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Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

A. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, E. Cattaneo, M. Barile, V. Pensotti, B. Pasini, R. Dolcetti, G. Giannini, A. Putignano, L. Varesco, P. Radice, P. Mai, M. Greene, I. Andrulis, G. Glendon, H. Ozcelik, M. Thomassen, A. Gerdes, T. Kruse, U. Birk Jensen, D. Crüger, M. Caligo, Y. Laitman, R. Milgrom, B. Kaufman, S. Paluch-Shimon, E. Friedman, N. Loman, K. Harbst, A. Lindblom, B. Arver, H. Ehrencrona, B. Melin, K. Nathanson, S. Domchek, T. Rebbeck, A. Jakubowska, J. Lubinski, J. Gronwald, T. Huzarski, T. Byrski, C. Cybulski, B. Gorski, A. Osorio, Ramón y Cajal, Teresa, F. Fostira, R. Andrés, J. Benitez, U. Hamann, F. Hogervorst, M. Rookus, M. Hooning, M. Nelen, van der Luijt, Rob B, van Os, Theo A M, van Asperen, Christi J, P. Devilee, Meijers-Heijboer, Hanne E J, Gómez Garcia, Encarna B, S. Peock, M. Cook, D. Frost, R. Platte, J. Leyland, D. Evans, F. Lalloo, R. Eeles, L. Izatt, J. Adlard, R. Davidson, D. Eccles, K. Ong, J. Cook, F. Douglas, J. Paterson, M. Kennedy, Z. Miedzybrodzka, A. Godwin, D. Stoppa-Lyonnet, B. Buecher, M. Belotti, C. Tirapo, S. Mazoyer, L. Barjhoux, C. Lasset, D. Leroux, L. Faivre, M. Bronner, F. Prieur, C. Nogues, E. Rouleau, P. Pujol, I. Coupier, M. Frénay, J. Hopper, M. Daly, M. Terry, E. John, S. Buys, Y. Yassin, A. Miron, D. Goldgar, C. Singer, M. Tea, G. Pfeiler, A. Dressler, Hansen, Thomas V O, L. Jønson, B. Ejlertsen, R. Barkardottir, T. Kirchhoff, K. Offit, M. Piedmonte, G. Rodriguez, L. Small, J. Boggess, S. Blank, J. Basil, M. Azodi, A. Toland, M. Montagna, S. Tognazzo, S. Agata, E. Imyanitov, R. Janavicius, C. Lazaro, I. Blanco, Pharoah, Paul D P, L. Sucheston, B. Karlan, C. Walsh, E. Olah, A. Bozsik, S. Teo, J. Seldon, M. Beattie, van Rensburg, Elizabeth J, M. Sluiter, O. Diez, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, I. Ruehl, R. Varon-Mateeva, K. Kast, H. Deissler, D. Niederacher, N. Arnold, D. Gadzicki, I. Schönbuchner, T. Caldes, de la Hoya, Miguel, H. Nevanlinna, K. Aittomäki, M. Dumont, J. Chiquette, M. Tischkowitz, X. Chen, J. Beesley, A. Spurdle, S. Neuhausen, Y. Chun Ding, Z. Fredericksen, X. Wang, V. Pankratz, F. Couch, J. Simard, D. Easton, и G. Chenevix-Trench. Human molecular genetics, 20 (16): 3304–3321 (2011)

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Lazaro Pinol

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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)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 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)SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population.J. Moreno-Cabrera, L. Feliubadaló, M. Pineda, P. Prada-Dacasa, M. Ramos-Muntada, J. del Valle, J. Brunet, B. Gel, M. Currás-Freixes, B. Calsina и 35 other автор(ы). Database J. Biol. Databases Curation, (января 2024)CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools.J. Moreno-Cabrera, J. del Valle, E. Castellanos, L. Feliubadaló, M. Pineda, E. Serra, G. Capellá, C. Lázaro, и B. Gel. Bioinform., 37 (22): 4227-4229 (ноября 2021)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)

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