Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/23833
Title: 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 BRCA1/2.
Authors: Mulligan, A. M.
Couch, F. J.
Barrowdale, D.
Domchek, S. M.
Eccles, D.
Nevanlinna, H.
Ramus, S. J.
Robson, M.
Sherman, M.
Spurdle, A. B.
Wappenschmidt, B.
Hansen, T. V.
Karlsson, P.
Ding, Y. C.
Neuhausen, S. L.
Ontario Cancer Genetics Network
Beattie, M.
Pharoah, P. D.
Ejlertsen, B.
Moysich, K. B.
Southey, M. C.
Niederacher, D.
Andrulis, I. L.
Schoenbuchner, I.
CIMBA
Mazoyer, S.
Osorio, A.
Coupier, I.
Muñoz-Repeto, I.
Durán, M.
Godino, J.
Pertesi, M.
Sutter, C.
Benítez, J.
Peterlongo, P.
Fiebig, B.
Manoukian, S.
Peissel, B.
Léoné, M.
Zaffaroni, D.
Cattaneo, E.
Lebrun, M.
Bonanni, B.
Deissler, H.
Viel, A.
Pasini, B.
Papi, L.
Heinritz, W.
Ottini, L.
Savarese, A.
Bernard, L.
Boutry-Kryza, N.
Radice, P.
Hamann, U.
Gadzicki, D.
Verheus, M.
Kientz, C.
Meijers-Heijboer, H. E.
Wijnen, J.
Schäfer, D.
Gómez García, E. B.
Nelen, M. R.
Kets, C. M.
Seynaeve, C.
Hardouin, A.
Isaacs, C.
Tilanus-Linthorst, M. M.
van der Luijt, R. B.
van Os, T.
Rookus, M.
Longy, M.
Gevensleben, H.
Frost, D.
Jones, J. L.
Evans, D. G.
Lalloo, F.
Kast, K.
Eeles, R.
Berthet, P.
Izatt, L.
Adlard, J.
Davidson, R.
Cook, J.
Caux-Moncoutier, V.
Donaldson, A.
Sevenet, N.
Dorkins, H.
Preisler-Adams, S.
Gregory, H.
Eason, J.
Houghton, C.
Muller, D.
Barwell, J.
Side, L. E.
McCann, E.
Fassy-Colcombet, M.
Murray, A.
Peock, S.
Mortemousque, I.
Godwin, A. K.
Stoppa-Lyonnet, D.
Schmutzler, R. K.
Rhiem, K.
Engel, C.
Fricker, J. P.
Meindl, A.
Ruehl, I.
Caldes, T.
Arnold, N.
Varon-Mateeva, R.
Cornelis, F.
Nathanson, K. L.
Pujol, P.
Hopper, J. L.
de la Hoya, M.
Antoniou, A. C.
Heikkinen, T.
Lee, A.
Aittomäki, K.
Blanco, I.
Lazaro, C.
Barkardottir, R. B.
Karlan, B. Y.
Soucy, P.
Dumont, M.
Terry, M. B.
Simard, J.
Montagna, M.
Breast Cancer Family Registry
Tognazzo, S.
D'Andrea, E.
McGuffog, L.
Fox, S.
Gross, J.
Yan, M.
Rebbeck, T.
Olopade, O.
Chung, W.
Weitzel, J. N.
Lynch, H. T.
Ganz, P. A.
EMBRACE
Tomlinson, G. E.
Wang, X.
John, E. M.
Fredericksen, Z.
Healey, S.
Pankratz, V. S.
Lindor, N. M.
Miron, A. F.
Szabo, C.
Offit, K.
Sakr, R.
Gaudet, M.
GEMO Study Collaborators
Nielsen, F. C.
Bhatia, J.
Kauff, N.
Singer, C. F.
Tea, M. K.
Sinilnikova, O. M.
Goldgar, D.
Gschwantler-Kaulich, D.
Fink-Retter, A.
Mai, P. L.
Greene, M. H.
Daly, M. B.
Imyanitov, E.
HEBON
O'Malley, F. P.
Ozcelik, H.
Glendon, G.
Toland, A. E.
Chenevix-Trench, G.
Gerdes, A. M.
Janavicius, R.
Thomassen, M.
Buys, S. M.
Kruse, T. A.
Jensen, U. B.
Skytte, A. B.
kConFab, Investigators
Caligo, M. A.
Soller, M.
Henriksson, K.
Easton, D. F.
Wachenfeldt, V. A.
Arver, B.
SWE-BRCA
Stenmark-Askmalm, M.
First Published: 2-Nov-2011
Publisher: BioMed Central
Citation: Breast Cancer Research, 2011, 13 (6), pp. R110-R110
Abstract: Previous studies have demonstrated that common breast cancer susceptibility alleles are differentially associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. It is currently unknown how these alleles are associated with different breast cancer subtypes in BRCA1 and BRCA2 mutation carriers defined by estrogen (ER) or progesterone receptor (PR) status of the tumour.
DOI Link: 10.1186/bcr3052
eISSN: 1465-542X
Links: http://hdl.handle.net/2381/23833
http://breast-cancer-research.biomedcentral.com/articles/10.1186/bcr3052
Type: Journal Article
Rights: © Mulligan et al.; licensee BioMed Central Ltd. 2011 This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Appears in Collections:Published Articles, Dept. of Cancer Studies and Molecular Medicine

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