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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, и O. Sinilnikova. Human molecular genetics, 20 (23): 4732–4747 (2011)

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Maria A Martin

Maria A Slowinska

Maria A Diefenbach

Boris Mariacher

Petra Marialke-Kandaouroff

Другие публикации лиц с тем же именем

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 и 252 other автор(ы). PLoS genetics, 9 (3): e1003212 (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 и 172 other автор(ы). Breast cancer research : BCR, 13 (6): R110 (2011)Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriersS. Ramus, A. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, O. Sinilnikova, S. Healey, D. Barrowdale и 176 other автор(ы). Human mutation, 33 (4): 690–702 (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 и 76 other автор(ы). American journal of human genetics, 82 (4): 937–948 (2008)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 и 180 other автор(ы). 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)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 и 99 other автор(ы). Human molecular genetics, 20 (23): 4732–4747 (2011)Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel и 169 other автор(ы). Human molecular genetics, 20 (16): 3304–3321 (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 и 171 other автор(ы). 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 и 168 other автор(ы). Nature genetics, 42 (10): 885–892 (2010)Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, O. Sinilnikova, L. McGuffog, S. Healey, H. Nevanlinna, T. Heikkinen, J. Simard, A. Spurdle, J. Beesley, X. Chen и 127 other автор(ы). Human molecular genetics, 18 (22): 4442–4456 (2009)

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