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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 population

A. Antoniou, X. Wang, Z. Fredericksen, L. McGuffog, R. Tarrell, O. Sinilnikova, S. Healey, J. Morrison, C. Kartsonaki, T. Lesnick, M. Ghoussaini, D. Barrowdale, S. Peock, M. Cook, C. Oliver, D. Frost, D. Eccles, D. Evans, R. Eeles, L. Izatt, C. Chu, F. Douglas, J. Paterson, D. Stoppa-Lyonnet, C. Houdayer, S. Mazoyer, S. Giraud, C. Lasset, A. Remenieras, O. Caron, A. Hardouin, P. Berthet, Hogervorst, Frans B L, M. Rookus, A. Jager, van den Ouweland, Ans, N. Hoogerbrugge, van der Luijt, Rob B, H. Meijers-Heijboer, Gómez García, Encarna B, P. Devilee, Vreeswijk, Maaike P G, J. Lubinski, A. Jakubowska, J. Gronwald, T. Huzarski, T. Byrski, B. Górski, C. Cybulski, A. Spurdle, H. Holland, D. Goldgar, E. John, J. Hopper, M. Southey, S. Buys, M. Daly, M. Terry, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, S. Preisler-Adams, N. Arnold, D. Niederacher, C. Sutter, S. Domchek, K. Nathanson, T. Rebbeck, J. Blum, M. Piedmonte, G. Rodriguez, K. Wakeley, J. Boggess, J. Basil, S. Blank, E. Friedman, B. Kaufman, Y. Laitman, R. Milgrom, I. Andrulis, G. Glendon, H. Ozcelik, T. Kirchhoff, J. Vijai, M. Gaudet, D. Altshuler, C. Guiducci, N. Loman, K. Harbst, J. Rantala, H. Ehrencrona, A. Gerdes, M. Thomassen, L. Sunde, P. Peterlongo, S. Manoukian, B. Bonanni, A. Viel, P. Radice, T. Caldes, de la Hoya, Miguel, C. Singer, A. Fink-Retter, M. Greene, P. Mai, J. Loud, L. Guidugli, N. Lindor, Hansen, Thomas V O, F. Nielsen, I. Blanco, C. Lazaro, J. Garber, S. Ramus, S. Gayther, C. Phelan, S. Narod, C. Szabo, J. Benitez, A. Osorio, H. Nevanlinna, T. Heikkinen, M. Caligo, M. Beattie, U. Hamann, A. Godwin, M. Montagna, C. Casella, S. Neuhausen, B. Karlan, N. Tung, A. Toland, J. Weitzel, O. Olopade, J. Simard, P. Soucy, W. Rubinstein, A. Arason, G. Rennert, N. Martin, G. Montgomery, J. Chang-Claude, D. Flesch-Janys, H. Brauch, G. Severi, L. Baglietto, A. Cox, S. Cross, P. Miron, S. Gerty, W. Tapper, D. Yannoukakos, G. Fountzilas, P. Fasching, M. Beckmann, dos Santos Silva, Isabel, J. Peto, D. Lambrechts, R. Paridaens, T. Rüdiger, A. Försti, R. Winqvist, K. Pylkäs, R. Diasio, A. Lee, J. Eckel-Passow, C. Vachon, F. Blows, K. Driver, A. Dunning, Pharoah, Paul P D, K. Offit, V. Pankratz, H. Hakonarson, G. Chenevix-Trench, D. Easton, and F. Couch. Nature genetics, 42 (10): 885–892 (2010)

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Amanda Smith

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Other publications of authors with the same name

BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer riskA. Spurdle, P. Whiley, B. Thompson, B. Feng, S. Healey, M. Brown, C. Pettigrew, van Asperen, Christi J, Ausems, Margreet G E M, A. Kattentidt-Mouravieva and 23 other author(s). Journal of medical genetics, 49 (8): 525–532 (2012)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 and 171 other author(s). Breast cancer research : BCR, 14 (1): R33 (2012)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 and 127 other author(s). Human molecular genetics, 18 (22): 4442–4456 (2009)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)mrSNP: Software to detect SNP effects on microRNA binding.M. Deveci, Ü. Çatalyürek, and A. Toland. BMC Bioinform., (2014)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)Benchmarking short sequence mapping tools.A. Hatem, D. Bozdag, A. Toland, and Ü. Çatalyürek. BMC Bioinform., (2013)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 and 201 other author(s). 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 and 99 other author(s). Human molecular genetics, 20 (23): 4732–4747 (2011)

BibSonomy

Disambiguation of "Toland, Amanda E."