1. 2024
  2. 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 journalArticlepeer-review

  3. 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 journalArticlepeer-review

  4. 2023
  5. 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 journalArticlepeer-review

  6. 2021
  7. 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 journalArticlepeer-review

  8. 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 journalArticlepeer-review

  9. 2020
  10. 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 journalMeeting Abstractpeer-review

  11. 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 journalArticlepeer-review

  12. 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 journalArticlepeer-review

  13. 2019
  14. Assessment of the phenylketonuria (PKU)-associated mutation p.R155H biochemical manifestations by mass spectrometry-based blood metabolite profiling

    Baturina, O. A., Chernonosov, A. A., Koval, V. V. & Morozov, I. V., 16 Aug 2019, In: Acta Naturae. 11, 2, p. 42-46 5 p.

    Research output: Contribution to journalArticlepeer-review

  15. Bacterial Communities in Areas of Oil and Methane Seeps in Pelagic of Lake Baikal

    Zakharenko, A. S., Galachyants, Y. P., Morozov, I. V., Shubenkova, O. V., Morozov, A. A., Ivanov, V. G., Pimenov, N. V., Krasnopeev, A. Y. & Zemskaya, T. I., 15 Aug 2019, In: Microbial Ecology. 78, 2, p. 269-285 17 p.

    Research output: Contribution to journalArticlepeer-review

  16. Experimental transformation of organic matter by the microbial community from the bottom sediments of Akademichesky Ridge (Lake Baikal)

    Pavlova, O. N., Bukin, S. V., Kostyreva, E., Moskvin, V. I., Manakov, A. Y., Morozov, I. V., Galachyants, Y. P., Khabuev, A. V. & Zemskaya, T. I., Aug 2019, In: Russian Geology and Geophysics. 60, 8, p. 926-937 12 p.

    Research output: Contribution to journalArticlepeer-review

  17. Waardenburg syndrome in the Sakha Republic (Eastern Siberia, Russia): mutation analyses of genes PAX3, MITF, SOX10 and SNAI2

    Барашков, Н., Борисова, У., Романов, Г., Соловьев, А., Пшенникова, В., Терютин, Ф., Бондарь, А., Морозов, И. В., Джемилева, Л., Хуснутдинова, Э., Посух, О. Л. & Федорова, С., 1 Jul 2019, In: European journal of human genetics. 26, p. 852 2 p., E-P02.25.

    Research output: Contribution to journalConference articlepeer-review

  18. Allelic diversity of the GJB2 gene in deaf patients and ethnically matched controls from Turkic-speaking populations of South Siberia

    Zytsar, M. V., Bady-Khoo, M. S., Maslova, E. A., Danilchenko, V. Y., Barashkov, N. A., Morozov, I. V., Bondar, A. A. & Posukh, O. L., Jul 2019, In: European journal of human genetics. 27, p. 894-895 2 p.

    Research output: Contribution to journalMeeting Abstractpeer-review

  19. Unique mutational spectrum of the GJB2 gene and its pathogenic contribution to deafness in tuvinians (Southern siberia, russia): A high prevalence of rare variant c.516G>C (p.trp172Cys)

    Posukh, O. L., Zytsar, M. V., Bady-Khoo, M. S., Danilchenko, V. Y., Maslova, E. A., Barashkov, N. A., Bondar, A. A., Morozov, I. V., Maximov, V. N. & Voevoda, M. I., 5 Jun 2019, In: Genes. 10, 6, 17 p., 429.

    Research output: Contribution to journalArticlepeer-review

  20. The effect of 16S rRNA region choice on bacterial community metabarcoding results

    Букин, Ю., Галачьянц, Ю., Морозов, И. В., Букин, С., Захаренко, А. & Земская, Т., 5 Feb 2019, In: Scientific Data. 6, p. 190007 14 p., 190007.

    Research output: Contribution to journalArticlepeer-review

  21. A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the MITF gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia)

    Barashkov, N. A., Romanov, G. P., Borisova, U. P., Solovyev, A. V., Pshennikova, V. G., Teryutin, F. M., Bondar, A. A., Morozov, I. V., Khusnutdinova, E. K., Posukh, O. L., Burtseva, T. E., Odland, J. Ø. & Fedorova, S. A., 1 Jan 2019, In: International Journal of Circumpolar Health. 78, 1, p. 1630219 1630219.

    Research output: Contribution to journalArticlepeer-review

  22. Comparison of Predictive in Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A)

    Pshennikova, V. G., Barashkov, N. A., Romanov, G. P., Teryutin, F. M., Solov'ev, A. V., Gotovtsev, N. N., Nikanorova, A. A., Nakhodkin, S. S., Sazonov, N. N., Morozov, I. V., Bondar, A. A., Dzhemileva, L. U., Khusnutdinova, E. K., Posukh, O. L. & Fedorova, S. A., 1 Jan 2019, In: Scientific World Journal. 2019, p. 5198931 5198931.

    Research output: Contribution to journalArticlepeer-review

  23. Genome constitution and differentiation of subgenomes in Siberian and Far Eastern endemic species of the genus Elymus (Poaceae) according to the sequencing of the nuclear gene waxy

    Agafonov, A. V., Asbaganov, S. V., Shabanova, E. V., Morozov, I. V. & Bondar, A. A., 1 Jan 2019, In: Вавиловский журнал генетики и селекции. 23, 7, p. 817-826 10 p.

    Research output: Contribution to journalArticlepeer-review

  24. 2018
  25. Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

    Zytsar, M. V., Barashkov, N. A., Bady-Khoo, M. S., Shubina-Olejnik, O. A., Danilenko, N. G., Bondar, A. A., Morozov, I. V., Solovyev, A. V., Danilchenko, V. Y., Maximov, V. N. & Posukh, O. L., 7 Aug 2018, In: BMC Medical Genetics. 19, 1, p. 138 9 p., 138.

    Research output: Contribution to journalArticlepeer-review

  26. Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia)

    Romanov, G. P., Barashkov, N. A., Teryutin, F. M., Lashin, S. A., Solovyev, A. V., Pshennikova, V. G., Bondar, A. A., Morozov, I. V., Sazonov, N. N., Tomsky, M. I., Dzhemileva, L. U., Khusnutdinova, E. K., Posukh, O. L. & Fedorova, S. A., 1 May 2018, In: Russian Journal of Genetics. 54, 5, p. 554-561 8 p.

    Research output: Contribution to journalArticlepeer-review

  27. Diversity of Archaea in Bottom Sediments of the Discharge Areas With Oil- and Gas-Bearing Fluids in Lake Baikal

    Lomakina, A. V., Mamaeva, E. V., Galachyants, Y. P., Petrova, D. P., Pogodaeva, T. V., Shubenkova, O. V., Khabuev, A. V., Morozov, I. V. & Zemskaya, T. I., 2 Jan 2018, In: Geomicrobiology Journal. 35, 1, p. 50-63 14 p.

    Research output: Contribution to journalArticlepeer-review

  28. A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2)

    Barashkov, N. A., Klarov, L. A., Teryutin, F. M., Solovyev, A. V., Pshennikova, V. G., Konnikova, E. E., Romanov, G. P., Tobokhov, A. V., Morozov, I. V., Bondar, A. A., Posukh, O. L., Dzhemileva, L. U., Tomsky, M. I., Khusnutdinova, E. K. & Fedorova, S. A., 1 Jan 2018, In: International Journal of Pediatric Otorhinolaryngology. 104, p. 94-97 4 p.

    Research output: Contribution to journalArticlepeer-review

  29. A novel pathogenic variant c.975G > A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2)

    Barashkov, N. A., Klarov, L. A., Teryutin, F. M., Solovyev, A. V., Pshennikova, V. G., Konnikova, E. E., Romanov, G. P., Tobokhov, A. V., Morozov, I. V., Bondar, A. A., Posukh, O. L., Dzhemileva, L. U., Tomsky, M. I., Khusnutdinova, E. K. & Fedorova, S. A., Jan 2018, In: International Journal of Pediatric Otorhinolaryngology. 104, p. 94-97 4 p.

    Research output: Contribution to journalArticlepeer-review

  30. 2017
  31. Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations

    Solovyev, A. V., Dzhemileva, L. U., Posukh, O. L., Barashkov, N. A., Bady-Khoo, M. S., Lobov, S. L., Popova, N. Y., Romanov, G. P., Sazonov, N. N., Bondar, A. A., Morozov, I. V., Tomsky, M. I., Fedorova, S. A. & Khusnutdinova, E. K., 1 Jul 2017, In: Journal of Community Genetics. 8, 3, p. 167-171 5 p.

    Research output: Contribution to journalArticlepeer-review

  32. 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

ID: 3436381