IORS Dept. for Department of Genetic Counseling for Hereditary Cancer published the first systematic analysis of a clinically selected high-risk Serbian cohort related to Lynch syndrome. The manuscript provides novel data on the spectrum of LS-associated variants in this referral population, demonstrates the predominance of MLH1 variants, and supports broader implementation of genetic testing, tumor screening, and genetic counseling.
Djordjic Crnogorac M, Karadzic V, Cato T, Cavic M, Nikolic N, Spasic J, Djordjevic F, Jokic V, Kocic M, Djurasinovic M, Kukic B, Nikolic S, Ristic M, Milovic M, Krivokuca A. Genetic Landscape of Lynch Syndrome in a High-Risk Serbian Cohort: Predominance of MLH1 Variants and Implications for Risk-Based Testing. International Journal of Molecular Sciences. 2026; 27(15):6652. https://doi.org/10.3390/ijms27156652.


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Project ID:  101079217 (HORIZON-WIDERA-2021-ACCESS-03)

Funded by the European Union. Views and opinions expressed are those of the author(s) only and do not necessarily reflect those of the European Union or the European Research Executive Agency. Neither the European Union nor the European Research Executive Agency can be held responsible for them

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