Su Wol Chung

5.2k total citations · 3 hit papers
77 papers, 4.3k citations indexed

About

Su Wol Chung is a scholar working on Molecular Biology, Immunology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Su Wol Chung has authored 77 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 23 papers in Immunology and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Su Wol Chung's work include Heme Oxygenase-1 and Carbon Monoxide (14 papers), Immune Response and Inflammation (10 papers) and Immune Cell Function and Interaction (7 papers). Su Wol Chung is often cited by papers focused on Heme Oxygenase-1 and Carbon Monoxide (14 papers), Immune Response and Inflammation (10 papers) and Immune Cell Function and Interaction (7 papers). Su Wol Chung collaborates with scholars based in South Korea, United States and Taiwan. Su Wol Chung's co-authors include Eunhee Park, Seon‐Jin Lee, Mark A. Perrella, Bok Yun Kang, Min‐Young Kwon, Tae Sung Kim, Eun‐Hee Park, Xiaoli Liu, Giorgio Trinchieri and Rebecca M. Baron and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Journal of Clinical Investigation.

In The Last Decade

Su Wol Chung

77 papers receiving 4.2k citations

Hit Papers

ROS-mediated autophagy increases intracellular iron lev... 2015 2026 2018 2022 2019 2015 2023 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Su Wol Chung South Korea 32 2.5k 1.1k 1.0k 753 400 77 4.3k
Xiang Xue China 40 1.8k 0.7× 548 0.5× 1.1k 1.1× 405 0.5× 423 1.1× 111 4.1k
Dan Xu China 35 2.8k 1.1× 590 0.5× 1.8k 1.8× 515 0.7× 528 1.3× 234 5.1k
Zili Zhang China 41 2.5k 1.0× 1.2k 1.1× 1.2k 1.2× 736 1.0× 1.4k 3.5× 132 5.1k
Ning Li China 36 2.2k 0.9× 1.2k 1.0× 1.0k 1.0× 464 0.6× 497 1.2× 137 4.4k
Ting Wang China 35 2.4k 1.0× 765 0.7× 1.1k 1.0× 419 0.6× 559 1.4× 267 4.3k
Mary E. Choi United States 41 2.9k 1.2× 707 0.6× 557 0.5× 658 0.9× 1.3k 3.2× 73 5.6k
Lei Zhao China 33 1.7k 0.7× 1.0k 0.9× 895 0.9× 518 0.7× 519 1.3× 120 3.9k
Minghua Yang China 29 2.3k 0.9× 1.1k 1.0× 1.2k 1.1× 749 1.0× 737 1.8× 95 4.0k
Sandeep Kumar United States 38 2.1k 0.8× 537 0.5× 1.0k 1.0× 705 0.9× 309 0.8× 129 4.1k
Hua Yang China 37 1.9k 0.8× 509 0.5× 685 0.7× 597 0.8× 323 0.8× 179 4.1k

Countries citing papers authored by Su Wol Chung

Since Specialization
Citations

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

Fields of papers citing papers by Su Wol Chung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Su Wol Chung. 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 Su Wol Chung. The network helps show where Su Wol Chung may publish in the future.

Co-authorship network of co-authors of Su Wol Chung

This figure shows the co-authorship network connecting the top 25 collaborators of Su Wol Chung. A scholar is included among the top collaborators of Su Wol Chung 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 Su Wol Chung. Su Wol Chung 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.
Kim, Yong Hwan, Mi Jeong Kim, Su Wol Chung, et al.. (2025). Phosphorylation of eIF2α suppresses the impairment of GSH/NADPH homeostasis and mitigates the activation of cell death pathways, including ferroptosis, during ER stress. Molecules and Cells. 48(5). 100210–100210. 2 indexed citations
2.
Park, Min‐Kyung, et al.. (2024). The mechanism underlying correlation of particulate matter-induced ferroptosis with inflammasome activation and iron accumulation in macrophages. Cell Death Discovery. 10(1). 144–144. 9 indexed citations
3.
Park, Min‐Kyung, Young‐Jun Park, In‐Ah Lee, et al.. (2024). Anti-Inflammatory Effects of Idebenone Attenuate LPS-Induced Systemic Inflammatory Diseases by Suppressing NF-κB Activation. Antioxidants. 13(2). 151–151. 2 indexed citations
4.
Kim, Hee‐Ju, Joon Ho Moon, Su Wol Chung, & Ivo Abraham. (2023). The role of cytokines and Indolamine-2.3 dioxygenase in experiencing a psycho-neurological symptom cluster in hematological cancer patients: IL-1alpha, IL-1beta, IL-4, IL-6, TNF-alpha, kynurenine, and tryptophan. Journal of Psychosomatic Research. 173. 111455–111455. 6 indexed citations
5.
Lee, Seunghee, et al.. (2023). Autophagy mediates an amplification loop during ferroptosis. Cell Death and Disease. 14(7). 464–464. 136 indexed citations breakdown →
6.
Kwon, Min‐Young, Sailaja Ghanta, Julie Ng, et al.. (2021). Mesenchymal stromal cells expressing a dominant-negative high mobility group A1 transgene exhibit improved function during sepsis. Journal of Leukocyte Biology. 110(4). 711–722. 4 indexed citations
7.
Yoon, Sung‐Jin, Dong Hyun Jo, Seung Ho Park, et al.. (2019). Thioredoxin-Interacting Protein Promotes Phagosomal Acidification Upon Exposure to Escherichia coli Through Inflammasome-Mediated Caspase-1 Activation in Macrophages. Frontiers in Immunology. 10. 2636–2636. 4 indexed citations
8.
Woo, Je Moon, et al.. (2013). Human retinal pigment epithelial cells express the long pentraxin PTX3.. PubMed. 19. 303–10. 30 indexed citations
9.
Baron, Rebecca M., Silvia López-Guzmán, Dario F. Riascos‐Bernal, et al.. (2010). Distamycin A Inhibits HMGA1-Binding to the P-Selectin Promoter and Attenuates Lung and Liver Inflammation during Murine Endotoxemia. PLoS ONE. 5(5). e10656–e10656. 26 indexed citations
10.
Agiostratidou, Georgia, Maomi Li, Kimita Suyama, et al.. (2009). Loss of Retinal Cadherin Facilitates Mammary Tumor Progression and Metastasis. Cancer Research. 69(12). 5030–5038. 38 indexed citations
11.
Fredenburgh, Laura E., Olin D. Liang, Alvaro A. Macias, et al.. (2008). Absence of Cyclooxygenase-2 Exacerbates Hypoxia-Induced Pulmonary Hypertension and Enhances Contractility of Vascular Smooth Muscle Cells. Circulation. 117(16). 2114–2122. 67 indexed citations
12.
Geraldes, Pedro, Kunimasa Yagi, Yuzuru Ohshiro, et al.. (2008). Selective Regulation of Heme Oxygenase-1 Expression and Function by Insulin through IRS1/Phosphoinositide 3-Kinase/Akt-2 Pathway. Journal of Biological Chemistry. 283(49). 34327–34336. 60 indexed citations
13.
Hulit, James, Kimita Suyama, Su Wol Chung, et al.. (2007). N-Cadherin Signaling Potentiates Mammary Tumor Metastasis via Enhanced Extracellular Signal-Regulated Kinase Activation. Cancer Research. 67(7). 3106–3116. 173 indexed citations
14.
Chung, Su Wol, Yen‐Hsu Chen, Shaw‐Fang Yet, Matthew D. Layne, & Mark A. Perrella. (2006). Endotoxin-Induced Down-Regulation of Elk-3 Facilitates Heme Oxygenase-1 Induction in Macrophages. The Journal of Immunology. 176(4). 2414–2420. 26 indexed citations
17.
18.
Kang, Bok Yun, Su Wol Chung, Seung Hyun Kim, Shi Yong Ryu, & Tae Sung Kim. (2000). Inhibition of interleukin-12 and interferon-γ production in immune cells by tanshinones from Salvia miltiorrhiza. Immunopharmacology. 49(3). 355–361. 111 indexed citations
19.
Chung, Su Wol, et al.. (2000). Retinoid‐mediated inhibition of interleukin‐12 production in mouse macrophages suppresses Th1 cytokine profile in CD4+ T cells. British Journal of Pharmacology. 130(3). 581–586. 50 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026