Davide Calebiro

6.7k total citations
92 papers, 4.1k citations indexed

About

Davide Calebiro is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Cellular and Molecular Neuroscience. According to data from OpenAlex, Davide Calebiro has authored 92 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 34 papers in Endocrinology, Diabetes and Metabolism and 26 papers in Cellular and Molecular Neuroscience. Recurrent topics in Davide Calebiro's work include Receptor Mechanisms and Signaling (45 papers), Neuropeptides and Animal Physiology (18 papers) and Hormonal Regulation and Hypertension (14 papers). Davide Calebiro is often cited by papers focused on Receptor Mechanisms and Signaling (45 papers), Neuropeptides and Animal Physiology (18 papers) and Hormonal Regulation and Hypertension (14 papers). Davide Calebiro collaborates with scholars based in Germany, United Kingdom and Italy. Davide Calebiro's co-authors include Martin J. Lohse, Luca Persani, Viacheslav O. Nikolaev, Titiwat Sungkaworn, Tiziana de Filippis, Amod Godbole, Marie‐Lise Jobin, Isabella Maiellaro, Christian Dees and Carlo Tacchetti and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Davide Calebiro

89 papers receiving 4.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Davide Calebiro 2.8k 1.3k 1.1k 515 338 92 4.1k
Anthony Carruthers 2.7k 1.0× 578 0.5× 556 0.5× 1.0k 2.0× 285 0.8× 87 4.6k
Ronald M. Lynch 2.0k 0.7× 469 0.4× 223 0.2× 422 0.8× 346 1.0× 88 3.6k
Sadashiva S. Karnik 4.9k 1.8× 2.4k 1.9× 755 0.7× 289 0.6× 199 0.6× 116 6.9k
Manuela Zaccolo 6.4k 2.3× 1.4k 1.1× 203 0.2× 349 0.7× 510 1.5× 143 8.4k
Carine Maenhaut 3.3k 1.2× 749 0.6× 1.9k 1.7× 266 0.5× 305 0.9× 110 5.7k
Juan M. Pascual 2.3k 0.8× 584 0.5× 287 0.3× 417 0.8× 141 0.4× 107 5.1k
Walter Rosenthal 7.3k 2.6× 2.0k 1.6× 442 0.4× 718 1.4× 923 2.7× 151 9.0k
Éric Reiter 4.2k 1.5× 2.2k 1.8× 722 0.7× 295 0.6× 268 0.8× 103 5.8k
Erin J. Whalen 4.0k 1.4× 2.1k 1.7× 285 0.3× 274 0.5× 228 0.7× 48 5.2k
Peter R. Allegrini 2.8k 1.0× 679 0.5× 172 0.2× 413 0.8× 329 1.0× 75 5.3k

Countries citing papers authored by Davide Calebiro

Since Specialization
Citations

This map shows the geographic impact of Davide Calebiro's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Davide Calebiro with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Davide Calebiro more than expected).

Fields of papers citing papers by Davide Calebiro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Davide Calebiro. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Davide Calebiro. The network helps show where Davide Calebiro may publish in the future.

Co-authorship network of co-authors of Davide Calebiro

This figure shows the co-authorship network connecting the top 25 collaborators of Davide Calebiro. A scholar is included among the top collaborators of Davide Calebiro based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Davide Calebiro. Davide Calebiro is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
O’Brien, Shannon, Jennie Roberts, Jeremy A. Pike, et al.. (2025). Intracrine FFA4 signaling controls lipolysis at lipid droplets. Nature Chemical Biology. 22(1). 109–119. 1 indexed citations
2.
Kőszegi, Zsombor, Harald Hübner, Damien Maurel, et al.. (2024). Design, Synthesis, and Characterization of New δ Opioid Receptor-Selective Fluorescent Probes and Applications in Single-Molecule Microscopy of Wild-Type Receptors. Journal of Medicinal Chemistry. 67(15). 12618–12631. 1 indexed citations
3.
Ast, Julia, Daniela Nasteska, Nicholas H. F. Fine, et al.. (2023). Revealing the tissue-level complexity of endogenous glucagon-like peptide-1 receptor expression and signaling. Nature Communications. 14(1). 301–301. 12 indexed citations
4.
Lafont, Chrystel, Pierre Fontanaud, Davide Calebiro, et al.. (2023). TSH Pulses Finely Tune Thyroid Hormone Release and TSH Receptor Transduction. Endocrinology. 165(1). 2 indexed citations
5.
Lanoiselée, Yann, A. A. Stanislavsky, Davide Calebiro, & Aleksander Weron. (2022). Temperature and friction fluctuations inside a harmonic potential. Physical review. E. 106(6). 64127–64127. 9 indexed citations
6.
Novikoff, Aaron, Shannon O’Brien, Gerald Grandl, et al.. (2021). Spatiotemporal GLP-1 and GIP receptor signaling and trafficking/recycling dynamics induced by selected receptor mono- and dual-agonists. Molecular Metabolism. 49. 101181–101181. 60 indexed citations
7.
Kőszegi, Zsombor, Yann Lanoiselée, Harald Hübner, et al.. (2020). Investigation of Inactive-State κ Opioid Receptor Homodimerization via Single-Molecule Microscopy Using New Antagonistic Fluorescent Probes. Journal of Medicinal Chemistry. 63(7). 3596–3609. 16 indexed citations
8.
Husted, Anna Sofie, Jeppe H. Ekberg, Shannon O’Brien, et al.. (2020). Autocrine negative feedback regulation of lipolysis through sensing of NEFAs by FFAR4/GPR120 in WAT. Molecular Metabolism. 42. 101103–101103. 20 indexed citations
9.
Buenaventura, Teresa, Stavroula Bitsi, Thomas Burgoyne, et al.. (2019). Agonist-induced membrane nanodomain clustering drives GLP-1 receptor responses in pancreatic beta cells. PLoS Biology. 17(8). e3000097–e3000097. 66 indexed citations
10.
Walker, Caitlin, Yingjie Wang, Cristina Olivieri, et al.. (2019). Cushing’s syndrome driver mutation disrupts protein kinase A allosteric network, altering both regulation and substrate specificity. Science Advances. 5(8). eaaw9298–eaaw9298. 45 indexed citations
11.
Monteagudo, Silvia, et al.. (2018). A cholecystokinin receptor antagonist inhibits the osteoarthritis features induced by GPR22 in vitro and in vivo. Osteoarthritis and Cartilage. 26. S32–S33. 2 indexed citations
12.
Godbole, Amod, et al.. (2017). Internalized TSH receptors en route to the TGN induce local Gs-protein signaling and gene transcription. Nature Communications. 8(1). 443–443. 123 indexed citations
13.
Sungkaworn, Titiwat, Marie‐Lise Jobin, Krzysztof Burnecki, et al.. (2017). Single-molecule imaging reveals receptor–G protein interactions at cell surface hot spots. Nature. 550(7677). 543–547. 227 indexed citations
14.
Calebiro, Davide, et al.. (2016). A cholecystokinin receptor antagonist inhibits chondrocyte hypertrophy and protein kinase a activity decrease induced by activation of GPR22. Osteoarthritis and Cartilage. 24. S178–S179. 1 indexed citations
15.
Maiellaro, Isabella, Martin J. Lohse, Robert J. Kittel, & Davide Calebiro. (2016). cAMP Signals in Drosophila Motor Neurons Are Confined to Single Synaptic Boutons. Cell Reports. 17(5). 1238–1246. 50 indexed citations
16.
Calebiro, Davide, Julia Wagner, Titiwat Sungkaworn, et al.. (2012). Single-molecule analysis of fluorescently labeled G-protein–coupled receptors reveals complexes with distinct dynamics and organization. Proceedings of the National Academy of Sciences. 110(2). 743–748. 345 indexed citations
17.
Calebiro, Davide, Giulia Gelmini, Daniela Cordella, et al.. (2011). Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia. The Journal of Clinical Endocrinology & Metabolism. 97(1). E156–E160. 40 indexed citations
18.
Calebiro, Davide, Viacheslav O. Nikolaev, Maria Cristina Gagliani, et al.. (2009). Persistent cAMP-Signals Triggered by Internalized G-Protein–Coupled Receptors. PLoS Biology. 7(8). e1000172–e1000172. 446 indexed citations
19.
Cordella, Daniela, Alessandro De Marco, Davide Calebiro, et al.. (2007). Prevalence of inactivating TSH receptor (TSHR) mutations in a large series of pediatric subjects with non-autoimmune mild hyper-thyrotropinemia (hyperTSH). 14(11). 676–80. 2 indexed citations
20.
Calebiro, Davide, Tiziana de Filippis, Simona Lucchi, et al.. (2005). Intracellular entrapment of wild-type TSH receptor by oligomerization with mutants linked to dominant TSH resistance. Human Molecular Genetics. 14(20). 2991–3002. 95 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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