Nikolay A Barashkov (Nikolay Barashkov)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 23

Top Venues

International journal of molecular sciences

Genes

International journal of circumpolar health

TheScientificWorldJournal

Yakut Science Centre of Complex Medical Problems

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Yakut Science Centre of Complex Medical Problems May 01 2015

Russia

Head of Laboratory of Molecular Genetics :: Department of Molecular Genetics

Publications

Alena A Nikanorova, Nikolay A Barashkov, Vera G Pshennikova, Fedor M Teryutin, Sergey S Nakhodkin, Aisen V Solovyev, Georgii P Romanov, Tatiana E Burtseva, Sardana A Fedorova
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? International journal of molecular sciences 24 (18) (2023)
Vera G Pshennikova, Fedor M Teryutin, Alexandra M Cherdonova, Tuyara V Borisova, Aisen V Solovyev, Georgii P Romanov, Igor V Morozov, Alexander A Bondar, Olga L Posukh, Sardana A Fedorova, Nikolay A Barashkov
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia). Genes 14 (5) (2023)
Leonid A Klarov, Vera G Pshennikova, Georgii P Romanov, Aleksandra M Cherdonova, Aisen V Solovyev, Fedor M Teryutin, Nikolay V Luginov, Petr M Kotlyarov, Nikolay A Barashkov
Analysis of SLC26A4,&nbsp;FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. International journal of molecular sciences 23 (23) (2022)
Leonid A Klarov, Vera G Pshennikova, Georgii P Romanov, Aleksandra M Cherdonova, Aisen V Solovyev, Fedor M Teryutin, Nikolay V Luginov, Petr M Kotlyarov, Nikolay A Barashkov
Analysis of SLC26A4,&nbsp;FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. International journal of molecular sciences 23 (23) (2022)
Leonid A Klarov, Vera G Pshennikova, Georgii P Romanov, Aleksandra M Cherdonova, Aisen V Solovyev, Fedor M Teryutin, Nikolay V Luginov, Petr M Kotlyarov, Nikolay A Barashkov
Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies International journal of molecular sciences 23 (23) (2022)
Georgii P Romanov, Anna A Smirnova, Vladimir I Zamyatin, Aleksei M Mukhin, Fedor V Kazantsev, Vera G Pshennikova, Fedor M Teryutin, Aisen V Solovyev, Sardana A Fedorova, Olga L Posukh, Sergey A Lashin, Nikolay A Barashkov
Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population. Biology 11 (2) (2022)
Alena A Nikanorova, Nikolay A Barashkov, Vera G Pshennikova, Nyurgun N Gotovtsev, Georgii P Romanov, Aisen V Solovyev, Sargylana S Kuzmina, Nikolay N Sazonov, Sardana A Fedorova
Relationships between Uncoupling Protein Genes UCP1 , UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia. Genes 13 (9) (2022)
Leonid A Klarov, Vera G Pshennikova, Georgii P Romanov, Aleksandra M Cherdonova, Aisen V Solovyev, Fedor M Teryutin, Nikolay V Luginov, Petr M Kotlyarov, Nikolay A Barashkov
Analysis of SLC26A4,&nbsp;FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. International journal of molecular sciences 23 (23) (2022)
Leonid A Klarov, Vera G Pshennikova, Georgii P Romanov, Aleksandra M Cherdonova, Aisen V Solovyev, Fedor M Teryutin, Nikolay V Luginov, Petr M Kotlyarov, Nikolay A Barashkov
Analysis of SLC26A4,&nbsp;FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. International journal of molecular sciences 23 (23) (2022)
Leonid A Klarov, Vera G Pshennikova, Georgii P Romanov, Aleksandra M Cherdonova, Aisen V Solovyev, Fedor M Teryutin, Nikolay V Luginov, Petr M Kotlyarov, Nikolay A Barashkov
Analysis of SLC26A4,&nbsp;FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. International journal of molecular sciences 23 (23) (2022)
Sardana Kononova, Dekabrina Vinokurova, Nikolay A Barashkov, Ariadna Semenova, Sargylana Sofronova, Sidorova Oksana, Davydova Tatiana, Valentin Struchkov, Tatiana Burtseva, Anna Romanova, Sardana A Fedorova
The attitude of young people in the city of Yakutsk to DNA-testing. International journal of circumpolar health 80 (1) (2021)
Valeriia Yu Danilchenko, Marina V Zytsar, Ekaterina A Maslova, Marita S Bady-Khoo, Nikolay A Barashkov, Igor V Morozov, Alexander A Bondar, Olga L Posukh
Different Rates of the SLC26A4 -Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia). Diagnostics (Basel, Switzerland) 11 (12) (2021)
Alena A Nikanorova, Nikolay A Barashkov, Vera G Pshennikova, Sergey S Nakhodkin, Nyurgun N Gotovtsev, Georgii P Romanov, Aisen V Solovyev, Sargylana S Kuzmina, Nikolay N Sazonov, Sardana A Fedorova
The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of Siberia. International journal of molecular sciences 22 (9) (2021)
Aisen V Solovyev, Alena Kushniarevich, Elena A Bliznetz, Marita Bady-Khoo, Maria R Lalayants, Tatiana G Markova, Gabriel Minárik, L'udevít Kádasi, Ene Metspalu, Vera G Pshennikova, Fedor M Teryutin, Elza K Khusnutdinova, Alexander Poliakov, Mait Metspalu, Olga L Posukh, Nikolay A Barashkov, Sardana A Fedorova
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia. Human genetics (2021)
Nikolay A Barashkov, Fedor A Konovalov, Tuyara V Borisova, Fedor M Teryutin, Aisen V Solovyev, Vera G Pshennikova, Nadejda V Sapojnikova, Lyubov S Vychuzhina, Georgii P Romanov, Nyurgun N Gotovtsev, Igor V Morozov, Alexander A Bondar, Fedor A Platonov, Tatiana E Burtseva, Elza K Khusnutdinova, Olga L Posukh, Sardana A Fedorova
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene. European journal of human genetics : EJHG 29 (6) (2021)
Sergey S Nakhodkin, Vera G Pshennikova, Paraskovia S Dyachkovskaya, Nikolay A Barashkov, Alena A Nikanorova, Fedor M Teryutin, Olga A Melnichuk, Eric Crubézy, Sardana A Fedorova, Jean-François Magnaval
A serological survey of echinococcosis, toxocariasis and trichinellosis among rural inhabitants of Central Yakutia. International journal of circumpolar health 78 (1) (2020)
Alena A Nikanorova, Nikolay A Barashkov, Sergey S Nakhodkin, Vera G Pshennikova, Aisen V Solovyev, Georgii P Romanov, Sargylana S Kuzmina, Nikolay N Sazonov, Tatyana E Burtseva, Jon Øyvind Odland, Sardana A Fedorova
The Role of Leptin Levels in Adaptation to Cold Climates. International journal of environmental research and public health 17 (6) (2020)
Georgii P Romanov, Vera G Pshennikova, Sergey A Lashin, Aisen V Solovyev, Fedor M Teryutin, Aleksandra M Cherdonova, Tuyara V Borisova, Nikolay N Sazonov, Elza K Khusnutdinova, Olga L Posukh, Sardana A Fedorova, Nikolay A Barashkov
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. PloS one 15 (11) (2020)
Vincent Zvénigorosky, Sylvie Duchesne, Liubomira Romanova, Patrice Gérard, Christiane Petit, Michel Petit, Anatoly Alexeev, Olga A Melnichuk, Angéla Gonzalez, Jean-Luc Fausser, Aisen Solovyev, Georgii P Romanov, Nikolay A Barashkov, Sardana A Fedorova, Bertrand Ludes, Eric Crubézy, Christine Keyser
The genetic legacy of legendary and historical Siberian chieftains. Communications biology 3 (1) (2020)
Nikolay A Barashkov, Georgii P Romanov, Uigulaana P Borisova, Aisen V Solovyev, Vera G Pshennikova, Fedor M Teryutin, Alexander A Bondar, Igor V Morozov, Elza K Khusnutdinova, Olga L Posukh, Tatiana E Burtseva, Jon Øyvind Odland, Sardana A Fedorova
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). International journal of circumpolar health 78 (1) (2020)
Marina V Zytsar, Marita S Bady-Khoo, Valeriia Yu Danilchenko, Ekaterina A Maslova, Nikolay A Barashkov, Igor V Morozov, Alexander A Bondar, Olga L Posukh
High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect. Genes 11 (7) (2020)
Olga L Posukh, Marina V Zytsar, Marita S Bady-Khoo, Valeria Yu Danilchenko, Ekaterina A Maslova, Nikolay A Barashkov, Alexander A Bondar, Igor V Morozov, Vladimir N Maximov, Michael I Voevoda
Unique Mutational Spectrum of the GJB2 Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys). Genes 10 (6) (2019)
Vera G Pshennikova, Nikolay A Barashkov, Georgii P Romanov, Fedor M Teryutin, Aisen V Solov'ev, Nyurgun N Gotovtsev, Alena A Nikanorova, Sergey S Nakhodkin, Nikolay N Sazonov, Igor V Morozov, Alexander A Bondar, Lilya U Dzhemileva, Elza K Khusnutdinova, Olga L Posukh, Sardana A Fedorova
Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A). TheScientificWorldJournal 2019 (2019)

Nikolay A Barashkov.css-eqlu8i{font-size:small;padding-left:4px;} (Nikolay Barashkov)

Publication Activity (10 Years)

Top Topics

Top Venues

Nikolay A Barashkov (Nikolay Barashkov)