Genome-wide somatic mutation analysis of sinonasal adenocarcinoma with and without wood dust exposure

Sipilä, L. J., Katainen, R., Aavikko, M., Ravantti, J., Donner, I., Lehtonen, R., Leivo, I., Wolff, H., Holmila, R., Husgafvel-Pursiainen, K. & Aaltonen, L. A., 2024, I: Genes and Environment. 46, 1, 13 s., 12.

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Lynch syndrome-associated and sporadic microsatellite unstable colorectal cancers: different patterns of clonal evolution yield highly similar tumours

Martin, S., Katainen, R., Taira, A., Välimäki, N., Ristimäki, A., Seppälä, T., Renkonen-Sinisalo, L., Lepistö, A., Tahkola, K., Mattila, A., Koskensalo, S., Mecklin, J-P., Rajamäki, K., Palin, K. & Aaltonen, L. A., 1 aug. 2024, I: Human Molecular Genetics. 15 s., ddae124.

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Previously reported CCDC26 risk variant and novel germline variants in GALNT13, AR, and MYO10 associated with familial glioma in Finland

Nurminen, R., Afyounian, E., Paunu, N., Katainen, R., Isomäki, M., Nurminen, A., Scaravilli, M., Tolppanen, J., Fey, V., Kivinen, A., Helén, P., Välimäki, N., Kesseli, J., Aaltonen, L. A., Haapasalo, H., Nykter, M. & Rautajoki, K. J., 2024, I: Scientific Reports. 14, 1, 12 s., 11562.

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APOBEC mutagenesis is a common process in normal human small intestine

Wang, Y., Robinson, P. S., Coorens, T. H. H., Moore, L., Lee-Six, H., Noorani, A., Sanders, M. A., Jung, H., Katainen, R., Heuschkel, R., Brunton-Sim, R., Weston, R., Read, D., Nobbs, B., Fitzgerald, R. C., Saeb-Parsy, K., Martincorena, I., Campbell, P. J., Rushbrook, S., Zilbauer, M., & 2 andraBuczacki, S. J. A. & Stratton, M. R., 2023, I: Nature Genetics. 55, s. 246–254 23 s.

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Mutation-Attention (MuAt): deep representation learning of somatic mutations for tumour typing and subtyping

Sanjaya, P., Maljanen, K., Katainen, R., Waszak, S. A., Genomics England Research Consortium, O., Aaltonen, L. A., Stegle, O., Korbel, J. & Pitkänen, E., 7 juli 2023, I: Genome medicine. 15, 1, 18 s., 47.

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