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  1. 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 journal › Article › peer-review

  2. 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 journal › Article › peer-review

  3. A Method for Assessing the Efficiency of the Nucleotide Excision Repair System Ex Vivo

    Popov, A. A., Orishchenko, K. E., Naumenko, K. N., Evdokimov, A. N., Petruseva, I. O. & Lavrik, O. I., Sept 2021, In: Acta Naturae. 13, 3, p. 122-125 4 p., 13.

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

  4. A hypomorphic mutation in the mouse Csn1s1 gene generated by CRISPR/Cas9 pronuclear microinjection

    Smirnov, A. V., Shnaider, T., Korablev, A. N., Yunusova, A. M., Serova, I. A. & Battulin, N. R., Mar 2021, In: Vavilovskii Zhurnal Genetiki i Selektsii. 25, 3, p. 331-336 6 p., 10.

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

  5. A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

    Koksharova, G., Kokh, N., Gridina, M., Khapaev, R., Nimaev, V. & Fishman, V., May 2024, In: International Journal of Molecular Sciences. 25, 10, 5464.

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

  6. Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population

    Romanov, G. P., Smirnova, A. A., Zamyatin, V. I., Mukhin, A. M., Kazantsev, F. V., Pshennikova, V. G., Teryutin, F. M., Solovyev, A. V., Fedorova, S. A., Posukh, O. L., Lashin, S. A. & Barashkov, N. A., Feb 2022, In: Biology. 11, 2, 257.

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

  7. Adaptation of CRISPR/Cas9 system for directed elimination of mitochondrial DNA copies with mutations

    Zakirova, E., Mazunin, I. & Orishchenko, K., Jul 2021, In: FEBS Open Bio. 11, p. 118-118 1 p.

    Research output: Contribution to journal › Meeting Abstract › peer-review

  8. A Cre-LoxP-based approach for combinatorial chromosome rearrangements in human HAP1 cells

    Khabarova, A., Koksharova, G., Salnikov, P., Belokopytova, P., Mungalov, R., Pristyazhnuk, I., Nurislamov, A., Gridina, M. & Fishman, V., 26 Feb 2023, In: Chromosome Research. 31, 1, 15 p., 11.

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

  9. A cookbook for DNase Hi-C

    Gridina, M., Mozheiko, E., Valeev, E., Nazarenko, L. P., Lopatkina, M. E., Markova, Z. G., Yablonskaya, M. I., Voinova, V. Y., Shilova, N. V., Lebedev, I. N. & Fishman, V., 20 Mar 2021, In: Epigenetics and Chromatin. 14, 1, 15.

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

  10. A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

    Solovyev, A. V., Kushniarevich, A., Bliznetz, E., Bady-Khoo, M., Lalayants, M. R., Markova, T. G., Minárik, G., Kádasi, L., Metspalu, E., Pshennikova, V. G., Teryutin, F. M., Khusnutdinova, E. K., Poliakov, A., Metspalu, M., Posukh, O. L., Barashkov, N. A. & Fedorova, S. A., Apr 2022, In: Human Genetics. 141, 3-4, p. 697-707 11 p.

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

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