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Fedor M. Teryutin

Observed names: F M Teryutin, F. M. Teryutin, F.M. Teryutin, Fedor M Teryutin, Fedor Teryutin, T.M. Teryutin
ORCID: 0000-0002-8659-0886
Observed ORCID: 0000-0002-8659-0886
OpenAlex ID: A5003413548
Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect
2011 · Nikolay A Barashkov, Lilya U Dzhemileva, et al. · Journal of Human Genetics · 48
Comparison of PredictiveIn SilicoTools on Missense Variants inGJB2,GJB6, andGJB3Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A)
2019 · Vera G. Pshennikova, Nikolay A. Barashkov, et al. · The Scientific World JOURNAL · 28
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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)
2016 · Nikolay A. Barashkov, Vera G. Pshennikova, et al. · PLoS ONE · 27
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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?
2023 · Alena Nikanorova, Nikolay Barashkov, et al. · International Journal of Molecular Sciences · 18
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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
2011 · L U Dzhemileva, O L Posukh, et al. · Acta Naturae · 16
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene
2021 · Nikolay A. Barashkov, Fedor A. Konovalov, et al. · European Journal of Human Genetics · 14
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Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies
2022 · Leonid A. Klarov, Vera G. Pshennikova, et al. · International Journal of Molecular Sciences · 13
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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
2023 · A. V. Solovyev, T. V. Borisova, et al. · Russian Journal of Genetics · 10
High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect
2024 · Tuyara V. Borisova, Aleksandra M. Cherdonova, et al. · Scientific Reports · 9
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
2023 · Vera G. Pshennikova, Fedor M. Teryutin, et al. · Genes · 8
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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)
2017 · Nikolay A. Barashkov, Leonid A. Klarov, et al. · International Journal of Pediatric Otorhinolaryngology · 8
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia
2021 · Aisen V Solovyev, Alena Kushniarevich, et al. · Human Genetics · 7
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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)
2019 · Nikolay A. Barashkov, Georgii P. Romanov, et al. · International Journal of Circumpolar Health · 7
Age-Related Hearing Impairment (ARHI) Associated with GJB2 Single Mutation IVS1+1G>A in the Yakut Population Isolate in Eastern Siberia
2014 · Nikolay A. Barashkov, Fedor M. Teryutin, et al. · PLoS ONE · 7
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A serological survey of echinococcosis, toxocariasis and trichinellosis among rural inhabitants of Central Yakutia
2019 · Sergey S. Nakhodkin, Vera G. Pshennikova, et al. · International Journal of Circumpolar Health · 5
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Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia)
2018 · G. P. Romanov, N. A. Barashkov, et al. · Russian Journal of Genetics · 5
Genotype–phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26)
2024 · Fedor M. Teryutin, Vera G. Pshennikova, et al. · PLoS ONE · 4
Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population
2022 · Georgii P. Romanov, Anna A. Smirnova, et al. · Biology · 3
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The Russian Old-Settlers in the Arctic Coast of Eastern Siberia: Family Name Diversity in the Context of Their Origin
2021 · Aisen V. Solovyev, Tuyara V. Borisova, et al. · Sustainability · 3
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Clinical, audiological and genealogical analysis of hearing disorders in the Republic of Buryatia
2020 · V.G. Pshennikova, F.M. Teryutin, et al. · Yakut Medical Journal · 3
Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A
2019 · A. V. Solovyev, N. A. Barashkov, et al. · Bulletin of Experimental Biology and Medicine · 3
Analysis of the Mitochondrial Gene Pool Structure of Russian Old-Settlers of the Arctic Coast of Yakutia from the Village of Russkoye Ust’ye
2024 · T. V. Borisova, A. V. Solovyev, et al. · Russian Journal of Genetics · 2
The Spectrum and Frequency of Inner Ear Anomalies in Patients with Congenital Hearing Impairment in Yakutia
2020 · L. A. Klarov, N. A. Barashkov, et al. · Journal of radiology and nuclear medicine · 2
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The Genetic History of the Russian Old Settlers of the Arctic Coast of Yakutia from the Village Russkoye Ust’ye
2023 · A. V. Solovyev, T. V. Borisova, et al. · Генетика · 1
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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
2020 · Georgii P. Romanov, Vera G. Pshennikova, et al. · PLoS ONE · 1
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Works count: 40
Citation count: 254
H-index: 9
I10-index: 8
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