Thomas S. Reger

1.4k total citations
20 papers, 972 citations indexed

About

Thomas S. Reger is a scholar working on Organic Chemistry, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Thomas S. Reger has authored 20 papers receiving a total of 972 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 7 papers in Molecular Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Thomas S. Reger's work include Chemical Synthesis and Analysis (5 papers), Neuroscience and Neuropharmacology Research (4 papers) and Synthetic Organic Chemistry Methods (4 papers). Thomas S. Reger is often cited by papers focused on Chemical Synthesis and Analysis (5 papers), Neuroscience and Neuropharmacology Research (4 papers) and Synthetic Organic Chemistry Methods (4 papers). Thomas S. Reger collaborates with scholars based in United States, Japan and China. Thomas S. Reger's co-authors include Kim D. Janda, Bruce Clapham, Albert Padwa, C. Oliver Kappe, Nicholas Stock, Patrick H. Toy, Mitchell Green, Christopher D. King, John J. Renger and Anthony L. Gotter and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Clinical Investigation and Journal of Pharmacology and Experimental Therapeutics.

In The Last Decade

Thomas S. Reger

19 papers receiving 944 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas S. Reger United States 12 581 326 175 172 95 20 972
Ling Ma China 19 268 0.5× 245 0.8× 89 0.5× 71 0.4× 102 1.1× 53 934
Sung‐Gon Kim South Korea 27 1.4k 2.4× 351 1.1× 112 0.6× 273 1.6× 96 1.0× 161 2.3k
Frédéric Buron France 21 754 1.3× 362 1.1× 245 1.4× 130 0.8× 47 0.5× 79 1.4k
Brian C. Shook United States 18 1.5k 2.7× 509 1.6× 89 0.5× 347 2.0× 60 0.6× 25 2.1k
Marvin M. Hansen United States 17 623 1.1× 389 1.2× 66 0.4× 77 0.4× 219 2.3× 30 1.0k
Holger Monenschein Germany 18 864 1.5× 505 1.5× 92 0.5× 157 0.9× 45 0.5× 32 1.1k
Bin Huang China 21 598 1.0× 136 0.4× 143 0.8× 104 0.6× 28 0.3× 81 1.0k
Michael T. Scerba United States 18 871 1.5× 298 0.9× 63 0.4× 304 1.8× 57 0.6× 36 1.5k
Jianming Bao United States 16 523 0.9× 250 0.8× 84 0.5× 110 0.6× 63 0.7× 28 812
David G. Melillo United States 14 440 0.8× 289 0.9× 36 0.2× 76 0.4× 158 1.7× 37 939

Countries citing papers authored by Thomas S. Reger

Since Specialization
Citations

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

Fields of papers citing papers by Thomas S. Reger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas S. Reger. 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 Thomas S. Reger. The network helps show where Thomas S. Reger may publish in the future.

Co-authorship network of co-authors of Thomas S. Reger

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas S. Reger. A scholar is included among the top collaborators of Thomas S. Reger 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 Thomas S. Reger. Thomas S. Reger 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.
Reger, Thomas S., et al.. (2020). Science of Sealing: Advanced Materials for High-Temperature Applications. 1–5. 1 indexed citations
2.
Kraus, Richard L., Yuxing Li, Anthony L. Gotter, et al.. (2010). In Vitro Characterization of T-Type Calcium Channel Antagonist TTA-A2 and In Vivo Effects on Arousal in Mice. Journal of Pharmacology and Experimental Therapeutics. 335(2). 409–417. 88 indexed citations
3.
Reger, Thomas S., Nicholas Stock, Bowei Wang, et al.. (2009). Heterocycle-substituted proline dipeptides as potent VLA-4 antagonists. Bioorganic & Medicinal Chemistry Letters. 20(3). 1173–1176. 7 indexed citations
4.
Uebele, Victor N., Anthony L. Gotter, Cindy E. Nuss, et al.. (2009). Antagonism of T-type calcium channels inhibits high-fat diet–induced weight gain in mice. Journal of Clinical Investigation. 119(6). 1659–1667. 61 indexed citations
5.
Smith, Nicholas D., Thomas S. Reger, Joseph E. Payne, et al.. (2005). Water soluble prodrug of a COX-2 selective inhibitor suitable for intravenous administration in models of cerebral ischemia. Bioorganic & Medicinal Chemistry Letters. 15(13). 3197–3200. 3 indexed citations
6.
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Green, Mitchell, et al.. (2004). Glucuronidation of carboxylic acid containing compounds by UDP-glucuronosyltransferase isoforms. Archives of Biochemistry and Biophysics. 424(2). 219–225. 96 indexed citations
8.
Huang, Dehua, Steve F. Poon, Deborah F. Chapman, et al.. (2004). 2-{2-[3-(Pyridin-3-yloxy)phenyl]-2H-tetrazol-5-yl}pyridine: a highly potent, orally active, metabotropic glutamate subtype 5 (mGlu5) receptor antagonist. Bioorganic & Medicinal Chemistry Letters. 14(22). 5473–5476. 25 indexed citations
9.
Reger, Thomas S. & Kim D. Janda. (2002). Parallel suspension polymerization for high-throughput resin synthesis. Bioorganic & Medicinal Chemistry Letters. 12(6). 837–840. 6 indexed citations
10.
Clapham, Bruce, Thomas S. Reger, & Kim D. Janda. (2001). Polymer-supported catalysis in synthetic organic chemistry. Tetrahedron. 57(22). 4637–4662. 260 indexed citations
11.
Clapham, Bruce, Thomas S. Reger, & Kim D. Janda. (2001). ChemInform Abstract: Polymer‐Supported Catalysis in Synthetic Organic Chemistry. ChemInform. 32(39). 1 indexed citations
12.
Padwa, Albert & Thomas S. Reger. (2000). Construction of bicyclic tetrahydroisoquinolinones by combination of an IMDAF-ring cleavage reaction of N-allyl-2-furan-2-yl-acetamides. Canadian Journal of Chemistry. 78(6). 749–756. 13 indexed citations
13.
Toy, Patrick H., Thomas S. Reger, & Kim D. Janda. (2000). Soluble Polymer Bound Cleavage Reagents:  A Multipolymer Strategy for the Cleavage of Tertiary Amines from REM Resin. Organic Letters. 2(15). 2205–2207. 25 indexed citations
14.
Reger, Thomas S. & Kim D. Janda. (2000). Polymer-Supported (Salen)Mn Catalysts for Asymmetric Epoxidation:  A Comparison between Soluble and Insoluble Matrices. Journal of the American Chemical Society. 122(29). 6929–6934. 201 indexed citations
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18.
Toy, Patrick H., Thomas S. Reger, Patrick Garibay, et al.. (2000). Polytetrahydrofuran Cross-Linked Polystyrene Resins for Solid-Phase Organic Synthesis. Journal of Combinatorial Chemistry. 3(1). 117–124. 55 indexed citations
19.
Padwa, Albert, et al.. (1998). A Triple Cascade Sequence as a Strategy for the Construction of the Erythrinane Skeleton. The Journal of Organic Chemistry. 63(4). 1144–1155. 68 indexed citations
20.
Padwa, Albert, C. Oliver Kappe, & Thomas S. Reger. (1996). Tandem Diels−Alder N-Acyliminium Ion Cyclization Reactions. A New Entry into the Erythrinane Skeleton. The Journal of Organic Chemistry. 61(15). 4888–4889. 36 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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