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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

A. Antoniou, J. Beesley, L. McGuffog, O. Sinilnikova, S. Healey, S. Neuhausen, Y. Ding, T. Rebbeck, J. Weitzel, H. Lynch, C. Isaacs, P. Ganz, G. Tomlinson, O. Olopade, F. Couch, X. Wang, N. Lindor, V. Pankratz, P. Radice, S. Manoukian, B. Peissel, D. Zaffaroni, M. Barile, A. Viel, A. Allavena, V. Dall'Olio, P. Peterlongo, C. Szabo, M. Zikan, K. Claes, B. Poppe, L. Foretova, P. Mai, M. Greene, G. Rennert, F. Lejbkowicz, G. Glendon, H. Ozcelik, I. Andrulis, M. Thomassen, A. Gerdes, L. Sunde, D. Cruger, U. Birk Jensen, M. Caligo, E. Friedman, B. Kaufman, Y. Laitman, R. Milgrom, M. Dubrovsky, S. Cohen, A. Borg, H. Jernström, A. Lindblom, J. Rantala, M. Stenmark-Askmalm, B. Melin, K. Nathanson, S. Domchek, A. Jakubowska, J. Lubinski, T. Huzarski, A. Osorio, A. Lasa, M. Durán, M. Tejada, J. Godino, J. Benitez, U. Hamann, M. Kriege, N. Hoogerbrugge, van der Luijt, Rob B, van Asperen, Christi J, P. Devilee, E. Meijers-Heijboer, M. Blok, C. Aalfs, F. Hogervorst, M. Rookus, M. Cook, C. Oliver, D. Frost, D. Conroy, D. Evans, F. Lalloo, G. Pichert, R. Davidson, T. Cole, J. Cook, J. Paterson, S. Hodgson, P. Morrison, M. Porteous, L. Walker, M. Kennedy, H. Dorkins, S. Peock, A. Godwin, D. Stoppa-Lyonnet, A. Pauw, S. Mazoyer, V. Bonadona, C. Lasset, H. Dreyfus, D. Leroux, A. Hardouin, P. Berthet, L. Faivre, C. Loustalot, T. Noguchi, H. Sobol, E. Rouleau, C. Nogues, M. Frénay, L. Vénat-Bouvet, J. Hopper, M. Daly, M. Terry, E. John, S. Buys, Y. Yassin, A. Miron, D. Goldgar, C. Singer, A. Dressler, D. Gschwantler-Kaulich, G. Pfeiler, Hansen, Thomas V O, L. Jønson, B. Agnarsson, T. Kirchhoff, K. Offit, V. Devlin, A. Dutra-Clarke, M. Piedmonte, G. Rodriguez, K. Wakeley, J. Boggess, J. Basil, P. Schwartz, S. Blank, A. Toland, M. Montagna, C. Casella, E. Imyanitov, L. Tihomirova, I. Blanco, C. Lazaro, S. Ramus, L. Sucheston, B. Karlan, J. Gross, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, M. Lochmann, N. Arnold, S. Heidemann, R. Varon-Mateeva, D. Niederacher, C. Sutter, H. Deissler, D. Gadzicki, S. Preisler-Adams, K. Kast, I. Schönbuchner, T. Caldes, de la Hoya, Miguel, K. Aittomäki, H. Nevanlinna, J. Simard, A. Spurdle, H. Holland, X. Chen, R. Platte, G. Chenevix-Trench, and D. Easton. Cancer research, 70 (23): 9742–9754 (2010)

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Christoph Engel

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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)Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancerS. Krüger, C. Engel, A. Bier, E. Mangold, C. Pagenstecher, Doeberitz, Magnus von Knebel, E. Holinski-Feder, G. Moeslein, G. Keller, E. Kunstmann and 4 other author(s). Cancer letters, 236 (2): 191–197 (2006)Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancerE. Mangold, C. Pagenstecher, W. Friedl, M. Mathiak, R. Buettner, C. Engel, M. Loeffler, E. Holinski-Feder, Y. Müller-Koch, G. Keller and 10 other author(s). International journal of cancer. Journal international du cancer, 116 (5): 692–702 (2005)Association of the BRCA1 missense variant R1699W with a malignant phyllodes tumor of the breastK. Rhiem, U. Flucke, C. Engel, B. Wappenschmidt, A. Reinecke-Lüthge, R. Büttner, and R. Schmutzler. Cancer genetics and cytogenetics, 176 (1): 76–79 (2007)BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative familiesC. Fischer, C. Engel, C. Sutter, S. Zachariae, R. Schmutzler, A. Meindl, S. Heidemann, T. Grimm, T. Goecke, I. Debatin and 7 other author(s). Clinical genetics, 82 (5): 478–483 (2012)Endogenous thrombopoietin serum levels during multicycle chemotherapyC. Engel, M. Loeffler, H. Franke, and S. Schmitz. British journal of haematology, 105 (3): 832–838 (1999)Hemotoxicity by prolonged etoposide administration to mice can be prevented by simultaneous growth factor therapyG. Haan, C. Engel, B. Dontje, M. Loeffler, and W. Nijhof. Cancer research, 55 (2): 324–329 (1995)The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC)S. Krüger, A. Bier, C. Engel, E. Mangold, C. Pagenstecher, von Knebel Doeberitz, M, E. Holinski-Feder, G. Moeslein, K. Schulmann, J. Plaschke and 2 other author(s). Journal of medical genetics, 42 (10): 769–773 (2005)The internet and the nation state{. Engel. Lectiones Jenenses Max-Planck-Inst. zur Erforschung von Wirtschaftssystemen, Jena, 1. Aufl edition, (1999)

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Disambiguation of "Engel, Christoph"

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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

Please choose a person to relate this publication to

Christoph Engel

Christoph Engel

Christoph Engel

Christoph Engel

Christoph Engel

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Engel, Christoph"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

Please choose a person to relate this publication to

Christoph Engel

Christoph Engel

Christoph Engel

Christoph Engel

Christoph Engel

Other publications of authors with the same name

Disambiguation

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URL
DOI
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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction