Nailya M. Galeeva

Moscow, MOW, Russian Federation

Last Updated: 09/26/2026

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Found 8 publications

Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas.

Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas.

Journal: Frontiers in genetics
Published: May 20, 2024

The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study.

The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study.

Journal: Human mutation
Published: June 09, 2023

Spectrum of Genes for Non-GJB2-Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel.

Spectrum of Genes for Non-GJB2-Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel.

Journal: International journal of molecular sciences
Published: October 31, 2022

Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.

Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.

Journal: Journal of personalized medicine
Published: September 28, 2022

Clinical and genetic characterization of three Russian patients with pycnodysostosis due to pathogenic variants in the CTSK gene.

Clinical and genetic characterization of three Russian patients with pycnodysostosis due to pathogenic variants in the CTSK gene.

Journal: Molecular genetics & genomic medicine
Published: November 16, 2021

Early audiological phenotype in patients with mutations in the USH2A gene.

Early audiological phenotype in patients with mutations in the USH2A gene.

Journal: International journal of pediatric otorhinolaryngology
Published: October 18, 2021

Ehlers-Danlos syndrome kyphoscoliotic type 2 caused by mutations in the FKBP14 gene: an analysis of five cases.

Ehlers-Danlos syndrome kyphoscoliotic type 2 caused by mutations in the FKBP14 gene: an analysis of five cases.

Journal: F1000Research
Published: June 15, 2021

Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population.

Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population.

Journal: International journal of pediatric otorhinolaryngology
Published: June 17, 2020
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Last Updated: 09/26/2026