Associated Papers
Molecular dynamics of select missense mutations of Apolipoprotein E and their implications in Hyperlipoproteinemia type III.
Thakur S et al.
Biochemistry and Biophysics Reports, 2025
Association of VDR and TMPRSS2 gene polymorphisms with COVID-19 severity: a computational and clinical study.
Verma S et al.
Molecular Biology 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
Corrigendum to "APOE gene variants in primary dyslipidemia" [Atherosclerosis (2021 Jul) 328 11-22].
Abou Khalil Y et al.
Atherosclerosis, 2023
Genetics of Alzheimer's disease: an East Asian perspective.
Miyashita A et al.
Journal of Human Genetics, 2023
Orthogonal analysis of variants in APOE gene using in-silico approaches reveals novel disrupting variants.
Li C et al.
Frontiers in Bioinformatics, 2023
Establishing the relationship between familial dysbetalipoproteinemia and genetic variants in the APOE gene.
Heidemann BE et al.
Clinical Genetics, 2022
35781703 (PubMed )
Supplement: CGE-102-253-s001.docx
A pleiotropic effect of the APOE gene: association of APOE polymorphisms with multibacillary leprosy in Han Chinese from Southwest China.
Wang D et al.
The British Journal of Dermatology, 2018
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses.
Dasari S et al.
Journal of Proteome Research, 2014
24650283 (PubMed )
Supplement: pr4011475_si_001.pdf
Association analysis of peroxisome proliferator-activated receptor gamma polymorphisms and late onset Alzheimer's disease in the Finnish population.
Koivisto AM et al.
Dementia and Geriatric Cognitive Disorders, 2006
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