Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients за авторством Chernushyn, S.Yu., Hryshchenko, N.V.

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Development of MLPA approach for SNP detection in MTHFR, F5 and F2 genes за авторством Kravchenko, S.A., Chernushyn, S.Yu., Kucherenko, A.M., Soloviov, O.O., Livshits, L.A.

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Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis за авторством Livshits, L.A., Kravchenko, S.A., Nechyporenko, M.V., Pampukha, V.M., Hryshchenko, N.V., Livshyts, G.B., Soloviov, O.O., Tatarskyy, P.F., Fesai, O.A., Chernushyn, S.Yu., Kucherenko, A.M., Gulkovskyy, R.V.

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