1. An experimental study of the effect of rare polymorphisms of human HBB, HBD and F9 promoter TATA boxes on the kinetics of interaction with the TATA-binding protein

    Sharypova, E. B., Drachkova, I. A., Kashina, E. V., Rasskazov, D. A., Ponomarenko, M. P., Ponomarenko, M. P., Kolchanov, N. A. & Savinkova, L. K., 1 Jan 2018, In: Вавиловский журнал генетики и селекции. 22, 1, p. 145-152 8 p.

    Research output: Contribution to journalArticlepeer-review

  2. A new molecular marker including parts of conservative histone H3 and H4 genes and the spacer between them for phylogenetic studies in dragonflies (Insecta, Odonata), extendable to other organisms

    Mglinets, A. V., Bulgakova, V. S. & Kosterin, O. E., Oct 2025, In: Vavilovskii Zhurnal Genetiki i Selektsii. 29, 6, p. 868-882 15 p., 14.

    Research output: Contribution to journalArticlepeer-review

  3. A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

    Romanov, G. P., Pshennikova, V. G., Lashin, S. A., Solovyev, A. V., Teryutin, F. M., Cherdonova, A. M., Borisova, T. V., Sazonov, N. N., Khusnutdinova, E. K., Posukh, O. L., Fedorova, S. A. & Barashkov, N. A., Nov 2020, In: PLoS ONE. 15, 11 November, p. e0242219 e0242219.

    Research output: Contribution to journalArticlepeer-review

  4. A network-based conditional genetic association analysis of the human metabolome

    Tsepilov, Y. A., Sharapov, S. Z., Zaytseva, O. O., Krumsek, J., Prehn, C., Adamski, J., Kastenmüller, G., Wang-Sattler, R., Strauch, K., Gieger, C. & Aulchenko, Y. S., 29 Nov 2018, In: GigaScience. 7, 12, 11 p., 137.

    Research output: Contribution to journalArticlepeer-review

  5. Analysis of SDC2 and SEPT9 promoters methylation in plasma cfDNA to detect colorectal and precancerous lesions

    Borobova, V., Aksamentov, A., Sazonov, D., Baklaushev, V., Indinok, D., Valuyskikh, E., Valuiskikh, A., Oleynikova, N., Laktionov, P. & Kovalenko, S., 21 May 2025, In: Exploration of Medicine. 6, 1001322.

    Research output: Contribution to journalArticlepeer-review

  6. Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia)

    Pshennikova, V. G., Barashkov, N. A., Solovyev, A. V., Romanov, G. P., Diakonov, E. E., Sazonov, N. N., Morozov, I. V., Bondar, A. A., Posukh, O. L., Dzhemileva, L. U., Khusnutdinova, E. K., Tomsky, M. I. & Fedorova, S. A., 1 Jun 2017, In: Russian Journal of Genetics. 53, 6, p. 688-697 10 p.

    Research output: Contribution to journalArticlepeer-review

  7. Analysis of Genome Structure and Its Variations in Potato Cultivars Grown in Russia

    Karetnikov, D. I., Vasiliev, G. V., Toshchakov, S. V., Shmakov, N. A., Genaev, M. A., Nesterov, M. A., Ibragimova, S. M., Rybakov, D. A., Gavrilenko, T. A., Salina, E. A., Patrushev, M. V., Kochetov, A. V. & Afonnikov, D. A., 16 Mar 2023, In: International Journal of Molecular Sciences. 24, 6, 5713.

    Research output: Contribution to journalArticlepeer-review

  8. Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions

    Tsepilov, Y. A., Freidin, M. B., Shadrina, A. S., Sharapov, S. Z., Elgaeva, E. E., Zundert, J. V., Karssen, L., Suri, P., Williams, F. M. K. & Aulchenko, Y. S., 25 Jun 2020, In: Communications Biology. 3, 1, 13 p., 329.

    Research output: Contribution to journalArticlepeer-review

  9. Analysis of differential expression of matrix metalloproteases in stable and unstable atherosclerotic lesions by a method of full genome sequencing of RNA: Pilot study

    Ivanoschuk, D. E., Ragino, Y. I., Shakhtshneider, E. V., Mikhailova, S. V., Fishman, V. S., Polonskaya, Y. V., Kashtanova, E. V., Chernyavsky, A. M., Murashov, I. S. & Voevoda, M. I., 1 Jan 2018, In: Russian Journal of Cardiology. 23, 8, p. 52-58 7 p.

    Research output: Contribution to journalArticlepeer-review

  10. Analysis by Minigene Assay of the Splicing Effect of a Novel Variant c.1545T>G in the SLC26A4 Gene Associated with Hearing Loss

    Panina, E. A., Danilchenko, V. Y., Zytsar, M. V., Orishchenko, K. E. & Posukh, O. L., 10 Jun 2025, In: Russian Journal of Genetics. 61, 5, p. 602-607 6 p.

    Research output: Contribution to journalArticlepeer-review

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