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A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer.
Bogdanova N, Cybulski C, Bermisheva M, Datsyuk I, Yamini P, Hillemanns P, Antonenkova NN, Khusnutdinova E, Lubinski J, Dörk T. Bogdanova N, et al. Among authors: dork t. Breast Cancer Res Treat. 2009 Nov;118(1):207-11. doi: 10.1007/s10549-008-0189-9. Epub 2008 Sep 21. Breast Cancer Res Treat. 2009. PMID: 18807267
Association of two mutations in the CHEK2 gene with breast cancer.
Bogdanova N, Enssen-Dubrowinskaja N, Feshchenko S, Lazjuk GI, Rogov YI, Dammann O, Bremer M, Karstens JH, Sohn C, Dörk T. Bogdanova N, et al. Among authors: dork t. Int J Cancer. 2005 Aug 20;116(2):263-6. doi: 10.1002/ijc.21022. Int J Cancer. 2005. PMID: 15810020
A common coding variant in CASP8 is associated with breast cancer risk.
Cox A, Dunning AM, Garcia-Closas M, Balasubramanian S, Reed MW, Pooley KA, Scollen S, Baynes C, Ponder BA, Chanock S, Lissowska J, Brinton L, Peplonska B, Southey MC, Hopper JL, McCredie MR, Giles GG, Fletcher O, Johnson N, dos Santos Silva I, Gibson L, Bojesen SE, Nordestgaard BG, Axelsson CK, Torres D, Hamann U, Justenhoven C, Brauch H, Chang-Claude J, Kropp S, Risch A, Wang-Gohrke S, Schürmann P, Bogdanova N, Dörk T, Fagerholm R, Aaltonen K, Blomqvist C, Nevanlinna H, Seal S, Renwick A, Stratton MR, Rahman N, Sangrajrang S, Hughes D, Odefrey F, Brennan P, Spurdle AB, Chenevix-Trench G; Kathleen Cunningham Foundation Consortium for Research into Familial Breast Cancer; Beesley J, Mannermaa A, Hartikainen J, Kataja V, Kosma VM, Couch FJ, Olson JE, Goode EL, Broeks A, Schmidt MK, Hogervorst FB, Van't Veer LJ, Kang D, Yoo KY, Noh DY, Ahn SH, Wedrén S, Hall P, Low YL, Liu J, Milne RL, Ribas G, Gonzalez-Neira A, Benitez J, Sigurdson AJ, Stredrick DL, Alexander BH, Struewing JP, Pharoah PD, Easton DF; Breast Cancer Association Consortium. Cox A, et al. Among authors: dork t. Nat Genet. 2007 Mar;39(3):352-8. doi: 10.1038/ng1981. Epub 2007 Feb 11. Nat Genet. 2007. PMID: 17293864
ATM missense variant P1054R predisposes to prostate cancer.
Meyer A, Wilhelm B, Dörk T, Bremer M, Baumann R, Karstens JH, Machtens S. Meyer A, et al. Among authors: dork t. Radiother Oncol. 2007 Jun;83(3):283-8. doi: 10.1016/j.radonc.2007.04.029. Epub 2007 May 14. Radiother Oncol. 2007. PMID: 17502119
CHEK2 mutation and hereditary breast cancer.
Bogdanova N, Feshchenko S, Cybulski C, Dörk T. Bogdanova N, et al. Among authors: dork t. J Clin Oncol. 2007 Jul 1;25(19):e26. doi: 10.1200/JCO.2007.11.4223. J Clin Oncol. 2007. PMID: 17602067 No abstract available.
Nijmegen Breakage Syndrome mutations and risk of breast cancer.
Bogdanova N, Feshchenko S, Schürmann P, Waltes R, Wieland B, Hillemanns P, Rogov YI, Dammann O, Bremer M, Karstens JH, Sohn C, Varon R, Dörk T. Bogdanova N, et al. Among authors: dork t. Int J Cancer. 2008 Feb 15;122(4):802-6. doi: 10.1002/ijc.23168. Int J Cancer. 2008. PMID: 17957789
NBS1 variant I171V and breast cancer risk.
Bogdanova N, Schürmann P, Waltes R, Feshchenko S, Zalutsky IV, Bremer M, Dörk T. Bogdanova N, et al. Among authors: dork t. Breast Cancer Res Treat. 2008 Nov;112(1):75-9. doi: 10.1007/s10549-007-9820-4. Epub 2007 Nov 30. Breast Cancer Res Treat. 2008. PMID: 18049891
394 results