Nikita A. Kolesnikov
Tomsk, TOM, Russian Federation
Last Updated: 09/26/2026
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Found 13 publications
A novel homozygous variant in the ATP7B gene in a patient with Wilson's disease: a case report.
Journal: Frontiers in medicine
Published: March 11, 2026
From North Asia to South America: Tracing the longest human migration through genomic sequencing.
Journal: Science (New York, N.Y.)
Published: May 15, 2025
Case Report: A Novel Homozygous Variant of the CTSK Gene in Rare Pycnodysostosis.
Journal: International journal of molecular sciences
Published: October 04, 2024
Traces of Paleolithic expansion in the Nivkh gene pool based on data on autosomal SNP and Y chromosome polymorphism.
Journal: Vavilovskii zhurnal genetiki i selektsii
Published: April 03, 2024
A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication.
Journal: Frontiers in genetics
Published: October 31, 2023
Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI.
Journal: International journal of molecular sciences
Published: February 22, 2023
Blocks identical by descent in the genomes of the indigenous population of Siberia demonstrate genetic links between populations.
Journal: Vavilovskii zhurnal genetiki i selektsii
Published: October 21, 2022
Relationship of the gene pool of the Khants with the peoples of Western Siberia, Cis-Urals and the Altai-Sayan Region according to the data on the polymorphism of autosomic locus and the Y-chromosome.
Journal: Vavilovskii zhurnal genetiki i selektsii
Published: October 14, 2022
Structure and origin of Tuvan gene pool according to autosome SNP and Y-chromosome haplogroups.
Journal: Vavilovskii zhurnal genetiki i selektsii
Published: October 13, 2022
Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene.
Journal: Stem cell research
Published: September 09, 2021
NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss.
Journal: Journal of assisted reproduction and genetics
Published: April 19, 2021
Structural Variability, Expression Profile, and Pharmacogenetic Properties of TMPRSS2 Gene as a Potential Target for COVID-19 Therapy.
Journal: Genes
Published: November 16, 2020
Last Updated: 09/26/2026