Alexey N. Meshkov

1, Ostrovityanova Str
Moscow, MOW 117997, Russian Federation

Last Updated: 09/26/2026

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Found 51 publications

Genetic Determinants of Severe Hypertriglyceridemia: Rare Variants in LPL, APOC2, APOA5, GPIHBP1, LMF1, APOE and Polygenic Risk.

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

Insights from GWAS, TWAS, and DEG analysis: CDKN2B-AS1, MAP3K4, and P2RX2-encoded P2X2 receptor identified as potential therapeutic targets for ischemic heart disease in Russian adults and long-living individuals.

Insights from GWAS, TWAS, and DEG analysis: CDKN2B-AS1, MAP3K4, and P2RX2-encoded P2X2 receptor identified as potential therapeutic targets for ischemic heart disease in Russian adults and long-living individuals.

Journal: Frontiers in cardiovascular medicine

Published: March 26, 2026

Cardiomyopathies, heart rhythm and conduction disorders as phenotypic manifestation of genetic variants in large cohort of cardiac patients: results of whole-genome study.

Cardiomyopathies, heart rhythm and conduction disorders as phenotypic manifestation of genetic variants in large cohort of cardiac patients: results of whole-genome study.

Journal: Gene

Published: July 25, 2025

Genetic and Metabolic Factors of Familial Dysbetalipoproteinemia Phenotype: Insights from a Cross-Sectional Study.

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.

On Penetrance Estimation in Family, Clinical, and Population Cohorts.

Journal: Circulation. Genomic and precision medicine

Published: March 28, 2025

Prevalence and penetrance of pathogenic and likely pathogenic LDLR and APOB gene variants linked to familial hypercholesterolemia and increased risk of ischemic heart disease.

Prevalence and penetrance of pathogenic and likely pathogenic LDLR and APOB gene variants linked to familial hypercholesterolemia and increased risk of ischemic heart disease.

Journal: Frontiers in genetics

Published: March 06, 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.

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

Blood Lipid Polygenic Risk Score Development and Application for Atherosclerosis Ultrasound Parameters.

Blood Lipid Polygenic Risk Score Development and Application for Atherosclerosis Ultrasound Parameters.

Journal: Biomedicines

Published: November 21, 2024

Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia.

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.

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

New pathogenic mutation in LMNA gene: Clinical case of familial cardiomyopathy

New pathogenic mutation in LMNA gene: Clinical case of familial cardiomyopathy

Journal: Terapevticheskii arkhiv

Published: September 13, 2024

Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study.

Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study.

Journal: PloS one

Published: July 24, 2024

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Last Updated: 09/26/2026