Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A
Solovyev, A. V., Barashkov, N. A., Teryutin, F. M., Pshennikova, V. G., Romanov, G. P., Rafailov, A. M., Sazonov, N. N., Dzhemileva, L. U., Tomsky, M. I., Posukh, O. L., Khusnutdinova, E. K., Fedorova, S. A.
Published in Bulletin of experimental biology and medicine (01.07.2019)
Published in Bulletin of experimental biology and medicine (01.07.2019)
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The Spectrum and Frequency of Inner Ear Anomalies in Patients with Congenital Hearing Impairment in Yakutia
Klarov, L. A., Barashkov, N. A., Teryutin, F. M., Romanov, G. P., Popov, M. M., Solov’ev, A. V., Luginov, N. V., Tobokhov, A. V., Kotlyarov, P. M.
Published in Vestnik rentgenologii i radiologii (17.05.2020)
Published in Vestnik rentgenologii i radiologii (17.05.2020)
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The audiological analysis in the patients homozygous for the c.-23+1G>A mutation in the GJB2 gene presenting with the loss of hearing in Yakutiya
Teryutin, F M, Barashkov, N A, Kunel'skaya, N L, Pshennikova, V G, Solov'ev, A V
Published in Vestnik otorinolaringologii (2016)
Published in Vestnik otorinolaringologii (2016)
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The impact of the sociodemographic structure of deaf people communities on the prevalence of hereditary hearing loss
Posukh, O. L., Bady-Khoo, M. S., Zytsar, M. V., Mikhalskaia, V. Yu, Lashin, S. A., Barashkov, N. A., Romanov, G. P.
Published in Russian journal of genetics. Applied research (01.12.2016)
Published in Russian journal of genetics. Applied research (01.12.2016)
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Impact of socio-demographic structure of the deaf people communities in prevalence of hereditary hearing loss
O. L. Posukh, M. S. Bady-Khoo, M. V. Zytsar, V. Yu. Mikhalskaia, S. A. Lashin, N. A. Barashkov, G. P. Romanov
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (11.03.2016)
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (11.03.2016)
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Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia
Dzhemileva, L U, Posukh, O L, Barashkov, N A, Fedorova, S A, Teryutin, F M, Akhmetova, V L, Khidiyatova, I M, Khusainova, R I, Lobov, S L, Khusnutdinova, E K
Published in Actanaturae (01.07.2011)
Published in Actanaturae (01.07.2011)
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Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia
Dzhemileva, L U, Posukh, O L, Tazetdinov, A M, Barashkov, N A, Zhuravskiĭ, S G, Ponidelko, S N, Markova, T G, Tadinova, V N, Fedorova, S A, Maksimova, N R, Khusnutdinova, E K
Published in Genetika (01.07.2009)
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Published in Genetika (01.07.2009)
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Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia)
Barashkov, N A, Dzhemileva, L U, Fedorova, S A, Maksimova, N R, Khusnutdinova, E K
Published in Vestnik otorinolaringologii (2008)
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Published in Vestnik otorinolaringologii (2008)
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Analysis of mitochondrial 12S rRNA and tRNASer(UCN) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia
Dzhemilova, L. U., Posukh, O. L., Tazetdinov, A. M., Barashkov, N. A., Zhuravskii, S. A., Ponidelko, S. N., Markova, T. G., Tadinova, V. N., Fedorova, S. A., Maksimova, N. R., Khusnutdinova, E. K.
Published in Russian journal of genetics (01.07.2009)
Published in Russian journal of genetics (01.07.2009)
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Cochlear implantation in a child with congenital sensorineural deafness due to 35 DELG mutation in GJB2 (connexin 26) gene
Teriutin, F M, Barashkov, N A, Dzhemileva, L U, Posukh, O L, Fedotova, E E, Gurinova, E E, Fedorova, S A, Tavartkiladze, G A, Khusnutdinova, E K
Published in Vestnik otorinolaringologii (2009)
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Published in Vestnik otorinolaringologii (2009)
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Genetic History of Russian Old-Settlers of the Arctic Coast of Yakutia from the Settlement of Russkoe Ust’ye Inferred from Y Chromosome Data and Genome-Wide Analysis
Solovyev, A. V., Borisova, T. V., Romanov, G. P., Teryutin, F. M., Pshennikova, V. G., Nikitina, S. E., Alekseev, A. N., Barashkov, N. A., Fedorova, S. A.
Published in Russian journal of genetics (01.09.2023)
Published in Russian journal of genetics (01.09.2023)
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Estimation of the mutation age c.1621C>T p.(Gln541) in the FYCO1 gene responsible for the development of autosomal recessive congenital cataract in the Yakut population
Borisova, T.V., Pshennikova, V.G., Teryutin, F.M., Solovyov, A.V., Romanov, G.P., Fedorova, S.A., Barashkov, N.A.
Published in Yakut Medical Journal (2022)
Published in Yakut Medical Journal (2022)
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Association of polymorphic variant rs1800849 of the UCP3 gene with deficit and excess of body weight in the Yakut population
Nikanorova, A.A., Barashkov, N.A., Pshennikova, V.G., Gotovtsev, N.N., Romanov, G.P., Solovyov, A.V., Fedorova, S.A.
Published in Yakut Medical Journal (2022)
Published in Yakut Medical Journal (2022)
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Analysis of Y-chromosome lines of Russian old-residents in the village Russkoye Ustye
Borisova, T.V., Solovyov, A.V., Cherdonova, A.M., Romanov, G.P., Teryutin, F.M., Pshennikova, V.G., Gotovtsev, N.N., Barashkov, N.A., Alekseev, A.N., Fedorova, S.A.
Published in Yakut Medical Journal (2022)
Published in Yakut Medical Journal (2022)
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