Nikolay Barashkov
21PUBLICATIONS
40CO-AUTHORS

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Publications (21)
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|Sep 16, 2025
The c.644 G > A p.(Trp215*) founder variant in the CLIC5 gene causes progressive autosomal recessive deafness 103 (DFNB103) in Eastern Siberia.Vera G Pshennikova, Fedor M Teryutin, Tuyara V Borisova
|Oct 22, 2024
Genotype-phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26).Fedor M Teryutin, Vera G Pshennikova, Aisen V Solovyev
|Sep 28, 2023
A Systematic Review and Meta-Analysis of Free Triiodothyronine (FT3) Levels in Humans Depending on Seasonal Air Temperature Changes: Is the Variation in FT3 Levels Related to Nonshivering Thermogenesis?Alena A Nikanorova, Nikolay A Barashkov, Vera G Pshennikova
|May 27, 2023
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).Vera G Pshennikova, Fedor M Teryutin, Alexandra M Cherdonova
|Dec 11, 2022
Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) AnomaliesLeonid A Klarov, Vera G Pshennikova, Georgii P Romanov
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Frequent Collaborators
10 joint publications
Georgii Romanov
9 joint publications
Sardana Fedorova
8 joint publications
Vera G Pshennikova
7 joint publications
Alena A Nikanorova
7 joint publications
Alexander A Bondar
7 joint publications
Olga L Posukh
4 joint publications
Igor V Morozov
3 joint publications
Fedor M Teryutin
2 joint publications
Elza K Khusnutdinova
2 joint publications
Sergey A Lashin