Tammy C. Wang

525 total citations
16 papers, 278 citations indexed

About

Tammy C. Wang is a scholar working on Organic Chemistry, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Tammy C. Wang has authored 16 papers receiving a total of 278 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Organic Chemistry, 7 papers in Molecular Biology and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Tammy C. Wang's work include Chemical Synthesis and Analysis (3 papers), Antiplatelet Therapy and Cardiovascular Diseases (3 papers) and Adenosine and Purinergic Signaling (3 papers). Tammy C. Wang is often cited by papers focused on Chemical Synthesis and Analysis (3 papers), Antiplatelet Therapy and Cardiovascular Diseases (3 papers) and Adenosine and Purinergic Signaling (3 papers). Tammy C. Wang collaborates with scholars based in United States, Germany and Sweden. Tammy C. Wang's co-authors include Jennifer X. Qiao, Ruth R. Wexler, Patrick Y. S. Lam, Jianqing Li, John S. Sack, Laura A. Price, Robert M. Knabb, Daniel G. Roberts, Steven M. Seiler and Chong‐Qing Sun and has published in prestigious journals such as Journal of Molecular Biology, Journal of Medicinal Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Tammy C. Wang

16 papers receiving 271 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tammy C. Wang United States 10 113 98 52 46 36 16 278
Bernd Jablonka Germany 7 233 2.1× 159 1.6× 69 1.3× 93 2.0× 17 0.5× 14 508
Daisy Pireh United States 8 172 1.5× 119 1.2× 44 0.8× 16 0.3× 40 1.1× 14 347
Barry Teobald United Kingdom 6 287 2.5× 136 1.4× 53 1.0× 115 2.5× 14 0.4× 6 535
Yumi Matsui Japan 13 68 0.6× 242 2.5× 10 0.2× 21 0.5× 20 0.6× 21 342
Peter Raddatz Germany 14 239 2.1× 185 1.9× 15 0.3× 41 0.9× 20 0.6× 30 445
Herman J. Crowley United States 13 145 1.3× 157 1.6× 10 0.2× 24 0.5× 11 0.3× 24 369
Shuichi Mori Japan 14 111 1.0× 240 2.4× 4 0.1× 51 1.1× 25 0.7× 33 442
Taisuke Hamamoto Japan 9 122 1.1× 115 1.2× 41 0.8× 106 2.3× 10 0.3× 11 441
Szymon Kłossowski Poland 12 131 1.2× 301 3.1× 51 1.0× 8 0.2× 5 0.1× 22 410
Xiaozhang Zheng United States 13 102 0.9× 249 2.5× 10 0.2× 17 0.4× 3 0.1× 26 448

Countries citing papers authored by Tammy C. Wang

Since Specialization
Citations

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

Fields of papers citing papers by Tammy C. Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tammy C. Wang. 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 Tammy C. Wang. The network helps show where Tammy C. Wang may publish in the future.

Co-authorship network of co-authors of Tammy C. Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Tammy C. Wang. A scholar is included among the top collaborators of Tammy C. Wang 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 Tammy C. Wang. Tammy C. Wang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Qiao, Jennifer X., Mark R. Witmer, Tammy C. Wang, et al.. (2023). Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1). Bioorganic & Medicinal Chemistry Letters. 98. 129589–129589. 3 indexed citations
2.
Wang, Tammy C., Jennifer X. Qiao, David S. Taylor, et al.. (2018). Discovery and synthesis of tetrahydropyrimidinedione-4-carboxamides as endothelial lipase inhibitors. Bioorganic & Medicinal Chemistry Letters. 28(23-24). 3721–3725. 7 indexed citations
3.
4.
Wang, Tammy C. & Jennifer X. Qiao. (2016). Microwave-assisted transamidation of ureas. Tetrahedron Letters. 57(18). 1941–1943. 10 indexed citations
5.
Qiao, Jennifer X., Kenneth J. Fraunhoffer, Yi Hsiao, et al.. (2016). Synthesis of Fmoc-Protected Arylphenylalanines (Bip Derivatives) via Nonaqueous Suzuki-Miyaura Cross-Coupling Reactions. The Journal of Organic Chemistry. 81(19). 9499–9506. 8 indexed citations
6.
Qiao, Jennifer X., Ying Han, Tammy C. Wang, et al.. (2014). 2-Amino-1,3,4-thiadiazoles in the 7-hydroxy-N-neopentyl spiropiperidine indolinyl series as potent P2Y1 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 24(11). 2481–2485. 8 indexed citations
7.
Yang, Wu, Jennifer X. Qiao, Tammy C. Wang, et al.. (2014). Discovery of 4-Aryl-7-Hydroxyindoline-Based P2Y1 Antagonists as Novel Antiplatelet Agents. Journal of Medicinal Chemistry. 57(14). 6150–6164. 38 indexed citations
8.
Wang, Tammy C., Jennifer X. Qiao, Charles G. Clark, et al.. (2013). Discovery of diarylurea P2Y1 antagonists with improved aqueous solubility. Bioorganic & Medicinal Chemistry Letters. 23(11). 3239–3243. 14 indexed citations
9.
Qiao, Jennifer X., et al.. (2011). Transformation of Anionically Activated Trifluoromethyl Groups to Heterocycles under Mild Aqueous Conditions. Organic Letters. 13(7). 1804–1807. 33 indexed citations
10.
Qiao, Jennifer X., Chong‐Hwan Chang, Daniel L. Cheney, et al.. (2007). SAR and X-ray structures of enantiopure 1,2-cis-(1R,2S)-cyclopentyldiamine and cyclohexyldiamine derivatives as inhibitors of coagulation Factor Xa. Bioorganic & Medicinal Chemistry Letters. 17(16). 4419–4427. 29 indexed citations
11.
Qiao, Jennifer X., Tammy C. Wang, Daniel L. Cheney, et al.. (2007). Enantiopure five-membered cyclicdiamine derivatives as potent and selective inhibitors of factor Xa. Improving in vitro metabolic stability via core modifications. Bioorganic & Medicinal Chemistry Letters. 17(18). 5041–5048. 17 indexed citations
12.
Sun, Chong‐Qing, Jeffrey A. Robl, Tammy C. Wang, et al.. (2006). Discovery of Potent, Orally-Active, and Muscle-Selective Androgen Receptor Modulators Based on an N-Aryl-hydroxybicyclohydantoin Scaffold. Journal of Medicinal Chemistry. 49(26). 7596–7599. 46 indexed citations
13.
Das, Jagabandhu, S. David Kimball, Tammy C. Wang, et al.. (2002). Thrombin active site inhibitors: chemical synthesis, in vitro and in vivo pharmacological profile of a novel and selective agent BMS-189090 and analogues. Bioorganic & Medicinal Chemistry Letters. 12(1). 41–44. 8 indexed citations
14.
Iwanowicz, Edwin J., S. David Kimball, James C. Lin, et al.. (2002). Retro-Binding thrombin active site inhibitors: identification of an orally active inhibitor of thrombin catalytic activity. Bioorganic & Medicinal Chemistry Letters. 12(21). 3183–3186. 1 indexed citations
15.
Sun, Chong‐Qing, Peter T. W. Cheng, Tamara Dejneka, et al.. (2002). A general synthesis of dioxolenone prodrug moieties. Tetrahedron Letters. 43(7). 1161–1164. 13 indexed citations
16.
Iwanowicz, Edwin J., et al.. (1995). Structure of a Retro-binding Peptide Inhibitor Complexed with Human α-Thrombin. Journal of Molecular Biology. 246(1). 14–20. 29 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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