Long‐Liu Lin

2.2k total citations
120 papers, 1.9k citations indexed

About

Long‐Liu Lin is a scholar working on Molecular Biology, Materials Chemistry and Biotechnology. According to data from OpenAlex, Long‐Liu Lin has authored 120 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 87 papers in Molecular Biology, 44 papers in Materials Chemistry and 43 papers in Biotechnology. Recurrent topics in Long‐Liu Lin's work include Enzyme Structure and Function (44 papers), Enzyme Production and Characterization (40 papers) and Amino Acid Enzymes and Metabolism (37 papers). Long‐Liu Lin is often cited by papers focused on Enzyme Structure and Function (44 papers), Enzyme Production and Characterization (40 papers) and Amino Acid Enzymes and Metabolism (37 papers). Long‐Liu Lin collaborates with scholars based in Taiwan, South Africa and United States. Long‐Liu Lin's co-authors include Wen-Hwei Hsu, Meng‐Chun Chi, Huei‐Fen Lo, Jennifer A. Thomson, Min-Guan Lin, Yiyu Chen, Huiyu Hu, Wenlung Chen, Wen‐Ching Wang and Wen‐Shen Chu and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Agricultural and Food Chemistry and Biochemical and Biophysical Research Communications.

In The Last Decade

Long‐Liu Lin

120 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Long‐Liu Lin Taiwan 25 1.2k 779 417 369 354 120 1.9k
Mamoru Wakayama Japan 24 1.4k 1.1× 647 0.8× 302 0.7× 425 1.2× 214 0.6× 111 2.0k
Wen-Hwei Hsu Taiwan 23 1.1k 0.9× 381 0.5× 164 0.4× 367 1.0× 210 0.6× 78 1.5k
Pekka Mäntsälä Finland 37 2.2k 1.8× 673 0.9× 483 1.2× 167 0.5× 122 0.3× 113 3.2k
Sakuzo Fukui Japan 25 1.8k 1.5× 651 0.8× 368 0.9× 127 0.3× 596 1.7× 180 2.4k
Ashraf S. A. El‐Sayed Egypt 30 657 0.5× 452 0.6× 352 0.8× 176 0.5× 89 0.3× 85 1.8k
Shigeru Nakamori Japan 29 2.0k 1.6× 250 0.3× 285 0.7× 394 1.1× 412 1.2× 103 2.6k
Kenzo Yokozeki Japan 27 1.7k 1.4× 262 0.3× 156 0.4× 501 1.4× 256 0.7× 114 2.4k
Hiroshi Tsujibo Japan 34 1.9k 1.5× 1.2k 1.5× 841 2.0× 71 0.2× 377 1.1× 140 3.0k
Thorsten Eggert Germany 29 3.3k 2.7× 550 0.7× 354 0.8× 166 0.4× 622 1.8× 49 3.8k
Hirosuke Okada Japan 30 1.6k 1.3× 647 0.8× 337 0.8× 219 0.6× 711 2.0× 106 2.5k

Countries citing papers authored by Long‐Liu Lin

Since Specialization
Citations

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

Fields of papers citing papers by Long‐Liu Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Long‐Liu Lin. 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 Long‐Liu Lin. The network helps show where Long‐Liu Lin may publish in the future.

Co-authorship network of co-authors of Long‐Liu Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Long‐Liu Lin. A scholar is included among the top collaborators of Long‐Liu Lin 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 Long‐Liu Lin. Long‐Liu Lin 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.. (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
2.
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
3.
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
4.
Lo, Huei‐Fen, et al.. (2011). Contribution of conserved Glu255 and Cys289 residues to catalytic activity of recombinant aldehyde dehydrogenase from Bacillus licheniformis. Biochemistry (Moscow). 76(11). 1233–1241. 2 indexed citations
5.
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
6.
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
7.
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
8.
9.
Weng, Yih‐Ming, et al.. (2007). Residues Arg114 and Arg337 are critical for the proper function of Escherichia coli γ-glutamyltranspeptidase. Biochemical and Biophysical Research Communications. 366(2). 294–300. 15 indexed citations
10.
Yang, Hsin‐Ling, Ruey-Shyang Chen, Wenlung Chen, & Long‐Liu Lin. (2006). Identification of glutamate residues important for catalytic activity of Bacillus stearothermophilus leucine aminopeptidase II. Antonie van Leeuwenhoek. 90(2). 195–199. 3 indexed citations
11.
Lin, Long‐Liu, et al.. (2005). Phylogenetic Analysis and Biochemical Characterization of a Thermostable Dihydropyrimidinase from Alkaliphilic Bacillus sp. TS-23. Antonie van Leeuwenhoek. 88(3-4). 189–197. 4 indexed citations
12.
Hwang, Guang‐Yuh, et al.. (2005). Histidines 345 and 378 of Bacillus stearotheromophilus leucine aminopeptidase II are essential for the catalytic activity of the enzyme. Antonie van Leeuwenhoek. 87(4). 355–359. 9 indexed citations
13.
Lin, Long‐Liu, et al.. (2004). A thermostable leucine aminopeptidase from Bacillus kaustophilus CCRC 11223. Extremophiles. 8(1). 79–87. 24 indexed citations
14.
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
15.
16.
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
17.
Lin, Long‐Liu, et al.. (2001). Serine 187 is a crucial residue for allosteric regulation ofCorynebacterium glutamicum3-deoxy-D-arabino-heptulosonate-7-phosphate synthase. FEMS Microbiology Letters. 194(1). 59–64. 20 indexed citations
18.
Lin, Long‐Liu, et al.. (1999). The role of a conserved histidine residue, His324, inTrigonopsis variabilisd-amino acid oxidase. FEMS Microbiology Letters. 176(2). 443–448. 2 indexed citations
19.
Lin, Long‐Liu, et al.. (1997). A gene encoding for an α‐amylase from thermophilic Bacillus sp. strain TS‐23 and its expression in Escherichia coli . Journal of Applied Microbiology. 82(3). 325–334. 46 indexed citations
20.
Lin, Long‐Liu. (1991). An analysis of the extracellular xylanases and cellulases of Butyrivibrio fibrisolvens H17c. FEMS Microbiology Letters. 84(2). 197–203. 4 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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