Autor der Publikation

Kopieren Löschen Diese Publikation zur Ablage hinzufügen
Community-Eintrag
Versionsverlauf dieses Eintrags
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

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 carriers

F. Couch, M. Gaudet, A. Antoniou, S. Ramus, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, X. Wang, T. Kirchhoff, L. McGuffog, D. Barrowdale, A. Lee, S. Healey, O. Sinilnikova, I. Andrulis, H. Ozcelik, A. Mulligan, M. Thomassen, A. Gerdes, U. Jensen, A. Skytte, T. Kruse, M. Caligo, A. Wachenfeldt, G. Barbany-Bustinza, N. Loman, M. Soller, H. Ehrencrona, P. Karlsson, K. Nathanson, T. Rebbeck, S. Domchek, A. Jakubowska, J. Lubinski, K. Jaworska, K. Durda, E. Zlowocka, T. Huzarski, T. Byrski, J. Gronwald, C. Cybulski, B. Górski, A. Osorio, M. Durán, M. Tejada, J. Benitez, U. Hamann, Hogervorst, Frans B L, van Os, Theo A, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, J. Wijnen, M. Blok, M. Kets, M. Hooning, R. Oldenburg, Ausems, Margreet G E M, S. Peock, D. Frost, S. Ellis, R. Platte, E. Fineberg, D. Evans, C. Jacobs, R. Eeles, J. Adlard, R. Davidson, D. Eccles, T. Cole, J. Cook, J. Paterson, C. Brewer, F. Douglas, S. Hodgson, P. Morrison, L. Walker, M. Porteous, M. Kennedy, L. Side, B. Bove, A. Godwin, D. Stoppa-Lyonnet, M. Fassy-Colcombet, L. Castera, F. Cornelis, S. Mazoyer, M. Léoné, N. Boutry-Kryza, B. Bressac-de Paillerets, O. Caron, P. Pujol, I. Coupier, C. Delnatte, L. Akloul, H. Lynch, C. Snyder, S. Buys, M. Daly, M. Terry, W. Chung, E. John, A. Miron, M. Southey, J. Hopper, D. Goldgar, C. Singer, C. Rappaport, M. Tea, A. Fink-Retter, Hansen, Thomas V O, F. Nielsen, A. Arason, J. Vijai, S. Shah, K. Sarrel, M. Robson, M. Piedmonte, K. Phillips, J. Basil, W. Rubinstein, J. Boggess, K. Wakeley, A. Ewart-Toland, M. Montagna, S. Agata, E. Imyanitov, C. Isaacs, R. Janavicius, C. Lazaro, I. Blanco, L. Feliubadalo, J. Brunet, S. Gayther, Pharoah, Paul P D, K. Odunsi, B. Karlan, C. Walsh, E. Olah, S. Teo, P. Ganz, M. Beattie, van Rensburg, Elizabeth J, C. Dorfling, 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, W. Heinritz, T. Caldes, de la Hoya, Miguel, T. Muranen, H. Nevanlinna, M. Tischkowitz, A. Spurdle, S. Neuhausen, Y. Ding, N. Lindor, Z. Fredericksen, V. Pankratz, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, M. Barile, L. Bernard, A. Viel, G. Giannini, L. Varesco, P. Radice, M. Greene, P. Mai, D. Easton, G. Chenevix-Trench, K. Offit, und J. Simard. 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)

Bitte wählen Sie eine Person um die Publikation zuzuordnen

Um zwischen Personen mit demselben Namen zu unterscheiden, wird der akademische Grad und der Titel einer wichtigen Publikation angezeigt. Zudem lassen sich über den Button neben dem Namen einige der Person bereits zugeordnete Publikationen anzeigen.

Alfons Meindl

Antonie Meindl

Karl Meindl

Thomas Meindl

Ralf Meindl

Weitere Publikationen von Autoren mit dem selben Namen

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 und 69 andere Autor(en). 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 und 8 andere Autor(en). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 27 (35): 5887–5892 (2009)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 und 252 andere Autor(en). 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 und 13 andere Autor(en). Journal of medical genetics, 50 (6): 360–367 (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 und 172 andere Autor(en). Breast cancer research : BCR, 13 (6): R110 (2011)Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patientsK. Hemminki, B. Müller-Myhsok, P. Lichtner, C. Engel, B. Chen, B. Burwinkel, A. Försti, C. Sutter, B. Wappenschmidt, H. Hellebrand und 13 andere Autor(en). International journal of cancer. Journal international du cancer, 126 (12): 2858–2862 (2010)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriersA. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, A. Lee, D. Barrowdale, S. Healey, O. Sinilnikova und 171 andere Autor(en). Breast cancer research : BCR, 14 (1): R33 (2012)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 und 168 andere Autor(en). Nature genetics, 42 (10): 885–892 (2010)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 und 58 andere Autor(en). 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)Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriersX. Wang, V. Pankratz, Z. Fredericksen, R. Tarrell, M. Karaus, L. McGuffog, Pharaoh, Paul D P, Ponder, Bruce A J, A. Dunning, S. Peock und 34 andere Autor(en). Human molecular genetics, 19 (14): 2886–2897 (2010)

BibSonomy

Disambiguierung von "Meindl, Alfons"