John Saunders

4.1k total citations
139 papers, 3.1k citations indexed

About

John Saunders is a scholar working on Molecular Biology, Organic Chemistry and Endocrine and Autonomic Systems. According to data from OpenAlex, John Saunders has authored 139 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 48 papers in Organic Chemistry and 25 papers in Endocrine and Autonomic Systems. Recurrent topics in John Saunders's work include Receptor Mechanisms and Signaling (35 papers), Regulation of Appetite and Obesity (25 papers) and Biochemical Analysis and Sensing Techniques (25 papers). John Saunders is often cited by papers focused on Receptor Mechanisms and Signaling (35 papers), Regulation of Appetite and Obesity (25 papers) and Biochemical Analysis and Sensing Techniques (25 papers). John Saunders collaborates with scholars based in United States, United Kingdom and Netherlands. John Saunders's co-authors include Chen Chen, Angus M. MacLeod, Fábio C. Tucci, Clare O. Kneen, Kevin J. Merchant, Yunfei Zhu, R. Scott Struthers, R. BAKER, Val S. Goodfellow and Christine M. Tarby and has published in prestigious journals such as Scientific Reports, FEBS Letters and Annals of the New York Academy of Sciences.

In The Last Decade

John Saunders

138 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John Saunders United States 28 1.3k 1.3k 410 384 337 139 3.1k
Jean‐Alain Fehrentz France 39 1.1k 0.8× 2.1k 1.6× 782 1.9× 1.3k 3.5× 941 2.8× 149 4.3k
Erich Wünsch Germany 31 965 0.7× 2.2k 1.8× 841 2.1× 98 0.3× 142 0.4× 167 3.6k
Chiara Cabrele Germany 28 932 0.7× 1.8k 1.4× 610 1.5× 143 0.4× 49 0.1× 78 2.9k
Jesper Lau Denmark 31 843 0.6× 2.2k 1.7× 802 2.0× 214 0.6× 112 0.3× 74 4.2k
Panayotis G. Katsoyannis United States 37 733 0.5× 2.9k 2.3× 181 0.4× 158 0.4× 124 0.4× 141 4.2k
Gianfranco Balboni Italy 35 781 0.6× 2.2k 1.7× 1.6k 4.0× 166 0.4× 33 0.1× 163 3.6k
Raymond S.L. Chang United States 31 1.6k 1.2× 2.7k 2.2× 1.6k 3.9× 119 0.3× 61 0.2× 114 4.7k
Hidehiko Nakagawa Japan 40 1.2k 0.9× 2.4k 1.9× 347 0.8× 130 0.3× 135 0.4× 170 4.9k
Zbigniew Grzonka Poland 28 305 0.2× 1.3k 1.0× 251 0.6× 235 0.6× 221 0.7× 104 2.4k
Donald J. Wolff United States 30 259 0.2× 1.7k 1.3× 572 1.4× 72 0.2× 113 0.3× 50 2.8k

Countries citing papers authored by John Saunders

Since Specialization
Citations

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

Fields of papers citing papers by John Saunders

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Saunders

This figure shows the co-authorship network connecting the top 25 collaborators of John Saunders. A scholar is included among the top collaborators of John Saunders 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 Saunders. John Saunders 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.
Chen, Chen, Fábio C. Tucci, Wanlong Jiang, et al.. (2008). Pharmacological and pharmacokinetic characterization of 2-piperazine-α-isopropyl benzylamine derivatives as melanocortin-4 receptor antagonists. Bioorganic & Medicinal Chemistry. 16(10). 5606–5618. 18 indexed citations
2.
Chen, Chen, Joe A. Tran, Beth A. Fleck, et al.. (2008). Studies on the Structure-Activity Relationship of the Basic Amine of Phenylpiperazines as Melanocortin-4 Receptor Antagonists. Medicinal Chemistry. 4(1). 67–74. 4 indexed citations
3.
Moorjani, M. N., Xiaohu Zhang, Yongsheng Chen, et al.. (2008). 2,6-Diaryl-4-phenacylaminopyrimidines as potent and selective adenosine A2A antagonists with reduced hERG liability. Bioorganic & Medicinal Chemistry Letters. 18(4). 1269–1273. 5 indexed citations
4.
Jiang, Wanlong, Fábio C. Tucci, Joe A. Tran, et al.. (2007). Pyrrolidinones as potent functional antagonists of the human melanocortin-4 receptor. Bioorganic & Medicinal Chemistry Letters. 17(20). 5610–5613. 16 indexed citations
5.
Rowbottom, Martin W., Mingzhu Zhang, Brian Dyck, et al.. (2007). Synthesis and structure–activity relationships of spirohydantoin-derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1). Bioorganic & Medicinal Chemistry Letters. 17(8). 2171–2178. 8 indexed citations
6.
Chen, Caroline W., Joe A. Tran, Wanlong Jiang, et al.. (2006). Propionylpiperazines as human melanocortin-4 receptor ligands. Bioorganic & Medicinal Chemistry Letters. 16(18). 4800–4803. 12 indexed citations
7.
Tran, Joe A., Joseph Pontillo, Beth A. Fleck, et al.. (2006). Design, synthesis, and SAR studies on a series of 2-pyridinylpiperazines as potent antagonists of the melanocortin-4 receptor. Bioorganic & Medicinal Chemistry Letters. 16(14). 3693–3696. 4 indexed citations
8.
Pontillo, Joseph, Beth A. Fleck, Fábio C. Tucci, et al.. (2005). Structure–activity relationship of a series of cyclohexylpiperidines bearing an amide side chain as antagonists of the human melanocortin-4 receptor. Bioorganic & Medicinal Chemistry Letters. 15(14). 3434–3438. 9 indexed citations
9.
Guo, Zhiqiang, Yongsheng Chen, Charles Q. Huang, et al.. (2005). Uracils as potent antagonists of the human gonadotropin-releasing hormone receptor without atropisomers. Bioorganic & Medicinal Chemistry Letters. 15(10). 2519–2522. 20 indexed citations
10.
Pontillo, Joseph, Joe A. Tran, Beth A. Fleck, et al.. (2005). Structure–activity relationship studies on a series of cyclohexylpiperazines bearing a phanylacetamide as ligands of the human melanocortin-4 receptor. Bioorganic & Medicinal Chemistry Letters. 15(23). 5237–5240. 7 indexed citations
11.
Pontillo, Joseph, Stacy Markison, Margaret Joppa, et al.. (2005). A potent and selective nonpeptide antagonist of the melanocortin-4 receptor induces food intake in satiated mice. Bioorganic & Medicinal Chemistry Letters. 15(10). 2541–2546. 19 indexed citations
12.
Tucci, Fábio C., Stacy Markison, Margaret Joppa, et al.. (2005). Potent and orally active non-peptide antagonists of the human melanocortin-4 receptor based on a series of trans-2-disubstituted cyclohexylpiperazines. Bioorganic & Medicinal Chemistry Letters. 15(19). 4389–4395. 30 indexed citations
13.
Tran, Joe A., Joseph Pontillo, Beth A. Fleck, et al.. (2004). Identification of agonists and antagonists of the human melanocortin-4 receptor from piperazinebenzylamines. Bioorganic & Medicinal Chemistry Letters. 15(3). 833–837. 12 indexed citations
14.
Moree, Wilna J., Ken-ichiro Kataoka, Tatsuki Shiota, et al.. (2004). Small molecule antagonists of the CCR2b receptor. Part 2: Discovery process and initial structure–activity relationships of diamine derivatives. Bioorganic & Medicinal Chemistry Letters. 14(21). 5413–5416. 33 indexed citations
15.
Dyck, Brian, Val S. Goodfellow, Teresa A. Phillips, et al.. (2004). Potent imidazole and triazole CB 1 receptor antagonists related to SR141716. Bioorganic & Medicinal Chemistry Letters. 14(5). 1151–1154. 56 indexed citations
16.
Shiota, Tatsuki, Ken-ichiro Kataoka, Christine M. Tarby, et al.. (2004). Small molecule inhibitors of the CCR2b receptor. Part 1: Discovery and optimization of homopiperazine derivatives. Bioorganic & Medicinal Chemistry Letters. 14(21). 5407–5411. 22 indexed citations
17.
Rowbottom, Martin W., Fábio C. Tucci, Patrick J. Connors, et al.. (2004). Synthesis and structure–activity relationships of uracil derived human GnRH receptor antagonists: (R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6-methyluracils containing a substituted thiophene or thiazole at C-5. Bioorganic & Medicinal Chemistry Letters. 14(19). 4967–4973. 13 indexed citations
18.
Guo, Zhiqiang, Yongsheng Chen, Dongpei Wu, et al.. (2003). Synthesis and structure–Activity relationships of thieno[2,3-d]pyrimidine-2,4-dione derivatives as potent GnRH receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 13(20). 3617–3622. 20 indexed citations
19.
Saunders, John. (2000). Top Drugs. Oxford University Press eBooks. 6 indexed citations
20.
Wätjen, Frank, R. BAKER, Richard H. Herbert, et al.. (1989). Novel benzodiazepine receptor partial agonists: oxadiazolylimidazobenzodiazepines. Journal of Medicinal Chemistry. 32(10). 2282–2291. 114 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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