Yihua Chen

3.7k total citations · 1 hit paper
123 papers, 2.8k citations indexed

About

Yihua Chen is a scholar working on Molecular Biology, Pharmacology and Organic Chemistry. According to data from OpenAlex, Yihua Chen has authored 123 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 61 papers in Pharmacology and 30 papers in Organic Chemistry. Recurrent topics in Yihua Chen's work include Microbial Natural Products and Biosynthesis (55 papers), Genomics and Phylogenetic Studies (13 papers) and Carbohydrate Chemistry and Synthesis (12 papers). Yihua Chen is often cited by papers focused on Microbial Natural Products and Biosynthesis (55 papers), Genomics and Phylogenetic Studies (13 papers) and Carbohydrate Chemistry and Synthesis (12 papers). Yihua Chen collaborates with scholars based in China, United States and Canada. Yihua Chen's co-authors include Ben Shen, Zhengyan Guo, Evelyn Wendt-Pienkowski, Geoff P. Horsman, Brett F. Carver, Liuling Yan, Yuwei Zhang, Michael J. Smanski, Scott R. Rajski and Shuwen Wang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Yihua Chen

116 papers receiving 2.7k citations

Hit Papers

Identification of antimicrobial peptides from the human g... 2022 2026 2023 2024 2022 50 100 150 200 250

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yihua Chen China 29 1.7k 1.1k 484 482 328 123 2.8k
Andreas Kulik Germany 25 1.1k 0.7× 1.0k 0.9× 605 1.3× 329 0.7× 349 1.1× 82 2.1k
Xiaoying Bian China 28 1.9k 1.1× 1.2k 1.1× 380 0.8× 253 0.5× 444 1.4× 91 2.7k
Satoshi Ōmura Japan 35 2.3k 1.3× 1.5k 1.4× 553 1.1× 909 1.9× 457 1.4× 121 4.0k
In‐Kyoung Lee South Korea 30 1.3k 0.8× 1.2k 1.1× 486 1.0× 420 0.9× 210 0.6× 120 3.0k
Xuefu You China 29 1.4k 0.8× 1.1k 1.0× 257 0.5× 483 1.0× 138 0.4× 102 2.8k
Xiaofei Shang China 29 1.2k 0.7× 581 0.5× 1.2k 2.4× 729 1.5× 72 0.2× 89 3.3k
Ming Ma China 29 1.2k 0.7× 868 0.8× 255 0.5× 697 1.4× 254 0.8× 86 2.4k
Thorsten Heinekamp Germany 40 2.3k 1.3× 1.4k 1.2× 1.6k 3.3× 315 0.7× 273 0.8× 83 4.5k
Christoph Freiberg Germany 22 909 0.5× 262 0.2× 636 1.3× 172 0.4× 84 0.3× 33 2.0k
Changlin Zhou China 35 1.6k 0.9× 436 0.4× 326 0.7× 220 0.5× 96 0.3× 108 2.9k

Countries citing papers authored by Yihua Chen

Since Specialization
Citations

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

Fields of papers citing papers by Yihua Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yihua Chen. 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 Yihua Chen. The network helps show where Yihua Chen may publish in the future.

Co-authorship network of co-authors of Yihua Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Yihua Chen. A scholar is included among the top collaborators of Yihua Chen 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 Yihua Chen. Yihua Chen 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
2.
Li, Chao, Junying Ma, Chao Xu, et al.. (2025). Selective Synthesis of Cyclopeptides with a 2-Oxindole or 3a-Hydroxy-hexahydropyrrolo-[2,3-b]indole Structure by Cytochrome P450 Enzymes. Journal of the American Chemical Society. 147(4). 3304–3314. 3 indexed citations
3.
Sun, Yanhong, Sijia Li, Shu Zhang, et al.. (2024). Quantitative Characterization of Gene Regulatory Circuits Associated With Fungal Secondary Metabolism to Discover Novel Natural Products. Advanced Science. 11(47). e2407195–e2407195. 2 indexed citations
4.
Tang, Yue, et al.. (2024). Characterization of the ADP-β-d-manno-heptose biosynthetic enzymes from two pathogenic Vibrio strains. Applied Microbiology and Biotechnology. 108(1). 267–267. 2 indexed citations
5.
Miao, Lili, Tingting Hou, Lan Ma, et al.. (2023). N-Hydroxylation and Hydrolysis by the DnfA/B/C Multienzyme System Involved in the Aerobic N2 Formation Process. ACS Catalysis. 13(18). 11963–11976. 8 indexed citations
6.
Dai, Huanqin, Junjie Han, Tao Wang, et al.. (2023). Recent advances in gut microbiota-associated natural products: structures, bioactivities, and mechanisms. Natural Product Reports. 40(6). 1078–1093. 20 indexed citations
7.
Ma, Yue, Zhengyan Guo, Binbin Xia, et al.. (2022). Identification of antimicrobial peptides from the human gut microbiome using deep learning. Nature Biotechnology. 40(6). 921–931. 296 indexed citations breakdown →
9.
Zhang, Yuwei, et al.. (2022). Artificial intelligence accelerates the mining of bioactive small molecules from human microbiome. Clinical and Translational Medicine. 12(8). e1011–e1011. 8 indexed citations
10.
Chen, Dongwei, Wei Tang, Yuwei Zhang, et al.. (2022). Whole lifecycle observation of single‐spore germinated Streptomyces using a nanogap‐stabilized microfluidic chip. SHILAP Revista de lepidopterología. 1(3). 341–349. 2 indexed citations
11.
Guo, Zhengyan, Yue Tang, Wei Tang, & Yihua Chen. (2021). Heptose-containing bacterial natural products: structures, bioactivities, and biosyntheses. Natural Product Reports. 38(10). 1887–1909. 14 indexed citations
12.
Tang, Yue, Min Wang, Zhengyan Guo, et al.. (2020). Deciphering the Biosynthesis of TDP-β-l-oleandrose in Avermectin. Journal of Natural Products. 83(10). 3199–3206. 9 indexed citations
13.
Wang, Min, Zhoujie Xie, Shoubin Tang, et al.. (2020). Reductase of Mutanobactin Synthetase Triggers Sequential C–C Macrocyclization, C–S Bond Formation, and C–C Bond Cleavage. Organic Letters. 22(3). 960–964. 6 indexed citations
14.
Du, Pei, Haoqian Zhang, Jianyi H. Huang, et al.. (2020). De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation. Nature Communications. 11(1). 4226–4226. 73 indexed citations
15.
Yang, Keqian, et al.. (2019). Characterization of a Bi-directional Promoter OtrRp Involved in Oxytetracycline Biosynthesis. Current Microbiology. 76(11). 1264–1269. 5 indexed citations
16.
Tang, Wei, Zhengyan Guo, Min Wang, et al.. (2018). d -Sedoheptulose-7-phosphate is a common precursor for the heptoses of septacidin and hygromycin B. Proceedings of the National Academy of Sciences. 115(11). 2818–2823. 41 indexed citations
17.
Yang, Yanlong, Shasha Zhang, Ke Ma, et al.. (2017). Discovery and Characterization of a New Family of Diterpene Cyclases in Bacteria and Fungi. Angewandte Chemie. 129(17). 4827–4830. 18 indexed citations
18.
Zheng, Feng, et al.. (2011). A quantitative method for the measurement of membrane affinity by polydiacetylene-based colorimetric assay. Analytical Biochemistry. 420(2). 171–176. 18 indexed citations
19.
Chen, Yihua, Michael J. Smanski, & Ben Shen. (2010). Improvement of secondary metabolite production in Streptomyces by manipulating pathway regulation. Applied Microbiology and Biotechnology. 86(1). 19–25. 86 indexed citations
20.
Chen, Yihua, et al.. (2000). Inducing somatic meiosis-like reduction at high frequency by caffeine in root-tip cells of Vicia faba. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 452(1). 67–72. 11 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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