Hak Joong Kim

2.0k total citations
60 papers, 1.6k citations indexed

About

Hak Joong Kim is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Hak Joong Kim has authored 60 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 22 papers in Organic Chemistry and 16 papers in Pharmacology. Recurrent topics in Hak Joong Kim's work include Microbial Natural Products and Biosynthesis (15 papers), Antibiotic Resistance in Bacteria (9 papers) and Synthetic Organic Chemistry Methods (8 papers). Hak Joong Kim is often cited by papers focused on Microbial Natural Products and Biosynthesis (15 papers), Antibiotic Resistance in Bacteria (9 papers) and Synthetic Organic Chemistry Methods (8 papers). Hak Joong Kim collaborates with scholars based in South Korea, United States and Japan. Hak Joong Kim's co-authors include Hung‐wen Liu, Mark W. Ruszczycky, Sei-hyun Choi, Robert Stroup, John P. Fruehauf, Ainura Kyshtoobayeva, Eugene Mechetner, Svetlana Zonis, R. J. Parker and Reinaldo de la Noval García and has published in prestigious journals such as Nature, Journal of the American Chemical Society and Chemical Society Reviews.

In The Last Decade

Hak Joong Kim

59 papers receiving 1.6k citations

Peers

Hak Joong Kim

PHARM

ONCOL

BIOTE

Michael Brands Germany

Jian Ding China

Rodrigo J. Carbajo Spain

Yoko Tachibana Japan

Shilong Zheng United States

Nace Zidar Slovenia

Alfonso Carotenuto Italy

Brian Y. Feng United States

Qingfei Zheng United States

Michael Brands Germany

Hak Joong Kim

1.1k ×1.2

601 ×1.4

353 ×1.0

PHARM

360 ×1.4

ONCOL

112 ×1.0

BIOTE

Citations per year, relative to Hak Joong Kim Hak Joong Kim (= 1×) peers Michael Brands

Countries citing papers authored by Hak Joong Kim

Since Specialization

Citations

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

Fields of papers citing papers by Hak Joong Kim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hak Joong Kim. 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 Hak Joong Kim. The network helps show where Hak Joong Kim may publish in the future.

Co-authorship network of co-authors of Hak Joong Kim

This figure shows the co-authorship network connecting the top 25 collaborators of Hak Joong Kim. A scholar is included among the top collaborators of Hak Joong Kim 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 Hak Joong Kim. Hak Joong Kim 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

Kim, Seung‐Woo, Ji Yeon Oh, Dong Ho Kim, et al.. (2025). Siderophore-based targeted antibody recruitment for promoting immune responses towards Gram-negative pathogens. RSC Chemical Biology. 6(3). 387–393. 1 indexed citations

Kim, Jiseong, et al.. (2024). Targeted protein degradation directly engaging lysosomes or proteasomes. Chemical Society Reviews. 53(7). 3253–3272. 42 indexed citations

Park, Jimin, et al.. (2023). Cytoplasmic Delivery of an Antibiotic, Trimethoprim, with a Simple Bidentate Catechol Analog as a Siderophore Mimetic. ACS Infectious Diseases. 9(3). 554–566. 14 indexed citations

Kim, Seungwoo, et al.. (2023). Carboxylate-Directed Pd-Catalyzed β-C(sp³)–H Arylation of N-Methyl Alanine Derivatives for Diversification of Bioactive Peptides. Organic Letters. 25(50). 9008–9013. 2 indexed citations

Kim, Jaehwan, Hyeon Jeong Kim, Seon Hee Seo, et al.. (2023). Exploration of Tetrahydroisoquinoline- and Benzo[c]azepine-Based Sphingosine 1-Phosphate Receptor 1 Agonists for the Treatment of Multiple Sclerosis. Journal of Medicinal Chemistry. 66(15). 10381–10412. 5 indexed citations

Sengupta, Sandip, et al.. (2023). Synthesis and antibacterial activities of baulamycin A inspired derivatives. European Journal of Medicinal Chemistry. 259. 115592–115592. 5 indexed citations

Lee, Jieon, Do-Young Kim, Ha Eun Lee, et al.. (2021). Discovery of G Protein-Biased Antagonists against 5-HT₇R. Journal of Medicinal Chemistry. 64(18). 13766–13779. 6 indexed citations

Kim, Juhyeon, Ahmed Z. Abdelazem, Hak Joong Kim, et al.. (2019). Development of carbapenem-based fluorogenic probes for the clinical screening of carbapenemase-producing bacteria. Bioorganic Chemistry. 94. 103405–103405. 16 indexed citations

Kim, Ji Hye, et al.. (2019). Evaluation of anti-depressant effects of phthalazinone-based triple-acting small molecules against 5-HT2A, 5-HT2C, and the serotonin transporter. Bioorganic & Medicinal Chemistry Letters. 30(4). 126882–126882. 4 indexed citations

10.

Kim, Ji Hyeon, Jung Hoon Lee, Young Hoon Son, et al.. (2017). Docosahexaenoic acid-mediated protein aggregates may reduce proteasome activity and delay myotube degradation during muscle atrophy in vitro. Experimental & Molecular Medicine. 49(1). e287–e287. 26 indexed citations

11.

Lee, Hyun, Nga Nguyen, Jin Hee Hong, et al.. (2016). MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) Interaction Disruptor Sensitizes Insulin Signaling in Skeletal Muscle. Journal of Biological Chemistry. 291(52). 26627–26635. 13 indexed citations

12.

Kim, YoungJae, Hyeri Park, Jinsung Tae, et al.. (2016). 5-HT 7 receptor modulators: Amino groups attached to biphenyl scaffold determine functional activity. European Journal of Medicinal Chemistry. 123. 180–190. 14 indexed citations

13.

Kim, Hak Joong, et al.. (2014). Development of a novel fluorescence probe capable of assessing the cytoplasmic entry of siderophore-based conjugates. Organic & Biomolecular Chemistry. 13(1). 73–76. 10 indexed citations

14.

Kim, Hak Joong, et al.. (2014). Chemoenzymatic Synthesis of Spinosyn A. Angewandte Chemie International Edition. 53(49). 13553–13557. 30 indexed citations

15.

Kim, Chan Hyuk, Mingchao Kang, Hak Joong Kim, Abhishek Chatterjee, & Peter G. Schultz. (2012). Site‐Specific Incorporation of ε‐N‐Crotonyllysine into Histones. Angewandte Chemie International Edition. 51(29). 7246–7249. 101 indexed citations

16.

Kim, Hak Joong, et al.. (2011). Enzyme-catalysed [4+2] cycloaddition is a key step in the biosynthesis of spinosyn A. Nature. 473(7345). 109–112. 267 indexed citations

17.

Choi, Suck‐Chei, Jung‐Hee Lee, Ji Hoon Phi, et al.. (2011). Therapeutic targeting of subdural medulloblastomas using human neural stem cells expressing carboxylesterase. Cancer Gene Therapy. 18(11). 817–824. 21 indexed citations

18.

Borisova, Svetlana A., Hak Joong Kim, Xiaotao Pu, & Hung‐wen Liu. (2008). Glycosylation of Acyclic and Cyclic Aglycone Substrates by Macrolide Glycosyltransferase DesVII/DesVIII: Analysis and Implications. ChemBioChem. 9(10). 1554–1558. 22 indexed citations

19.

Choi, Byung Ock, Hak Joong Kim, Bum‐Soo Kim, et al.. (2002). New subtraction algorithms for evaluation of lesions on dynamic contrast-enhanced MR mammography. European Radiology. 12(12). 3018–3022. 14 indexed citations

20.

Lee, Eun, Cheol Hwan Yoon, Young‐Jin Lee, & Hak Joong Kim. (1997). Synthesis of Iridolactones via Stereoselective Favorskii Rearrangement: (+)-Dolicholactone, (+)-Alyxialactone, and (-)-4-epi-Alyxialactone. Bulletin of the Korean Chemical Society. 18(12). 1247–1248. 3 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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