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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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Christian Singer

Dominique Singer

Jörg Singer

Susanne Singer

Siegfried Singer

Other publications of authors with the same name

Automatische Synthese von Familienmodellen durch Analyse von block-basierten Funktionsmodellen.S. Holthusen, P. Manhart, I. Schaefer, S. Schulze, C. Singer, and D. Wille. GI-Jahrestagung, volume P-220 of LNI, page 2443-2457. GI, (2013)Artificial Intelligence-Based Decision Support in Laboratory Diagnostics.A. Scherrer, M. Helmling, C. Singer, S. Riedel, and K. Küfer. OR, page 229-235. Springer, (2021)A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activityL. Guidugli, V. Pankratz, N. Singh, J. Thompson, C. Erding, C. Engel, R. Schmutzler, S. Domchek, K. Nathanson, P. Radice and 5 other author(s). Cancer research, 73 (1): 265–275 (2013)Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, O. Sinilnikova, L. McGuffog, S. Healey, H. Nevanlinna, T. Heikkinen, J. Simard, A. Spurdle, J. Beesley, X. Chen and 127 other author(s). Human molecular genetics, 18 (22): 4442–4456 (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 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)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 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)

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Disambiguation of "Singer, Christian"

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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

Christian Singer

Dominique Singer

Jörg Singer

Susanne Singer

Siegfried Singer

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Singer, Christian"

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

Christian Singer

Dominique Singer

Jörg Singer

Susanne Singer

Siegfried Singer

Other publications of authors with the same name

Disambiguation

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