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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

A. Antoniou, O. Sinilnikova, L. McGuffog, S. Healey, H. Nevanlinna, T. Heikkinen, J. Simard, A. Spurdle, J. Beesley, X. Chen, S. Neuhausen, Y. Ding, F. Couch, X. Wang, Z. Fredericksen, P. Peterlongo, B. Peissel, B. Bonanni, A. Viel, L. Bernard, P. Radice, C. Szabo, L. Foretova, M. Zikan, K. Claes, M. Greene, P. Mai, G. Rennert, F. Lejbkowicz, I. Andrulis, H. Ozcelik, G. Glendon, A. Gerdes, M. Thomassen, L. Sunde, M. Caligo, Y. Laitman, T. Kontorovich, S. Cohen, B. Kaufman, E. Dagan, R. Baruch, E. Friedman, K. Harbst, G. Barbany-Bustinza, J. Rantala, H. Ehrencrona, P. Karlsson, S. Domchek, K. Nathanson, A. Osorio, I. Blanco, A. Lasa, J. Benítez, U. Hamann, Hogervorst, Frans B L, M. Rookus, J. Collee, P. Devilee, M. Ligtenberg, van der Luijt, Rob B, C. Aalfs, Q. Waisfisz, J. Wijnen, van Roozendaal, Cornelis E P, S. Peock, M. Cook, D. Frost, C. Oliver, R. Platte, D. Evans, F. Lalloo, R. Eeles, L. Izatt, R. Davidson, C. Chu, D. Eccles, T. Cole, S. Hodgson, A. Godwin, D. Stoppa-Lyonnet, B. Buecher, M. Léoné, B. Bressac-de Paillerets, A. Remenieras, O. Caron, G. Lenoir, N. Sevenet, M. Longy, S. Ferrer, F. Prieur, D. Goldgar, A. Miron, E. John, S. Buys, M. Daly, J. Hopper, M. Terry, Y. Yassin, C. Singer, D. Gschwantler-Kaulich, C. Staudigl, Hansen, Thomas V O, R. Barkardottir, T. Kirchhoff, P. Pal, K. Kosarin, K. Offit, M. Piedmonte, G. Rodriguez, K. Wakeley, J. Boggess, J. Basil, P. Schwartz, S. Blank, A. Toland, M. Montagna, C. Casella, E. Imyanitov, A. Allavena, R. Schmutzler, B. Versmold, C. Engel, A. Meindl, N. Ditsch, N. Arnold, D. Niederacher, H. Deissler, B. Fiebig, C. Suttner, I. Schönbuchner, D. Gadzicki, T. Caldes, de la Hoya, Miguel, K. Pooley, D. Easton, and G. Chenevix-Trench. Human molecular genetics, 18 (22): 4442–4456 (2009)

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Alfons Meindl

Antonie Meindl

Karl Meindl

Thomas Meindl

Ralf Meindl

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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)Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer ConsortiumC. Fischer, K. Kuchenbäcker, C. Engel, S. Zachariae, K. Rhiem, A. Meindl, N. Rahner, N. Dikow, H. Plendl, I. Debatin and 13 other author(s). Journal of medical genetics, 50 (6): 360–367 (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)Contralateral breast cancer risk in BRCA1 and BRCA2 mutation carriersM. Graeser, C. Engel, K. Rhiem, D. Gadzicki, U. Bick, K. Kast, U. Froster, B. Schlehe, A. Bechtold, N. Arnold and 8 other author(s). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 27 (35): 5887–5892 (2009)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)Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility geneA. Meindl, H. Hellebrand, C. Wiek, V. Erven, B. Wappenschmidt, D. Niederacher, M. Freund, P. Lichtner, L. Hartmann, H. Schaal and 14 other author(s). Nature genetics, 42 (5): 410–414 (2010)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)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)Association of death receptor 4 variant (683A C) with ovarian cancer risk in BRCA1 mutation carriersM. Dick, B. Versmold, C. Engel, A. Meindl, N. Arnold, R. Varon-Mateeva, C. Sutter, D. Niederacher, H. Deissler, S. Preisler-Adams and 6 other author(s). International journal of cancer. Journal international du cancer, 130 (6): 1314–1318 (2012)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)

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Disambiguation of "Meindl, Alfons"

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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

Please choose a person to relate this publication to

Alfons Meindl

Antonie Meindl

Karl Meindl

Thomas Meindl

Ralf Meindl

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Meindl, Alfons"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

Please choose a person to relate this publication to

Alfons Meindl

Antonie Meindl

Karl Meindl

Thomas Meindl

Ralf Meindl

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
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APA
Chicago
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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers