de la Hoya, Miguel, T. Muranen, H. Nevanlinna, M. Tischkowitz, A. Spurdle, S. Neuhausen, Y. Ding, N. Lindor, Z. Fredericksen, V. Pankratz, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, M. Barile, L. Bernard, A. Viel, G. Giannini, L. Varesco, P. Radice, M. Greene, P. Mai, D. Easton, G. Chenevix-Trench, K. Offit, and J. Simard. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (4): 645–657 (2012)

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To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

Amitay Isaacs

Claudine Vahle

Claudine Loisel

Cueni Claudine

Claudine Robert

Other publications of authors with the same name

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 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 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)AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 studyF. Couch, O. Sinilnikova, R. Vierkant, V. Pankratz, Z. Fredericksen, D. Stoppa-Lyonnet, I. Coupier, D. Hughes, A. Hardouin, P. Berthet and 61 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 16 (7): 1416–1421 (2007)Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2A. Mulligan, F. Couch, D. Barrowdale, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, M. Robson, M. Sherman, A. Spurdle and 172 other author(s). Breast cancer research : BCR, 13 (6): R110 (2011)RAD51 135G--C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studiesA. Antoniou, O. Sinilnikova, J. Simard, M. Léoné, M. Dumont, S. Neuhausen, J. Struewing, D. Stoppa-Lyonnet, L. Barjhoux, D. Hughes and 69 other author(s). American journal of human genetics, 81 (6): 1186–1200 (2007)Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriersF. Couch, M. Gaudet, A. Antoniou, S. Ramus, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, X. Wang, T. Kirchhoff and 180 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (4): 645–657 (2012)Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)N. Mavaddat, D. Barrowdale, I. Andrulis, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, A. Spurdle, M. Robson, M. Sherman and 123 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (1): 134–147 (2012)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)

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Disambiguation of "Isaacs, Claudine"

Please choose a person to relate this publication to

Amitay Isaacs

Claudine Vahle

Claudine Loisel

Cueni Claudine

Claudine Robert

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Isaacs, Claudine"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Please choose a person to relate this publication to

Amitay Isaacs

Claudine Vahle

Claudine Loisel

Cueni Claudine

Claudine Robert

Other publications of authors with the same name

Disambiguation