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Page 1
Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia.
Fedorova SA, Reidla M, Metspalu E, Metspalu M, Rootsi S, Tambets K, Trofimova N, Zhadanov SI, Hooshiar Kashani B, Olivieri A, Voevoda MI, Osipova LP, Platonov FA, Tomsky MI, Khusnutdinova EK, Torroni A, Villems R. Fedorova SA, et al. Among authors: tomsky mi. BMC Evol Biol. 2013 Jun 19;13:127. doi: 10.1186/1471-2148-13-127. BMC Evol Biol. 2013. PMID: 23782551 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: tomsky mi. 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
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: tomsky mi. 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: tomsky mi. 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: tomsky mi. 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
Key indicators of obstetric and neonatal care in the Republic of Sakha (Yakutia).
Burtseva TE, Odland JØ, Douglas NI, Grigoreva AN, Pavlova TY, Chichahov DA, Afanasieva LN, Baisheva NS, Rad YG, Tomsky MI, Postoev VA. Burtseva TE, et al. Among authors: tomsky mi. Int J Circumpolar Health. 2016 Dec 13;75:33956. doi: 10.3402/ijch.v75.33956. eCollection 2016. Int J Circumpolar Health. 2016. PMID: 27974143 Free PMC article.