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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 BRCA1/2

A. Mulligan, F. Couch, D. Barrowdale, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, M. Robson, M. Sherman, A. Spurdle, B. Wappenschmidt, A. Lee, L. McGuffog, S. Healey, O. Sinilnikova, R. Janavicius, T. Hansen, F. Nielsen, B. Ejlertsen, A. Osorio, I. Muñoz-Repeto, M. Durán, J. Godino, M. Pertesi, J. Benítez, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, E. Cattaneo, B. Bonanni, A. Viel, B. Pasini, L. Papi, L. Ottini, A. Savarese, L. Bernard, P. Radice, U. Hamann, M. Verheus, Meijers-Heijboer, Hanne E J, J. Wijnen, Gómez García, Encarna B, M. Nelen, C. Kets, C. Seynaeve, Tilanus-Linthorst, Madeleine M A, van der Luijt, Rob B, T. van Os, M. Rookus, D. Frost, J. Jones, D. Evans, F. Lalloo, R. Eeles, L. Izatt, J. Adlard, R. Davidson, J. Cook, A. Donaldson, H. Dorkins, H. Gregory, J. Eason, C. Houghton, J. Barwell, L. Side, E. McCann, A. Murray, S. Peock, A. Godwin, R. Schmutzler, K. Rhiem, C. Engel, A. Meindl, I. Ruehl, N. Arnold, D. Niederacher, C. Sutter, H. Deissler, D. Gadzicki, K. Kast, S. Preisler-Adams, R. Varon-Mateeva, I. Schoenbuchner, B. Fiebig, W. Heinritz, D. Schäfer, H. Gevensleben, V. Caux-Moncoutier, M. Fassy-Colcombet, F. Cornelis, S. Mazoyer, M. Léoné, N. Boutry-Kryza, A. Hardouin, P. Berthet, D. Muller, J. Fricker, I. Mortemousque, P. Pujol, I. Coupier, M. Lebrun, C. Kientz, M. Longy, N. Sevenet, D. Stoppa-Lyonnet, C. Isaacs, T. Caldes, de la Hoya, Miguel, T. Heikkinen, K. Aittomäki, I. Blanco, C. Lazaro, R. Barkardottir, P. Soucy, M. Dumont, J. Simard, M. Montagna, S. Tognazzo, E. D'Andrea, S. Fox, M. Yan, T. Rebbeck, O. Olopade, J. Weitzel, H. Lynch, P. Ganz, G. Tomlinson, X. Wang, Z. Fredericksen, V. Pankratz, N. Lindor, C. Szabo, K. Offit, R. Sakr, M. Gaudet, J. Bhatia, N. Kauff, C. Singer, M. Tea, D. Gschwantler-Kaulich, A. Fink-Retter, P. Mai, M. Greene, E. Imyanitov, F. O'Malley, H. Ozcelik, G. Glendon, A. Toland, A. Gerdes, M. Thomassen, T. Kruse, U. Jensen, A. Skytte, M. Caligo, M. Soller, K. Henriksson, v. Wachenfeldt, B. Arver, M. Stenmark-Askmalm, P. Karlsson, Y. Ding, S. Neuhausen, M. Beattie, Pharoah, Paul D P, K. Moysich, K. Nathanson, B. Karlan, J. Gross, E. John, M. Daly, S. Buys, M. Southey, J. Hopper, M. Terry, W. Chung, A. Miron, D. Goldgar, G. Chenevix-Trench, D. Easton, I. Andrulis, and A. Antoniou. Breast cancer research : BCR, 13 (6): R110 (2011)

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Philipp Josef Wendy

Wendy Danner

Wendy Wagner

Wendy Hildebrandt

Wendy Lossow

Other publications of authors with the same name

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)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 and 176 other author(s). Human mutation, 33 (4): 690–702 (2012)Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network.X. Zhang, Y. Veturi, S. Verma, W. Bone, A. Verma, A. Lucas, S. Hebbring, J. Denny, I. Stanaway, G. Jarvik and 14 other author(s). PSB, page 272-283. (2019)ORE identifies extreme expression effects enriched for rare variants.F. Richter, G. Hoffman, K. Manheimer, N. Patel, A. Sharp, D. McKean, S. Morton, S. DePalma, J. Gorham, A. Kitaygorodksy and 8 other author(s). Bioinform., 35 (20): 3906-3912 (2019)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 and 252 other author(s). PLoS genetics, 9 (3): e1003212 (2013)Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.P. Dexter, H. Ong, A. Elsey, G. Bell, N. Walton, W. Chung, L. Rasmussen, J. Hicks, A. Owusu obeng, S. Scott and 2 other author(s). AMIA, AMIA, (2019)User engagement with web-based genomics education videos and implications for designing scalable patient education materials.J. Wynn, W. Wei, X. Li, Y. So, S. Bakken, C. Weng, and W. Chung. AMIA, AMIA, (2019)Promoting equity in clinical research: The role of social determinants of health.B. Idnay, Y. Fang, E. Stanley, B. Ruotolo, W. Chung, K. Marder, and C. Weng. J. Biomed. Informatics, (2024)Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study.A. Casillan, M. Florido, J. Galarza-Cornejo, S. Bakken, J. Lynch, W. Chung, K. Mittendorf, E. Berner, J. Connolly, C. Weng and 7 other author(s). J. Am. Medical Informatics Assoc., 31 (2): 306-316 (January 2024)Predicting functional effect of missense variants using graph attention neural networks.H. Zhang, M. Xu, X. Fan, W. Chung, and Y. Shen. Nat. Mac. Intell., 4 (11): 1017-1028 (November 2022)

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Disambiguation of "Chung, Wendy"