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Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility.
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.
Optical Genome Mapping as an Alternative to FISH-Based Cytogenetic Assessment in Chronic Lymphocytic Leukemia.
Valkama A, Vorimo S, Kumpula TA, Räsänen H, Savolainen ER, Pylkäs K, Mantere T.
Valkama A, et al. Among authors: vorimo s.
Cancers (Basel). 2023 Feb 17;15(4):1294. doi: 10.3390/cancers15041294.
Cancers (Basel). 2023.
PMID: 36831635
Free PMC article.
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Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predisposition.
Kumpula TA, Koivuluoma S, Soikkonen L, Vorimo S, Moilanen J, Winqvist R, Mantere T, Kuismin O, Pylkäs K.
Kumpula TA, et al. Among authors: vorimo s.
Fam Cancer. 2023 Jul;22(3):291-294. doi: 10.1007/s10689-023-00327-2. Epub 2023 Jan 19.
Fam Cancer. 2023.
PMID: 36653541
Free PMC article.
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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.
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