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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

D. Cox, J. Simard, D. Sinnett, Y. Hamdi, P. Soucy, M. Ouimet, L. Barjhoux, C. Verny-Pierre, L. McGuffog, S. Healey, C. Szabo, M. Greene, P. Mai, I. Andrulis, M. Thomassen, A. Gerdes, M. Caligo, E. Friedman, Y. Laitman, B. Kaufman, S. Paluch, Å. Borg, P. Karlsson, M. Askmalm, G. Bustinza, K. Nathanson, S. Domchek, T. Rebbeck, J. Benítez, U. Hamann, M. Rookus, van den Ouweland, Ans M W, Ausems, Margreet G E M, C. Aalfs, van Asperen, Christi J, P. Devilee, Gille, Hans J J P, S. Peock, D. Frost, D. Evans, R. Eeles, L. Izatt, J. Adlard, J. Paterson, J. Eason, A. Godwin, M. Remon, V. Moncoutier, M. Gauthier-Villars, C. Lasset, S. Giraud, A. Hardouin, P. Berthet, H. Sobol, F. Eisinger, Bressac de Paillerets, Brigitte, O. Caron, C. Delnatte, D. Goldgar, A. Miron, H. Ozcelik, S. Buys, M. Southey, M. Terry, C. Singer, A. Dressler, M. Tea, Hansen, Thomas V O, O. Johannsson, M. Piedmonte, G. Rodriguez, J. Basil, S. Blank, A. Toland, M. Montagna, C. Isaacs, I. Blanco, S. Gayther, K. Moysich, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, N. Ditsch, N. Arnold, D. Niederacher, C. Sutter, D. Gadzicki, B. Fiebig, T. Caldes, R. Laframboise, H. Nevanlinna, X. Chen, J. Beesley, A. Spurdle, S. Neuhausen, Y. Ding, F. Couch, X. Wang, P. Peterlongo, S. Manoukian, L. Bernard, P. Radice, D. Easton, G. Chenevix-Trench, A. Antoniou, D. Stoppa-Lyonnet, S. Mazoyer, and O. Sinilnikova. Human molecular genetics, 20 (23): 4732–4747 (2011)

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Csilla Anna Szabó

Csilla Kiss

Csilla Wolter

Csilla Jeszenszky

Csilla Hoffmüller

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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)Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes.S. Hart, K. Maxwell, T. Thomas, V. Ravichandran, B. Wubberhorst, R. Klein, K. Schrader, C. Szabo, J. Weitzel, S. Neuhausen and 4 other author(s). Briefings Bioinform., 17 (4): 672-677 (2016)Language choice in note-taking for consecutive interpretingC. Szabo. Interpreting, (2006)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)No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort studyT. Rebbeck, A. Antoniou, T. Llopis, H. Nevanlinna, K. Aittomäki, J. Simard, A. Spurdle, F. Couch, Pereira, Lutecia H Mateus, M. Greene and 34 other author(s). Breast cancer research and treatment, 115 (1): 185–192 (2009)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)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)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 "Szabo, Csilla"

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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

Please choose a person to relate this publication to

Csilla Anna Szabó

Csilla Kiss

Csilla Wolter

Csilla Jeszenszky

Csilla Hoffmüller

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Szabo, Csilla"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

Please choose a person to relate this publication to

Csilla Anna Szabó

Csilla Kiss

Csilla Wolter

Csilla Jeszenszky

Csilla Hoffmüller

Other publications of authors with the same name

Disambiguation

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history of this post
URL
DOI
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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers