Associated Papers
Trans-ancestral rare variant association study with machine learning-based phenotyping for metabolic dysfunction-associated steatotic liver disease.
Chen R et al.
Genome Biology, 2025
40065360 (PubMed )
Supplement: 13059_2025_3518_MOESM1_ESM.xlsx › Table_S23
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.
Akbari P et al.
Nature Communications, 2022
Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity.
Deaton AM et al.
Nature Communications, 2022
Select a paper to view details