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
Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features.
Matsunaga A et al.
Journal of Atherosclerosis and Thrombosis, 2025
Is it time for a paradigm shift? Inclusion of APOE on genetic dyslipidemia panels.
Ison HE et al.
Journal of Genetic Counseling, 2025
Association between cytokine polymorphisms and recurrent pregnancy loss: A review of current evidence.
Stavros S et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics, 2024
Genetics of Alzheimer's disease: an East Asian perspective.
Miyashita A et al.
Journal of Human Genetics, 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
In silico analyses of deleterious missense SNPs of human apolipoprotein E3.
Pires AS et al.
Scientific Reports, 2017
28559539 (PubMed )
Supplement: 41598_2017_1737_MOESM1_ESM.docx
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
Screening and Evaluation of Deleterious SNPs in APOE Gene of Alzheimer's Disease.
Masoodi TA et al.
Neurology Research International, 2012
Select a paper to view details