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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

A. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, A. Lee, D. Barrowdale, S. Healey, O. Sinilnikova, M. Caligo, N. Loman, K. Harbst, A. Lindblom, B. Arver, R. Rosenquist, P. Karlsson, K. Nathanson, S. Domchek, T. Rebbeck, A. Jakubowska, J. Lubinski, K. Jaworska, K. Durda, E. Złowowcka-Perłowska, A. Osorio, M. Durán, R. Andrés, J. Benítez, U. Hamann, F. Hogervorst, van Os, Theo A, S. Verhoef, Meijers-Heijboer, Hanne E J, J. Wijnen, Gómez Garcia, Encarna B, M. Ligtenberg, M. Kriege, J. Collée, Ausems, Margreet G E M, J. Oosterwijk, S. Peock, D. Frost, S. Ellis, R. Platte, E. Fineberg, D. Evans, F. Lalloo, C. Jacobs, R. Eeles, J. Adlard, R. Davidson, T. Cole, J. Cook, J. Paterson, F. Douglas, C. Brewer, S. Hodgson, P. Morrison, L. Walker, M. Rogers, A. Donaldson, H. Dorkins, A. Godwin, B. Bove, D. Stoppa-Lyonnet, C. Houdayer, B. Buecher, A. Pauw, S. Mazoyer, A. Calender, M. Léoné, B. Bressac-de Paillerets, O. Caron, H. Sobol, M. Frenay, F. Prieur, S. Ferrer, I. Mortemousque, S. Buys, M. Daly, A. Miron, M. Terry, J. Hopper, E. John, M. Southey, D. Goldgar, C. Singer, A. Fink-Retter, M. Tea, D. Kaulich, T. Hansen, F. Nielsen, R. Barkardottir, M. Gaudet, T. Kirchhoff, V. Joseph, A. Dutra-Clarke, K. Offit, M. Piedmonte, J. Kirk, D. Cohn, J. Hurteau, J. Byron, J. Fiorica, A. Toland, M. Montagna, C. Oliani, E. Imyanitov, C. Isaacs, L. Tihomirova, I. Blanco, C. Lazaro, A. Teulé, J. Valle, S. Gayther, K. Odunsi, J. Gross, B. Karlan, E. Olah, S. Teo, P. Ganz, M. Beattie, C. Dorfling, van Rensburg, Elizabeth U, O. Diez, A. Kwong, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, N. Ditsch, N. Arnold, S. Heidemann, D. Niederacher, S. Preisler-Adams, D. Gadzicki, R. Varon-Mateeva, H. Deissler, A. Gehrig, C. Sutter, K. Kast, B. Fiebig, D. Schäfer, T. Caldes, de la Hoya, Miguel, H. Nevanlinna, T. Muranen, B. Lespérance, A. Spurdle, S. Neuhausen, Y. Ding, X. Wang, Z. Fredericksen, V. Pankratz, N. Lindor, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, B. Bonanni, L. Bernard, R. Dolcetti, L. Papi, L. Ottini, P. Radice, M. Greene, J. Loud, I. Andrulis, H. Ozcelik, A. Mulligan, G. Glendon, M. Thomassen, A. Gerdes, U. Jensen, A. Skytte, T. Kruse, G. Chenevix-Trench, F. Couch, J. Simard, and D. Easton. Breast cancer research : BCR, 14 (1): R33 (2012)

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Üstün Olgay

Olga Arzberger

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriersL. Walker, Z. Fredericksen, X. Wang, R. Tarrell, V. Pankratz, N. Lindor, J. Beesley, S. Healey, X. Chen, D. Stoppa-Lyonnet and 63 other author(s). Breast cancer research : BCR, 12 (6): R102 (2010)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)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)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)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)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)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)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 and 180 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 (4): 645–657 (2012)

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Disambiguation of "Sinilnikova, Olga M."

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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Please choose a person to relate this publication to

Üstün Olgay

Olga Munteanu

Olga Bruskina

Olga Osetska

Olga Arzberger

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Sinilnikova, Olga M."

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Please choose a person to relate this publication to

Üstün Olgay

Olga Munteanu

Olga Bruskina

Olga Osetska

Olga Arzberger

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
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history of this post
URL
DOI
BibTeX
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APA
Chicago
DIN 1505
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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers