Varaico: Literature-Extracted Genetic Variants

Gene:ANGPTL4
Variant:p.E40K
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ANGPTL4

NM_139314.3:p.E40K

Associated Papers

Angiopoietin-like protein inhibitors: Promising agents for the treatment of familial hypercholesterolemia and atherogenic dyslipidemia.

Vahdat-Lasemi F et al.

Atherosclerosis, 2025

Evaluating the Cardiometabolic Efficacy and Safety of Lipoprotein Lipase Pathway Targets in Combination With Approved Lipid-Lowering Targets: A Drug Target Mendelian Randomization Study.

Gagnon E et al.

Circulation. Genomic and Precision Medicine, 2025

Identifying novel drug targets for calcific aortic valve disease through Mendelian randomization.

Xu D et al.

Atherosclerosis, 2025

Exome wide association study for blood lipids in 1,158,017 individuals from diverse populations.

Koyama S et al.

Medrxiv : the Preprint Server for Health Sciences, 2024

Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery disease.

Lee PC et al.

Iscience, 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

Impact of loss-of-function in angiopoietin-like 4 on the human phenome.

Gagnon E et al.

Atherosclerosis, 2024

Drug-target Mendelian randomization analysis supports lowering plasma ANGPTL3, ANGPTL4, and APOC3 levels as strategies for reducing cardiovascular disease risk.

Landfors F et al.

European Heart Journal Open, 2024

Association of a genetic variant in angiopoietin-like 3 with serum HDL-C and risk of cardiovascular disease: A study of the MASHAD cohort over 6 years.

Aghasizadeh M et al.

Molecular Genetics & Genomic Medicine, 2024

Inhibition of Angiopoietin-Like Protein 3 or 3/8 Complex and ApoC-III in Severe Hypertriglyceridemia.

Larouche M et al.

Current Atherosclerosis Reports, 2023

Elucidation of Increased Cervical Cancer Risk Due to Polymorphisms in XRCC1 (R399Q and R194W), ERCC5 (D1104H), and NQO1 (P187S).

Das AP et al.

Reproductive Sciences (thousand Oaks, Calif.), 2023

Genetic Mimicry Analysis Reveals the Specific Lipases Targeted by the ANGPTL3-ANGPTL8 Complex and ANGPTL4.

Landfors F et al.

Journal of Lipid Research, 2023

Evinacumab, an ANGPTL3 Inhibitor, in the Treatment of Dyslipidemia.

Sosnowska B et al.

Journal of Clinical Medicine, 2022

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

Aragam KG et al.

Nature Genetics, 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

Common and Rare 5'UTR Variants Altering Upstream Open Reading Frames in Cardiovascular Genomics.

Soukarieh O et al.

Frontiers in Cardiovascular Medicine, 2022

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

Natarajan P et al.

Nature Communications, 2021

Cross-talk between ANGPTL4 gene SNP Rs1044250 and weight management is a risk factor of metabolic syndrome.

Tong Z et al.

Journal of Translational Medicine, 2021

Quantile-Dependent Expressivity and Gene-Lifestyle Interactions Involving High-Density Lipoprotein Cholesterol.

Williams PT

Lifestyle Genomics, 2021

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.

Nielsen JB et al.

Nature Communications, 2020

Association of a genetic variant in the angiopoietin-like protein 4 gene with cervical cancer.

Rahmani F et al.

Pathology, Research and Practice, 2020

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

The influence of rare variants in circulating metabolic biomarkers.

Riveros-Mckay F et al.

Plos Genetics, 2020

32150548 (PubMed )
Supplement: pgen.1008605.s004.xlsx › Supp_Table_1

Association of a genetic variant in the angiopoietin-like protein 4 gene with metabolic syndrome.

Kharazmi-Khorassani S et al.

Bmc Medical Genetics, 2019

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.

Justice AE et al.

Nature Genetics, 2019

ANGPTL4 gene E40K variation protects against obesity-associated dyslipidemia in participants with obesity.

Bailetti D et al.

Obesity Science & Practice, 2019

Rare BANF1 Alleles and Relatively Frequent EMD Alleles Including 'Healthy Lipid' Emerin p.D149H in the ExAC Cohort.

Dharmaraj T et al.

Frontiers in Cell and Developmental Biology, 2019

Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.

Klarin D et al.

Nature Genetics, 2018

Association of Genetically Enhanced Lipoprotein Lipase-Mediated Lipolysis and Low-Density Lipoprotein Cholesterol-Lowering Alleles With Risk of Coronary Disease and Type 2 Diabetes.

Lotta LA et al.

Jama Cardiology, 2018

A subregion-based burden test for simultaneous identification of susceptibility loci and subregions within.

Zhu B et al.

Genetic Epidemiology, 2018

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.

Natarajan P et al.

Nature Communications, 2018

30140000 (PubMed )
Supplement: 41467_2018_5747_MOESM1_ESM.pdf

Genomic insights into the causes of type 2 diabetes.

Langenberg C et al.

Lancet (london, England), 2018

Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.

Gusarova V et al.

Nature Communications, 2018

1–50 of 113 papers
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."