Meng‐Chun Chi

688 total citations
55 papers, 599 citations indexed

About

Meng‐Chun Chi is a scholar working on Molecular Biology, Oncology and Biochemistry. According to data from OpenAlex, Meng‐Chun Chi has authored 55 papers receiving a total of 599 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 19 papers in Oncology and 19 papers in Biochemistry. Recurrent topics in Meng‐Chun Chi's work include Amino Acid Enzymes and Metabolism (19 papers), Enzyme Structure and Function (19 papers) and Peptidase Inhibition and Analysis (18 papers). Meng‐Chun Chi is often cited by papers focused on Amino Acid Enzymes and Metabolism (19 papers), Enzyme Structure and Function (19 papers) and Peptidase Inhibition and Analysis (18 papers). Meng‐Chun Chi collaborates with scholars based in Taiwan, Italy and United States. Meng‐Chun Chi's co-authors include Long‐Liu Lin, Huei‐Fen Lo, Yiyu Chen, Min-Guan Lin, Wen-Hwei Hsu, Antonello Merlino, Hsien‐Bin Huang, Yufen Huang, Huiyu Hu and Andrea Pica and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Applied Microbiology and Biotechnology.

In The Last Decade

Meng‐Chun Chi

55 papers receiving 591 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Meng‐Chun Chi Taiwan 15 424 168 153 121 92 55 599
Huei‐Fen Lo Taiwan 14 343 0.8× 99 0.6× 267 1.7× 119 1.0× 135 1.5× 44 510
M Kossmann Germany 8 278 0.7× 56 0.3× 105 0.7× 153 1.3× 59 0.6× 8 479
Haibo Weng China 14 435 1.0× 145 0.9× 256 1.7× 72 0.6× 64 0.7× 28 851
Peter Poulsen Denmark 19 567 1.3× 29 0.2× 59 0.4× 125 1.0× 96 1.0× 32 782
Pieter de Geus Netherlands 12 578 1.4× 34 0.2× 92 0.6× 78 0.6× 66 0.7× 13 829
Alexander W.M. Strasser Germany 13 600 1.4× 50 0.3× 159 1.0× 97 0.8× 232 2.5× 14 796
Sebastiana Angelaccio Italy 17 534 1.3× 304 1.8× 73 0.5× 373 3.1× 61 0.7× 38 734
Yasuhiro Mihara Japan 14 370 0.9× 74 0.4× 42 0.3× 32 0.3× 29 0.3× 21 490
Kirill Piotukh Germany 13 526 1.2× 25 0.1× 156 1.0× 50 0.4× 64 0.7× 14 665
Susumu Morigasaki Japan 16 590 1.4× 77 0.5× 30 0.2× 42 0.3× 205 2.2× 30 893

Countries citing papers authored by Meng‐Chun Chi

Since Specialization
Citations

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

Fields of papers citing papers by Meng‐Chun Chi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meng‐Chun Chi

This figure shows the co-authorship network connecting the top 25 collaborators of Meng‐Chun Chi. A scholar is included among the top collaborators of Meng‐Chun Chi 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 Meng‐Chun Chi. Meng‐Chun Chi 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.
Chi, Meng‐Chun, et al.. (2018). High-level expression and molecular characterization of a recombinant prolidase from Escherichia coli NovaBlue. PeerJ. 6. e5863–e5863. 5 indexed citations
2.
Lo, Huei‐Fen, et al.. (2018). Protective Effect of Biological Osmolytes against Heat- and Chaotropic Agent-Induced Denaturation of Bacillus licheniformis ��-Glutamyl Transpeptidase. Journal of Microbiology and Biotechnology. 28(9). 1457–1466. 2 indexed citations
3.
Lin, Long‐Liu, et al.. (2017). Facile immobilization of Bacillus licheniformis γ-glutamyltranspeptidase onto graphene oxide nanosheets and its application to the biocatalytic synthesis of γ-l-glutamyl peptides. International Journal of Biological Macromolecules. 117. 1326–1333. 13 indexed citations
4.
Lin, Min-Guan, et al.. (2016). Site-directed mutagenesis of a conserved Asn450 residue of Bacillus licheniformis γ-glutamyltranspeptidase. International Journal of Biological Macromolecules. 91. 416–425. 13 indexed citations
5.
Chi, Meng‐Chun, et al.. (2014). γ-Glutamyl transpeptidase architecture: Effect of extra sequence deletion on autoprocessing, structure and stability of the protein from Bacillus licheniformis. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1844(12). 2290–2297. 14 indexed citations
6.
Lin, Min-Guan, et al.. (2014). Residues Phe103 and Phe149 are critical for the co-chaperone activity of Bacillus licheniformis GrpE. International Journal of Biological Macromolecules. 72. 724–731. 1 indexed citations
7.
Lin, Long‐Liu, Yiyu Chen, Meng‐Chun Chi, & Antonello Merlino. (2014). Low resolution X-ray structure of γ-glutamyltranspeptidase from Bacillus licheniformis: Opened active site cleft and a cluster of acid residues potentially involved in the recognition of a metal ion. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1844(9). 1523–1529. 22 indexed citations
8.
Chi, Meng‐Chun, Yiyu Chen, Huei‐Fen Lo, & Long‐Liu Lin. (2012). Experimental evidence for the involvement of amino acid residue Glu398 in the autocatalytic processing of Bacillus licheniformis γ‐glutamyltranspeptidase. FEBS Open Bio. 2(1). 298–304. 10 indexed citations
9.
Huang, Hsien‐Bin, et al.. (2012). Molecular characterization of a novel trehalose-6-phosphate hydrolase, TreA, from Bacillus licheniformis. International Journal of Biological Macromolecules. 50(3). 459–470. 7 indexed citations
10.
Chen, Yiyu, et al.. (2011). Biophysical characterization of Bacillus licheniformis and Escherichia coli γ-glutamyltranspeptidases: A comparative analysis. International Journal of Biological Macromolecules. 48(3). 414–422. 22 indexed citations
11.
Chi, Meng‐Chun, et al.. (2010). Biophysical Characterization of a Recombinant α-Amylase from Thermophilic Bacillus sp. strain TS-23. The Protein Journal. 29(8). 572–582. 4 indexed citations
12.
Chi, Meng‐Chun, et al.. (2010). Biophysical characterization of a recombinant leucyl aminopeptidase from Bacillus kaustophilus. Biochemistry (Moscow). 75(5). 642–647. 1 indexed citations
13.
Lin, Min-Guan, et al.. (2009). Deletion analysis of the C-terminal region of a molecular chaperone DnaK from Bacillus licheniformis. Archives of Microbiology. 191(7). 583–593. 8 indexed citations
14.
Chi, Meng‐Chun, et al.. (2009). Engineering of a truncated α-amylase of Bacillus sp. strain TS-23 for the simultaneous improvement of thermal and oxidative stabilities. Journal of Bioscience and Bioengineering. 109(6). 531–538. 37 indexed citations
15.
Chi, Meng‐Chun, et al.. (2006). Residues threonine 346 and leucine 352 are critical for the proper function of Bacillus kaustophilus leucine aminopeptidase. FEMS Microbiology Letters. 260(2). 156–161. 8 indexed citations
16.
Lin, Long‐Liu, et al.. (2004). A thermostable leucine aminopeptidase from Bacillus kaustophilus CCRC 11223. Extremophiles. 8(1). 79–87. 24 indexed citations
17.
Chi, Meng‐Chun, et al.. (2004). Identification of Amino Acid Residues Essential for the Catalytic Reaction ofBacillus kaustophilusLeucine Aminopeptidase. Bioscience Biotechnology and Biochemistry. 68(8). 1794–1797. 7 indexed citations
18.
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20.
Chang, Chen-Tien, et al.. (2003). Identification of essential histidine residues in a recombinant ?-amylase of thermophilic and alkaliphilic Bacillus sp. strain TS-23. Extremophiles. 7(6). 505–509. 13 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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