Eric T. Sun

1.4k total citations
20 papers, 1.0k citations indexed

About

Eric T. Sun is a scholar working on Molecular Biology, Oncology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Eric T. Sun has authored 20 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Oncology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Eric T. Sun's work include Chemical Synthesis and Analysis (7 papers), Neuroscience and Neuropharmacology Research (4 papers) and Cancer-related Molecular Pathways (4 papers). Eric T. Sun is often cited by papers focused on Chemical Synthesis and Analysis (7 papers), Neuroscience and Neuropharmacology Research (4 papers) and Cancer-related Molecular Pathways (4 papers). Eric T. Sun collaborates with scholars based in United States and Singapore. Eric T. Sun's co-authors include Daniel H. Rich, E H Ulm, Anthony D. William, Brian Dymock, Ramesh Jayaraman, Kantharaj Ethirajulu, Daniel J. Garland, Paul H. Taghert, Kee Chuan Goh and D. S. KEMP and has published in prestigious journals such as The Journal of Comparative Neurology, Biochemical and Biophysical Research Communications and Journal of Medicinal Chemistry.

In The Last Decade

Eric T. Sun

20 papers receiving 949 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric T. Sun United States 16 596 265 264 191 125 20 1.0k
Shin‐ichi Tsukamoto Japan 22 765 1.3× 147 0.6× 652 2.5× 119 0.6× 139 1.1× 71 1.6k
Haile Tecle United States 14 1.1k 1.9× 403 1.5× 423 1.6× 161 0.8× 42 0.3× 27 1.7k
Wang‐Qing Liu France 20 805 1.4× 283 1.1× 194 0.7× 122 0.6× 48 0.4× 54 1.2k
Roland Neuhaus Germany 16 732 1.2× 191 0.7× 123 0.5× 193 1.0× 54 0.4× 35 1.1k
Geoffrey Lawton United Kingdom 13 904 1.5× 166 0.6× 275 1.0× 176 0.9× 48 0.4× 20 1.4k
Roland Feifel Switzerland 21 769 1.3× 164 0.6× 338 1.3× 206 1.1× 41 0.3× 36 1.3k
Kelli Glenn United States 13 895 1.5× 690 2.6× 182 0.7× 126 0.7× 69 0.6× 20 1.4k
Paul Rose United States 17 634 1.1× 329 1.2× 94 0.4× 124 0.6× 77 0.6× 21 1.1k
Karima Bettayeb France 18 731 1.2× 316 1.2× 397 1.5× 101 0.5× 59 0.5× 21 1.5k
Christopher H. Hill United Kingdom 14 960 1.6× 152 0.6× 353 1.3× 177 0.9× 49 0.4× 22 1.5k

Countries citing papers authored by Eric T. Sun

Since Specialization
Citations

This map shows the geographic impact of Eric T. Sun'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 Eric T. Sun with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric T. Sun more than expected).

Fields of papers citing papers by Eric T. Sun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric T. Sun. 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 Eric T. Sun. The network helps show where Eric T. Sun may publish in the future.

Co-authorship network of co-authors of Eric T. Sun

This figure shows the co-authorship network connecting the top 25 collaborators of Eric T. Sun. A scholar is included among the top collaborators of Eric T. Sun 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 Eric T. Sun. Eric T. Sun 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
3.
Novotny‐Diermayr, Veronica, Stefan Hart, Yung Kiang Loh, et al.. (2011). TG02, a novel oral multi-kinase inhibitor of CDKs, JAK2 and FLT3 with potent anti-leukemic properties. Leukemia. 26(2). 236–243. 105 indexed citations
6.
Blanchard, Stéphanie, Anthony D. William, Anders Poulsen, et al.. (2010). Synthesis and evaluation of alkenyl indazoles as selective Aurora kinase inhibitors. Bioorganic & Medicinal Chemistry Letters. 20(8). 2443–2447. 15 indexed citations
7.
Wang, Haishan, Yan Zhou, Ting Lu, et al.. (2010). Acylurea connected straight chain hydroxamates as novel histone deacetylase inhibitors: Synthesis, SAR, and in vivo antitumor activity. Bioorganic & Medicinal Chemistry Letters. 20(11). 3314–3321. 24 indexed citations
8.
Poulsen, Anders, Anthony D. William, Stéphanie Blanchard, et al.. (2008). Structure-based design of Aurora A & B inhibitors. Journal of Computer-Aided Molecular Design. 22(12). 897–906. 8 indexed citations
9.
Li, Haitao, Kenna Anderes, Eugenia Kraynov, et al.. (2006). Discovery of a Novel, Orally Active, Small Molecule Gonadotropin-Releasing Hormone (GnRH) Receptor Antagonist. Journal of Medicinal Chemistry. 49(11). 3362–3367. 14 indexed citations
10.
Sun, Eric T., et al.. (1993). An immunocytochemical study of the FMRFamide neuropeptide gene products in Drosophila. The Journal of Comparative Neurology. 337(3). 446–460. 81 indexed citations
11.
Vazquez, Michael L., Danny J. Garland, Eric T. Sun, et al.. (1992). Characterization of 3-carboxy-5-phosphono-1,2,3,4-tetrahydroisoquinoline (SC-48981), a potent competitive (NMDA) receptor antagonist, in vitro and in vivo. Neuroscience Letters. 135(2). 149–152. 4 indexed citations
12.
Rao, Tadimeti S., Julie A. Cler, Robert P. Compton, et al.. (1990). Neuropharmacological characterization of 1-Aminocyclopropane-1-carboxylate and 1-Aminocyclobutane-1-carboxylate, Ligands of the N-Methyl-D-Aspartate-associated Glycine Receptor. Neuropharmacology. 29(3). 305–309. 28 indexed citations
13.
Wood, Paul L., Tadimeti S. Rao, Smriti Iyengar, et al.. (1990). A review of the in vitro and in vivo neurochemical characterization of the NMDA/PCP/Glycine/Ion channel receptor macrocomplex. Neurochemical Research. 15(2). 217–230. 54 indexed citations
14.
Hood, William F., et al.. (1989). 1-Aminocyclobutane-1-carboxylate (ACBC): a specific antagonist of the N-methyl-D-aspartate receptor coupled glycine receptor. European Journal of Pharmacology. 161(2-3). 281–282. 47 indexed citations
15.
KEMP, D. S. & Eric T. Sun. (1982). Amino acids derivatives that stabilize secondary structures of polypeptides--. Tetrahedron Letters. 23(37). 3759–3760. 40 indexed citations
16.
Rich, Daniel H., Eric T. Sun, & E H Ulm. (1980). Synthesis of analogs of the carboxyl protease inhibitor pepstatin. Effect of structure on inhibition of pepsin and renin. Journal of Medicinal Chemistry. 23(1). 27–33. 119 indexed citations
17.
Rich, Daniel H. & Eric T. Sun. (1980). Mechanism of inhibition of pepsin by pepstatin. Biochemical Pharmacology. 29(16). 2205–2212. 68 indexed citations
18.
Rich, Daniel H., et al.. (1979). ChemInform Abstract: SYNTHESIS OF (3S,4S)‐4‐AMINO‐3‐HYDROXY‐6‐METHYLHEPTANOIC ACID DERIVATIVES. ANALYSIS OF DIASTEREOMERIC PURITY. Chemischer Informationsdienst. 10(8). 15 indexed citations
19.
Rich, Daniel H., et al.. (1978). Synthesis of (3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid derivatives. Analysis of diastereomeric purity. The Journal of Organic Chemistry. 43(18). 3624–3626. 81 indexed citations
20.
Rich, Daniel H., Eric T. Sun, & Jasbir Singh. (1977). Synthesis of dideoxy-pepstatin. Mechanism of inhibition of porcine pepsin. Biochemical and Biophysical Research Communications. 74(2). 762–767. 23 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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