GCK-MODY diabetes course in persons over 18 years of age: prospective observation by A. K. Ovsyannikova, E. V. Shakhtshneider, D. E. Ivanoshchuk, M. I. Voevoda, O. D. Rymar

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Screening of West Siberian patients with primary congenital glaucoma for CYP1B1 gene mutations by D. E. Ivanoshchuk, S. V. Mikhailova, O. G. Fenkova, E. V. Shakhtshneider, A. Z. Fursova, I. V. Bychkov, M. I. Voevoda

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CASCADE GENETIC SCREENING IN DIAGNOSTICS OF HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA: CLINICAL CASE by E. V. Shakhtshneider, D. E. Ivanoshchuk, K. V. Makarenkova, P. S. Orlov, O. V. Timoshchenko, S. S. Bazhan, Yu. P. Nikitin, M. I. Voevoda

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Expression analysis of microRNA and lncRNA in visceral adipose tissue of obese and non-obese individuals by A. Bairqdar, D. E. Ivanoshchuk, O. V. Tuzovskaya, N. S. Shirokova, E. Kashtanova, Y. V. Polonskaya, Y. I. Ragino, E. V. Shakhtshneider

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A rare splice site mutation in the gene encoding glucokinase/hexokinase 4 in a patient with MODY type 2 by D. E. Ivanoshchuk, E. V. Shakhtshneider, A. K. Ovsyannikova, S. V. Mikhailova, O. D. Rymar, V. I. Oblaukhova, A. A. Yurchenko, M. I. Voevoda

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Next generation sequencing in sudden cardiac death (pilot study) by V. N. Maksimov, D. E. Ivanoshchuk, P. S. Orlov, A. A. Ivanova, S. K. Malyutina, S. V. Maksimova, I. A. Rodina, O. V. Khamovich, V. P. Novoselov, M. I. Voevoda

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