All Stories

  1. Semaglutide in MASH with F2-F3 fibrosis: a holistic perspective on the ESSENCE phase 3 trial
  2. Sex-specific cardiometabolic phenotypes in MASLD: 3PM-centric stratification and trajectory mapping for proactive risk assessment
  3. Therapeutic targets for metabolic dysfunction-associated steatohepatitis: a personalized approach to disease management
  4. Panomics in metabolic dysfunction-associated steatotic liver disease: unravelling the drivers of disease heterogeneity
  5. Proteomic signature of MASLD heterogeneity reveals sex-driven endotypes and predicts all-cause mortality
  6. Focus on Semaglutide 2.4 mg/week for the Treatment of Metabolic Dysfunction‐Associated Steatohepatitis
  7. Organ damage proteomic signature identifies patients with MASLD at-risk of systemic complications
  8. Identifying molecular pathways of olfactory dysfunction in Parkinson’s disease through a systems biology framework
  9. Global Burden of Major Chronic Liver Diseases in 2021
  10. MASLD as a non-communicable disease
  11. Global, regional, and national burden of primary liver cancer attributable to metabolic risks: an analysis of the Global Burden of Disease Study 1990-2021
  12. The Proteomics of MASLD Progression: Insights From Functional Analysis to Drive the Development of New Therapeutic Solutions
  13. Corrigendum to “Cross talk between the liver microbiome and epigenome in patients with metabolic dysfunction-associated steatotic liver disease”
  14. Metabolic dysfunction-associated steatotic liver disease exhibits sex-specific microbial heterogeneity within intestinal compartments
  15. Organ damage proteomic signature identifies patients with MASLD at-risk of systemic complications
  16. Global Epidemiological Impact of PNPLA3 I148M on Liver Disease
  17. Genetics of MASLD: The State of Art Update.
  18. The gene expression signature of metabolic dysfunction- associated steatotic liver disease from a multiomics perspective
  19. Cross talk between the liver microbiome and epigenome in patients with metabolic dysfunction-associated steatotic liver disease
  20. Drug repurposing in MASLD and MASH-cirrhosis: Targets and treatment approaches based on pathways analysis
  21. From NAFLD to MASLD: Updated Naming and Diagnosis Criteria for Fatty Liver Disease
  22. Non‐alcoholic fatty liver disease mediates the effect of obesity on arterial hypertension
  23. SARS-CoV-2 targets the liver and manipulates glucose metabolism
  24. Editorial: NAFLD , chronic kidney disease, and pleiotropy—Why is PNPLA3 omnipresent?
  25. Advances in our understanding of the molecular heterogeneity of fatty liver disease: towards informed treatment decision making
  26. Genetics in non-alcoholic fatty liver disease: The role of risk alleles through the lens of immune response
  27. COVID ‐19 and NAFLD : biological insights from multi‐omics data
  28. Personalized medicine in nonalcoholic fatty liver disease
  29. Repurposing drugs to target nonalcoholic steatohepatitis: Auranofin, a gold-organic molecule complex for the treatment of a specifc complex trait
  30. Geographical similarity and differences in the burden and genetic predisposition of NAFLD
  31. Alcohol consumption and metabolic syndrome: Clinical and epidemiological impact on liver disease
  32. Single cell gene expression profiling of nasal ciliated cells reveals distinctive biological processes related to epigenetic mechanisms in patients with severe COVID-19
  33. The serum uric acid/creatinine ratio is associated with nonalcoholic fatty liver disease in the general population
  34. PNPLA3 rs738409 and risk of fibrosis in NAFLD: Exploring mediation pathways through intermediate histological features
  35. MicroRNAs as messengers of liver diseases: has the message finally been decrypted?
  36. The influence of host genetics on liver microbiome composition in patients with NAFLD
  37. Computational Pipeline for Next-Generation Sequencing (NGS) Studies in Genetics of NASH
  38. Single cell gene expression profiling of nasal ciliated cells reveals distinctive biological processes related to epigenetic mechanisms in patients with severe COVID-19
  39. Genome‐wide association study of liver‐related enzymes suggests putative pleiotropic effects on diverse traits and diseases
  40. PNPLA3 and COVID‐19 outcomes: Thinking outside the box might explain the biology behind pleiotropic effects of rs738409 on the immune system
  41. Editorial: bariatric surgery to reduce the risk of liver cancer
  42. The lipidome in nonalcoholic fatty liver disease: actionable targets
  43. NAFLD and cardiometabolic risk factors: The liver fibrosis trajectory through the lens of biological interactions
  44. Liver mitochondrial DNA damage and genetic variability of Cytochrome b ‐ a key component of the respirasome ‐ drive the severity of fatty liver disease
  45. Epigenetics factors in nonalcoholic fatty liver disease
  46. ADH1B∗2 Is Associated With Reduced Severity of Nonalcoholic Fatty Liver Disease in Adults, Independent of Alcohol Consumption
  47. SARS‐CoV‐2 virus and liver expression of host receptors: Putative mechanisms of liver involvement in COVID‐19
  48. COVID-19 and ACE2 in the Liver and Gastrointestinal Tract: Putative Biological Explanations of Sexual Dimorphism
  49. Genetic pathways in nonalcoholic fatty liver disease: Insights from systems biology
  50. Liver tissue microbiota linked to nonalcoholic fatty liver disease
  51. Review article: shared disease mechanisms between non-alcoholic fatty liver disease and metabolic syndrome - translating knowledge from systems biology to the bedside
  52. Splice variant rs72613567 prevents worst histologic outcomes in patients with nonalcoholic fatty liver disease
  53. Editorial: surviving your genes-the role of PNPLA3 variation in end-stage liver disease
  54. A Rare Nonsense Mutation in the Glucokinase Regulator Gene Is Associated With a Rapidly Progressive Clinical Form of Nonalcoholic Steatohepatitis
  55. Metastasis-associated lung adenocarcinoma transcript 1 as a common molecular driver in the pathogenesis of nonalcoholic steatohepatitis and chronic immune-mediated liver damage
  56. Lack of evidence supporting a role of TMC4-rs641738 missense variant—MBOAT7- intergenic downstream variant—in the Susceptibility to Nonalcoholic Fatty Liver Disease
  57. The nonalcoholic steatohepatitis metabotype: Imbalance of circulating amino acids and transamination reactions reflect impaired mitochondrial function
  58. Systematic review with meta-analysis: the significance of histological disease severity in lean patients with nonalcoholic fatty liver disease
  59. Letter: Mendelian randomisation to investigate moderate alcohol consumption in nonalcoholic fatty liver disease; modest effects need large numbers-authors' reply
  60. Systematic review with meta-analysis: risk factors for non-alcoholic fatty liver disease suggest a shared altered metabolic and cardiovascular profile between lean and obese patients
  61. How Safe Is Moderate Alcohol Consumption in Overweight and Obese Individuals?
  62. Serum aminotransferases in nonalcoholic fatty liver disease are a signature of liver metabolic perturbations at the amino acid and Krebs cycle level,