Associated Papers
Role of genetic variants and DNA methylation of lipid metabolism-related genes in metabolic dysfunction-associated steatotic liver disease.
Wang JJ et al.
Frontiers in Physiology, 2025
40166716 (PubMed )
Supplement: Table1.xlsx › Table_S1__
Sirtuin3 rs28365927 functional variant confers to the high risk of non-alcoholic fatty liver disease in Chinese Han population.
Chen LJ et al.
Lipids in Health and Disease, 2021
Lrp6 Genotype affects Individual Susceptibility to Nonalcoholic Fatty Liver Disease and Silibinin Therapeutic Response via Wnt/β-catenin-Cyp2e1 Signaling.
Chen LJ et al.
International Journal of Biological Sciences, 2021
34671210 (PubMed )
Supplement: ijbsv17p3936s1.pdf
The role of the folate pathway in pancreatic cancer risk.
Chittiboyina S et al.
Plos One, 2018
Exome-wide association study of plasma lipids in >300,000 individuals.
Liu DJ et al.
Nature Genetics, 2017
Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population.
Edelman D et al.
Molecular Genetics & Genomic Medicine, 2015
Aberrant estrogen regulation of PEMT results in choline deficiency-associated liver dysfunction.
Resseguie ME et al.
The Journal of Biological Chemistry, 2011
Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD).
Song J et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2005
Whole-Exome Sequencing Identifies a Variant in Phosphatidylethanolamine N-Methyltransferase Gene to be Associated With Lean-Nonalcoholic Fatty Liver Disease.
Bale G et al.
Journal of Clinical and Experimental Hepatology, 0
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