| 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 … NA Barashkov, VG Pshennikova, OL Posukh, FM Teryutin, AV Solovyev, ... PLoS One 11 (5), e0156300, 2016 | 40 | 2016 |
| Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A) VG Pshennikova, NA Barashkov, GP Romanov, FM Teryutin, AV Solov’ev, ... The Scientific World Journal 2019, 2019 | 37 | 2019 |
| Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene NA Barashkov, FA Konovalov, TV Borisova, FM Teryutin, AV Solovyev, ... European Journal of Human Genetics 29 (6), 965-976, 2021 | 13 | 2021 |
| The genetic legacy of legendary and historical Siberian chieftains V Zvénigorosky, S Duchesne, L Romanova, P Gérard, C Petit, M Petit, ... Communications Biology 3 (1), 1-9, 2020 | 10 | 2020 |
| The role of leptin levels in adaptation to cold climates AA Nikanorova, NA Barashkov, SS Nakhodkin, VG Pshennikova, ... International Journal of Environmental Research and Public Health 17 (6), 1854, 2020 | 10 | 2020 |
| 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 … NA Barashkov, GP Romanov, UP Borisova, AV Solovyev, ... International journal of circumpolar health 78 (1), 1630219, 2019 | 10 | 2019 |
| The limitations of kinship determinations using STR data in ill-defined populations V Zvénigorosky, A Sabbagh, A Gonzalez, JL Fausser, F Palstra, ... International Journal of Legal Medicine 134, 1981-1990, 2020 | 9 | 2020 |
| 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) NA Barashkov, LA Klarov, FM Teryutin, AV Solovyev, VG Pshennikova, ... International Journal of Pediatric Otorhinolaryngology 104, 94-97, 2018 | 9 | 2018 |
| The role of nonshivering thermogenesis genes on leptin levels regulation in residents of the coldest region of Siberia AA Nikanorova, NA Barashkov, VG Pshennikova, SS Nakhodkin, ... International Journal of Molecular Sciences 22 (9), 4657, 2021 | 8 | 2021 |
| Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia) GP Romanov, NA Barashkov, FM Teryutin, SA Lashin, AV Solovyev, ... Russian Journal of Genetics 54, 554-561, 2018 | 7 | 2018 |
| Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia) VG Pshennikova, NA Barashkov, AV Solovyev, GP Romanov, ... Russian Journal of Genetics 53, 688-697, 2017 | 7 | 2017 |
| 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 NA Barashkov, AV Solovyev, FM Teryutin, VG Pshennikova, LA Klarov, ... J Genet Genome Res 1 (001), 2014 | 7 | 2014 |
| Persistence and disappearance of traditional patrilocality: matrimonial strategies and postnuptial residence patterns in two eastern Siberian communities of the twenty-first … V Zvénigorosky, D Nikolaeva, G Romanov, A Solovev, N Barashkov, ... Sibirica 18 (1), 53-70, 2019 | 5 | 2019 |
| Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations AV Solovyev, LU Dzhemileva, OL Posukh, NA Barashkov, MS Bady-Khoo, ... Journal of Community Genetics 8, 167-171, 2017 | 5 | 2017 |
| Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies LA Klarov, VG Pshennikova, GP Romanov, AM Cherdonova, AV Solovyev, ... International Journal of Molecular Sciences 23 (23), 15372, 2022 | 4 | 2022 |
| Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A AV Solovyev, NA Barashkov, FM Teryutin, VG Pshennikova, GP Romanov, ... Bulletin of Experimental Biology and Medicine 167, 380-383, 2019 | 4 | 2019 |
| Reconstruction of SNP haplotypes with mutation c.-23+1G>A in human gene GJB2 (Chromosome 13) in some populations of Eurasia AV Solovyev, NA Barashkov, MS Bady-Khoo, MV Zytsar, OL Posukh, ... Russian Journal of Genetics 53, 936-941, 2017 | 4 | 2017 |
| 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 AV Solovyev, TV Borisova, GP Romanov, FM Teryutin, VG Pshennikova, ... Russian Journal of Genetics 59 (9), 949-955, 2023 | 3 | 2023 |
| The impact of the sociodemographic structure of deaf people communities on the prevalence of hereditary hearing loss OL Posukh, MS Bady-Khoo, MV Zytsar, VY Mikhalskaia, SA Lashin, ... Russian Journal of Genetics: Applied Research 6, 854-863, 2016 | 3 | 2016 |
| Comparison of Predictive In Silico Tools on Missense Variants in GJB2 VG Pshennikova, NA Barashkov, GP Romanov, FM Teryutin, AV Solov’ev, ... GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness A 1, 0 | 3 | |
Lilya U DzhemilevaN. D. Zelinsky Institute of Organic Chemistry在 ioc.ac.ru 的电子邮件经过验证
