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AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study

F. Couch, O. Sinilnikova, R. Vierkant, V. Pankratz, Z. Fredericksen, D. Stoppa-Lyonnet, I. Coupier, D. Hughes, A. Hardouin, P. Berthet, S. Peock, M. Cook, C. Baynes, S. Hodgson, P. Morrison, M. Porteous, A. Jakubowska, J. Lubinski, J. Gronwald, A. Spurdle, R. Schmutzler, B. Versmold, C. Engel, A. Meindl, C. Sutter, J. Horst, D. Schaefer, K. Offit, T. Kirchhoff, I. Andrulis, E. Ilyushik, G. Glendon, P. Devilee, Vreeswijk, Maaike P G, Vasen, Hans F A, A. Borg, K. Backenhorn, J. Struewing, M. Greene, S. Neuhausen, T. Rebbeck, K. Nathanson, S. Domchek, T. Wagner, J. Garber, C. Szabo, M. Zikan, L. Foretova, J. Olson, T. Sellers, N. Lindor, H. Nevanlinna, J. Tommiska, K. Aittomaki, U. Hamann, M. Rashid, D. Torres, J. Simard, F. Durocher, F. Guenard, H. Lynch, C. Isaacs, J. Weitzel, O. Olopade, S. Narod, M. Daly, A. Godwin, G. Tomlinson, D. Easton, G. Chenevix-Trench, and A. Antoniou. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 16 (7): 1416–1421 (2007)

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Helena Peters

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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 and 427 other author(s). Nature genetics, 45 (4): 371-84, 384e1-2 (2013)RAD51 135G--C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studiesA. Antoniou, O. Sinilnikova, J. Simard, M. Léoné, M. Dumont, S. Neuhausen, J. Struewing, D. Stoppa-Lyonnet, L. Barjhoux, D. Hughes and 69 other author(s). American journal of human genetics, 81 (6): 1186–1200 (2007)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)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 and 92 other author(s). Nature, 447 (7148): 1087--1093 (June 2007)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)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)AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 studyF. Couch, O. Sinilnikova, R. Vierkant, V. Pankratz, Z. Fredericksen, D. Stoppa-Lyonnet, I. Coupier, D. Hughes, A. Hardouin, P. Berthet and 61 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 16 (7): 1416–1421 (2007)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)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)

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Disambiguation of "Devilee, Peter"

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AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study

Please choose a person to relate this publication to

Tanja Elisabeth Peters

Jillian Petersen

Andre Peters

Robert Martin Peterreins

Helena Peters

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Devilee, Peter"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study

Please choose a person to relate this publication to

Tanja Elisabeth Peters

Jillian Petersen

Andre Peters

Robert Martin Peterreins

Helena Peters

Other publications of authors with the same name

Disambiguation

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AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study