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Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility.
Kumpula TA, Vorimo S, Mattila TT, O'Gorman L, Astuti G, Tervasmäki A, Koivuluoma S, Mattila TM, Grip M, Winqvist R, Kuismin O, Moilanen J, Hoischen A, Gilissen C, Mantere T, Pylkäs K. Kumpula TA, et al. Among authors: vorimo s. PLoS Genet. 2023 Aug 14;19(8):e1010889. doi: 10.1371/journal.pgen.1010889. eCollection 2023 Aug. PLoS Genet. 2023. PMID: 37578974 Free PMC article.
Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility.
Koivuluoma S, Vorimo S, Mattila TM, Tervasmäki A, Kumpula T, Kuismin O, Winqvist R, Moilanen J, Mantere T, Pylkäs K. Koivuluoma S, et al. Among authors: vorimo s. Fam Cancer. 2023 Jan;22(1):13-17. doi: 10.1007/s10689-022-00295-z. Epub 2022 May 20. Fam Cancer. 2023. PMID: 35590014 Free PMC article.