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  1. 2025

  2. Analysis of the Spectrum of the mtDNA Haplogroups in Patients with Hearing Loss Carrying the Likely Pathogenic Ultra-Rare m.1494C>T Variant in the MT-RNR1 Gene

    Borisova, T. V., Cherdonova, A. M., Pshennikova, V. G., Teryutin, F. M., Morozov, I. V., Bondar, A. A., Baturina, O. A., Kabilov, M. R., Romanov, G. P., Solovyev, A. V., Fedorova, S. A. & Barashkov, N. A., Aug 2025, In: Russian Journal of Genetics. 61, 8, p. 974-986 13 p., 9.

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

  3. The c.644 G > A p.(Trp215*) founder variant in the CLIC5 gene causes progressive autosomal recessive deafness 103 (DFNB103) in Eastern Siberia

    Pshennikova, V. G., Teryutin, F. M., Borisova, T. V., Romanov, G. P., Cherdonova, A. M., Nikanorova, A. A., Morozov, I. V., Bondar, A. A., Solovyev, A. V., Fedorova, S. A. & Barashkov, N. A., 2025, In: Journal of human genetics.

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

  4. 2024

  5. High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect

    Borisova, T. V., Cherdonova, A. M., Pshennikova, V. G., Teryutin, F. M., Morozov, I. V., Bondar, A. A., Baturina, O. A., Kabilov, M. R., Romanov, G. P., Solovyev, A. V., Fedorova, S. A. & Barashkov, N. A., Dec 2024, In: Scientific Reports. 14, 1, 10 p., 15342.

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

  6. Phylogenetic and taxonomic relationships between morphotypes related to Elymus caninus (Poaceae) based on sequence of a nuclear gene GBSS1 (waxy) and sexual hybridization

    Agafonov, A. V., Shabanova, E. V., Emtseva, M. V., Asbaganov, S. V., Morozov, I. V., Bondar, A. A. & Dorogina, O. V., May 2024, In: Journal of Systematics and Evolution. 62, 3, p. 520-533 14 p.

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

  7. 2023

  8. The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)

    Pshennikova, V. G., Teryutin, F. M., Cherdonova, A. M., Borisova, T. V., Solovyev, A. V., Romanov, G. P., Morozov, I. V., Bondar, A. A., Posukh, O. L., Fedorova, S. A. & Barashkov, N. A., 28 Apr 2023, In: Genes. 14, 5, 1001.

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

  9. 2021

  10. Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia)

    Danilchenko, V. Y., Zytsar, M. V., Maslova, E. A., Bady-Khoo, M. S., Barashkov, N. A., Morozov, I. V., Bondar, A. A. & Posukh, O. L., Dec 2021, In: Diagnostics. 11, 12, 2378.

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

  11. Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

    Barashkov, N. A., Konovalov, F. A., Borisova, T. V., Teryutin, F. M., Solovyev, A. V., Pshennikova, V. G., Sapojnikova, N. V., Vychuzhina, L. S., Romanov, G. P., Gotovtsev, N. N., Morozov, I. V., Bondar, A. A., Platonov, F. A., Burtseva, T. E., Khusnutdinova, E. K., Posukh, O. L. & Fedorova, S. A., Jun 2021, In: European journal of human genetics. 29, 6, p. 965-976 12 p.

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

  12. 2020

  13. Mutational spectrum of the SLC26A4 gene and its contribution to the etiology of hearing loss in the indigenous peoples of Southern Siberia (Russia)

    Danilchenko, V. Y., Zytsar, M. V., Bady-Khoo, M. S., Maslova, E. A., Bondar, A. A., Morozov, I. V., Barashkov, N. A. & Posukh, O. L., 1 Dec 2020, In: European journal of human genetics. 28, Suppl 1, p. 810-811 2 p., P02.14.

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

  14. Genetic legacy of cultures indigenous to the Northeast Asian coast in mitochondrial genomes of nearly extinct maritime tribes

    Dryomov, S. V., Starikovskaya, E. B., Nazhmidenova, A. M., Morozov, I. V. & Sukernik, R. I., 13 Jul 2020, In: BMC Evolutionary Biology. 20, 1, 8 p., 83.

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

  15. High rates of three common GJB2 mutations c.516g>c, c.-23+1g>a, c.235delc in deaf patients from southern siberia are due to the founder effect

    Zytsar, M. V., Bady-Khoo, M. S., Danilchenko, V. Y., Maslova, E. A., Barashkov, N. A., Morozov, I. V., Bondar, A. A. & Posukh, O. L., 1 Jul 2020, In: Genes. 11, 7, p. 1-17 17 p., 833.

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

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