Associated Papers
Steatotic liver disease associated with 2,4-dienoyl-CoA reductase 1 deficiency.
Kohlmaier B et al.
International Journal of Obesity (2005), 2024
39277655 (PubMed )
Supplement: 41366_2024_1634_MOESM1_ESM.docx
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis.
Ghouse J et al.
Nature Genetics, 2024
38632349 (PubMed )
Supplement: 41588_2024_1720_MOESM4_ESM.xlsx › S16
Multiomics study of nonalcoholic fatty liver disease.
Sveinbjornsson G et al.
Nature Genetics, 2022
36280732 (PubMed )
Supplement: 41588_2022_1199_MOESM4_ESM.xlsx › Supplementary_Table_1
Insights into genetic variants associated with NASH-fibrosis from metabolite profiling.
Mann JP et al.
Human Molecular Genetics, 2020
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