Get started
Author

Alexandra M. Cherdonova

Observed names: A. M. Cherdonova, A.M. Cherdonova, А.М. ЧЕРДОНОВА, А.М. Чердонова
Observed institution: North-Eastern Federal University
ORCID: 0000-0002-4168-9516
Observed ORCID: 0000-0002-4168-9516
OpenAlex ID: A5071665712
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
PDF
Analysis of Y-chromosome lines of Russian old-residents in the village Russkoye Ustye
2022 · T.V. Borisova, A.V. Solovyov, et al. · Yakut Medical Journal · 6
Some bioethical issues of molecular genetic diagnosis of autosomal recessive deafness of 1 A type common in the Yakut population
2018 · S.K. Kononova, N.A. Barashkov, et al. · Yakut Medical Journal · 1
Analysis of the Origin of mtDNA Lineages Carrying the Pathogenic m.1555A>G Variant in the MT-RNR1 Gene, Causing Mitochondrial Form of Deafness in Eastern Siberia
2026 · T. V. Borisova, A. M. Cherdonova, et al. · Russian Journal of Genetics
The c.644 G > A p.(Trp215*) founder variant in the CLIC5 gene causes progressive autosomal recessive deafness 103 (DFNB103) in Eastern Siberia
2025 · Vera G. Pshennikova, Fedor M. Teryutin, et al. · Journal of Human Genetics
Analysis of the Spectrum of the mtDNA Haplogroups in Patients with Hearing Loss Carrying the Likely Pathogenic Ultra-Rare m.1494C>T Variant in the MT-RNR1 Gene
2025 · T. V. Borisova, A. M. Cherdonova, et al. · Russian Journal of Genetics
Atypical cases of hearing loss in patients with the mitochondrial variant m.1555A>G of the MT-RNR1 gene in the Republic of Buryatia
2025 · F. M. Teryutin, T. V. Borisova, et al. · Yakut Medical Journal
PDF
A rare variant of p.7636C>T p.(Gln2546*) of the MYO15A gene in two patients from Buryatia with sensorineural deafness
2024 · A.M. Cherdonova, T.V. Borisova, et al. · Yakut Medical Journal
Analysis of pathogenic variants of the mtDNA MT-TS1 gene in patients with hearing loss in Buryatia
2023 · T.V. Borisova, A.M. Cherdonova, et al. · Yakut Medical Journal
Analysis of the c.757A>G p.(Ile253Val) variant of the SLC26A4 gene in GJB2-negative patients with hearing loss in Yakutia
2023 · V.G. Pshennikova, F.M. Teryutin, et al. · Yakut Medical Journal
Analysis of the frequency of heterozygous carriage of six mutations of autosomal recessive diseases among Russian old-timers of Yakutia
2022 · N.A. Barashkov, A.M. Cherdonova, et al. · Yakut Medical Journal
A novel mutation in the COL4A5 gene in the Yakut family with Alport syndrome
2022 · A.M. Cherdonova, N.A. Barashkov, et al. · Yakut Medical Journal
Mutation analysis of the SLC26A4 gene in patients in Yakutia with inner ear abnormalities: IP-I, IP-II (Mondini) and/or EVA
2021 · Л.А. Кларов, К.Ю. Николаева, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
PDF
Medical and social aspects of molecular genetic studies of hereditary deafness in the Sakha Rrepublic (Yakutia)
2018 · С.К. КОНОНОВА, Н.А. БАРАШКОВ, et al. · Vestnik of North-Eastern Federal University Medical Sciences
Opinion of young people on the potential risk of the birth of deaf child
2018 · A.M. Cherdonova, V.G. Pshennikova, et al. · Yakut Medical Journal
Works count: 15
Citation count: 15
H-index: 2
I10-index:
Year
Topic
Type