Chia‐Fu Chang

681 total citations
20 papers, 570 citations indexed

About

Chia‐Fu Chang is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Chia‐Fu Chang has authored 20 papers receiving a total of 570 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Organic Chemistry and 4 papers in Pharmacology. Recurrent topics in Chia‐Fu Chang's work include Signaling Pathways in Disease (4 papers), Bioactive natural compounds (3 papers) and Synthetic Organic Chemistry Methods (3 papers). Chia‐Fu Chang is often cited by papers focused on Signaling Pathways in Disease (4 papers), Bioactive natural compounds (3 papers) and Synthetic Organic Chemistry Methods (3 papers). Chia‐Fu Chang collaborates with scholars based in United States, Taiwan and Norway. Chia‐Fu Chang's co-authors include Jia‐Yaw Chang, Christina M. Woo, Chun‐Wei Huang, Chung‐Hua Chiu, Wen‐Wei Wu, Yean‐Jang Lee, Hope A. Flaxman, Anya Maan‐Yuh Lin, Hsin‐Chen Lee and Ping‐Hung Yeh and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and ACS Applied Materials & Interfaces.

In The Last Decade

Chia‐Fu Chang

20 papers receiving 564 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chia‐Fu Chang United States 14 171 169 137 123 83 20 570
Charles R. Robertson United States 8 245 1.4× 73 0.4× 160 1.2× 336 2.7× 21 0.3× 9 657
Debashree Das India 14 127 0.7× 38 0.2× 83 0.6× 70 0.6× 52 0.6× 46 478
De‐Ping Yang United States 17 262 1.5× 57 0.3× 93 0.7× 42 0.3× 13 0.2× 28 636
Jianfei Kan China 9 102 0.6× 71 0.4× 231 1.7× 30 0.2× 73 0.9× 11 428
Thomas S. Reger United States 12 326 1.9× 24 0.1× 175 1.3× 581 4.7× 14 0.2× 20 972
Alpesh K. Sharma India 19 190 1.1× 43 0.3× 167 1.2× 595 4.8× 45 0.5× 37 1.1k
M. Takayama Japan 11 509 3.0× 87 0.5× 152 1.1× 253 2.1× 16 0.2× 22 1.1k
Ulla Björkroth Sweden 16 361 2.1× 47 0.3× 47 0.3× 171 1.4× 23 0.3× 71 890
Pui Shan Chan Hong Kong 12 196 1.1× 20 0.1× 184 1.3× 41 0.3× 8 0.1× 14 680
Qunxing Huang China 7 120 0.7× 66 0.4× 280 2.0× 43 0.3× 60 0.7× 7 546

Countries citing papers authored by Chia‐Fu Chang

Since Specialization
Citations

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

Fields of papers citing papers by Chia‐Fu Chang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chia‐Fu Chang. 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 Chia‐Fu Chang. The network helps show where Chia‐Fu Chang may publish in the future.

Co-authorship network of co-authors of Chia‐Fu Chang

This figure shows the co-authorship network connecting the top 25 collaborators of Chia‐Fu Chang. A scholar is included among the top collaborators of Chia‐Fu Chang 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 Chia‐Fu Chang. Chia‐Fu Chang 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.
Ichikawa, Saki, N. Connor Payne, Chia‐Fu Chang, et al.. (2024). The cyclimids: Degron-inspired cereblon binders for targeted protein degradation. Cell chemical biology. 31(6). 1162–1175.e10. 17 indexed citations
2.
Flaxman, Hope A., Hongwei Han, Chia‐Fu Chang, et al.. (2024). Sanglifehrin A mitigates multiorgan fibrosis by targeting the collagen chaperone cyclophilin B. JCI Insight. 9(15). 4 indexed citations
3.
Wilson, Robert M., et al.. (2023). A Versatile Isocyanate-Mediated Strategy for Appending Chemical Tags onto Drug-Like Small Molecules. Bioconjugate Chemistry. 34(12). 2181–2186. 1 indexed citations
4.
Chang, Chia‐Fu, Hope A. Flaxman, & Christina M. Woo. (2021). Enantioselective Synthesis and Biological Evaluation of Sanglifehrin A and B and Analogs. Angewandte Chemie International Edition. 60(31). 17045–17052. 14 indexed citations
5.
Chang, Chia‐Fu, Hope A. Flaxman, & Christina M. Woo. (2021). Enantioselective Synthesis and Biological Evaluation of Sanglifehrin A and B and Analogs. Angewandte Chemie. 133(31). 17182–17189. 2 indexed citations
6.
Chang, Chia‐Fu, et al.. (2021). Enantioselective Total Synthesis of the Putative Biosynthetic Intermediate Ambruticin J. Chemistry - A European Journal. 27(43). 11126–11131. 13 indexed citations
7.
Flaxman, Hope A., et al.. (2019). A Binding Site Hotspot Map of the FKBP12–Rapamycin–FRB Ternary Complex by Photoaffinity Labeling and Mass Spectrometry-Based Proteomics. Journal of the American Chemical Society. 141(30). 11759–11764. 40 indexed citations
8.
Chang, Chia‐Fu, Adelphe M. Mfuh, Jinxu Gao, Hung‐Yi Wu, & Christina M. Woo. (2018). Synthesis of an electronically-tuned minimally interfering alkynyl photo-affinity label to measure small molecule–protein interactions. Tetrahedron. 74(26). 3273–3277. 18 indexed citations
9.
Larsen, Erik, et al.. (2018). Conformation-guided analogue design identifies potential antimalarial compounds through inhibition of mitochondrial respiration. Organic & Biomolecular Chemistry. 16(30). 5403–5406. 6 indexed citations
10.
Chang, Chia‐Fu, Jui‐Yuan Chen, Chun‐Wei Huang, et al.. (2017). Direct Observation of Dual‐Filament Switching Behaviors in Ta2O5‐Based Memristors. Small. 13(15). 100 indexed citations
11.
Chiu, Chung‐Hua, et al.. (2017). In-situ TEM observation of Multilevel Storage Behavior in low power FeRAM device. Nano Energy. 34. 103–110. 34 indexed citations
12.
Chang, Chia‐Fu, Eric Stefan, & Richard E. Taylor. (2015). Total Synthesis and Structural Reassignment of Lyngbyaloside C Highlighted by Intermolecular Ketene Esterification. Chemistry - A European Journal. 21(30). 10681–10686. 21 indexed citations
13.
Chang, Jia‐Yaw, et al.. (2013). Improved Performance of CuInS2 Quantum Dot-Sensitized Solar Cells Based on a Multilayered Architecture. ACS Applied Materials & Interfaces. 5(17). 8740–8752. 101 indexed citations
14.
Chang, Chia‐Fu, et al.. (2011). Melatonin attenuates kainic acid‐induced neurotoxicity in mouse hippocampus via inhibition of autophagy and α‐synuclein aggregation. Journal of Pineal Research. 52(3). 312–321. 89 indexed citations
15.
Luo, Yiwei, Yean‐Jang Lee, Chia‐Fu Chang, et al.. (2011). Total synthesis of moniliformediquinone and calanquinone A as potent inhibitors for breast cancer. Tetrahedron. 67(34). 6166–6172. 16 indexed citations
16.
Chang, Chia‐Fu, et al.. (2010). Total Synthesis of (±)-Armepavines and (±)-Nuciferines From (2-Nitroethenyl)benzene Derivatives. Synthetic Communications. 40(23). 3452–3466. 15 indexed citations
17.
Lee, Yean‐Jang, et al.. (2009). The First Total Synthesis Of Morusin And Himanimide D As Arachidonate 5-lipoxygenase Inhibitor In Automated Docking. Biophysical Journal. 96(3). 86a–86a. 1 indexed citations
18.
Tseng, Tsui‐Hwa, et al.. (2009). The synthesis of morusin as a potent antitumor agent. Tetrahedron. 66(6). 1335–1340. 41 indexed citations
19.
Lee, Yean‐Jang, et al.. (2009). The First Total Synthesis of Kynapcin-24 by Palladium Catalysis. Synthesis. 2009(7). 1175–1179. 4 indexed citations
20.
Chang, Chia‐Fu, et al.. (2008). Total synthesis of demethylwedelolactone and wedelolactone by Cu-mediated/Pd(0)-catalysis and oxidative-cyclization. Tetrahedron. 64(17). 3661–3666. 33 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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