Ming‐Fu Chang

5.5k total citations · 1 hit paper
90 papers, 4.4k citations indexed

About

Ming‐Fu Chang is a scholar working on Hepatology, Molecular Biology and Epidemiology. According to data from OpenAlex, Ming‐Fu Chang has authored 90 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Hepatology, 27 papers in Molecular Biology and 27 papers in Epidemiology. Recurrent topics in Ming‐Fu Chang's work include Hepatitis C virus research (25 papers), Hepatitis B Virus Studies (23 papers) and SARS-CoV-2 and COVID-19 Research (14 papers). Ming‐Fu Chang is often cited by papers focused on Hepatitis C virus research (25 papers), Hepatitis B Virus Studies (23 papers) and SARS-CoV-2 and COVID-19 Research (14 papers). Ming‐Fu Chang collaborates with scholars based in Taiwan, United States and China. Ming‐Fu Chang's co-authors include Shan‐Chwen Chang, John E. Cronan, Takeshi Ichinohe, Miyu Moriyama, Shinji Makino, Sugantha Govindarajan, Shin C. Chang, Susan C. Baker, Michael M. C. Lai and L H Soe and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Ming‐Fu Chang

88 papers receiving 4.3k citations

Hit Papers

Severe Acute Respiratory Syndrome Coronavirus Viroporin 3... 2019 2026 2021 2023 2019 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ming‐Fu Chang Taiwan 38 1.5k 1.4k 1.3k 1.2k 618 90 4.4k
Sunil K. Lal India 36 1.6k 1.0× 2.0k 1.4× 1.0k 0.8× 702 0.6× 700 1.1× 120 4.7k
Sandrine Belouzard France 31 1.1k 0.7× 2.5k 1.7× 1.2k 0.9× 939 0.8× 422 0.7× 69 5.0k
Miguel Ángel Martı́nez Spain 43 1.8k 1.2× 2.0k 1.4× 1.0k 0.8× 653 0.6× 391 0.6× 172 6.0k
Sui‐Yuan Chang Taiwan 36 1.9k 1.2× 2.2k 1.5× 1.5k 1.1× 626 0.5× 505 0.8× 247 5.7k
Yoshio Mori Japan 30 816 0.5× 1.2k 0.9× 788 0.6× 823 0.7× 294 0.5× 176 3.5k
Seung‐Yong Park South Korea 35 860 0.6× 1.3k 0.9× 887 0.7× 277 0.2× 949 1.5× 177 4.1k
Koichi Watashi Japan 43 2.5k 1.6× 1.2k 0.8× 4.2k 3.2× 3.8k 3.3× 1.1k 1.7× 192 7.7k
Dale L. Barnard United States 34 1.0k 0.7× 2.4k 1.7× 1.6k 1.2× 108 0.1× 764 1.2× 110 5.0k
Peter Wutzler Germany 41 569 0.4× 989 0.7× 3.8k 2.9× 532 0.5× 524 0.8× 197 5.1k
Clyde S. Crumpacker United States 44 961 0.6× 1.6k 1.1× 3.4k 2.5× 262 0.2× 878 1.4× 115 5.9k

Countries citing papers authored by Ming‐Fu Chang

Since Specialization
Citations

This map shows the geographic impact of Ming‐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 Ming‐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 Ming‐Fu Chang more than expected).

Fields of papers citing papers by Ming‐Fu Chang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Ming‐Fu Chang. A scholar is included among the top collaborators of Ming‐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 Ming‐Fu Chang. Ming‐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.
Wan, Hao, Ming‐Fu Chang, C. Chris Yun, et al.. (2025). Therapeutic targets in aging-related osteoarthritis: A focus on the extracellular matrix homeostasis. Life Sciences. 368. 123487–123487. 5 indexed citations
3.
Huang, Jian, et al.. (2023). Comparative prevalence of oral bacteria and protozoa in patients with periodontitis in Taiwan. Oral Diseases. 30(3). 1483–1487. 4 indexed citations
4.
Algaissi, Abdullah, Jr‐Shiuan Lin, Wei‐Ting Chen, et al.. (2023). Subunit vaccines with a saponin-based adjuvant boost humoral and cellular immunity to MERS coronavirus. Vaccine. 41(21). 3337–3346. 8 indexed citations
5.
Chen, Jui‐Chieh, et al.. (2023). Ergosterol peroxide blocks HDV infection as a novel entry inhibitor by targeting human NTCP receptor. Biomedicine & Pharmacotherapy. 170. 116077–116077. 2 indexed citations
6.
Shen, Hao, Shuning Liu, Min Ding, et al.. (2021). A quadruple recombination event discovered in hepatitis E virus. Archives of Virology. 166(12). 3405–3408. 3 indexed citations
7.
Peng, Wei‐Hao, et al.. (2018). Nucleocapsid protein-dependent assembly of the RNA packaging signal of Middle East respiratory syndrome coronavirus. Journal of Biomedical Science. 25(1). 47–47. 42 indexed citations
8.
Chang, Ming‐Fu, Wang‐Huei Sheng, Jann‐Tay Wang, et al.. (2017). Prognostic factors of health care–associated bloodstream infection in adult patients ≥40 years of age. American Journal of Infection Control. 46(1). 111–114. 8 indexed citations
9.
Chang, Shan‐Chwen, et al.. (2010). Upregulation of the Chemokine (C-C Motif) Ligand 2 via a Severe Acute Respiratory Syndrome Coronavirus Spike-ACE2 Signaling Pathway. Journal of Virology. 84(15). 7703–7712. 95 indexed citations
10.
Yu, Chun-Hsien, et al.. (2009). Impaired Hepatocyte Regeneration in Acute Severe Hepatic Injury Enhances Effective Repopulation by Transplanted Hepatocytes. Cell Transplantation. 18(10-11). 1081–1092. 13 indexed citations
11.
Huang, Shaoyong, et al.. (2006). Hepatitis C virus NS4A inhibits cap-dependent and the viral IRES-mediated translation through interacting with eukaryotic elongation factor 1A. Journal of Biomedical Science. 13(6). 861–874. 40 indexed citations
12.
Chen, Yee‐Chun, Li‐Min Huang, Chang‐Chuan Chan, et al.. (2004). SARS in Hospital Emergency Room. Emerging infectious diseases. 10(5). 782–788. 115 indexed citations
13.
Cheng, Ming‐Jen, et al.. (2003). Chemical and cytotoxic constituents from Peperomia sui. Phytochemistry. 63(5). 603–608. 52 indexed citations
14.
Stunz, Laura L., Petar Lenert, D. W. Peckham, et al.. (2002). Inhibitory oligonucleotides specifically block effects of stimulatory CpG oligonucleotides in B cells. European Journal of Immunology. 32(5). 1212–1212. 132 indexed citations
15.
Lee, Chia‐Huei, Shan‐Chwen Chang, Chih‐Feng Wu, & Ming‐Fu Chang. (2001). A Novel Chromosome Region Maintenance 1-independent Nuclear Export Signal of the Large Form of Hepatitis Delta Antigen That Is Required for the Viral Assembly. Journal of Biological Chemistry. 276(11). 8142–8148. 74 indexed citations
16.
Yi, Ae‐Kyung, Ming‐Fu Chang, D. W. Peckham, Arthur Μ. Krieg, & Robert F. Ashman. (1998). CpG Oligodeoxyribonucleotides Rescue Mature Spleen B Cells from Spontaneous Apoptosis and Promote Cell Cycle Entry. The Journal of Immunology. 160(12). 5898–5906. 198 indexed citations
17.
Yen, Jui-Hung, et al.. (1995). Cellular Proteins Specifically Bind to the 5′-Noncoding Region of Hepatitis C Virus RNA. Virology. 208(2). 723–732. 39 indexed citations
18.
Xia, Yuping, Ming‐Fu Chang, David C. Wei, Sugantha Govindarajan, & Michael M. C. Lai. (1990). Heterogeneity of hepatitis delta antigen. Virology. 178(1). 331–336. 40 indexed citations
19.
Baldarelli, Richard M., et al.. (1988). Transcripts of the Drosophila blastoderm-specific locus, terminus, are concentrated posteriorly and encode a potential DNA-binding finger. Developmental Biology. 125(1). 85–95. 26 indexed citations
20.
Ling, K H, et al.. (1987). Chromatographic quantitation of territrems A, B, and C, tremorgenic mycotoxins from Aspergillus terreus. Mycotoxin Research. 3(1). 7–12. 3 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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