W C Shen

524 total citations
11 papers, 446 citations indexed

About

W C Shen is a scholar working on Molecular Biology, Organic Chemistry and Biochemistry. According to data from OpenAlex, W C Shen has authored 11 papers receiving a total of 446 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 3 papers in Organic Chemistry and 2 papers in Biochemistry. Recurrent topics in W C Shen's work include RNA Research and Splicing (3 papers), Amino Acid Enzymes and Metabolism (2 papers) and Click Chemistry and Applications (2 papers). W C Shen is often cited by papers focused on RNA Research and Splicing (3 papers), Amino Acid Enzymes and Metabolism (2 papers) and Click Chemistry and Applications (2 papers). W C Shen collaborates with scholars based in United States, Denmark and United Kingdom. W C Shen's co-authors include Hugues J.‐P. Ryser, Anita K. Hopper, Ann R. Kennedy, David R. Stanford, S. Selvakumar, Chen Gao, Elena Milgröm, Chris L. Greer, Nicola Martin and Susan M. Dallabrida and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Agricultural and Food Chemistry.

In The Last Decade

W C Shen

11 papers receiving 429 citations

Peers

W C Shen
Wei‐Chiang Shen United States
Christine Davis United Kingdom
Huang China
Mario Ariatti South Africa
Taylor Fuselier United States
Wei‐Chiang Shen United States
W C Shen
Citations per year, relative to W C Shen W C Shen (= 1×) peers Wei‐Chiang Shen

Countries citing papers authored by W C Shen

Since Specialization
Citations

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

Fields of papers citing papers by W C Shen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W C Shen

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

All Works

11 of 11 papers shown
1.
Shen, W C, Paul A. Dalby, Zheng Guo, et al.. (2023). Residue Effect-Guided Design: Engineering of S. Solfataricus β-Glycosidase to Enhance Its Thermostability and Bioproduction of Ginsenoside Compound K. Journal of Agricultural and Food Chemistry. 71(44). 16669–16680. 5 indexed citations
2.
Gao, Chen, et al.. (2004). On the Mechanism of Constitutive Pdr1 Activator-mediated PDR5 Transcription in Saccharomyces cerevisiae. Journal of Biological Chemistry. 279(41). 42677–42686. 33 indexed citations
3.
Shen, W C, Lynne Apone, Ching-Man Virbasius, et al.. (1998). Functional Analysis of TFIID Components. Cold Spring Harbor Symposia on Quantitative Biology. 63(0). 219–228. 2 indexed citations
4.
O’Connor, J. Patrick, et al.. (1996). Nucleus-associated pools of Rna1p, the Saccharomyces cerevisiae Ran/TC4 GTPse activating protein involved in nucleus/cytosol transit.. Proceedings of the National Academy of Sciences. 93(15). 7667–7672. 25 indexed citations
5.
Shen, W C, et al.. (1995). Location of N2, N2-dimethylguanosine-specific tRNA methyltransferase. Biochimie. 77(1-2). 45–53. 34 indexed citations
6.
Kennedy, Ann R., et al.. (1995). Water‐soluble fatty acid derivatives as acylating agents for reversible lipidization of polypeptides. FEBS Letters. 371(3). 283–286. 46 indexed citations
7.
Shen, W C, S. Selvakumar, David R. Stanford, & Anita K. Hopper. (1993). The Saccharomyces cerevisiae LOS1 gene involved in pre-tRNA splicing encodes a nuclear protein that behaves as a component of the nuclear matrix.. Journal of Biological Chemistry. 268(26). 19436–19444. 35 indexed citations
8.
Shen, W C, et al.. (1985). Disulfide spacer between methotrexate and poly(D-lysine). A probe for exploring the reductive process in endocytosis.. Journal of Biological Chemistry. 260(20). 10905–10908. 66 indexed citations
9.
Shen, W C & Hugues J.‐P. Ryser. (1984). Selective killing of Fc-receptor-bearing tumor cells through endocytosis of a drug-carrying immune complex.. Proceedings of the National Academy of Sciences. 81(5). 1445–1447. 8 indexed citations
10.
Shen, W C & Hugues J.‐P. Ryser. (1981). Poly(L-lysine) has different membrane transport and drug-carrier properties when complexed with heparin.. Proceedings of the National Academy of Sciences. 78(12). 7589–7593. 37 indexed citations
11.
Shen, W C & Hugues J.‐P. Ryser. (1978). Conjugation of poly-L-lysine to albumin and horseradish peroxidase: a novel method of enhancing the cellular uptake of proteins.. Proceedings of the National Academy of Sciences. 75(4). 1872–1876. 155 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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