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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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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)ngALL database: a flexible framework for the management and integration of childhood leukemia next generation sequencing data.P. St-Onge, R. Hamon, V. Saillour, J. Healy, P. Beaulieu, and D. Sinnett. BCB, page 542-544. ACM, (2012)Joint genotype inference with germline and somatic mutations.E. Bareke, V. Saillour, J. Spinella, R. Vidal, J. Healy, D. Sinnett, and M. Csürös. BMC Bioinform., 14 (S-5): S3 (2013)A novel mathematical basis for predicting somatic single nucleotide variants from next-generation sequencing.E. Bareke, J. Spinella, R. Vidal, J. Healy, D. Sinnett, and M. Csürös. BCB, page 533-535. ACM, (2012)Bayesian joint modeling for causal mediation analysis with a binary outcome and a binary mediator: Exploring the role of obesity in the association between cranial radiation therapy for childhood acute lymphoblastic leukemia treatment and the long-term risk of insulin resistance.M. Caubet, M. Samoilenko, S. Drouin, D. Sinnett, M. Krajinovic, C. Laverdière, V. Marcil, and G. Lefebvre. Comput. Stat. Data Anal., (2023)Mining Heterogeneous Associations from Pediatric Cancer Data by Relational Concept Analysis.M. Wajnberg, P. Valtchev, A. Massé, A. Benmoussa, M. Krajinovic, C. Laverdière, E. Levy, D. Sinnett, and V. Marcil. ICDM (Workshops), page 597-604. IEEE, (2020)

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

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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

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Daniel

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Disambiguation

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