Associated Papers
Association of HindIII Polymorphism of the Lipoprotein Lipase (LPL) Gene (rs320) and Plasma Metabolic Parameters in a Nigerian Population.
Faleti JO et al.
Biochemical Genetics, 2026
Contemporary Management of Familial and Multifactorial Chylomicronemia Syndromes in Italy: Insights From the National LIPIGEN Registry.
D'Erasmo L et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2025
The Ongoing Utility of lipoprotein lipase activity in diagnosing familial Chylomicronemia Syndrome.
Fariña G et al.
Biochemistry and Biophysics Reports, 2025
Uncovering rare somatic variants in olfactory receptor genes in Pakistani triple-negative breast cancer patients.
Shawana S et al.
Bmc Cancer, 2025
Adult genomic medicine: lessons from a multisite study of 2700 patients.
Bakur K et al.
Genome Medicine, 2025
Gene-Diet Interactions in High-Density Lipoprotein Cholesterol-Related Polymorphisms and Cardiovascular Disease Risk: Insights from the Korean Genome and Epidemiology Study.
Lee JH et al.
Nutrients, 2025
Genetic Polymorphisms and Genetic Risk Scores Contribute to the Risk of Coronary Artery Disease (CAD) in a North Indian Population.
Mastana S et al.
International Journal of Molecular Sciences, 2024
Elevated plasma triglycerides increase the risk of psoriasis: a cohort and Mendelian randomization study.
Greve AM et al.
The British Journal of Dermatology, 2024
Association between APOA5 polymorphisms and susceptibility to metabolic syndrome: a systematic review and meta-analysis.
Mozafari S et al.
Bmc Genomics, 2024
Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry.
Jiang L et al.
Journal of Lipid Research, 2024
Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry.
Jiang L et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Genetic variation in apolipoprotein A-V in hypertriglyceridemia.
Perera SD et al.
Current Opinion in Lipidology, 2024
Understanding Hypertriglyceridemia: Integrating Genetic Insights.
Alves M et al.
Genes, 2024
Competing Genetic Traits and Their Influence on LDL Cholesterol Concentration in Familial Hypercholesterolemia.
Song C et al.
Jacc. Case Reports, 2024
Human apolipoprotein E glycosylation and sialylation: from structure to function.
Moon HJ et al.
Frontiers in Molecular Neuroscience, 2024
Genome-wide analysis identifies novel loci influencing plasma apolipoprotein E concentration and Alzheimer's disease risk.
Aslam MM et al.
Molecular Psychiatry, 2023
Association of S19W polymorphism in APOA5 gene and serum lipid levels in patients with type 2 diabetic nephropathy.
Mirabedini S et al.
Hormone Molecular Biology and Clinical Investigation, 2023
Lipid-Related Genetic Variants for Personalized Dietary Interventions: A Systematic Review.
Rivera-Íñiguez I et al.
Molecular Nutrition & Food Research, 2023
Effect of genetic variations in drug transporters, metabolizing enzyme and regulatory genes on the development of HIV-associated lipodystrophy.
Shyamveer et al.
The Journal of Gene Medicine, 2023
Screening program for familial hyperchylomicronemia syndrome detection: Experience of a university health system.
Masson W et al.
Archives of Endocrinology and Metabolism, 2023
Comprehensive in-silico analysis of deleterious SNPs in APOC2 and APOA5 and their differential expression in cancer and cardiovascular diseases conditions.
Deng H et al.
Genomics, 2023
Evinacumab in severe hypertriglyceridemia with or without lipoprotein lipase pathway mutations: a phase 2 randomized trial.
Rosenson RS et al.
Nature Medicine, 2023
Investigation of associations between apolipoprotein A5 and C3 gene polymorphisms with plasma triglyceride and lipid levels.
Taşkin E et al.
Revista Da Associacao Medica Brasileira (1992), 2023
Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency.
Rodríguez-Gutiérrez PG et al.
International Journal of Molecular Sciences, 2022
Sensitization of Patient-Derived Colorectal Cancer Organoids to Photon and Proton Radiation by Targeting DNA Damage Response Mechanisms.
Pape K et al.
Cancers, 2022
Apolipoprotein A5 gene polymorphism (rs662799) and cardiovascular disease in end-stage kidney disease patients.
Jacob J et al.
Bmc Nephrology, 2022
Identification of New Copy Number Variation and the Evaluation of a CNV Detection Tool for NGS Panel Data in Polish Familial Hypercholesterolemia Patients.
Rutkowska L et al.
Genes, 2022
Metabolic syndrome and underlying genetic determinants-A systematic review.
Rana S et al.
Journal of Diabetes and Metabolic Disorders, 2022
Apolipoprotein A-V is a potential target for treating coronary artery disease: evidence from genetic and metabolomic analyses.
Ibi D et al.
Journal of Lipid Research, 2022
Genetics of Familial Combined Hyperlipidemia (FCHL) Disorder: An Update.
Taghizadeh E et al.
Biochemical Genetics, 2022
Genetics and regulation of HDL metabolism.
Kardassis D et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids, 2022
Genetic polymorphisms associated with obesity in the Arab world: a systematic review.
Younes S et al.
International Journal of Obesity (2005), 2021
Exome-Wide Search for Genes Associated With Central Nervous System Inflammatory Demyelinating Diseases Following CHIKV Infection: The Tip of the Iceberg.
Alves-Leon SV et al.
Frontiers in Genetics, 2021
Genetic Regulatory Networks of Apolipoproteins and Associated Medical Risks.
Basavaraju P et al.
Frontiers in Cardiovascular Medicine, 2021
Triglycerides and remnant cholesterol associated with risk of aortic valve stenosis: Mendelian randomization in the Copenhagen General Population Study.
Kaltoft M et al.
European Heart Journal, 2020
Population History and Gene Divergence in Native Mexicans Inferred from 76 Human Exomes.
Ávila-Arcos MC et al.
Molecular Biology and Evolution, 2020
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Hu Y et al.
Plos Genetics, 2020
Association of single nucleotide polymorphisms with dyslipidemia in antiretroviral exposed HIV patients in a Ghanaian population: A case-control study.
Obirikorang C et al.
Plos One, 2020
Genetic polymorphisms of superoxide dismutase 1 are associated with the serum lipid profiles of Han Chinese adults in a sexually dimorphic manner.
Xu P et al.
Plos One, 2020
Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis.
Morjane I et al.
Cardiology Research and Practice, 2020
Pharmacogenetics of statins treatment: Efficacy and safety.
Guan ZW et al.
Journal of Clinical Pharmacy and Therapeutics, 2019
Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia Syndromes.
D'Erasmo L et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2019