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Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

S. Ramus, A. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, O. Sinilnikova, S. Healey, D. Barrowdale, A. Lee, M. Thomassen, A. Gerdes, T. Kruse, U. Jensen, A. Skytte, M. Caligo, A. Liljegren, A. Lindblom, H. Olsson, U. Kristoffersson, M. Stenmark-Askmalm, B. Melin, S. Domchek, K. Nathanson, T. Rebbeck, A. Jakubowska, J. Lubinski, K. Jaworska, K. Durda, E. Złowocka, J. Gronwald, T. Huzarski, T. Byrski, C. Cybulski, A. Toloczko-Grabarek, A. Osorio, J. Benitez, M. Duran, M. Tejada, U. Hamann, M. Rookus, van Leeuwen, Flora E, C. Aalfs, Meijers-Heijboer, Hanne E J, van Asperen, Christi J, van Roozendaal, K E P, N. Hoogerbrugge, J. Collée, M. Kriege, van der Luijt, Rob B, S. Peock, D. Frost, S. Ellis, R. Platte, E. Fineberg, D. Evans, F. Lalloo, C. Jacobs, R. Eeles, J. Adlard, R. Davidson, D. Eccles, T. Cole, J. Cook, J. Paterson, F. Douglas, C. Brewer, S. Hodgson, P. Morrison, L. Walker, M. Porteous, M. Kennedy, H. Pathak, A. Godwin, D. Stoppa-Lyonnet, V. Caux-Moncoutier, A. Pauw, M. Gauthier-Villars, S. Mazoyer, M. Léoné, A. Calender, C. Lasset, V. Bonadona, A. Hardouin, P. Berthet, Y. Bignon, N. Uhrhammer, L. Faivre, C. Loustalot, S. Buys, M. Daly, A. Miron, M. Terry, W. Chung, E. John, M. Southey, D. Goldgar, C. Singer, M. Tea, G. Pfeiler, A. Fink-Retter, Hansen, Thomas V O, B. Ejlertsen, O. Johannsson, K. Offit, T. Kirchhoff, M. Gaudet, J. Vijai, M. Robson, M. Piedmonte, K. Phillips, L. van Le, J. Hoffman, A. Ewart Toland, M. Montagna, S. Tognazzo, E. Imyanitov, C. Issacs, R. Janavicius, C. Lazaro, I. Blanco, E. Tornero, M. Navarro, K. Moysich, B. Karlan, J. Gross, E. Olah, T. Vaszko, S. Teo, P. Ganz, M. Beattie, C. Dorfling, van Rensburg, Elizabeth J, 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, D. Schäfer, T. Caldes, de la Hoya, Miguel, H. Nevanlinna, K. Aittomäki, M. Plante, A. Spurdle, S. Neuhausen, Y. Ding, X. Wang, N. Lindor, Z. Fredericksen, V. Pankratz, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, B. Bonanni, L. Bernard, R. Dolcetti, L. Papi, L. Ottini, P. Radice, M. Greene, P. Mai, I. Andrulis, G. Glendon, H. Ozcelik, Pharoah, Paul D P, S. Gayther, J. Simard, D. Easton, F. Couch, и G. Chenevix-Trench. Human mutation, 33 (4): 690–702 (2012)

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Ute Hamann

Ute Hamann

Helga Uterharck

Joseph Utewsky

Axel Utermann

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Genome-wide association study identifies novel breast cancer susceptibility lociD. Easton, K. Pooley, A. Dunning, P. Pharoah, D. Thompson, D. Ballinger, J. Struewing, J. Morrison, H. Field, R. Luben и 92 other автор(ы). Nature, 447 (7148): 1087--1093 (июня 2007)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)19p13.1 is a triple-negative-specific breast cancer susceptibility locusK. Stevens, Z. Fredericksen, C. Vachon, X. Wang, S. Margolin, A. Lindblom, H. Nevanlinna, D. Greco, K. Aittomäki, C. Blomqvist и 144 other автор(ы). Cancer research, 72 (7): 1795–1803 (2012)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 и 168 other автор(ы). Cancer research, 70 (23): 9742–9754 (2010)Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancersJ. French, M. Ghoussaini, S. Edwards, K. Meyer, K. Michailidou, S. Ahmed, S. Khan, M. Maranian, M. O'Reilly, K. Hillman и 201 other автор(ы). American journal of human genetics, 92 (4): 489–503 (2013)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)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 и 123 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 (1): 134–147 (2012)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)Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancerS. Bojesen, K. Pooley, S. Johnatty, J. Beesley, K. Michailidou, J. Tyrer, S. Edwards, H. Pickett, H. Shen, C. Smart и 427 other автор(ы). Nature genetics, 45 (4): 371-84, 384e1-2 (2013)

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