Author

Robert P. Doyle

SUNY Upstate Medical UniversityORCID 0000-0001-6786-5656Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Pharmacology & Toxicology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 1 Research Focus:metabolism & bioenergetics· 1 Organism:mouse· 1 Organism:rat· 1

Frequent Co-Authors

Christian Ludwig RothiD· 2 shared Clinton T. ElfersiD· 2 shared Emily F. AshlawiD· 2 shared James Ernest BlevinsiD· 2 shared Kylie S. Chichura· 2 shared Matvey GoldbergiD· 2 shared Andrew Dale Dodson· 1 shared Edison W. TsuiiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersPhysiology

Christian Ludwig RothORCID

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2 papers

Recent·Most cited

The Chimeric Peptide (GEP44) Reduces Body Weight and Both Energy Intake, and Energy Expenditure in Diet-Induced Obese Rats

Matvey Goldberg, James Ernest Blevins, Tami Wolden‐Hanson, Clinton Elfers, Kylie S. Chichura, Emily F. Ashlaw, Laura J. den Hartigh, Christian Ludwig Roth, Robert P. Doyle

International Journal of Molecular Sciences · Mar 26, 2025Peer-reviewedPhysiology

The Novel Chimeric Multi-Agonist Peptide (GEP44) Reduces Energy Intake and Body Weight in Male and Female Diet-Induced Obese Mice in a Glucagon-Like Peptide-1 Receptor-Dependent Manner

James Ernest Blevins, Mackenzie K. Honeycutt, Jared D. Slattery, Matvey Goldberg, June R. Rambousek, Edison W. Tsui, Andrew Dale Dodson, Kyra A. Shelton, Therese S. Salemeh, Clinton T. Elfers, Kylie S. Chichura, Emily F. Ashlaw, Sakeneh Zraika, Robert P. Doyle, Christian Ludwig Roth

This study shows that the chimeric peptide GEP44 reduces body weight and energy intake in diet-induced obese mice, primarily through GLP-1R signaling, with some GLP-1R-independent effects in males.

Frontiers in Endocrinology · Jul 22, 2024Peer-reviewedPharmacology & Toxicology