Associated Papers
PSEN1 His214Asn Mutation in a Korean Patient with Familial EOAD and the Importance of Histidine-Tryptophan Interactions in TM-4 Stability.
Bagyinszky E et al.
International Journal of Molecular Sciences, 2023
38203287 (PubMed )
Supplement: ijms-25-00116-s001.zip › ijms-2769595-supplementary.pdf
Lack of significant associations between single nucleotide polymorphisms in LPAL2-LPA genetic region and all cancer incidence and mortality in Japanese population: The Japan public health center-based prospective study.
Mieno MN et al.
Cancer Epidemiology, 2023
Hypercholesterolemia in the Malaysian Cohort Participants: Genetic and Non-Genetic Risk Factors.
Abdul Murad NA et al.
Genes, 2023
The HUNT study: A population-based cohort for genetic research.
Brumpton BM et al.
Cell Genomics, 2022
Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular Risk.
Coassin S et al.
Circulation. Genomic and Precision Medicine, 2022
35133173 (PubMed )
Supplement: hcg-15-e003489-s001.pdf
Mutations in SORL1 and MTHFDL1 possibly contribute to the development of Alzheimer's disease in a multigenerational Colombian Family.
Tejada Moreno JA et al.
Plos One, 2022
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
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study.
Dewey FE et al.
Science (new York, N.y.), 2016
28008009 (PubMed )
Supplement: aaf6814-dewey-tabless1-s14.xlsx › Table_S5
Influence of Genetic Risk Factors on Coronary Heart Disease Occurrence in Afro-Caribbeans.
Larifla L et al.
The Canadian Journal of Cardiology, 2016
Structure, function, and genetics of lipoprotein (a).
Schmidt K et al.
Journal of Lipid Research, 2016
Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels.
Lu W et al.
Human Molecular Genetics, 2015
LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography.
Santos PC et al.
Lipids in Health and Disease, 2014
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