Sungbeom Lee

2.3k total citations
52 papers, 1.8k citations indexed

About

Sungbeom Lee is a scholar working on Molecular Biology, Plant Science and Biotechnology. According to data from OpenAlex, Sungbeom Lee has authored 52 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 25 papers in Plant Science and 7 papers in Biotechnology. Recurrent topics in Sungbeom Lee's work include Plant biochemistry and biosynthesis (14 papers), Plant Stress Responses and Tolerance (9 papers) and Plant Gene Expression Analysis (7 papers). Sungbeom Lee is often cited by papers focused on Plant biochemistry and biosynthesis (14 papers), Plant Stress Responses and Tolerance (9 papers) and Plant Gene Expression Analysis (7 papers). Sungbeom Lee collaborates with scholars based in South Korea, United States and Germany. Sungbeom Lee's co-authors include Dorothea Tholl, Reza Sohrabi, Byung Yeoup Chung, Adela M. Sánchez‐Moreiras, Jonathan Gershenzon, Christian Abel, Joseph Chappell, Seung Sik Lee, Kyoungwhan Back and Moon‐Soo Chung and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and PLANT PHYSIOLOGY.

In The Last Decade

Sungbeom Lee

51 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sungbeom Lee South Korea 21 977 909 262 244 201 52 1.8k
Muhammad Ali China 30 1.1k 1.2× 2.2k 2.5× 96 0.4× 93 0.4× 116 0.6× 101 2.8k
Hugo Peña‐Cortés Chile 24 993 1.0× 1.8k 2.0× 164 0.6× 437 1.8× 179 0.9× 44 2.3k
Sam T. Mugford United Kingdom 26 1.5k 1.5× 1.4k 1.5× 127 0.5× 362 1.5× 61 0.3× 41 2.5k
James W. Sims United States 20 669 0.7× 455 0.5× 98 0.4× 207 0.8× 53 0.3× 29 1.5k
Nobuhiro Hirai Japan 31 2.0k 2.0× 3.2k 3.5× 298 1.1× 154 0.6× 141 0.7× 111 4.2k
Andrew Maxwell Phineas Jones Canada 29 1.2k 1.2× 1.3k 1.5× 76 0.3× 58 0.2× 139 0.7× 77 2.0k
Antje Klempien United States 8 1.2k 1.2× 1.0k 1.1× 525 2.0× 298 1.2× 348 1.7× 8 2.0k
Michael Gutensohn United States 23 1.7k 1.8× 1.0k 1.1× 139 0.5× 120 0.5× 146 0.7× 35 2.1k
Raju Datla Canada 30 1.7k 1.7× 1.9k 2.0× 113 0.4× 44 0.2× 104 0.5× 58 2.9k
Joëlle K. Mühlemann United States 14 1.6k 1.6× 1.4k 1.6× 733 2.8× 336 1.4× 390 1.9× 16 2.7k

Countries citing papers authored by Sungbeom Lee

Since Specialization
Citations

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

Fields of papers citing papers by Sungbeom Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sungbeom Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Sungbeom Lee. A scholar is included among the top collaborators of Sungbeom Lee 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 Sungbeom Lee. Sungbeom Lee 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.
Park, Chan Mi, Gun Su, Yujin Lee, et al.. (2024). Epoxidation of perillyl alcohol by engineered bacterial cytochrome P450 BM3. Enzyme and Microbial Technology. 180. 110487–110487. 2 indexed citations
2.
Kaur, Shubhpreet, Youngchul Yoo, Young Bae Ryu, et al.. (2024). Effects of Gamma Irradiation on Changes in Chemical Composition and Antioxidant Activity of Euphorbia maculata Callus. Plants. 13(16). 2306–2306. 2 indexed citations
3.
Kim, Jin‐Hong, Shubham Dubey, Kwon Hwangbo, et al.. (2023). Application of ionizing radiation as an elicitor to enhance the growth and metabolic activities in Chlamydomonas reinhardtii. Frontiers in Plant Science. 14. 1087070–1087070. 4 indexed citations
4.
Chung, Moon‐Soo, et al.. (2023). Comparative Analysis of Volatile Terpenoids Composition in Lavender Leaves in Response to Gamma Irradiation and Anticancer Effect of α-Santalene against Prostate Cancer. Journal of Essential Oil Bearing Plants. 26(2). 244–252. 2 indexed citations
5.
Wang, Dexin, Baek-Rock Oh, Sungbeom Lee, Dae‐Hyuk Kim, & Min-Ho Joe. (2021). Process optimization for mass production of 2,3-butanediol by Bacillus subtilis CS13. Biotechnology for Biofuels. 14(1). 15–15. 20 indexed citations
6.
Jung, Kwang‐Woo, et al.. (2021). Investigation of Antifungal Mechanisms of Thymol in the Human Fungal Pathogen, Cryptococcus neoformans. Molecules. 26(11). 3476–3476. 18 indexed citations
7.
Kim, Hyangmi, et al.. (2020). Simultaneous production of poly-γ-glutamic acid and 2,3-butanediol by a newly isolated Bacillus subtilis CS13. Applied Microbiology and Biotechnology. 104(16). 7005–7021. 14 indexed citations
8.
Kim, Hyangmi, et al.. (2020). High-level production of poly-γ-glutamic acid from untreated molasses by Bacillus siamensis IR10. Microbial Cell Factories. 19(1). 101–101. 19 indexed citations
9.
Chung, Moon‐Soo, et al.. (2020). Comparative Analysis of Volatile Terpenoids Composition in Rosemary Leaves in Response to Ionizing Radiation. Journal of Essential Oil Bearing Plants. 23(3). 594–600. 6 indexed citations
10.
Choi, Seung Hee, et al.. (2019). Mutation in DDM1 inhibits the homology directed repair of double strand breaks. PLoS ONE. 14(2). e0211878–e0211878. 14 indexed citations
11.
12.
Min, Ji‐Hee, et al.. (2019). A basic helix-loop-helix 104 (bHLH104) protein functions as a transcriptional repressor for glucose and abscisic acid signaling in Arabidopsis. Plant Physiology and Biochemistry. 136. 34–42. 3 indexed citations
13.
14.
Min, Ji‐Hee, et al.. (2017). Arabidopsis Basic Helix-Loop-Helix 34 (bHLH34) Is Involved in Glucose Signaling through Binding to a GAGA Cis-Element. Frontiers in Plant Science. 8. 2100–2100. 14 indexed citations
15.
Chung, Moon‐Soo, et al.. (2017). Loss of Ribosomal Protein L24A (RPL24A) suppresses proline accumulation of Arabidopsis thaliana ring zinc finger 1 (atrzf1) mutant in response to osmotic stress. Biochemical and Biophysical Research Communications. 494(3-4). 499–503. 9 indexed citations
16.
Chung, Moon‐Soo, Sungbeom Lee, Ji‐Hee Min, et al.. (2016). Regulation of Arabidopsis thaliana plasma membrane glucose-responsive regulator (AtPGR) expression by A. thaliana storekeeper-like transcription factor, AtSTKL, modulates glucose response in Arabidopsis. Plant Physiology and Biochemistry. 104. 155–164. 9 indexed citations
17.
Chung, Moon‐Soo, et al.. (2015). Direct suppression of a rice bacterial blight (Xanthomonas oryzae pv. oryzae) by monoterpene (S)-limonene. PROTOPLASMA. 253(3). 683–690. 38 indexed citations
18.
Tholl, Dorothea, Reza Sohrabi, Jung‐Hyun Huh, & Sungbeom Lee. (2011). The biochemistry of homoterpenes – Common constituents of floral and herbivore-induced plant volatile bouquets. Phytochemistry. 72(13). 1635–1646. 95 indexed citations
19.
Tholl, Dorothea & Sungbeom Lee. (2011). Terpene Specialized Metabolism inArabidopsis thaliana. PubMed. 9. e0143–e0143. 184 indexed citations
20.
Kang, Kiyoon, Sangkyu Park, Young Soon Kim, et al.. (2009). Production of plant-specific tyramine derivatives by dual expression of tyramine N-hydroxycinnamoyltransferase and 4-coumarate:coenzyme A ligase in Escherichia coli. Biotechnology Letters. 31(9). 1469–1475. 6 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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