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Suggested authors matching "AUTH:Barashkov NA" with an ORCID

Nikolay A Barashkov
Yakut Science Centre of Complex Medical Problems
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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).
Teryutin FM, Pshennikova VG, Solovyev AV, Romanov GP, Fedorova SA, Barashkov NA
PLoS One, 19(10):e0309439, 22 Oct 2024
Cited by: 0 articles | PMID: 39436953 | PMCID: PMC11495561
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Associations of the AVPR1A RS1 Microsatellite Locus with the Level of Hormones of the Anterior Pituitary Gland and Personality Traits.
Nakhodkin SS, Barashkov NA, Kazantseva AV, Pshennikova VG, Nikanorova AA, Khusnutdinova EK, Fedorova SA
Biochem Genet, 28 Sep 2024
Cited by: 0 articles | PMID: 39340576
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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 TV, Cherdonova AM, Pshennikova VG, Teryutin FM, Morozov IV, Bondar AA, Baturina OA, Kabilov MR, Romanov GP, Solovyev AV, Fedorova SA, Barashkov NA
Sci Rep, 14(1):15342, 03 Jul 2024
Cited by: 0 articles | PMID: 38961196 | PMCID: PMC11222474
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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?
Nikanorova AA, Barashkov NA, Pshennikova VG, Teryutin FM, Nakhodkin SS, Solovyev AV, Romanov GP, Burtseva TE, Fedorova SA
Int J Mol Sci, 24(18):14052, 13 Sep 2023
Cited by: 0 articles | PMID: 37762355 | PMCID: PMC10531421
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The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).
Pshennikova VG, Teryutin FM, Cherdonova AM, Borisova TV, Solovyev AV, Romanov GP, Morozov IV, Bondar AA, Posukh OL, Fedorova SA, Barashkov NA
Genes (Basel), 14(5):1001, 28 Apr 2023
Cited by: 3 articles | PMID: 37239361 | PMCID: PMC10218609
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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
Klarov LA, Pshennikova VG, Romanov GP, Cherdonova AM, Solovyev AV, Teryutin FM, Luginov NV, Kotlyarov PM, Barashkov NA
Int J Mol Sci, 23(23):15372, 06 Dec 2022
Cited by: 3 articles | PMID: 36499699 | PMCID: PMC9740095
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Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia.
Nikanorova AA, Barashkov NA, Pshennikova VG, Gotovtsev NN, Romanov GP, Solovyev AV, Kuzmina SS, Sazonov NN, Fedorova SA
Genes (Basel), 13(9):1612, 08 Sep 2022
Cited by: 1 article | PMID: 36140780 | PMCID: PMC9498418
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A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.
Solovyev AV, Kushniarevich A, Bliznetz E, Bady-Khoo M, Lalayants MR, Markova TG, Minárik G, Kádasi L, Metspalu E, Pshennikova VG, Teryutin FM, Khusnutdinova EK, Poliakov A, Metspalu M, Posukh OL, Barashkov NA, Fedorova SA
Hum Genet, 141(3-4):697-707, 27 Nov 2021
Cited by: 3 articles | PMID: 34839402
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Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population.
Romanov GP, Smirnova AA, Zamyatin VI, Mukhin AM, Kazantsev FV, Pshennikova VG, Teryutin FM, Solovyev AV, Fedorova SA, Posukh OL, Lashin SA, Barashkov NA
Biology (Basel), 11(2):257, 07 Feb 2022
Cited by: 2 articles | PMID: 35205123 | PMCID: PMC8869167
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Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).
Danilchenko VY, Zytsar MV, Maslova EA, Bady-Khoo MS, Barashkov NA, Morozov IV, Bondar AA, Posukh OL
Diagnostics (Basel), 11(12):2378, 17 Dec 2021
Cited by: 10 articles | PMID: 34943614 | PMCID: PMC8699871
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The attitude of young people in the city of Yakutsk to DNA-testing.
Kononova S, Vinokurova D, Barashkov NA, Semenova A, Sofronova S, Oksana S, Tatiana D, Struchkov V, Burtseva T, Romanova A, Fedorova S
Int J Circumpolar Health, 80(1):1973697, 01 Dec 2021
Cited by: 1 article | PMID: 34544327 | PMCID: PMC8462860
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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?
Romanov GP, Smirnova AA, Zamyatin VI, Mukhin AM, Kazantsev FV, Pshennikova VG, Teryutin FM, Solovyev AV, Fedorova SA, Posukh OL, Lashin SA, Barashkov NA
medRxiv, 13 Aug 2021
Cited by: 0 articles | PPR: PPR382484
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A Common Founder Effect of the Splice Site Variant c.-23+1G>A in GJB2 Gene Causing Autosomal Recessive Deafness 1A (DFNB1A) in Eurasia
Solovyev AV, Kushniarevich A, Bliznetz E, Bady-Khoo M, Lalayants MR, Markova TG, Minárik G, Kádasi L, Metspalu E, Pshennikova VG, Teryutin FM, Alekseev AN, Khusnutdinova EK, Poliakov A, Мetspalu M, Posukh OL, Barashkov NA, Fedorova SA
Research Square, 07 Jul 2021
Cited by: 0 articles | PPR: PPR366558
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Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.
Barashkov NA, Konovalov FA, Borisova TV, Teryutin FM, Solovyev AV, Pshennikova VG, Sapojnikova NV, Vychuzhina LS, Romanov GP, Gotovtsev NN, Morozov IV, Bondar AA, Platonov FA, Burtseva TE, Khusnutdinova EK, Posukh OL, Fedorova SA
Eur J Hum Genet, 29(6):965-976, 25 Mar 2021
Cited by: 7 articles | PMID: 33767456 | PMCID: PMC8187664
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The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of Siberia.
Nikanorova AA, Barashkov NA, Pshennikova VG, Nakhodkin SS, Gotovtsev NN, Romanov GP, Solovyev AV, Kuzmina SS, Sazonov NN, Fedorova SA
Int J Mol Sci, 22(9):4657, 28 Apr 2021
Cited by: 4 articles | PMID: 33925025 | PMCID: PMC8124869
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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.
Romanov GP, Pshennikova VG, Lashin SA, Solovyev AV, Teryutin FM, Cherdonova AM, Borisova TV, Sazonov NN, Khusnutdinova EK, Posukh OL, Fedorova SA, Barashkov NA
PLoS One, 15(11):e0242219, 30 Nov 2020
Cited by: 0 articles | PMID: 33253245 | PMCID: PMC7703874
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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 MV, Bady-Khoo MS, Danilchenko VY, Maslova EA, Barashkov NA, Morozov IV, Bondar AA, Posukh OL
Genes (Basel), 11(7):E833, 21 Jul 2020
Cited by: 8 articles | PMID: 32708339 | PMCID: PMC7397271
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A serological survey of echinococcosis, toxocariasis and trichinellosis among rural inhabitants of Central Yakutia.
Nakhodkin SS, Pshennikova VG, Dyachkovskaya PS, Barashkov NA, Nikanorova AA, Teryutin FM, Melnichuk OA, Crubézy E, Fedorova SA, Magnaval JF
Int J Circumpolar Health, 78(1):1603550, 01 Dec 2019
Cited by: 1 article | PMID: 31046654 | PMCID: PMC6507814
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The Role of Leptin Levels in Adaptation to Cold Climates.
Nikanorova AA, Barashkov NA, Nakhodkin SS, Pshennikova VG, Solovyev AV, Romanov GP, Kuzmina SS, Sazonov NN, Burtseva TE, Odland JØ, Fedorova SA
Int J Environ Res Public Health, 17(6):E1854, 12 Mar 2020
Cited by: 4 articles | PMID: 32178438 | PMCID: PMC7143756
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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).
Barashkov NA, Romanov GP, Borisova UP, Solovyev AV, Pshennikova VG, Teryutin FM, Bondar AA, Morozov IV, Khusnutdinova EK, Posukh OL, Burtseva TE, Odland JØ, Fedorova SA
Int J Circumpolar Health, 78(1):1630219, 01 Dec 2019
Cited by: 4 articles | PMID: 31213145 | PMCID: PMC6586136
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Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A.
Solovyev AV, Barashkov NA, Teryutin FM, Pshennikova VG, Romanov GP, Rafailov AM, Sazonov NN, Dzhemileva LU, Tomsky MI, Posukh OL, Khusnutdinova EK, Fedorova SA
Bull Exp Biol Med, 167(3):380-383, 26 Jul 2019
Cited by: 3 articles | PMID: 31346875
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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 OL, Zytsar MV, Bady-Khoo MS, Danilchenko VY, Maslova EA, Barashkov NA, Bondar AA, Morozov IV, Maximov VN, Voevoda MI
Genes (Basel), 10(6):E429, 05 Jun 2019
Cited by: 8 articles | PMID: 31195736 | PMCID: PMC6627114
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Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A).
Pshennikova VG, Barashkov NA, Romanov GP, Teryutin FM, Solov'ev AV, Gotovtsev NN, Nikanorova AA, Nakhodkin SS, Sazonov NN, Morozov IV, Bondar AA, Dzhemileva LU, Khusnutdinova EK, Posukh OL, Fedorova SA
ScientificWorldJournal, 2019:5198931, 20 Mar 2019
Cited by: 19 articles | PMID: 31015822 | PMCID: PMC6446107
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Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
Zytsar MV, Barashkov NA, Bady-Khoo MS, Shubina-Olejnik OA, Danilenko NG, Bondar AA, Morozov IV, Solovyev AV, Danilchenko VY, Maximov VN, Posukh OL
BMC Med Genet, 19(1):138, 07 Aug 2018
Cited by: 10 articles | PMID: 30086704 | PMCID: PMC6081885
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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).
Barashkov NA, Klarov LA, Teryutin FM, Solovyev AV, Pshennikova VG, Konnikova EE, Romanov GP, Tobokhov AV, Morozov IV, Bondar AA, Posukh OL, Dzhemileva LU, Tomsky MI, Khusnutdinova EK, Fedorova SA
Int J Pediatr Otorhinolaryngol, 104:94-97, 06 Nov 2017
Cited by: 7 articles | PMID: 29287890
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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).

Associations of the AVPR1A RS1 Microsatellite Locus with the Level of Hormones of the Anterior Pituitary Gland and Personality Traits.

High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect.

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?

The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).

Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies

Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia.

A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.

Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population.

Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).

The attitude of young people in the city of Yakutsk to DNA-testing.

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?

A Common Founder Effect of the Splice Site Variant c.-23+1G>A in GJB2 Gene Causing Autosomal Recessive Deafness 1A (DFNB1A) in Eurasia

Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.

The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of Siberia.

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.

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.

A serological survey of echinococcosis, toxocariasis and trichinellosis among rural inhabitants of Central Yakutia.

The Role of Leptin Levels in Adaptation to Cold Climates.

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).

Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A.

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).

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

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

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).

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