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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

F. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis, M. Gaudet, E. Dicks, M. Kosel, S. Healey, O. Sinilnikova, A. Lee, F. Bacot, D. Vincent, Hogervorst, Frans B L, S. Peock, D. Stoppa-Lyonnet, A. Jakubowska, P. Radice, R. Schmutzler, S. Domchek, M. Piedmonte, C. Singer, E. Friedman, M. Thomassen, Hansen, Thomas V O, S. Neuhausen, C. Szabo, I. Blanco, M. Greene, B. Karlan, J. Garber, C. Phelan, J. Weitzel, M. Montagna, E. Olah, I. Andrulis, A. Godwin, D. Yannoukakos, D. Goldgar, T. Caldes, H. Nevanlinna, A. Osorio, M. Terry, M. Daly, van Rensburg, Elizabeth J, U. Hamann, S. Ramus, A. Toland, M. Caligo, O. Olopade, N. Tung, K. Claes, M. Beattie, M. Southey, E. Imyanitov, M. Tischkowitz, R. Janavicius, E. John, A. Kwong, O. Diez, J. Balmaña, R. Barkardottir, B. Arun, G. Rennert, S. Teo, P. Ganz, I. Campbell, van der Hout, Annemarie H, van Deurzen, Carolien H M, C. Seynaeve, Gómez Garcia, Encarna B, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, Gille, Johannes J P, Ausems, Margreet G E M, M. Blok, Ligtenberg, Marjolijn J L, M. Rookus, P. Devilee, S. Verhoef, van Os, Theo A M, J. Wijnen, D. Frost, S. Ellis, E. Fineberg, R. Platte, D. Evans, L. Izatt, R. Eeles, J. Adlard, D. Eccles, J. Cook, C. Brewer, F. Douglas, S. Hodgson, P. Morrison, L. Side, A. Donaldson, C. Houghton, M. Rogers, H. Dorkins, J. Eason, H. Gregory, E. McCann, A. Murray, A. Calender, A. Hardouin, P. Berthet, C. Delnatte, C. Nogues, C. Lasset, C. Houdayer, D. Leroux, E. Rouleau, F. Prieur, F. Damiola, H. Sobol, I. Coupier, L. Venat-Bouvet, L. Castera, M. Gauthier-Villars, M. Léoné, P. Pujol, S. Mazoyer, Y. Bignon, E. Złowocka-Perłowska, J. Gronwald, J. Lubinski, K. Durda, K. Jaworska, T. Huzarski, A. Spurdle, A. Viel, B. Peissel, B. Bonanni, G. Melloni, L. Ottini, L. Papi, L. Varesco, M. Tibiletti, P. Peterlongo, S. Volorio, S. Manoukian, V. Pensotti, N. Arnold, C. Engel, H. Deissler, D. Gadzicki, A. Gehrig, K. Kast, K. Rhiem, A. Meindl, D. Niederacher, N. Ditsch, H. Plendl, S. Preisler-Adams, S. Engert, C. Sutter, R. Varon-Mateeva, B. Wappenschmidt, Weber, Bernhard H F, B. Arver, M. Stenmark-Askmalm, N. Loman, R. Rosenquist, Z. Einbeigi, K. Nathanson, T. Rebbeck, S. Blank, D. Cohn, G. Rodriguez, L. Small, M. Friedlander, V. Bae-Jump, A. Fink-Retter, C. Rappaport, D. Gschwantler-Kaulich, G. Pfeiler, M. Tea, N. Lindor, B. Kaufman, S. Shimon Paluch, Y. Laitman, A. Skytte, A. Gerdes, I. Pedersen, S. Moeller, T. Kruse, U. Jensen, J. Vijai, K. Sarrel, M. Robson, N. Kauff, A. Mulligan, G. Glendon, H. Ozcelik, B. Ejlertsen, F. Nielsen, L. Jønson, M. Andersen, Y. Ding, L. Steele, L. Foretova, A. Teulé, C. Lazaro, J. Brunet, M. Pujana, P. Mai, J. Loud, C. Walsh, J. Lester, S. Orsulic, S. Narod, J. Herzog, S. Sand, S. Tognazzo, S. Agata, T. Vaszko, J. Weaver, A. Stavropoulou, S. Buys, A. Romero, de la Hoya, Miguel, K. Aittomäki, T. Muranen, M. Duran, W. Chung, A. Lasa, C. Dorfling, A. Miron, J. Benitez, L. Senter, D. Huo, S. Chan, A. Sokolenko, J. Chiquette, L. Tihomirova, T. Friebel, B. Agnarsson, K. Lu, F. Lejbkowicz, P. James, P. Hall, A. Dunning, D. Tessier, J. Cunningham, S. Slager, C. Wang, S. Hart, K. Stevens, J. Simard, T. Pastinen, V. Pankratz, K. Offit, D. Easton, G. Chenevix-Trench, and A. Antoniou. PLoS genetics, 9 (3): e1003212 (2013)

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Tuomas Aittomäki

Kristiina Kirtsi

Kristiina Holm

Kristiina Karvonen

Kristiina Niinivaara-Kreuzer

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Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriersC. Engel, B. Versmold, B. Wappenschmidt, J. Simard, D. Easton, S. Peock, M. Cook, C. Oliver, D. Frost, R. Mayes and 58 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 19 (11): 2859–2868 (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 and 201 other author(s). American journal of human genetics, 92 (4): 489–503 (2013)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 and 169 other author(s). Human molecular genetics, 20 (16): 3304–3321 (2011)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)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)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 and 144 other author(s). 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 and 168 other author(s). Cancer research, 70 (23): 9742–9754 (2010)No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort studyT. Rebbeck, A. Antoniou, T. Llopis, H. Nevanlinna, K. Aittomäki, J. Simard, A. Spurdle, F. Couch, Pereira, Lutecia H Mateus, M. Greene and 34 other author(s). Breast cancer research and treatment, 115 (1): 185–192 (2009)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 and 123 other author(s). 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)

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Disambiguation of "Aittomäki, Kristiina"

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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Please choose a person to relate this publication to

Tuomas Aittomäki

Kristiina Kirtsi

Kristiina Holm

Kristiina Karvonen

Kristiina Niinivaara-Kreuzer

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Aittomäki, Kristiina"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Please choose a person to relate this publication to

Tuomas Aittomäki

Kristiina Kirtsi

Kristiina Holm

Kristiina Karvonen

Kristiina Niinivaara-Kreuzer

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk