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Reetta Kariola

20032012
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Publications 2003 2012

Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients.

Kantelinen, J., Kansikas, M., Candelin, S., Hampel, H., Smith, B., Holm, L., Kariola, R. & Nyström, M., 2012, In : Human Mutation. 33, 8, p. 1294-1301 8 p.

Research output: Contribution to journalArticleScientificpeer-review

A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one

Kantelinen, J., Hansen, T. V. O., Kansikas, M., Krogh, L. N., Korhonen, M. K., Ollila, S., Nystrom, M., Gerdes, A-M. & Kariola, R., 2011, In : Familial Cancer. 2011, 10, p. 515-520 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Verification of the Three-Step Model in Assessing the Pathogenicity of Mismatch Repair Gene Variants

Kansikas, M., Kariola, R. & Nyström, M., 2011, In : Human Mutation. 32, 1, p. 107-115 9 p.

Research output: Contribution to journalArticleScientificpeer-review

MutSbeta exceeds MutSalpha in dinucleotide loop repair

Kantelinen, J., Kansikas, M., Korhonen, M., Ollila, S., Heinimann, K., Kariola, R. & Nyström, M., 2010, In : British Journal of Cancer. 102, 6, p. 1068–1073 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein

Ollila, S., Sarantaus, L., Kariola, R., Chan, P., Hampel, H., Holinski-Feder, E., Macrae, F., Kohonen-Corish, M., Gerdes, A-M., Peltomäki, P., Mangold, E., Chapelle, A. D. L., Greenblatt, M. & Nyström, M., 2006, In : Gastroenterology. 131, p. 1408-1417 10 p.

Research output: Contribution to journalArticleScientificpeer-review