Elizaveta V. Musatova
Moscow, MOW, Russian Federation
Last Updated: 09/26/2026
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Found 10 publications
Base editing in the AUTS2 gene and high-throughput NGS genotyping of clones: a strategy for generating a cellular model.
Journal: Vavilovskii zhurnal genetiki i selektsii
Published: June 14, 2025
Asymptomatic and oligosymptomatic states of dysferlinopathy.
Journal: Journal of neuromuscular diseases
Published: February 20, 2025
Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants.
Journal: Genome medicine
Published: May 04, 2024
Ultrastructural Abnormalities in Induced Pluripotent Stem Cell-Derived Neural Stem Cells and Neurons of Two Cohen Syndrome Patients.
Journal: Cells
Published: October 06, 2023
Genetic screening of an endemic mutation in the DYSF gene in an isolated, mountainous population in the Republic of Dagestan.
Journal: Molecular genetics & genomic medicine
Published: January 23, 2023
Corrigendum to "Generation of two iPSC lines from healthy donor with a heterozygous mutation in the VPS13B gene" [59 (2022) 102648].
Journal: Stem cell research
Published: April 24, 2022
A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing.
Journal: Genes
Published: March 29, 2022
Generation of two iPSC lines from healthy donor with a heterozygous mutation in the VPS13B gene.
Journal: Stem cell research
Published: November 26, 2021
Novel intronic variant in PALB2 gene and effective prevention of Fanconi anemia in family.
Journal: Familial cancer
Published: April 17, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026