Kuo‐Hsiung Lee

34.0k total citations · 1 hit paper
772 papers, 28.5k citations indexed

About

Kuo‐Hsiung Lee is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Kuo‐Hsiung Lee has authored 772 papers receiving a total of 28.5k indexed citations (citations by other indexed papers that have themselves been cited), including 512 papers in Molecular Biology, 261 papers in Organic Chemistry and 119 papers in Pharmacology. Recurrent topics in Kuo‐Hsiung Lee's work include Natural product bioactivities and synthesis (177 papers), Phytochemical compounds biological activities (101 papers) and Traditional and Medicinal Uses of Annonaceae (92 papers). Kuo‐Hsiung Lee is often cited by papers focused on Natural product bioactivities and synthesis (177 papers), Phytochemical compounds biological activities (101 papers) and Traditional and Medicinal Uses of Annonaceae (92 papers). Kuo‐Hsiung Lee collaborates with scholars based in United States, Taiwan and China. Kuo‐Hsiung Lee's co-authors include Susan L. Morris‐Natschke, Kenneth F. Bastow, Chin‐Ho Chen, Keduo Qian, L. Mark Cosentino, Yoshiki Kashiwada, Tian-Shung Wu, Zhiyan Xiao, Lan Xie and Kyoko Nakagawa‐Goto and has published in prestigious journals such as Science, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Kuo‐Hsiung Lee

750 papers receiving 27.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rational selection of training and test sets for the development of validated QSAR models

2003 568 citations Zhiyan Xiao, Kuo‐Hsiung Lee et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kuo‐Hsiung Lee United States	81	15.5k	9.8k	4.6k	3.9k	2.8k	772	28.5k
Gordon M. Cragg United States	60	17.2k 1.1×	7.6k 0.8×	7.3k 1.6×	10.1k 2.6×	4.3k 1.5×	148	35.2k
John M. Pezzuto United States	84	16.7k 1.1×	4.8k 0.5×	6.5k 1.4×	3.6k 0.9×	3.0k 1.1×	528	32.0k
M. Iqbal Choudhary Pakistan	69	10.7k 0.7×	9.3k 1.0×	7.0k 1.5×	4.4k 1.1×	3.7k 1.3×	1.5k	29.9k
A. Douglas Kinghorn United States	77	14.2k 0.9×	3.8k 0.4×	7.5k 1.6×	3.5k 0.9×	2.8k 1.0×	602	27.6k
Michael R. Boyd United States	81	12.6k 0.8×	9.5k 1.0×	3.0k 0.6×	4.3k 1.1×	2.6k 0.9×	389	28.6k
Vincent Zoete Switzerland	47	13.1k 0.8×	8.0k 0.8×	2.1k 0.5×	3.3k 0.8×	2.6k 0.9×	157	28.4k
Ruth Huey United States	15	18.7k 1.2×	8.9k 0.9×	2.0k 0.4×	3.5k 0.9×	2.1k 0.7×	23	34.2k
Oleg Trott United States	7	14.2k 0.9×	6.2k 0.6×	2.0k 0.4×	2.9k 0.7×	2.0k 0.7×	7	27.3k
Anne Monks United States	43	12.8k 0.8×	6.7k 0.7×	2.0k 0.4×	2.8k 0.7×	1.3k 0.4×	103	24.4k
Dominic A. Scudiero United States	50	16.3k 1.1×	6.9k 0.7×	2.2k 0.5×	2.9k 0.7×	1.3k 0.5×	95	28.1k

Countries citing papers authored by Kuo‐Hsiung Lee

Since Specialization

Citations

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

Fields of papers citing papers by Kuo‐Hsiung Lee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kuo‐Hsiung Lee

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

All Works

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20 of 20 papers shown

Sun, Lin, Alexej Dick, Megan E. Meuser, et al.. (2020). Design, synthesis and structure-activity relationships of 4-phenyl-1H-1,2,3-triazole phenylalanine derivatives as novel HIV-1 capsid inhibitors with promising antiviral activities. European Journal of Medicinal Chemistry. 190. 112085–112085. 92 indexed citations

Yi, Ping, Tao Yang, Fu‐Mei Yang, et al.. (2019). Ochrocephalamines B–D, Three Alkaloids from Oxytropis ochrocephala Bunge. Organic Letters. 21(13). 5051–5054. 17 indexed citations

Kang, Dongwei, Heng Zhang, Zhao Wang, et al.. (2019). Identification of Dihydrofuro[3,4-d]pyrimidine Derivatives as Novel HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors with Promising Antiviral Activities and Desirable Physicochemical Properties. Journal of Medicinal Chemistry. 62(3). 1484–1501. 75 indexed citations

Zhang, Yu, Masuo Goto, Akifumi Oda, et al.. (2019). Antiproliferative Aspidosperma-Type Monoterpenoid Indole Alkaloids from Bousigonia mekongensis Inhibit Tubulin Polymerization. Molecules. 24(7). 1256–1256. 18 indexed citations

Ling, Yong, Yu‐Ning Teng, Shi Chen, et al.. (2018). Development of novel amino-quinoline-5,8-dione derivatives as NAD(P)H:quinone oxidoreductase 1 (NQO1) inhibitors with potent antiproliferative activities. European Journal of Medicinal Chemistry. 154. 199–209. 31 indexed citations

Yan, Lei, Fangfang Lai, Xiaoguang Chen, et al.. (2017). Design, synthesis and biological evaluation of novel indolin-2-ones as potent anticancer compounds. Bioorganic & Medicinal Chemistry Letters. 27(15). 3326–3331. 16 indexed citations

Nakagawa‐Goto, Kyoko, et al.. (2016). A Novel Plant Sesquiterpene Lactone Derivative, DETD-35, Suppresses BRAFV600E Mutant Melanoma Growth and Overcomes Acquired Vemurafenib Resistance in Mice. Molecular Cancer Therapeutics. 15(6). 1163–1176. 19 indexed citations

Wang, Li‐Ting, Xiang Nan, Yang Liu, et al.. (2014). Toward synthesis of third-generation spin-labeled podophyllotoxin derivatives using isocyanide multicomponent reactions. European Journal of Medicinal Chemistry. 75. 282–288. 14 indexed citations

Shen, De-Yang, Chih‐Hua Chao, Hsiu-Hui Chan, et al.. (2012). Bioactive constituents of Clausena lansium and a method for discrimination of aldose enantiomers. Phytochemistry. 82. 110–117. 47 indexed citations

10.

Yang, Xiaoming, Qian Shi, Yi-Nan Liu, et al.. (2009). Antitumor Agents 268. Design, Synthesis, and Mechanistic Studies of New 9-Substituted Phenanthrene-Based Tylophorine Analogues as Potent Cytotoxic Agents. Journal of Medicinal Chemistry. 52(16). 5262–5268. 42 indexed citations

11.

Wu, Jianhui, Ming Zhao, Keduo Qian, et al.. (2009). Novel N-(3-carboxyl-9-benzyl-β-carboline-1-yl)ethylamino acids: Synthesis, anti-tumor evaluation, intercalating determination, 3D QSAR analysis and docking investigation. European Journal of Medicinal Chemistry. 44(10). 4153–4161. 87 indexed citations

12.

Nakagawa‐Goto, Kyoko, Seikou Nakamura, Kenneth F. Bastow, et al.. (2007). Antitumor agents. 256. Conjugation of paclitaxel with other antitumor agents: Evaluation of novel conjugates as cytotoxic agents. Bioorganic & Medicinal Chemistry Letters. 17(10). 2894–2898. 22 indexed citations

13.

Okasaka, Mamoru, Yoshihisa Takaishi, Yoshiki Kashiwada, et al.. (2006). Terpenoids from Juniperus polycarpus var. seravschanica. Phytochemistry. 67(24). 2635–2640. 48 indexed citations

14.

Nakamura, Seikou, Mutsuo Kozuka, Kenneth F. Bastow, et al.. (2005). Cancer preventive agents, Part 2: Synthesis and evaluation of 2-phenyl-4-quinolone and 9-oxo-9,10-dihydroacridine derivatives as novel antitumor promoters. Bioorganic & Medicinal Chemistry. 13(14). 4396–4401. 48 indexed citations

15.

Huang, Li, Phong Ho, Kuo‐Hsiung Lee, & Chin‐Ho Chen. (2005). Synthesis and anti-HIV activity of bi-functional betulinic acid derivatives. Bioorganic & Medicinal Chemistry. 14(7). 2279–2289. 70 indexed citations

16.

Wang, Xihong, Kenneth F. Bastow, Yun-Lian Lin, et al.. (2004). Antitumor Agents. 239. Isolation, Structure Elucidation, Total Synthesis, and Anti-Breast Cancer Activity of Neo-tanshinlactone from Salvia miltiorrhiza. Journal of Medicinal Chemistry. 47(23). 5816–5819. 192 indexed citations

17.

Lee, Kuo‐Hsiung. (2004). Research and Discovery Trends of Chinese Medicine in the New Century. 15(3). 151–160. 8 indexed citations

18.

Huang, Li-Jiau, Kuo‐Hsiung Lee, Zhiyan Xiao, et al.. (2004). Synthesis and biological relationships of 3′,6-substituted 2-phenyl-4-quinolone-3-carboxylic acid derivatives as antimitotic agents. Bioorganic & Medicinal Chemistry. 13(1). 265–275. 57 indexed citations

19.

Kashiwada, Yoshiki, Gen‐ichiro Nonaka, Itsuo Nishioka, et al.. (1993). Tannins as Potent Inhibitors of DNA Topoisomerase II In Vitro. Journal of Pharmaceutical Sciences. 82(5). 487–492. 82 indexed citations

20.

Hu, Changqi, et al.. (1990). The Cytotoxic Principles ofPseudolarix kaempferi: Pseudolaric Acid-A and -B and Related Derivatives¹. Planta Medica. 56(4). 383–385. 76 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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