Georgii Romanov
Ph.D. reseacher in computational population genetics
Research Interests
About
Publications
Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic)
PLOS ONE / May 25, 2016
Barashkov, N. A., Pshennikova, V. G., Posukh, O. L., Teryutin, F. M., Solovyev, A. V., Klarov, L. A., Romanov, G. P., Gotovtsev, N. N., Kozhevnikov, A. A., Kirillina, E. V., Sidorova, O. G., Vasilyevа, L. M., Fedotova, E. E., Morozov, I. V., Bondar, A. A., Solovyevа, N. A., Kononova, S. K., Rafailov, A. M., Sazonov, N. N., … Fedorova, S. A. (2016). Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic). PLOS ONE, 11(5), e0156300. https://doi.org/10.1371/journal.pone.0156300
Comparison of PredictiveIn SilicoTools on Missense Variants inGJB2,GJB6, andGJB3Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A)
The Scientific World Journal / Mar 20, 2019
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. (2019). Comparison of PredictiveIn SilicoTools on Missense Variants inGJB2,GJB6, andGJB3Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A). The Scientific World Journal, 2019, 1–9. https://doi.org/10.1155/2019/5198931
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene
European Journal of Human Genetics / Mar 25, 2021
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. (2021). Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene. European Journal of Human Genetics, 29(6), 965–976. https://doi.org/10.1038/s41431-021-00833-w
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)
International Journal of Circumpolar Health / Jan 01, 2019
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. (2019). 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). International Journal of Circumpolar Health, 78(1), 1630219. https://doi.org/10.1080/22423982.2019.1630219
The genetic legacy of legendary and historical Siberian chieftains
Communications Biology / Oct 16, 2020
Zvénigorosky, V., Duchesne, S., Romanova, L., Gérard, P., Petit, C., Petit, M., Alexeev, A., Melnichuk, O., Gonzalez, A., Fausser, J.-L., Solovyev, A., Romanov, G., Barashkov, N., Fedorova, S., Ludes, B., Crubézy, E., & Keyser, C. (2020). The genetic legacy of legendary and historical Siberian chieftains. Communications Biology, 3(1). https://doi.org/10.1038/s42003-020-01307-3
The Role of Leptin Levels in Adaptation to Cold Climates
International Journal of Environmental Research and Public Health / Mar 12, 2020
Nikanorova, A. A., Barashkov, N. A., Nakhodkin, S. S., Pshennikova, V. G., Solovyev, A. V., Romanov, G. P., Kuzmina, S. S., Sazonov, N. N., Burtseva, T. E., Odland, J. Ø., & Fedorova, S. A. (2020). The Role of Leptin Levels in Adaptation to Cold Climates. International Journal of Environmental Research and Public Health, 17(6), 1854. https://doi.org/10.3390/ijerph17061854
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)
International Journal of Pediatric Otorhinolaryngology / Jan 01, 2018
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. (2018). 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). International Journal of Pediatric Otorhinolaryngology, 104, 94–97. https://doi.org/10.1016/j.ijporl.2017.11.001
The limitations of kinship determinations using STR data in ill-defined populations
International Journal of Legal Medicine / Apr 21, 2020
Zvénigorosky, V., Sabbagh, A., Gonzalez, A., Fausser, J.-L., Palstra, F., Romanov, G., Solovyev, A., Barashkov, N., Fedorova, S., Crubézy, É., Ludes, B., & Keyser, C. (2020). The limitations of kinship determinations using STR data in ill-defined populations. International Journal of Legal Medicine, 134(6), 1981–1990. https://doi.org/10.1007/s00414-020-02298-w
The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of Siberia
International Journal of Molecular Sciences / Apr 28, 2021
Nikanorova, A. A., Barashkov, N. A., Pshennikova, V. G., Nakhodkin, S. S., Gotovtsev, N. N., Romanov, G. P., Solovyev, A. V., Kuzmina, S. S., Sazonov, N. N., & Fedorova, S. A. (2021). The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of Siberia. International Journal of Molecular Sciences, 22(9), 4657. https://doi.org/10.3390/ijms22094657
Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia)
Russian Journal of Genetics / May 01, 2018
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. (2018). Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia). Russian Journal of Genetics, 54(5), 554–561. https://doi.org/10.1134/s1022795418050071
Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia)
Russian Journal of Genetics / Jun 01, 2017
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. (2017). Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia). Russian Journal of Genetics, 53(6), 688–697. https://doi.org/10.1134/s1022795417030103
Extremely High Carrier Frequency of the GJB2 Splice Site IVS1+1G>A Mutation in Eastern Siberia is Comparable to the Carrier Frequency of the Sickle Cell Anemia in Africa
Journal of Genetics and Genome Research / Oct 31, 2014
Barashkov, N. A. (2014). Extremely High Carrier Frequency of the GJB2 Splice Site IVS1+1G>A Mutation in Eastern Siberia is Comparable to the Carrier Frequency of the Sickle Cell Anemia in Africa. Journal of Genetics and Genome Research, 1(1). https://doi.org/10.23937/2378-3648/1410001
Persistence and Disappearance of Traditional Patrilocality
Sibirica / Mar 01, 2019
Zvénigorosky, V., Nikolaeva, D., Romanov, G., Solovev, A., Barashkov, N., Crubézy, É., Fedorova, S., & Keyser, C. (2019). Persistence and Disappearance of Traditional Patrilocality. Sibirica, 18(1), 53–70. https://doi.org/10.3167/sib.2019.180104
Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations
Journal of Community Genetics / Mar 21, 2017
Solovyev, A. V., Dzhemileva, L. U., Posukh, O. L., Barashkov, N. A., Bady-Khoo, M. S., Lobov, S. L., Popova, N. Yu., Romanov, G. P., Sazonov, N. N., Bondar, A. A., Morozov, I. V., Tomsky, M. I., Fedorova, S. A., & Khusnutdinova, E. K. (2017). Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations. Journal of Community Genetics, 8(3), 167–171. https://doi.org/10.1007/s12687-017-0299-3
Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies
International Journal of Molecular Sciences / Dec 06, 2022
Klarov, L. A., Pshennikova, V. G., Romanov, G. P., Cherdonova, A. M., Solovyev, A. V., Teryutin, F. M., Luginov, N. V., Kotlyarov, P. M., & Barashkov, N. A. (2022). Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. International Journal of Molecular Sciences, 23(23), 15372. https://doi.org/10.3390/ijms232315372
Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A
Bulletin of Experimental Biology and Medicine / Jul 01, 2019
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. (2019). Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A. Bulletin of Experimental Biology and Medicine, 167(3), 380–383. https://doi.org/10.1007/s10517-019-04531-y
Reconstruction of SNP haplotypes with mutation c.-23+1G>A in human gene GJB2 (Chromosome 13) in some populations of Eurasia
Russian Journal of Genetics / Aug 01, 2017
Solovyev, A. V., Barashkov, N. A., Bady-Khoo, M. S., Zytsar, M. V., Posukh, O. L., Romanov, G. P., Rafailov, A. M., Sazonov, N. N., Alexeev, A. N., Dzhemileva, L. U., Khusnutdinova, E. K., & Fedorova, S. A. (2017). Reconstruction of SNP haplotypes with mutation c.-23+1G>A in human gene GJB2 (Chromosome 13) in some populations of Eurasia. Russian Journal of Genetics, 53(8), 936–941. https://doi.org/10.1134/s1022795417080099
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
Russian Journal of Genetics / Sep 01, 2023
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. (2023). 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. Russian Journal of Genetics, 59(9), 949–955. https://doi.org/10.1134/s1022795423090119
Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia
Genes / Sep 08, 2022
Nikanorova, A. A., Barashkov, N. A., Pshennikova, V. G., Gotovtsev, N. N., Romanov, G. P., Solovyev, A. V., Kuzmina, S. S., Sazonov, N. N., & Fedorova, S. A. (2022). Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia. Genes, 13(9), 1612. https://doi.org/10.3390/genes13091612
Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population
Biology / Feb 07, 2022
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. (2022). Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population. Biology, 11(2), 257. https://doi.org/10.3390/biology11020257
The Russian Old-Settlers in the Arctic Coast of Eastern Siberia: Family Name Diversity in the Context of Their Origin
Sustainability / Sep 30, 2021
Solovyev, A. V., Borisova, T. V., Cherdonova, A. M., Romanov, G. P., Teryutin, F. M., Pshennikova, V. G., Gotovtsev, N. N., Vasileva, O. V., Nikitina, S. E., Barashkov, N. A., Alekseev, A. N., & Fedorova, S. A. (2021). The Russian Old-Settlers in the Arctic Coast of Eastern Siberia: Family Name Diversity in the Context of Their Origin. Sustainability, 13(19), 10895. https://doi.org/10.3390/su131910895
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
PLOS ONE / Nov 30, 2020
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. (2020). 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. PLOS ONE, 15(11), e0242219. https://doi.org/10.1371/journal.pone.0242219
Agent-based modelling of genetic deafness propagation under various sociodemographic conditions
Симпозиум «Математическое моделирование и высокопроизводительные вычисления в биоинформатике, биомедицине и биотехнологии» / Aug 01, 2018
Agent-based modelling of genetic deafness propagation under various sociodemographic conditions. (2018). Симпозиум «Математическое Моделирование и Высокопроизводительные Вычисления в Биоинформатике, Биомедицине и Биотехнологии», 78–78. https://doi.org/10.18699/mm-hpc-bbb-2018-70
A local focus of accumulation of the mitochondrial form of hearing loss in Even-Bytantaysky district of Yakutia
Yakut Medical Journal / Jan 01, 2022
Pshennikova, V. G., Teryutin, F. M., Romanov, G. P., Solovyov, A. V., & Barashkov, N. A. (2022). A local focus of accumulation of the mitochondrial form of hearing loss in Even-Bytantaysky district of Yakutia. Yakut Medical Journal, 4, 91–95. https://doi.org/10.25789/ymj.2022.80.24
The impact of the sociodemographic structure of deaf people communities on the prevalence of hereditary hearing loss
Russian Journal of Genetics: Applied Research / Dec 01, 2016
Posukh, O. L., Bady-Khoo, M. S., Zytsar, M. V., Mikhalskaia, V. Yu., Lashin, S. A., Barashkov, N. A., & Romanov, G. P. (2016). The impact of the sociodemographic structure of deaf people communities on the prevalence of hereditary hearing loss. Russian Journal of Genetics: Applied Research, 6(8), 854–863. https://doi.org/10.1134/s2079059716070108
The Spectrum and Frequency of Inner Ear Anomalies in Patients with Congenital Hearing Impairment in Yakutia
Journal of radiology and nuclear medicine / May 17, 2020
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. (2020). The Spectrum and Frequency of Inner Ear Anomalies in Patients with Congenital Hearing Impairment in Yakutia. Journal of Radiology and Nuclear Medicine, 101(2), 90–102. https://doi.org/10.20862/0042-4676-2020-101-2-90-102
ANALYSIS OF LEVEL OF LEPTIN CIRCULATING IN BLOOD IN THE YAKUT POPULATION
Problems Of Biological, Medical And Pharmaceutical Chemistry / May 01, 2020
Nikanorova, A. A., Barashkov, N. A., Nakhodkin, S. S., Pshennikova, V. G., Solovyev, A. V., Romanov, G. P., Kuzmina, S. S., Sazonov, N. N., & Fedorova, S. A. (2020). ANALYSIS OF LEVEL OF LEPTIN CIRCULATING IN BLOOD IN THE YAKUT POPULATION. Problems Of Biological, Medical And Pharmaceutical Chemistry, 18(5). https://doi.org/10.29296/25877313-2020-05-02
Clinical, audiological and genealogical analysis of hearing disorders in the Republic of Buryatia
Yakut Medical Journal / Jan 01, 2020
Pshennikova, V. G., Teryutin, F. M., Barashkov, N. A., Kononova, S. K., Solovyov, A. V., Romanov, G. P., & Fedorova, S. A. (2020). Clinical, audiological and genealogical analysis of hearing disorders in the Republic of Buryatia. Yakut Medical Journal, 4, 44–49. https://doi.org/10.25789/ymj.2020.72.12
A novel nonsense mutation c.1121G>A (p.Trp374*) in the CLIC5 gene is the main cause of the juvenile autosomal recessive form of deafness (DFNB103) in the Arctic regions of Yakutia
Nauchno-prakticheskii zhurnal «Medicinskaia genetika» / Oct 30, 2019
Пшенникова, В. Г., Романов, Г. П., Николаева, Т. М., Терютин, Ф. М., Борисова, Т. В., Комарьков, И. Ф., Антонец, А. В., Соловьев, А. В., Кларов, Л. А., Бондарь, А. А., Морозов, И. В., Посух, О. Л., Хуснутдинова, Э. К., Федорова, С. А., & Барашков, Н. А. (2019). A novel nonsense mutation c.1121G>A (p.Trp374*) in the CLIC5 gene is the main cause of the juvenile autosomal recessive form of deafness (DFNB103) in the Arctic regions of Yakutia. Nauchno-Prakticheskii Zhurnal «Medicinskaia Genetika», 10(), 36–48. https://doi.org/10.25557/2073-7998.2019.10.36-48
Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome
Human Molecular Genetics / Aug 12, 2000
Bondurand, N. (2000). Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome. Human Molecular Genetics, 9(13), 1907–1917. https://doi.org/10.1093/hmg/9.13.1907
The analysis of the resistance of heterozygous carriers of the a-23+1G>A mutation in GJB2 gene to diarrhea
Yakut Medical Journal / Jan 01, 2018
Solovyev, A. V., Barashkov, N. A., Savvinova, K. E., Gotovtsev, N. N., Teryutin, F. M., Pshennikova, V. G., Romanov, G. P., Rafailov, A. M., Sazonov, N. N., Dzhemileva, L. U., Posukh, O. L., Khusnutdinova, E. K., & Fedorova, S. A. (2018). The analysis of the resistance of heterozygous carriers of the a-23+1G>A mutation in GJB2 gene to diarrhea. Yakut Medical Journal, 3, 15–17. https://doi.org/10.25789/ymj.2018.63.04
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
Genes / Apr 28, 2023
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. (2023). The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia). Genes, 14(5), 1001. https://doi.org/10.3390/genes14051001
A Systematic Review and Meta-Analysis of Free Triiodothyronine (FT3) Levels in Humans Depending on Seasonal Air Temperature Changes: Is the Variation in FT3 Levels Related to Nonshivering Thermogenesis?
International Journal of Molecular Sciences / Sep 13, 2023
Nikanorova, A., Barashkov, N., Pshennikova, V., Teryutin, F., Nakhodkin, S., Solovyev, A., Romanov, G., Burtseva, T., & Fedorova, S. (2023). A Systematic Review and Meta-Analysis of Free Triiodothyronine (FT3) Levels in Humans Depending on Seasonal Air Temperature Changes: Is the Variation in FT3 Levels Related to Nonshivering Thermogenesis? International Journal of Molecular Sciences, 24(18), 14052. https://doi.org/10.3390/ijms241814052
The influence of С.189G>A P.(Val66Met) polymorphism of the BDNF gene on serum leptin levels in Yakuts
Therapy / Dec 06, 2021
Nikanorova, N. A. A., Barashkov, B. N. A., Nakhodkin S, N. S. S., Pshennikova, P. V. G., Gotovtsev N, G. N. N., Solovyev, S. A. V., Romanov, R. G. P., Kuzmina, K. S. S., Sazonov, S. N. N., & Fedorova, F. S. A. (2021). The influence of С.189G>A P.(Val66Met) polymorphism of the BDNF gene on serum leptin levels in Yakuts. Therapy, 9_2021, 58–65. https://doi.org/10.18565/therapy.2021.9.58-65
Agent-based modeling of DFNB1A prevalence with regard to intensity of selection pressure in isolated human population: will cochlear implantation increase the cases of hereditary deafness?
Aug 13, 2021
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. (2021). Agent-based modeling of DFNB1A prevalence with regard to intensity of selection pressure in isolated human population: will cochlear implantation increase the cases of hereditary deafness? https://doi.org/10.1101/2021.08.11.21261942
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
Yakut Medical Journal / Jan 01, 2022
Borisova, T. V., Pshennikova, V. G., Teryutin, F. M., Solovyov, A. V., Romanov, G. P., Fedorova, S. A., & Barashkov, N. A. (2022). 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. Yakut Medical Journal, 4, 9–11. https://doi.org/10.25789/ymj.2022.80.02
Postlingual deafness in Eveno-Bytantaysky National District of the Sakha Republic (Yakutia): audiological and clinical-genealogical analysis
Yakut Medical Journal / Jan 01, 2018
Pshennikova, V. G., Teryutin, F. M., Barashkov, N. A., Gotovtsev, N. N., Nikanorova, A. A., Solovyev, A. V., Romanov, G. P., Posukh, O. L., Dzhemileva, L. U., Khusnutdinova, E. K., & Fedorova, S. A. (2018). Postlingual deafness in Eveno-Bytantaysky National District of the Sakha Republic (Yakutia): audiological and clinical-genealogical analysis. Yakut Medical Journal, 4, 47–52. https://doi.org/10.25789/ymj.2018.64.14
Opinion of young people on the potential risk of the birth of deaf child
Yakut Medical Journal / Jan 01, 2018
Cherdonova, A. M., Pshennikova, V. G., Solovyev, A. V., Barashkov, N. A., Rafailov, A. M., Romanov, G. P., Kononova, S. K., & Fedorova, S. A. (2018). Opinion of young people on the potential risk of the birth of deaf child. Yakut Medical Journal, 4, 62–65. https://doi.org/10.25789/ymj.2018.64.18
Impact of socio-demographic structure of the deaf people communities in prevalence of hereditary hearing loss
Vavilov Journal of Genetics and Breeding / Mar 11, 2016
Posukh, O. L., Bady-Khoo, M. S., Zytsar, M. V., Mikhalskaia, V. Yu., Lashin, S. A., Barashkov, N. A., & Romanov, G. P. (2016). Impact of socio-demographic structure of the deaf people communities in prevalence of hereditary hearing loss. Vavilov Journal of Genetics and Breeding, 20(1), 7–15. https://doi.org/10.18699/vj16/098
Some bioethical issues of molecular genetic diagnosis of autosomal recessive deafness of 1 A type common in the Yakut population
Yakut Medical Journal / Jan 01, 2018
Kononova, S. K., Barashkov, N. A., Pshennikova, V. G., Soloviev, A. V., Cherdonova, A. M., Nikanorova, A. A., Romanov, G. P., Khusnutdinova, E. K., Fedorova, S. A., & Teryutin, F. M. (2018). Some bioethical issues of molecular genetic diagnosis of autosomal recessive deafness of 1 A type common in the Yakut population. Yakut Medical Journal, 2, 79–82. https://doi.org/10.25789/ymj.2018.62.23
Analysis of hearing thresholds in patients with hearing impairments associated with mutations of the GJB2 gene (Sh26) in Buryatia
Yakut Medical Journal / Jan 01, 2022
Teryutin, F. M., Pshennikova, V. G., Romanov, G. P., Solovyov, A. V., Klarov, L. A., Lebedeva, N. A., & Barashkov, N. A. (2022). Analysis of hearing thresholds in patients with hearing impairments associated with mutations of the GJB2 gene (Sh26) in Buryatia. Yakut Medical Journal, 4, 36–39. https://doi.org/10.25789/ymj.2022.80.10
CHOLESTEROL AND RISK OF ATHEROSCLEROSIS IN RURAL INDIGENOUS POPULATION OF REPUBLIC OF SAKHA (YAKUTIA)
Ekologiya cheloveka (Human Ecology) / Apr 15, 2014
Klimova, T. M., Fedorova, V. I., Baltakhinova, M. E., & Krivoshapkin, V. G. (2014). CHOLESTEROL AND RISK OF ATHEROSCLEROSIS IN RURAL INDIGENOUS POPULATION OF REPUBLIC OF SAKHA (YAKUTIA). Ekologiya Cheloveka (Human Ecology), 21(4), 22–27. https://doi.org/10.17816/humeco17245
Gesamtverzeichnis des deutschsprachigen Schrifttums (GV) 1700 -1910: 142. Stud - Sv. Part 1
Stud - Sv / Dec 31, 1985
Gesamtverzeichnis des deutschsprachigen Schrifttums (GV) 1700 -1910: 142. Stud - Sv. Part 1. (1985). In Stud - Sv (pp. 1–172). De Gruyter Saur. https://doi.org/10.1515/9783111580647-001
Education
Ph. D., Genetics, Computational Biology / November, 2022
North-Eastern Federal University
Graduate, Biochemistry / May, 2018
North-Eastern Federal University
Masters, Biology / June, 2012
Experience
North-Eastern Federal University
Researcher / January, 2020 — Present
Junior Researcher / April, 2017 — December, 2019
Engineer / October, 2013 — April, 2017
Yakut Science Centre of Complex Medical Problems
Research Scientist / April, 2015 — October, 2022
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