Yang‐Sook Chun

2.3k total citations
41 papers, 1.9k citations indexed

About

Yang‐Sook Chun is a scholar working on Molecular Biology, Cancer Research and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Yang‐Sook Chun has authored 41 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 18 papers in Cancer Research and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Yang‐Sook Chun's work include Cancer, Hypoxia, and Metabolism (15 papers), Mitochondrial Function and Pathology (5 papers) and ATP Synthase and ATPases Research (5 papers). Yang‐Sook Chun is often cited by papers focused on Cancer, Hypoxia, and Metabolism (15 papers), Mitochondrial Function and Pathology (5 papers) and ATP Synthase and ATPases Research (5 papers). Yang‐Sook Chun collaborates with scholars based in South Korea, Ethiopia and Japan. Yang‐Sook Chun's co-authors include Jong‐Wan Park, Myung-Suk Kim, Eun-Jin Yeo, Hyunsung Choi, Young‐Suk Cho, Chan‐Hyung Kim, Seung Won Kim, Eunjoo Choi, Myung Kyu Lee and Dong Hoon Shin and has published in prestigious journals such as Nature Communications, Gastroenterology and Biomaterials.

In The Last Decade

Yang‐Sook Chun

38 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yang‐Sook Chun South Korea 24 1.1k 704 214 204 167 41 1.9k
Marco Colombi Switzerland 13 1.5k 1.3× 613 0.9× 371 1.7× 309 1.5× 123 0.7× 23 2.5k
Shizhong Bu China 30 1.5k 1.3× 626 0.9× 193 0.9× 298 1.5× 161 1.0× 86 2.6k
Javad Tavakkoly‐Bazzaz Iran 22 1.0k 0.9× 576 0.8× 120 0.6× 225 1.1× 64 0.4× 117 1.8k
Ju-Jun Xie China 27 1.5k 1.3× 722 1.0× 123 0.6× 378 1.9× 166 1.0× 42 2.5k
Dong Guo China 27 1.4k 1.2× 808 1.1× 233 1.1× 265 1.3× 86 0.5× 85 2.2k
Juan Du China 23 915 0.8× 380 0.5× 173 0.8× 126 0.6× 88 0.5× 73 1.5k
Qi Cao China 25 824 0.7× 299 0.4× 288 1.3× 314 1.5× 184 1.1× 74 2.4k
Xia Yang China 28 1.4k 1.2× 795 1.1× 117 0.5× 272 1.3× 107 0.6× 75 2.1k

Countries citing papers authored by Yang‐Sook Chun

Since Specialization
Citations

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

Fields of papers citing papers by Yang‐Sook Chun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yang‐Sook Chun. 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 Yang‐Sook Chun. The network helps show where Yang‐Sook Chun may publish in the future.

Co-authorship network of co-authors of Yang‐Sook Chun

This figure shows the co-authorship network connecting the top 25 collaborators of Yang‐Sook Chun. A scholar is included among the top collaborators of Yang‐Sook Chun 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 Yang‐Sook Chun. Yang‐Sook Chun 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.
Jeong, Do‐Won, Jong‐Wan Park, Jiyoung Kim, et al.. (2023). Palmitoylation-driven PHF2 ubiquitination remodels lipid metabolism through the SREBP1c axis in hepatocellular carcinoma. Nature Communications. 14(1). 6370–6370. 39 indexed citations
2.
Seo, Jieun, et al.. (2023). Hypoxia inducible factor-1α promotes trichogenic gene expression in human dermal papilla cells. Scientific Reports. 13(1). 1478–1478. 10 indexed citations
3.
Kageyama, Tatsuto, Hiroshi Yoshikawa, Makoto Hirota, et al.. (2022). Bone beads enveloped with vascular endothelial cells for bone regenerative medicine. Acta Biomaterialia. 165. 168–179. 13 indexed citations
4.
Seo, Jieun, et al.. (2021). Tumor-intrinsic FABP5 is a novel driver for colon cancer cell growth via the HIF-1 signaling pathway. Cancer Genetics. 258-259. 151–156. 15 indexed citations
5.
Lim, Ji‐Hong, et al.. (2010). Antihepatoma activity of chaetocin due to deregulated splicing of hypoxia-inducible factor 1α pre-mRNA in mice and in vitro. Hepatology. 53(1). 171–180. 51 indexed citations
6.
Min, Kyoungin, Hunho Jo, Kyung-Mi Song, et al.. (2010). Dual-aptamer-based delivery vehicle of doxorubicin to both PSMA (+) and PSMA (−) prostate cancers. Biomaterials. 32(8). 2124–2132. 106 indexed citations
7.
Shin, Dong Hoon, et al.. (2008). A novel mode of action of YC-1 in HIF inhibition: stimulation of FIH-dependent p300 dissociation from HIF-1α. Molecular Cancer Therapeutics. 7(12). 3729–3738. 138 indexed citations
8.
9.
Yeo, Eun-Jin, Jihye Ryu, Yang‐Sook Chun, et al.. (2006). YC-1 Induces S Cell Cycle Arrest and Apoptosis by Activating Checkpoint Kinases. Cancer Research. 66(12). 6345–6352. 55 indexed citations
10.
Kim, Kyungeun, et al.. (2006). FK506: An Immunosuppressive Agent Preserving HIF-1 Activity. Immunopharmacology and Immunotoxicology. 28(4). 609–620. 5 indexed citations
11.
Lim, Ji-Hong, et al.. (2006). Bafilomycin Induces the p21-Mediated Growth Inhibition of Cancer Cells under Hypoxic Conditions by Expressing Hypoxia-Inducible Factor-1α. Molecular Pharmacology. 70(6). 1856–1865. 60 indexed citations
12.
Chun, Yang‐Sook, et al.. (2004). Hypoxia-Inducible Factor 1alpha- Mediated Resistance to Phenolic Anticancer. Chemotherapy. 50(3). 119–126. 12 indexed citations
13.
Chun, Yang‐Sook, Eun-Jin Yeo, Hwa‐Jin Suh, & Jong‐Wan Park. (2004). Spontaneous Generation of Reactive Oxygen Species in the Mixture of Cyanide and Glycerol. Annals of the New York Academy of Sciences. 1030(1). 43–51. 1 indexed citations
14.
Chun, Yang‐Sook, et al.. (2003). Role of apoptosis-inducing factor in myocardial cell death by ischemia–reperfusion. Biochemical and Biophysical Research Communications. 309(3). 619–624. 69 indexed citations
15.
Kim, Chan‐Hyung, et al.. (2001). Hyperbaric oxygenation pretreatment induces catalase and reduces infarct size in ischemic rat myocardium. Pflügers Archiv - European Journal of Physiology. 442(4). 519–525. 76 indexed citations
16.
You, Ho Jin, et al.. (2000). Increased 8-Hydroxyguanine Formation and Endonuclease Activity for Its Repair in Ischemic-Reperfused Hearts of Rats. Journal of Molecular and Cellular Cardiology. 32(6). 1053–1059. 14 indexed citations
17.
Chun, Yang‐Sook & Jong‐Wan Park. (1999). Characterization of Plasma Membrane-associated NADPH and NADH Oxidoreductases in Bovine Liver. Laboratory Animal Research. 15(3). 289–296. 1 indexed citations
18.
Chun, Yang‐Sook, Jong‐Wan Park, Myung-Suk Kim, et al.. (1999). Role of the 78-kDa Glucose-Regulated Protein as an Activity Modulator of Protein Phosphatase1γ2. Biochemical and Biophysical Research Communications. 259(2). 300–304. 8 indexed citations
19.
Chun, Yang‐Sook, et al.. (1994). Effect of superoxide dismutase on the development of preimplantation mouse embryos. Theriogenology. 41(2). 511–520. 25 indexed citations
20.
Huh, Sung‐Oh, et al.. (1990). Cloning and analysis of the pseudogene for human epinephrine synthesizing enzyme, phenylethanolamine N-methyltransferase (PNMT). International Journal of Biochemistry. 22(8). 921–924.

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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