Associated Papers
Integrative bioinformatics analysis of APOE variants in Alzheimer's disease and clinical therapeutics.
Srivastava K et al.
Journal of Biomolecular Structure & Dynamics, 2025
Cytokine-induced reprogramming of human macrophages toward Alzheimer's disease-relevant molecular and cellular phenotypes in vitro.
Podleśny-Drabiniok A et al.
Cell Reports, 2025
Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features.
Matsunaga A et al.
Journal of Atherosclerosis and Thrombosis, 2025
Inherited Dyslipidemic Splenomegaly: A Genetic Macrophage Storage Disorder Caused by Disruptive Apolipoprotein E (APOE) Variants.
Ferreira EA et al.
Genes, 2025
Improved Genetic Characterization of Hypercholesterolemia in Latvian Patients with Familial Hypercholesterolemia: A Combined Monogenic and Polygenic Approach Using Whole-Genome Sequencing.
Atava I et al.
International Journal of Molecular Sciences, 2024
Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia.
Blokhina AV et al.
International Journal of Molecular Sciences, 2024
Alzheimer Disease Associated Loci: APOE Single Nucleotide Polymorphisms in Marmara Region.
Ismail AB et al.
Biomedicines, 2024
The current state of apolipoprotein E in dyslipidemia.
Rasmussen KL et al.
Current Opinion in Lipidology, 2024
APOE and vascular disease: Sequencing and genotyping in general population cohorts.
Rasmussen KL et al.
Atherosclerosis, 2023
Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia.
Marmontel O et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2023
Contribution of APOE Genetic Variants to Dyslipidemia.
Bea AM et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2023
Genetics of Alzheimer's disease: an East Asian perspective.
Miyashita A et al.
Journal of Human Genetics, 2023
Brain radiotoxicity-related 15CAcBRT gene expression signature predicts survival prognosis of glioblastoma patients.
Reyes-González J et al.
Neuro-oncology, 2023
Associations of Alzheimer Disease-Protective APOE Variants With Age-Related Macular Degeneration.
Rasmussen KL et al.
Jama Ophthalmology, 2023
Establishing the relationship between familial dysbetalipoproteinemia and genetic variants in the APOE gene.
Heidemann BE et al.
Clinical Genetics, 2022
APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia.
Abou Khalil Y et al.
International Journal of Molecular Sciences, 2022
Lysine acetylation regulates the interaction between proteins and membranes.
Okada AK et al.
Nature Communications, 2021
APOE and dementia - resequencing and genotyping in 105,597 individuals.
Rasmussen KL et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2020
The clinical and laboratory investigation of dysbetalipoproteinemia.
Boot CS et al.
Critical Reviews in Clinical Laboratory Sciences, 2020
Case Report: Hypertriglyceridemia and Premature Atherosclerosis in a Patient With Apolipoprotein E Gene ε2ε1 Genotype.
Limonova AS et al.
Frontiers in Cardiovascular Medicine, 2020
Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.
Zhou Y et al.
Journal of Lipid Research, 2018
Structural Biology Helps Interpret Variants of Uncertain Significance in Genes Causing Endocrine and Metabolic Disorders.
Ittisoponpisan S et al.
Journal of the Endocrine Society, 2018
In silico analyses of deleterious missense SNPs of human apolipoprotein E3.
Pires AS et al.
Scientific Reports, 2017
Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France.
Wintjens R et al.
Journal of Lipid Research, 2016
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses.
Dasari S et al.
Journal of Proteome Research, 2014
Structural and phylogenetic approaches to assess the significance of human Apolipoprotein E variation.
Corbo RM et al.
Molecular Genetics and Metabolism, 2006
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.
Cefalù AB et al.
Journal of Clinical Lipidology, 0
Severe Combined Dyslipidemia With a Complex Genetic Basis.
Le R et al.
Journal of Investigative Medicine High Impact Case Reports, 0