Shu‐Chun Cheng

784 total citations
18 papers, 608 citations indexed

About

Shu‐Chun Cheng is a scholar working on Molecular Biology, Aquatic Science and Ecology. According to data from OpenAlex, Shu‐Chun Cheng has authored 18 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Aquatic Science and 5 papers in Ecology. Recurrent topics in Shu‐Chun Cheng's work include Aquaculture Nutrition and Growth (5 papers), Physiological and biochemical adaptations (5 papers) and SARS-CoV-2 and COVID-19 Research (3 papers). Shu‐Chun Cheng is often cited by papers focused on Aquaculture Nutrition and Growth (5 papers), Physiological and biochemical adaptations (5 papers) and SARS-CoV-2 and COVID-19 Research (3 papers). Shu‐Chun Cheng collaborates with scholars based in Taiwan, Japan and United States. Shu‐Chun Cheng's co-authors include Chi‐Yuan Chou, Gu‐Gang Chang, Chiao-Yin Sun, Kai-Wen Cheng, Wei‐Yi Chen, Min-Han Lin, Athira Johnson, Zwe‐Ling Kong, Bo‐Lin Ho and Kuan‐I Ho and has published in prestigious journals such as PLoS ONE, Scientific Reports and FEBS Letters.

In The Last Decade

Shu‐Chun Cheng

17 papers receiving 593 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shu‐Chun Cheng Taiwan 12 263 201 135 104 98 18 608
Christel M. Olsen Norway 13 107 0.4× 168 0.8× 15 0.1× 249 2.4× 35 0.4× 19 734
Md. Shahadat Hossain Bangladesh 16 129 0.5× 179 0.9× 36 0.3× 178 1.7× 26 0.3× 49 701
Lindsay McDermott United Kingdom 17 60 0.2× 383 1.9× 11 0.1× 81 0.8× 12 0.1× 28 963
Jan Šilhán Czechia 15 319 1.2× 869 4.3× 80 0.6× 107 1.0× 2 0.0× 29 1.2k
Qin Tang China 12 78 0.3× 163 0.8× 6 0.0× 160 1.5× 61 0.6× 36 513
Shen Jean Lim United States 11 57 0.2× 364 1.8× 147 1.1× 34 0.3× 8 0.1× 27 667
Amanat Ali United Arab Emirates 12 147 0.6× 201 1.0× 77 0.6× 19 0.2× 3 0.0× 31 521
Anying Zhang China 19 14 0.1× 447 2.2× 31 0.2× 659 6.3× 169 1.7× 59 1.2k
Valentina Gallo Italy 15 27 0.1× 153 0.8× 21 0.2× 86 0.8× 12 0.1× 18 647

Countries citing papers authored by Shu‐Chun Cheng

Since Specialization
Citations

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

Fields of papers citing papers by Shu‐Chun Cheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shu‐Chun Cheng. 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 Shu‐Chun Cheng. The network helps show where Shu‐Chun Cheng may publish in the future.

Co-authorship network of co-authors of Shu‐Chun Cheng

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

All Works

18 of 18 papers shown
1.
Lee, Adam Shih‐Yuan, Ta-Hsien Lin, Yun‐Hsin Wang, et al.. (2025). Growth inhibition and toxicity assessments of cis-3,4-diaryl-α-methylene-γ-butyrolactams in cultured human renal cancer cells and zebrafish embryos. Biochimica et Biophysica Acta (BBA) - General Subjects. 1869(3). 130761–130761.
2.
Liu, Chun‐Fu, Hung‐Chi Chen, Shu‐Chun Cheng, et al.. (2022). Zebrafish (Danio rerio) Is an Economical and Efficient Animal Model for Screening Potential Anti-cataract Compounds. Translational Vision Science & Technology. 11(8). 21–21. 5 indexed citations
3.
Johnson, Athira, et al.. (2019). Attenuation of reproductive dysfunction in diabetic male rats with timber cultured Antrodia cinnamomea ethanol extract. Biomedicine & Pharmacotherapy. 112. 108684–108684. 20 indexed citations
4.
Cheng, Shu‐Chun, et al.. (2018). 6-Thioguanine is a noncompetitive and slow binding inhibitor of human deubiquitinating protease USP2. Scientific Reports. 8(1). 3102–3102. 45 indexed citations
5.
Kong, Zwe‐Ling, et al.. (2018). Effect of Cistanche Tubulosa Extracts on Male Reproductive Function in Streptozotocin–Nicotinamide-Induced Diabetic Rats. Nutrients. 10(10). 1562–1562. 36 indexed citations
6.
Ho, Bo‐Lin, et al.. (2015). Critical Assessment of the Important Residues Involved in the Dimerization and Catalysis of MERS Coronavirus Main Protease. PLoS ONE. 10(12). e0144865–e0144865. 54 indexed citations
7.
Chou, Chi‐Yuan, et al.. (2014). Structural basis for catalysis and ubiquitin recognition by theSevere acute respiratory syndrome coronaviruspapain-like protease. Acta Crystallographica Section D Biological Crystallography. 70(2). 572–581. 46 indexed citations
8.
Cheng, Kai-Wen, Shu‐Chun Cheng, Wei‐Yi Chen, et al.. (2014). Thiopurine analogs and mycophenolic acid synergistically inhibit the papain-like protease of Middle East respiratory syndrome coronavirus. Antiviral Research. 115. 9–16. 139 indexed citations
9.
Cheng, Shu‐Chun, et al.. (2012). Differential domain structure stability of the severe acute respiratory syndrome coronavirus papain-like protease. Archives of Biochemistry and Biophysics. 520(2). 74–80. 12 indexed citations
10.
Liou, Gunn‐Guang, Shu‐Chun Cheng, Chia‐Hui Chien, et al.. (2011). Role of a propeller loop in the quaternary structure and enzymatic activity of prolyl dipeptidases DPP-IV and DPP9. FEBS Letters. 585(21). 3409–3414. 11 indexed citations
11.
Cheng, Shu‐Chun, Gu‐Gang Chang, & Chi‐Yuan Chou. (2010). Mutation of Glu-166 Blocks the Substrate-Induced Dimerization of SARS Coronavirus Main Protease. Biophysical Journal. 98(7). 1327–1336. 112 indexed citations
12.
Chou, Chi‐Yuan, Chia-Hao Hsu, Yun‐Hsin Wang, et al.. (2010). Biochemical and structural properties of zebrafish Capsulin produced by Escherichia coli. Protein Expression and Purification. 75(1). 21–27. 3 indexed citations
13.
Cheng, Shu‐Chun, et al.. (2004). Increased Production and Excretion of Urea in the Kuruma Shrimp (Marsupenaeus japonicus) Exposed to Combined Environments of Increased Ammonia and Nitrite. Archives of Environmental Contamination and Toxicology. 47(3). 352–62. 20 indexed citations
14.
Huang, Li‐Tung, Chia‐Wei Liou, San Nan Yang, et al.. (2002). Aminophylline aggravates long-term morphological and cognitive damages in status epilepticus in immature rats. Neuroscience Letters. 321(3). 137–140. 4 indexed citations
15.
Cheng, Shu‐Chun, et al.. (2002). Accumulations of Nitrite and Nitrate in the Tissues of Penaeus monodon Exposed to a Combined Environment of Elevated Nitrite and Nitrate. Archives of Environmental Contamination and Toxicology. 43(1). 64–74. 9 indexed citations
16.
Cheng, Shu‐Chun, et al.. (2000). Accumulation of Nitrite in the Tissues of Penaeus monodon Exposed to Elevated Ambient Nitrite After Different Time Periods. Archives of Environmental Contamination and Toxicology. 39(2). 183–192. 22 indexed citations
17.
Cheng, Shu‐Chun, et al.. (1996). Hemolymph osmolality, acid-base balance, and ammonia excretion of Penaeus japonicus bate exposed to ambient nitrite. Archives of Environmental Contamination and Toxicology. 30(2). 151–155. 13 indexed citations
18.
Cheng, Shu‐Chun, et al.. (1995). Hemolymph oxygen content, oxyhemocyanin, protein levels and ammonia excretion in the shrimp Penaeus monodon exposed to ambient nitrite. Journal of Comparative Physiology B. 164(7). 57 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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