John W. Cuozzo

3.8k total citations
28 papers, 1.9k citations indexed

About

John W. Cuozzo is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, John W. Cuozzo has authored 28 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 6 papers in Oncology and 6 papers in Cell Biology. Recurrent topics in John W. Cuozzo's work include NF-κB Signaling Pathways (6 papers), Chemical Synthesis and Analysis (4 papers) and Cellular transport and secretion (4 papers). John W. Cuozzo is often cited by papers focused on NF-κB Signaling Pathways (6 papers), Chemical Synthesis and Analysis (4 papers) and Cellular transport and secretion (4 papers). John W. Cuozzo collaborates with scholars based in United States, United Kingdom and Canada. John W. Cuozzo's co-authors include Chris A. Kaiser, Alison R. Frand, G G Sahagian, Matthew Clark, Fredrik Åslund, Carolyn S. Sevier, Andrea Vala, Eric A. Sigel, Anthony D. Keefe and Zhengrong Zhu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Cell Biology.

In The Last Decade

John W. Cuozzo

28 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John W. Cuozzo United States 23 1.3k 483 337 220 187 28 1.9k
Stefan Müller Germany 28 1.6k 1.3× 247 0.5× 404 1.2× 296 1.3× 488 2.6× 51 2.4k
Frank J. Schoenen United States 27 1.5k 1.2× 543 1.1× 668 2.0× 103 0.5× 250 1.3× 76 3.0k
Piliang Hao China 27 1.6k 1.3× 285 0.6× 517 1.5× 207 0.9× 170 0.9× 72 2.3k
Jui‐Yoa Chang United States 29 1.8k 1.4× 334 0.7× 144 0.4× 174 0.8× 219 1.2× 93 2.8k
Lora Swenson United States 20 2.1k 1.7× 339 0.7× 252 0.7× 71 0.3× 130 0.7× 29 2.9k
Hiroshi Takemoto Japan 24 1.1k 0.9× 188 0.4× 364 1.1× 109 0.5× 139 0.7× 65 1.7k
Remigiusz Serwa Poland 22 1.2k 0.9× 245 0.5× 539 1.6× 160 0.7× 103 0.6× 56 1.8k
Fan Liu Germany 25 1.5k 1.2× 390 0.8× 210 0.6× 96 0.4× 108 0.6× 98 2.4k
Said A. Goueli United States 22 1.5k 1.2× 214 0.4× 137 0.4× 120 0.5× 142 0.8× 94 2.3k
HaJeung Park United States 27 1.7k 1.3× 157 0.3× 264 0.8× 121 0.6× 215 1.1× 68 2.4k

Countries citing papers authored by John W. Cuozzo

Since Specialization
Citations

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

Fields of papers citing papers by John W. Cuozzo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John W. Cuozzo. 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 John W. Cuozzo. The network helps show where John W. Cuozzo may publish in the future.

Co-authorship network of co-authors of John W. Cuozzo

This figure shows the co-authorship network connecting the top 25 collaborators of John W. Cuozzo. A scholar is included among the top collaborators of John W. Cuozzo 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 John W. Cuozzo. John W. Cuozzo 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.
Canè, Stefania, Roza Maria Barouni, Marina Fabbi, et al.. (2023). Neutralization of NET-associated human ARG1 enhances cancer immunotherapy. Science Translational Medicine. 15(687). eabq6221–eabq6221. 61 indexed citations
2.
Veerman, Johan J. N., Koen F. W. Hekking, Christopher D. Hupp, et al.. (2021). Discovery of 2,4-1H-Imidazole Carboxamides as Potent and Selective TAK1 Inhibitors. ACS Medicinal Chemistry Letters. 12(4). 555–562. 11 indexed citations
3.
McCloskey, Kevin, Eric A. Sigel, Steven Kearnes, et al.. (2020). Machine Learning on DNA-Encoded Libraries: A New Paradigm for Hit Finding. Journal of Medicinal Chemistry. 63(16). 8857–8866. 85 indexed citations
4.
Cuozzo, John W., Diana Gikunju, Sevan Habeshian, et al.. (2017). Discovery of a Potent BTK Inhibitor with a Novel Binding Mode by Using Parallel Selections with a DNA‐Encoded Chemical Library. ChemBioChem. 18(9). 864–871. 51 indexed citations
5.
Soutter, Holly H., Matthew Clark, John W. Cuozzo, et al.. (2016). Discovery of cofactor-specific, bactericidal Mycobacterium tuberculosis InhA inhibitors using DNA-encoded library technology. Proceedings of the National Academy of Sciences. 113(49). E7880–E7889. 46 indexed citations
6.
Litovchick, Alexander, Christoph E. Dumelin, Sevan Habeshian, et al.. (2015). Encoded Library Synthesis Using Chemical Ligation and the Discovery of sEH Inhibitors from a 334-Million Member Library. Scientific Reports. 5(1). 10916–10916. 87 indexed citations
7.
Cuozzo, John W. & Holly H. Soutter. (2014). Overview of Recent Progress in Protein-Expression Technologies for Small-Molecule Screening. SLAS DISCOVERY. 19(7). 1000–1013. 9 indexed citations
8.
Zhu, Zhengrong & John W. Cuozzo. (2009). High-Throughput Affinity-Based Technologies for Small-Molecule Drug Discovery. SLAS DISCOVERY. 14(10). 1157–1164. 44 indexed citations
9.
Kaila, Neelu, Neal Green, Huan‐Qiu Li, et al.. (2007). Identification of a novel class of selective Tpl2 kinase inhibitors: 4-Alkylamino-[1,7]naphthyridine-3-carbonitriles. Bioorganic & Medicinal Chemistry. 15(19). 6425–6442. 23 indexed citations
10.
Wang, Qin, Yuhua Zhang, J. Perry Hall, et al.. (2007). A rat pharmacokinetic/pharmacodynamic model for assessment of lipopolysaccharide-induced tumor necrosis factor-alpha production. Journal of Pharmacological and Toxicological Methods. 56(1). 67–71. 15 indexed citations
11.
Hall, J. Perry, Sang Hsu, John W. Cuozzo, et al.. (2007). Pharmacologic Inhibition of Tpl2 Blocks Inflammatory Responses in Primary Human Monocytes, Synoviocytes, and Blood. Journal of Biological Chemistry. 282(46). 33295–33304. 64 indexed citations
12.
Hu, Yonghan, Neal Green, Lori K. Gavrin, et al.. (2006). Inhibition of Tpl2 kinase and TNFα production with quinoline-3-carbonitriles for the treatment of rheumatoid arthritis. Bioorganic & Medicinal Chemistry Letters. 16(23). 6067–6072. 54 indexed citations
13.
Gavrin, Lori K., Neal Green, Yonghan Hu, et al.. (2005). Inhibition of Tpl2 kinase and TNF-α production with 1,7-naphthyridine-3-carbonitriles: Synthesis and structure–activity relationships. Bioorganic & Medicinal Chemistry Letters. 15(23). 5288–5292. 41 indexed citations
14.
Hsu, Sang, et al.. (2004). Phosphorylation of Threonine 290 in the Activation Loop of Tpl2/Cot Is Necessary but Not Sufficient for Kinase Activity. Journal of Biological Chemistry. 279(50). 52117–52123. 39 indexed citations
15.
Channavajhala, Padma L., Leeying Wu, John W. Cuozzo, et al.. (2003). Identification of a Novel Human Kinase Supporter of Ras (hKSR-2) That Functions as a Negative Regulator of Cot (Tpl2) Signaling. Journal of Biological Chemistry. 278(47). 47089–47097. 39 indexed citations
16.
Sevier, Carolyn S., John W. Cuozzo, Andrea Vala, Fredrik Åslund, & Chris A. Kaiser. (2001). A flavoprotein oxidase defines a new endoplasmic reticulum pathway for biosynthetic disulphide bond formation. Nature Cell Biology. 3(10). 874–882. 148 indexed citations
17.
Frand, Alison R., John W. Cuozzo, & Chris A. Kaiser. (2000). Pathways for protein disulphide bond formation. Trends in Cell Biology. 10(5). 203–210. 276 indexed citations
18.
Cuozzo, John W. & Chris A. Kaiser. (1999). Competition between glutathione and protein thiols for disulphide-bond formation. Nature Cell Biology. 1(3). 130–135. 267 indexed citations
19.
Cuozzo, John W., et al.. (1998). Lysine-based Structure Responsible for Selective Mannose Phosphorylation of Cathepsin D and Cathepsin L Defines a Common Structural Motif for Lysosomal Enzyme Targeting. Journal of Biological Chemistry. 273(33). 21067–21076. 53 indexed citations
20.
Cuozzo, John W., et al.. (1995). Lysine-based Structure in the Proregion of Procathepsin L Is the Recognition Site for Mannose Phosphorylation. Journal of Biological Chemistry. 270(26). 15611–15619. 46 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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