Marija Zaicenoka
Moscow, MOW 101000, Russian Federation
Last Updated: 09/26/2026
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Found 13 publications
Genetic Determinants of Severe Hypertriglyceridemia: Rare Variants in LPL, APOC2, APOA5, GPIHBP1, LMF1, APOE and Polygenic Risk.
Journal: International journal of molecular sciences
Published: April 27, 2026
Genetic and Metabolic Factors of Familial Dysbetalipoproteinemia Phenotype: Insights from a Cross-Sectional Study.
Journal: International journal of molecular sciences
Published: June 18, 2025
On Penetrance Estimation in Family, Clinical, and Population Cohorts.
Journal: Circulation. Genomic and precision medicine
Published: March 28, 2025
A Novel Bradycardia-Associated Variant in HCN4 as a Candidate Modifier in Type 3 Long QT Syndrome: Case Report and Deep In Silico Analysis.
Journal: Biomedicines
Published: March 03, 2025
Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia.
Journal: International journal of molecular sciences
Published: October 08, 2024
The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome Patients.
Journal: International journal of molecular sciences
Published: September 25, 2024
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.
Journal: International journal of molecular sciences
Published: June 21, 2024
Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot Study.
Journal: International journal of molecular sciences
Published: May 31, 2023
Genetic landscape in Russian patients with familial left ventricular noncompaction.
Journal: Frontiers in cardiovascular medicine
Published: April 14, 2023
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases.
Journal: Journal of personalized medicine
Published: June 06, 2022
Last Updated: 09/26/2026