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  1. A comparison of two approaches for autosomal recessive diseases carrier screening

    Sotnikova, E. A., Kiseleva, A. V., Kutsenko, V. A., Soplenkova, A., Zharikova, A. A., Ramensky, V. E., Вяткин, Ю. В., Ershova, A. I., Skirko, O. P., Zaicenoka, M., Pokrovskaya, M. S., Shalnova, S. A., Drapkina, O. M. & Meshkov, A. N., 2024, In: European journal of human genetics. 32, S1, p. 287 1 p., EP17.007.

    Research output: Contribution to journal › Conference article › peer-review

  2. A New MicroRNA Cluster Involved in the Reprogramming to a Pluripotent State

    Sherstyuk, V. V., Davletshina, G. I., Vyatkin, Y. V., Shtokalo, D. N., Vlasov, V. V. & Zakian, S. M., 16 Aug 2019, In: Acta Naturae. 11, 2, p. 92-97 6 p.

    Research output: Contribution to journal › Article › peer-review

  3. Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot Study

    Blokhina, A. V., Ershova, A. I., Kiseleva, A. V., Sotnikova, E. A., Zharikova, A. A., Zaicenoka, M., Vyatkin, Y. V., Ramensky, V. E., Kutsenko, V. A., Shalnova, S. A., Meshkov, A. N. & Drapkina, O. M., 24 Aug 2023, In: International Journal of Molecular Sciences. 24, 17, 13159.

    Research output: Contribution to journal › Article › peer-review

  4. Applying Patient-Specific Induced Pluripotent Stem Cells to Create a Model of Hypertrophic Cardiomyopathy

    Dementyeva, E. V., Medvedev, S. P., Kovalenko, V. R., Vyatkin, Y. V., Kretov, E. I., Slotvitsky, M. M., Shtokalo, D. N., Pokushalov, E. A. & Zakian, S. M., 1 Mar 2019, In: Biochemistry (Moscow). 84, 3, p. 291-298 8 p.

    Research output: Contribution to journal › Article › peer-review

  5. Assessment of polygenic risk of hypertension

    Limonova, A. S., Ershova, A. I., Kiseleva, A. V., Ramensky, V. E., Vyatkin, Y. V., Kutsenko, V. A., Meshkov, A. N. & Drapkina, O. M., 2022, In: Cardiovascular Therapy and Prevention (Russian Federation). 21, 12, 3464.

    Research output: Contribution to journal › Article › peer-review

  6. Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study

    Blokhina, A. V., Ershova, A. I., Kiseleva, A. V., Sotnikova, E. A., Zharikova, A. A., Zaicenoka, M., Vyatkin, Y. V., Ramensky, V. E., Kutsenko, V. A., Litinskaya, O. A., Pokrovskaya, M. S., Shalnova, S. A., Meshkov, A. N. & Drapkina, O. M., 20 Dec 2024, In: PLoS ONE. 19, 12, p. e0315693 e0315693.

    Research output: Contribution to journal › Article › peer-review

  7. Comparison of three approaches to autosomal recessive diseases carrier screening

    Sotnikova, E. A., Kiseleva, A. V., Soplenkova, A. G., Kutsenko, V. A., Zharikova, A. A., Ramensky, V. E., Vyatkin, Y. V., Zaicenoka, M., Ershova, A. I., Skirko, O. P., Pokrovskaya, M. S., Shalnova, S. A., Meshkov, A. N. & Drapkina, O. M., 2023, In: Profilakticheskaya Meditsina. 26, 10, p. 36-42 7 p.

    Research output: Contribution to journal › Article › peer-review

  8. Creation of Induced Pluripotent Stem Cells ICGi044-B and ICGi044-C Using Reprogramming of Peripheral Blood Mononuclear Cells of a Patient with Parkinson’s Disease Associated with c.1492T>G Mutation in the GLUD2 Gene

    Sorogina, D. A., Grigor’eva, E. V., Malakhova, A. A., Pavlova, S. V., Medvedev, S. P., Vyatkin, Y. V., Khabarova, E. A., Rzaev, J. A. & Zakian, S. M., 27 Jun 2023, In: Russian Journal of Developmental Biology. 54, 1, p. 104-111 8 p.

    Research output: Contribution to journal › Article › peer-review

  9. Generation of an induced pluripotent stem cell line, ICGi028-A, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.E510Q mutation in HADHA

    Dementyeva, E. V., Vyatkin, Y. V., Chernyavsky, A. M. & Zakian, S. M., May 2021, In: Stem Cell Research. 53, p. 102348 102348.

    Research output: Contribution to journal › Article › peer-review

  10. Generation of an Induced Pluripotent Stem Cell Line, ICGi042-A, by Reprogramming Peripheral Blood Mononuclear Cells from a Parkinson’s Disease Patient with c.1000G>A Mutation in the LRRK2 Gene

    Grigor’eva, E. V., Pavlova, S. V., Malakhova, A. A., Medvedev, S. P., Minina, J. M., Vyatkin, Y. V., Khabarova, E. A., Rzaev, J. A., Kovalenko, L. V. & Zakian, S. M., 2023, In: Russian Journal of Developmental Biology. 54, 1, p. 80-87 8 p.

    Research output: Contribution to journal › Article › peer-review

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