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Sims, E. K., et al. “Inhibition Of Polyamine Biosynthesis Preserves Β Cell Function In Type 1 Diabetes.”. Cell Reports. Medicine, p. 101261.
Indiana
Mooring, M., et al. “Hepatocyte Cyr61 Polarizes Profibrotic Macrophages To Orchestrate Nash Fibrosis.”. Science Translational Medicine, p. eade3157.
Yale
Sims, E. K., et al. “High Proinsulin:c-Peptide Ratio Identifies Individuals With Stage 2 Type 1 Diabetes At High Risk For Progression To Clinical Diagnosis And Responses To Teplizumab Treatment.”. Diabetologia, pp. 2283-2291.
Indiana
Rupp, A. C., et al. “Suppression Of Food Intake By Glp1R/Lepr-Coexpressing Neurons Prevents Obesity In Mouse Models.”. The Journal Of Clinical Investigation.
Michigan
Kaffe, E., et al. “Humanized Mouse Liver Reveals Endothelial Control Of Essential Hepatic Metabolic Functions.”. Cell, pp. 3793-3809.e26.
Yale
Ismail, H. M., et al. “Baseline Leptin Predicts Response To Metformin In Adolescents With Type 1 Diabetes And Increased Body Mass Index.”. Diabetes, Obesity & Metabolism, pp. 3420-3423.
Indiana
Cook, J. R., et al. “Liver Insulinization As A Driver Of Triglyceride Dysmetabolism.”. Nature Metabolism, pp. 1101-1110.
Columbia
Einstein
Rizk, A. A., et al. “Pancreatic Regional Blood Flow Links The Endocrine And Exocrine Diseases.”. The Journal Of Clinical Investigation.
Chicago
Patil, A. R., et al. “Single-Cell Expression Profiling Of Islets Generated By The Human Pancreas Analysis Program.”. Nature Metabolism, pp. 713-715.
Penn
Reynolds, E. L., et al. “The Effect Of Surgical Weight Loss On Diabetes Complications In Individuals With Class Ii/Iii Obesity.”. Diabetologia, pp. 1192-1207.
Michigan
Davidson, R. K., et al. “The Chd4 Helicase Regulates Chromatin Accessibility And Gene Expression Critical For Β-Cell Function In Vivo.”. Diabetes, pp. 746-757.
Indiana