Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants von Tatarskyy, P.F., Kucherenko, A.M., Kravchenko, S.A., Shulzhenko, D.V., Kuznetsova, S.M., Livshits, L.A.

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Study on possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children von Tatarskyy, P.F., Chumachenko, N.G., Kucherenko, A.M., Gulkovskyi, R.V., Arabskaya, L.P., Smirnova, O.A., Tolkach, S.I., Antipkin, Yu.G., Livshits, L.A.

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Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis von 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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