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

Generation of induced pluripotent stem cell line, ICGi034-A, by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease associated with GBA mutation

Grigor'eva, E. V., Drozdova, E. S., Sorogina, D. A., Malakhova, A. A., Pavlova, S. V., Vyatkin, Y. V., Khabarova, E. A., Rzaev, J. A., Medvedev, S. P. & Zakian, S. M., Mar 2022, In: Stem Cell Research. 59, 102651.

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

Generation of induced pluripotent stem cell lines ICGi021-A and ICGi022-A from peripheral blood mononuclear cells of two healthy individuals from Siberian population

Malakhova, A. A., Grigor'eva, E. V., Pavlova, S. V., Malankhanova, T. B., Valetdinova, K. R., Vyatkin, Y. V., Khabarova, E. A., Rzaev, J. A., Zakian, S. M. & Medvedev, S. P., 1 Oct 2020, In: Stem Cell Research. 48, 4 p., 101952.

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

Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C

Valetdinova, K. R., Maretina, M. A., Vyatkin, Y. V., Perepelkina, M. P., Egorova, A. A., Baranov, V. S., Kiselev, A. V., Gershovich, P. M. & Zakian, S. M., 1 Oct 2020, In: Stem Cell Research. 48, 5 p., 101941.

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

Generation of two clonal iPSC lines, ICGi019-A and ICGi019-B, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.M659I mutation in MYH7

Dementyeva, E. V., Kovalenko, V. R., Zhiven, M. K., Ustyantseva, E. I., Kretov, E. I., Vyatkin, Y. V. & Zakian, S. M., Jul 2020, In: Stem Cell Research. 46, 4 p., 101840.

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

Generation of two iPSC lines, (ICGi015-A and ICGi015-B), by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease

Sharipova, D. V., Kovalenko, V. R., Bairamova, E. M., Vartanova, V. A., Grigor'eva, E. V., Vyatkin, Y. V., Khabarova, E. A., Rzaev, D. A., Zakian, S. M. & Medvedev, S. P., 1 Dec 2019, In: Stem Cell Research. 41, 5 p., 101652.

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

Genetic analysis of patients with hypertrophic cardiomyopathy

Dementyeva, E. V., Vyatkin, Y. V., Kretov, E. I., Elisaphenko, E. A., Medvedev, S. P. & Zakian, S. M., 2020, In: Genes and Cells. 15, 3, p. 68-73 6 p.

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

Genetic and Metabolic Factors of Familial Dysbetalipoproteinemia Phenotype: Insights from a Cross-Sectional Study

Blokhina, A. V., Ershova, A. I., Kiseleva, A. V., Sotnikova, E. A., Zaicenoka, M., Zharikova, A. A., Vyatkin, Y. V., Ramensky, V. E., Novokhatskaya, E. A., Borisova, A. L., Shalnova, S. A., Meshkov, A. N. & Drapkina, O. M., 30 Jul 2025, In: International Journal of Molecular Sciences. 26, 15, 7376.

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

Genetic landscape in Russian patients with familial left ventricular noncompaction

Meshkov, A. N., Myasnikov, R. P., Kiseleva, A. V., Kulikova, O. V., Sotnikova, E. A., Kudryavtseva, M. M., Zharikova, A. A., Koretskiy, S. N., Mershina, E. A., Ramensky, V. E., Zaicenoka, M., Vyatkin, Y. V., Kharlap, M. S., Nikityuk, T. G., Sinitsyn, V. E., Divashuk, M. G., Kutsenko, V. A., Basargina, E. N., Barskiy, V. I., Sdvigova, N. A., & 4 othersSkirko, O. P., Efimova, I. A., Pokrovskaya, M. S. & Drapkina, O. M., 2023, In: Frontiers in cardiovascular medicine. 10, 1205787.

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

Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases

Sotnikova, E. A., Kiseleva, A. V., Kutsenko, V. A., Zharikova, A. A., Ramensky, V. E., Divashuk, M. G., Vyatkin, Y. V., Klimushina, M. V., Ershova, A. I., Revazyan, K. Z., Skirko, O. P., Zaicenoka, M., Efimova, I. A., Pokrovskaya, M. S., Kopylova, O. V., Glechan, A. M., Shalnova, S. A., Meshkov, A. N. & Drapkina, O. M., Jul 2022, In: Journal of Personalized Medicine. 12, 7, 1132.

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