Fiore Cattaruzza

2.4k total citations
49 papers, 1.9k citations indexed

About

Fiore Cattaruzza is a scholar working on Oncology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Fiore Cattaruzza has authored 49 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Oncology, 11 papers in Molecular Biology and 11 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Fiore Cattaruzza's work include Monoclonal and Polyclonal Antibodies Research (11 papers), Gastrointestinal motility and disorders (8 papers) and CAR-T cell therapy research (8 papers). Fiore Cattaruzza is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (11 papers), Gastrointestinal motility and disorders (8 papers) and CAR-T cell therapy research (8 papers). Fiore Cattaruzza collaborates with scholars based in United States, Australia and Canada. Fiore Cattaruzza's co-authors include Nigel W. Bunnett, Daniel P. Poole, Carlos U. Corvera, Farzad Alemi, Kristina Schoonjans, Graeme S. Cottrell, Stephen Vanner, Eileen F. Grady, Victoria Lyo and John R. Grider and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Fiore Cattaruzza

48 papers receiving 1.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Fiore Cattaruzza United States 21 631 557 442 387 361 49 1.9k
Weibiao Cao United States 27 623 1.0× 209 0.4× 826 1.9× 540 1.4× 298 0.8× 77 1.9k
Biljana Jovov United States 22 1.6k 2.6× 273 0.5× 383 0.9× 159 0.4× 255 0.7× 36 2.4k
C Cortesini Italy 30 542 0.9× 557 1.0× 938 2.1× 607 1.6× 315 0.9× 75 2.5k
Masayoshi Kajimura Japan 23 492 0.8× 250 0.4× 943 2.1× 606 1.6× 116 0.3× 58 1.8k
Pierre‐Yves von der Weid Canada 29 713 1.1× 1.1k 1.9× 485 1.1× 40 0.1× 704 2.0× 55 2.1k
Ferda Cevikbas United States 23 242 0.4× 200 0.4× 152 0.3× 39 0.1× 638 1.8× 33 2.8k
W. Keith Jones United States 27 1.7k 2.7× 69 0.1× 330 0.7× 61 0.2× 405 1.1× 43 2.9k
Muriel Jaquet Switzerland 16 1.3k 2.1× 786 1.4× 583 1.3× 46 0.1× 663 1.8× 20 2.4k
Roy B. Dyer United States 21 823 1.3× 95 0.2× 346 0.8× 389 1.0× 239 0.7× 46 1.7k
Jacqueline A. Koehler Canada 24 543 0.9× 186 0.3× 574 1.3× 108 0.3× 263 0.7× 29 1.6k

Countries citing papers authored by Fiore Cattaruzza

Since Specialization
Citations

This map shows the geographic impact of Fiore Cattaruzza'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 Fiore Cattaruzza with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fiore Cattaruzza more than expected).

Fields of papers citing papers by Fiore Cattaruzza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fiore Cattaruzza. 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 Fiore Cattaruzza. The network helps show where Fiore Cattaruzza may publish in the future.

Co-authorship network of co-authors of Fiore Cattaruzza

This figure shows the co-authorship network connecting the top 25 collaborators of Fiore Cattaruzza. A scholar is included among the top collaborators of Fiore Cattaruzza 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 Fiore Cattaruzza. Fiore Cattaruzza 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.
3.
Fischer, Marcus, Vincent Yeung, Fiore Cattaruzza, et al.. (2017). RSPO3 antagonism inhibits growth and tumorigenicity in colorectal tumors harboring common Wnt pathway mutations. Scientific Reports. 7(1). 15270–15270. 37 indexed citations
4.
Fischer, Marcus, Belinda Cancilla, Vincent Yeung, et al.. (2017). WNT antagonists exhibit unique combinatorial antitumor activity with taxanes by potentiating mitotic cell death. Science Advances. 3(6). e1700090–e1700090. 122 indexed citations
5.
7.
Page, Michael J., André Luiz Lourenço, Tovo David, et al.. (2015). Non-invasive imaging and cellular tracking of pulmonary emboli by near-infrared fluorescence and positron-emission tomography. Nature Communications. 6(1). 8448–8448. 38 indexed citations
9.
Jensen, Dane D., Michelle L. Halls, Meritxell Canals, et al.. (2014). Endothelin-converting Enzyme 1 and β-Arrestins Exert Spatiotemporal Control of Substance P-induced Inflammatory Signals. Journal of Biological Chemistry. 289(29). 20283–20294. 18 indexed citations
10.
Alemi, Farzad, Edwin Kwon, Daniel P. Poole, et al.. (2013). The TGR5 receptor mediates bile acid–induced itch and analgesia. Journal of Clinical Investigation. 123(4). 1513–1530. 300 indexed citations
11.
Alemi, Farzad, Daniel P. Poole, Jonathan Chiu, et al.. (2012). The Receptor TGR5 Mediates the Prokinetic Actions of Intestinal Bile Acids and Is Required for Normal Defecation in Mice. Gastroenterology. 144(1). 145–154. 279 indexed citations
12.
Cattaruzza, Fiore, Victoria Lyo, Ella F. Jones, et al.. (2011). Cathepsin S Is Activated During Colitis and Causes Visceral Hyperalgesia by a PAR2-Dependent Mechanism in Mice. Gastroenterology. 141(5). 1864–1874.e3. 82 indexed citations
13.
Ibeakanma, Charles, Fernando Ochoa‐Cortés, Marcela Miranda‐Morales, et al.. (2011). Brain–Gut Interactions Increase Peripheral Nociceptive Signaling in Mice With Postinfectious Irritable Bowel Syndrome. Gastroenterology. 141(6). 2098–2108.e5. 68 indexed citations
14.
Poole, Daniel P., Juan C. Pelayo, Fiore Cattaruzza, et al.. (2011). Transient Receptor Potential Ankyrin 1 Is Expressed by Inhibitory Motoneurons of the Mouse Intestine. Gastroenterology. 141(2). 565–575.e4. 67 indexed citations
15.
Eilers, Helge, Fiore Cattaruzza, Romina Nassini, et al.. (2010). Pungent General Anesthetics Activate Transient Receptor Potential-A1 to Produce Hyperalgesia and Neurogenic Bronchoconstriction. Anesthesiology. 112(6). 1452–1463. 53 indexed citations
16.
Poole, Daniel P., Catherine Godfrey, Fiore Cattaruzza, et al.. (2010). Expression and function of the bile acid receptor GpBAR1 (TGR5) in the murine enteric nervous system. Neurogastroenterology & Motility. 22(7). 814–e228. 195 indexed citations
17.
Vergnolle, Nathalie, Nicolas Cénac, Christophe Altier, et al.. (2010). A role for transient receptor potential vanilloid 4 in tonicity‐induced neurogenic inflammation. British Journal of Pharmacology. 159(5). 1161–1173. 78 indexed citations
18.
Cattaruzza, Fiore, G. Trevor Cottrell, Natalya Vaksman, & Nigel W. Bunnett. (2009). Endothelin‐converting enzyme 1 promotes re‐sensitization of neurokinin 1 receptor‐dependent neurogenic inflammation. British Journal of Pharmacology. 156(5). 730–739. 28 indexed citations
19.
Cattaruzza, Fiore, Nicolas Cénac, Elisabetta Barocelli, et al.. (2006). Protective Effect of Proteinase-Activated Receptor 2 Activation on Motility Impairment and Tissue Damage Induced by Intestinal Ischemia/Reperfusion in Rodents. American Journal Of Pathology. 169(1). 177–188. 53 indexed citations
20.
Barocelli, Elisabetta, Vigilio Ballabeni, Fiore Cattaruzza, et al.. (2006). The selective inhibition of inducible nitric oxide synthase prevents intestinal ischemia–reperfusion injury in mice. Nitric Oxide. 14(3). 212–218. 43 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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