Author

T.V. Borisova

Observed name: T. V. Borisova

Institution: North-Eastern Federal University

Observed institution: North-Eastern Federal University

ORCID: 0000-0002-5019-067X

Observed ORCID: 0000-0002-5019-067X

OpenAlex ID: A5034407829

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

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

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

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 Gene

2025 · T.V. Borisova · Генетика / Russian Journal of Genetics

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

Estimation of the mutation age c.1621C>T p.(Gln541*) in the FYCO1 gene responsible for the development of autosomal recessive congenital cataract in the Yakut population

2022 · T.V. Borisova, V.G. Pshennikova, 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

Works count: 10

Citation count: 6

H-index: 1

I10-index: