Being‐Sun Wung

3.5k total citations
43 papers, 3.0k citations indexed

About

Being‐Sun Wung is a scholar working on Molecular Biology, Physiology and Pharmacology. According to data from OpenAlex, Being‐Sun Wung has authored 43 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 9 papers in Physiology and 8 papers in Pharmacology. Recurrent topics in Being‐Sun Wung's work include Genomics, phytochemicals, and oxidative stress (10 papers), Nitric Oxide and Endothelin Effects (9 papers) and Heme Oxygenase-1 and Carbon Monoxide (8 papers). Being‐Sun Wung is often cited by papers focused on Genomics, phytochemicals, and oxidative stress (10 papers), Nitric Oxide and Endothelin Effects (9 papers) and Heme Oxygenase-1 and Carbon Monoxide (8 papers). Being‐Sun Wung collaborates with scholars based in Taiwan. Being‐Sun Wung's co-authors include Chia‐Wen Hsieh, H. J. Hsieh, Danny Ling Wang, Jen‐Fang Cheng, Jeng‐Jiann Chiu, Ming‐Chen Hsu, Jing‐Jy Cheng, D.L. Wang, Yeun-Jund Shyy and Yuen‐Jen Chao and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Circulation Research.

In The Last Decade

Being‐Sun Wung

43 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Being‐Sun Wung Taiwan 31 1.5k 627 510 366 259 43 3.0k
Hazel Lum United States 30 1.4k 0.9× 690 1.1× 442 0.9× 350 1.0× 113 0.4× 50 3.1k
Cuk‐Seong Kim South Korea 28 1.4k 1.0× 758 1.2× 400 0.8× 312 0.9× 282 1.1× 104 3.2k
Alejandra San Martín United States 28 1.2k 0.8× 902 1.4× 774 1.5× 404 1.1× 217 0.8× 58 3.0k
Manuela Bartoli United States 31 1.6k 1.1× 649 1.0× 511 1.0× 204 0.6× 155 0.6× 88 4.0k
Weili Shen China 31 1.4k 0.9× 807 1.3× 276 0.5× 338 0.9× 156 0.6× 71 3.0k
Stefano Menini Italy 41 1.3k 0.9× 889 1.4× 776 1.5× 392 1.1× 137 0.5× 72 4.0k
Laura Moreno Spain 35 1.2k 0.8× 806 1.3× 301 0.6× 645 1.8× 423 1.6× 95 3.2k
Chi Wai Lau Hong Kong 34 1.3k 0.9× 828 1.3× 388 0.8× 593 1.6× 123 0.5× 82 3.6k
Luisa Lenti Italy 24 948 0.6× 438 0.7× 474 0.9× 363 1.0× 234 0.9× 44 2.5k
Vincenzo Sica Italy 35 1.2k 0.8× 506 0.8× 361 0.7× 421 1.2× 173 0.7× 58 3.3k

Countries citing papers authored by Being‐Sun Wung

Since Specialization
Citations

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

Fields of papers citing papers by Being‐Sun Wung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Being‐Sun Wung. 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 Being‐Sun Wung. The network helps show where Being‐Sun Wung may publish in the future.

Co-authorship network of co-authors of Being‐Sun Wung

This figure shows the co-authorship network connecting the top 25 collaborators of Being‐Sun Wung. A scholar is included among the top collaborators of Being‐Sun Wung 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 Being‐Sun Wung. Being‐Sun Wung 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.
Cheng, Kai‐Chun, et al.. (2021). Sulforaphane inhibits blue light–induced inflammation and apoptosis by upregulating the SIRT1/PGC-1α/Nrf2 pathway and autophagy in retinal pigment epithelial cells. Toxicology and Applied Pharmacology. 421. 115545–115545. 38 indexed citations
2.
Liu, Yu‐Fan, et al.. (2017). Effect of acetic acid on ethanol production by Zymomonas mobilis mutant strains through continuous adaptation. BMC Biotechnology. 17(1). 63–63. 27 indexed citations
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Huang, Yu‐Ting, et al.. (2014). Carbon Monoxide Induces Heme Oxygenase-1 to Modulate STAT3 Activation in Endothelial Cells via S-Glutathionylation. PLoS ONE. 9(7). e100677–e100677. 29 indexed citations
5.
Hsieh, Chia‐Wen, et al.. (2012). The glutathionylation of p65 modulates NF-κB activity in 15-deoxy-Δ12,14-prostaglandin J2-treated endothelial cells. Free Radical Biology and Medicine. 52(9). 1844–1853. 28 indexed citations
6.
Hsieh, Chia‐Wen, et al.. (2010). The Glutaredoxin/Glutathione System Modulates NF-κB Activity by Glutathionylation of p65 in Cinnamaldehyde-Treated Endothelial Cells. Toxicological Sciences. 116(1). 151–163. 52 indexed citations
7.
Chuang, Jing-Jing, et al.. (2010). Dual mechanisms of NF-κB inhibition in carnosol-treated endothelial cells. Toxicology and Applied Pharmacology. 245(1). 21–35. 40 indexed citations
8.
Chen, Chih‐Cheng, et al.. (2010). Calcium- and phosphatidylinositol 3-kinase/Akt-dependent activation of endothelial nitric oxide synthase by apigenin. Life Sciences. 87(23-26). 743–749. 24 indexed citations
9.
Wei, Yushan, et al.. (2009). Isolating a Cytoprotective Compound fromGanoderma tsugae: Effects on Induction of Nrf-2-Related Genes in Endothelial Cells. Bioscience Biotechnology and Biochemistry. 73(8). 1757–1763. 12 indexed citations
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Liu, Yen‐Chin, et al.. (2007). Chalcone inhibits the activation of NF-κB and STAT3 in endothelial cells via endogenous electrophile. Life Sciences. 80(15). 1420–1430. 84 indexed citations
14.
Wung, Being‐Sun, et al.. (2005). Piceatannol upregulates endothelial heme oxygenase-1 expression via novel protein kinase C and tyrosine kinase pathways. Pharmacological Research. 53(2). 113–122. 62 indexed citations
15.
Wung, Being‐Sun, Ming‐Chen Hsu, Chia‐Ching Wu, & Chia‐Wen Hsieh. (2005). Resveratrol suppresses IL-6-induced ICAM-1 gene expression in endothelial cells: Effects on the inhibition of STAT3 phosphorylation. Life Sciences. 78(4). 389–397. 130 indexed citations
16.
Wu, Chean‐Ping, et al.. (2005). Upregulation of heme oxygenase-1 by Epigallocatechin-3-gallate via the phosphatidylinositol 3-kinase/Akt and ERK pathways. Life Sciences. 78(25). 2889–2897. 217 indexed citations
17.
Wung, Being‐Sun, et al.. (2005). ICAM-1 induction by TNFα and IL-6 is mediated by distinct pathways via Rac in endothelial cells. Journal of Biomedical Science. 12(1). 91–101. 120 indexed citations
18.
Hsieh, Hsyue‐Jen, et al.. (1998). Increase of reactive oxygen species (ROS) in endothelial cells by shear flow and involvement of ROS in shear‐induced c‐fos expression. Journal of Cellular Physiology. 175(2). 156–162. 23 indexed citations
19.
Chiu, Jeng‐Jiann, et al.. (1998). Increase of reactive oxygen species (ROS) in endothelial cells by shear flow and involvement of ROS in shear-induced c-fos expression. Journal of Cellular Physiology. 175(2). 156–162. 158 indexed citations
20.
Wang, D.L., et al.. (1993). Cyclical Strain Increases Endothelin-1 Secretion and Gene Expression in Human Endothelial Cells. Biochemical and Biophysical Research Communications. 195(2). 1050–1056. 48 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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