1. 2019
  2. Single nucleotide polymorphism rs110861313 in the intergenic region of chromosome 23 is associated with the development of leukosis in the Russian Black Pied cattle

    Aitnazarov, R. B., Ignatieva, E. V., Agarkova, T. A., Dvoeglazov, N. G., Osipova, N. A., Khramtsov, V. V. & Yudin, N. S., 1 Aug 2019, In: Вавиловский журнал генетики и селекции. 23, 8, p. 999-1005 7 p.

    Research output: Contribution to journalArticlepeer-review

  3. Hyperlipidemia in patients with Mody2 and Mody in Russia

    Shakhtshneider, E., Ivanoshchuk, D., Ovsyannikova, A., Mikhailova, S., Rymar, O., Ragino, Y. & Voevoda, M., Aug 2019, In: Atherosclerosis. 287, p. E131-E131 1 p.

    Research output: Contribution to journalMeeting Abstractpeer-review

  4. Computer genomics research at the bioinformatics conference series in Novosibirsk

    Orlov, Y. L., Galieva, E. R. & Melerzanov, A. V., 11 Jul 2019, In: BMC Genomics. 20, Suppl 7, p. 537 4 p., 537.

    Research output: Contribution to journalArticlepeer-review

  5. ESEEM Reveals Bound Substrate Histidine in the ABC Transporter HisQMP 2

    Isaev, N., Heuveling, J., Ivanisenko, N., Schneider, E. & Steinhoff, H. J., 1 Jul 2019, In: Applied Magnetic Resonance. 50, 7, p. 883-893 11 p.

    Research output: Contribution to journalArticlepeer-review

  6. 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

  7. 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

  8. Insight into genetic and social aspects of modern communities of deaf people in Siberia for forecasting the prevalence of hereditary deafness

    Posukh, O. L., Bady-Khoo, M. S., Romanov, G. P., Barashkov, N. A., Smirnova, A. A., Zytsar, M. V., Maslova, E. A., Danilchenko, V. Y., Posukh, O. V. & Lashin, S. A., Jul 2019, In: European journal of human genetics. 27, p. 1038-1038 1 p.

    Research output: Contribution to journalMeeting Abstractpeer-review

  9. Opinions of young hearing people living in the Sakha Republic (Russia) about potential risk of the birth of deaf child

    Cherdonova, A. M., Solovyev, A. V., Pshennikova, V. G., Barashkov, N. A., Romanov, G. P., Nikanorova, A. A., Kononova, S. K., Posukh, O. L., Fedorova, S. A. & Teryutin, F. M., Jul 2019, In: European journal of human genetics. 27, p. 717-717 1 p.

    Research output: Contribution to journalMeeting Abstractpeer-review

  10. Progressive post-lingual sensorineural hearing loss with unknown etiology in subarctic part of Russia (Sakha Republic)

    Barashkov, N. A., Romanov, G. P., Teryutin, F. M., Pshennikova, V. G., Solovyev, A. V., Gotovtsev, N. N., Nikanorova, A. A., Dzhemileva, L. U., Khusnutdinova, E. K., Posukh, O. L. & Fedorova, S. A., Jul 2019, In: European journal of human genetics. 27, p. 897-897 1 p.

    Research output: Contribution to journalMeeting Abstractpeer-review

  11. 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

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