Publications
295
Citations
20,423
Est. group size
—
Recurring co-author estimate
Active years
49
Publishing since 1978
Richard D. DiMarchi designs engineered peptide and protein drugs that target the hormone receptors controlling blood sugar, appetite, and body weight. Much of the work focuses on molecules that act on multiple receptors at once (such as GLP-1, GIP, and glucagon receptors) to treat obesity, type 2 diabetes, and related metabolic conditions, along with modified insulin formulations and other hormone analogs.
Publication output was highest in the late 2010s (around 18-22 per year) and has trended downward since, averaging about 10 papers per year over the last five years.
Generated by claude-opus-4-8 from public bibliographic data · Jul 9, 2026
Typically publishes in teams of ~8 · 8% small-team papers (≤3 authors) · across 61 venues
- GLP-1R–GIPR–PPARα/γ/δ quintuple agonism corrects obesity and diabetes in mice
Nature · 2026
- Discovery and characterization of canvuparatide, a once-weekly parathyroid hormone analog for the treatment of hypoparathyroidism
Molecular Metabolism · 2026
- A High-Potency Protein That Normalizes Body Weight in DIO Mice through Triple Agonism at FGF21, GLP1, and GIP Receptors
Biochemistry · 2026
- Publisher Correction: GLP-1R–GIPR–PPARα/γ/δ quintuple agonism corrects obesity and diabetes in mice
Nature · 2026
- GIPR:GCGR co-agonism restores normal weight in obese rodents
Molecular Metabolism · 2026
- Antagonism of β-klotho signaling by peptide 19 impairs wheel running in male mice and potentiates the cisplatin-induced decrease in wheel running
Frontiers in Pharmacology · 2026
- A Novel Class of Complement 3a Receptor Agonists and Antagonists Derived from the TLQP-21 Peptide
Journal of Medicinal Chemistry · 2025
- Celebrating Professor George Barany's Half Century in Science
2025
- Glucose-dependent insulinotropic polypeptide (GIP)
Molecular Metabolism · 2025
- GIPR agonism and antagonism decrease body weight and food intake via different mechanisms in male mice
Nature Metabolism · 2025
- A once-daily GLP-1/GIP/glucagon receptor tri-agonist (NN1706) lowers body weight in rodents, monkeys and humans
Molecular Metabolism · 2025
- Estrogenic activity of E2-conjugated GLP-1 is mediated by intracellular endolysosomal acidification and estrone metabolism
Molecular Metabolism · 2025
- Viral insulin/IGF-like peptides inhibit IGF-1 receptor signaling to enhance viral replication
Cell Reports · 2025
- Publisher Correction: GIPR agonism and antagonism decrease body weight and food intake via different mechanisms in male mice
Nature Metabolism · 2025
- Bile Acid Binding Resins Improve Glucagon Receptor Agonist‐Mediated Weight Loss in Diet‐Induced Obese Mice
Obesity · 2025
- Molecular Metabolism×21
- Diabetes×14
- Cell Metabolism×6
- Nature Metabolism×6
- Journal of Medicinal Chemistry×6
- David T. Broome
Medicine · University of Michigan
- Michael K. Hansen
Medicine · University of Michigan
- Curtis Triplitt
Medicine · University of Michigan
- Eugênio Cersósimo
Medicine · University of Michigan
- Kieren J. Mather
Medicine · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Sep 1, 2026.
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