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Page 1
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. Pshennikova VG, et al. Among authors: romanov gp. ScientificWorldJournal. 2019 Mar 20;2019:5198931. doi: 10.1155/2019/5198931. eCollection 2019. ScientificWorldJournal. 2019. PMID: 31015822 Free PMC article.
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).
Barashkov NA, Pshennikova VG, Posukh OL, Teryutin FM, Solovyev AV, Klarov LA, Romanov GP, Gotovtsev NN, Kozhevnikov AA, Kirillina EV, Sidorova OG, Vasilyevа LM, Fedotova EE, Morozov IV, Bondar AA, Solovyevа NA, Kononova SK, Rafailov AM, Sazonov NN, Alekseev AN, Tomsky MI, Dzhemileva LU, Khusnutdinova EK, Fedorova SA. Barashkov NA, et al. Among authors: romanov gp. PLoS One. 2016 May 25;11(5):e0156300. doi: 10.1371/journal.pone.0156300. eCollection 2016. PLoS One. 2016. PMID: 27224056 Free PMC article.
Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations.
Solovyev AV, Dzhemileva LU, Posukh OL, Barashkov NA, Bady-Khoo MS, Lobov SL, Popova NY, Romanov GP, Sazonov NN, Bondar AA, Morozov IV, Tomsky MI, Fedorova SA, Khusnutdinova EK. Solovyev AV, et al. Among authors: romanov gp. J Community Genet. 2017 Jul;8(3):167-171. doi: 10.1007/s12687-017-0299-3. Epub 2017 Mar 21. J Community Genet. 2017. PMID: 28324246 Free PMC article.
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. Barashkov NA, et al. Among authors: romanov gp. Int J Pediatr Otorhinolaryngol. 2018 Jan;104:94-97. doi: 10.1016/j.ijporl.2017.11.001. Epub 2017 Nov 6. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29287890
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. Barashkov NA, et al. Among authors: romanov gp. Int J Circumpolar Health. 2019 Dec;78(1):1630219. doi: 10.1080/22423982.2019.1630219. Int J Circumpolar Health. 2019. PMID: 31213145 Free PMC article.
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. Solovyev AV, et al. Among authors: romanov gp. Bull Exp Biol Med. 2019 Jul;167(3):380-383. doi: 10.1007/s10517-019-04531-y. Epub 2019 Jul 26. Bull Exp Biol Med. 2019. PMID: 31346875
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. Nikanorova AA, et al. Among authors: romanov gp. Int J Environ Res Public Health. 2020 Mar 12;17(6):1854. doi: 10.3390/ijerph17061854. Int J Environ Res Public Health. 2020. PMID: 32178438 Free PMC article.
The genetic legacy of legendary and historical Siberian chieftains.
Zvénigorosky V, Duchesne S, Romanova L, Gérard P, Petit C, Petit M, Alexeev A, Melnichuk O, Gonzalez A, Fausser JL, Solovyev A, Romanov G, Barashkov N, Fedorova S, Ludes B, Crubézy E, Keyser C. Zvénigorosky V, et al. Commun Biol. 2020 Oct 16;3(1):581. doi: 10.1038/s42003-020-01307-3. Commun Biol. 2020. PMID: 33067556 Free PMC article.
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. Romanov GP, et al. PLoS One. 2020 Nov 30;15(11):e0242219. doi: 10.1371/journal.pone.0242219. eCollection 2020. PLoS One. 2020. PMID: 33253245 Free PMC article.
18 results