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Biomedicines|January 8, 2025
Blood Lipid Polygenic Risk Score Development and Application for Atherosclerosis Ultrasound ParametersMarija Zaicenoka, Alexandra I Ershova, Anna V Kiseleva, et al.
International Journal of Molecular Sciences|August 14, 2025
Genetic and Metabolic Factors of Familial Dysbetalipoproteinemia Phenotype: Insights from a Cross-Sectional StudyAnastasia V Blokhina, Alexandra I Ershova, Anna V Kiseleva, et al.
Plos One|July 19, 2017
The prevalence of familial hypercholesterolemia in the West Siberian region of the Russian Federation: A substudy of the ESSE-RFAlexandra I Ershova, Alexey N Meshkov, Stepan S Bazhan, et al.
Plos One|December 20, 2024
Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative studyAnastasia V Blokhina, Alexandra I Ershova, Anna V Kiseleva, et al.
Biopreservation and Biobanking|October 15, 2020
National Association of Biobanks and Biobanking Specialists: New Community for Promoting Biobanking Ideas and Projects in RussiaSergey V Anisimov, Alexey N Meshkov, Andrey S Glotov, et al.
Journal of Personalized Medicine|September 25, 2020
A Data-Driven Approach to Carrier Screening for Common Recessive DiseasesAnna V Kiseleva, Marina V Klimushina, Evgeniia A Sotnikova, et al.
International Journal of Molecular Sciences|December 17, 2024
Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial DysbetalipoproteinemiaAnastasia V Blokhina, Alexandra I Ershova, Anna V Kiseleva, et al.
International Journal of Molecular Sciences|June 26, 2026
Genetic Determinants of Severe Hypertriglyceridemia: Rare Variants in LPL, APOC2, APOA5, GPIHBP1, LMF1, APOE and Polygenic RiskAnastasia V Blokhina, Alexey N Meshkov, Alexandra I Ershova, et al.
Frontiers in Genetics|October 25, 2021
Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo RegionVasily E Ramensky, Alexandra I Ershova, Marija Zaicenoka, et al.
Human Mutation|March 26, 2019
Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defectAndrey V Marakhonov, Andreas Brodehl, Roman P Myasnikov, et al.
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