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The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Weinhold N, Johnson DC, Chubb D, Chen B, Försti A, Hosking FJ, Broderick P, Ma YP, Dobbins SE, Hose D, Walker BA, Davies FE, Kaiser MF, Li NL, Gregory WA, Jackson GH, Witzens-Harig M, Neben K, Hoffmann P, Nöthen MM, Mühleisen TW, Eisele L, Ross FM, Jauch A, Goldschmidt H, Houlston RS, Morgan GJ, Hemminki K. Weinhold N, et al. Among authors: forsti a. Nat Genet. 2013 May;45(5):522-525. doi: 10.1038/ng.2583. Epub 2013 Mar 17. Nat Genet. 2013. PMID: 23502783 Free PMC article.
Use of twins in search for tumor suppressor genes.
Försti A, Söderberg M, Hemminki K. Försti A, et al. Environ Mol Mutagen. 1997;30(2):231-9. doi: 10.1002/(sici)1098-2280(1997)30:2<231::aid-em16>3.0.co;2-e. Environ Mol Mutagen. 1997. PMID: 9329648
Proper controls for SNP studies?
Hemminki K, Försti A. Hemminki K, et al. Among authors: forsti a. Carcinogenesis. 2002 Aug;23(8):1405. doi: 10.1093/carcin/23.8.1405. Carcinogenesis. 2002. PMID: 12151361 No abstract available.
Single nucleotide polymorphisms in breast cancer.
Försti A, Angelini S, Festa F, Sanyal S, Zhang Z, Grzybowska E, Pamula J, Pekala W, Zientek H, Hemminki K, Kumar R. Försti A, et al. Oncol Rep. 2004 Apr;11(4):917-22. Oncol Rep. 2004. PMID: 15010895
414 results