Svetlana I. Tarnovskaya
Saint Petersburg, SPE 194223, Russian Federation
Last Updated: 09/26/2026
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Found 25 publications
Role of TRPM4 ion channel in pediatric arrhythmic syndromes.
Journal: World journal of clinical pediatrics
Published: September 15, 2025
Predicting the Damaging Potential of Uncharacterized KCNQ1 and KCNE1 Variants.
Journal: International journal of molecular sciences
Published: May 31, 2025
The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis.
Journal: Journal of cardiovascular development and disease
Published: May 15, 2024
In silico analysis of TRPM4 variants of unknown clinical significance.
Journal: PloS one
Published: July 18, 2023
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.
Journal: Orphanet journal of rare diseases
Published: March 02, 2022
Family-specific analysis of variant pathogenicity prediction tools.
Journal: NAR genomics and bioinformatics
Published: December 19, 2019
Predicting novel disease mutations in the cardiac sodium channel.
Journal: Biochemical and biophysical research communications
Published: October 17, 2019
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.
Journal: Human mutation
Published: December 22, 2017
MutHTP: mutations in human transmembrane proteins.
Journal: Bioinformatics (Oxford, England)
Published: November 18, 2017
Last Updated: 09/26/2026