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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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Alfons Meindl

Antonie Meindl

Karl Meindl

Thomas Meindl

Ralf Meindl

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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)Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer ConsortiumC. Fischer, K. Kuchenbäcker, C. Engel, S. Zachariae, K. Rhiem, A. Meindl, N. Rahner, N. Dikow, H. Plendl, I. Debatin and 13 other author(s). Journal of medical genetics, 50 (6): 360–367 (2013)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)Contralateral breast cancer risk in BRCA1 and BRCA2 mutation carriersM. Graeser, C. Engel, K. Rhiem, D. Gadzicki, U. Bick, K. Kast, U. Froster, B. Schlehe, A. Bechtold, N. Arnold and 8 other author(s). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 27 (35): 5887–5892 (2009)Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patientsK. Hemminki, B. Müller-Myhsok, P. Lichtner, C. Engel, B. Chen, B. Burwinkel, A. Försti, C. Sutter, B. Wappenschmidt, H. Hellebrand and 13 other author(s). International journal of cancer. Journal international du cancer, 126 (12): 2858–2862 (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)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 populationA. Antoniou, X. Wang, Z. Fredericksen, L. McGuffog, R. Tarrell, O. Sinilnikova, S. Healey, J. Morrison, C. Kartsonaki, T. Lesnick and 168 other author(s). Nature genetics, 42 (10): 885–892 (2010)Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriersC. Engel, B. Versmold, B. Wappenschmidt, J. Simard, D. Easton, S. Peock, M. Cook, C. Oliver, D. Frost, R. Mayes and 58 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 19 (11): 2859–2868 (2010)Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriersX. Wang, V. Pankratz, Z. Fredericksen, R. Tarrell, M. Karaus, L. McGuffog, Pharaoh, Paul D P, Ponder, Bruce A J, A. Dunning, S. Peock and 34 other author(s). Human molecular genetics, 19 (14): 2886–2897 (2010)

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Disambiguation of "Meindl, Alfons"

Please choose a person to relate this publication to

Alfons Meindl

Antonie Meindl

Karl Meindl

Thomas Meindl

Ralf Meindl

Other publications of authors with the same name

Disambiguation

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Disambiguation of "Meindl, Alfons"

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

Alfons Meindl

Antonie Meindl

Karl Meindl

Thomas Meindl

Ralf Meindl

Other publications of authors with the same name

Disambiguation