Sanghwa Han

1.5k total citations
44 papers, 1.3k citations indexed

About

Sanghwa Han is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, Sanghwa Han has authored 44 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 9 papers in Physiology and 8 papers in Cell Biology. Recurrent topics in Sanghwa Han's work include Nitric Oxide and Endothelin Effects (8 papers), Photosynthetic Processes and Mechanisms (7 papers) and Photoreceptor and optogenetics research (5 papers). Sanghwa Han is often cited by papers focused on Nitric Oxide and Endothelin Effects (8 papers), Photosynthetic Processes and Mechanisms (7 papers) and Photoreceptor and optogenetics research (5 papers). Sanghwa Han collaborates with scholars based in South Korea, United States and Germany. Sanghwa Han's co-authors include Denis L. Rousseau, Young‐Guen Kwon, Young‐Myeong Kim, Roman S. Czernuszewicz, Thomas G. Spiro, Jeong‐Ki Min, Shin‐Jeong Lee, Tae‐Yoon Kim, Satoshi Takahashi and Syun‐Ru Yeh and has published in prestigious journals such as Nature, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Sanghwa Han

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sanghwa Han South Korea 18 723 231 173 163 119 44 1.3k
H. Diehl Germany 24 635 0.9× 177 0.8× 65 0.4× 46 0.3× 24 0.2× 66 1.4k
Mark C. Walker United States 18 473 0.7× 104 0.5× 81 0.5× 39 0.2× 102 0.9× 32 1.2k
Kyoji Furuta Japan 30 1.1k 1.5× 79 0.3× 119 0.7× 103 0.6× 288 2.4× 93 2.9k
Dayong Shi China 27 902 1.2× 63 0.3× 46 0.3× 37 0.2× 103 0.9× 137 2.3k
Huiying Li China 23 633 0.9× 126 0.5× 61 0.4× 177 1.1× 255 2.1× 81 1.9k
Giuseppe Calvaruso Italy 26 744 1.0× 66 0.3× 86 0.5× 97 0.6× 36 0.3× 92 1.8k
B.S.S. Masters United States 23 826 1.1× 307 1.3× 116 0.7× 296 1.8× 122 1.0× 53 2.0k
Jordi Bujons Spain 26 1.1k 1.6× 42 0.2× 130 0.8× 108 0.7× 87 0.7× 84 1.8k
Antonia F. Stepan United States 20 733 1.0× 313 1.4× 129 0.7× 84 0.5× 271 2.3× 37 2.9k
Thomas M. Shea United States 11 537 0.7× 273 1.2× 66 0.4× 125 0.8× 123 1.0× 16 1.1k

Countries citing papers authored by Sanghwa Han

Since Specialization
Citations

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

Fields of papers citing papers by Sanghwa Han

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sanghwa Han. 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 Sanghwa Han. The network helps show where Sanghwa Han may publish in the future.

Co-authorship network of co-authors of Sanghwa Han

This figure shows the co-authorship network connecting the top 25 collaborators of Sanghwa Han. A scholar is included among the top collaborators of Sanghwa Han 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 Sanghwa Han. Sanghwa Han 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.
Lim, Hye Jin, et al.. (2020). Small molecule inhibitors of IκB kinase β: A chip-based screening and molecular docking simulation. Bioorganic & Medicinal Chemistry. 28(9). 115440–115440. 3 indexed citations
2.
Myung, Yoochan, et al.. (2016). A niosomal bilayer of sorbitan monostearate in complex with flavones: a molecular dynamics simulation study. Journal of Liposome Research. 26(4). 336–344. 7 indexed citations
3.
Lee, Seungkoo, et al.. (2016). BIX02189 inhibits TGF-β1-induced lung cancer cell metastasis by directly targeting TGF-β type I receptor. Cancer Letters. 381(2). 314–322. 29 indexed citations
4.
Han, Sanghwa. (2015). Effect of Cholesterol on Ethanol‐induced Disruption of a POPC Bilayer: A Molecular Dynamics Simulation Study. Bulletin of the Korean Chemical Society. 36(10). 2569–2572. 2 indexed citations
5.
Cho, Young-Lai, Sung Mo Hur, Ji-Yoon Kim, et al.. (2014). Specific Activation of Insulin-like Growth Factor-1 Receptor by Ginsenoside Rg5 Promotes Angiogenesis and Vasorelaxation. Journal of Biological Chemistry. 290(1). 467–477. 59 indexed citations
6.
Han, Sanghwa. (2013). Molecular Dynamics Simulation of Sorbitan Monooleate Bilayers. Bulletin of the Korean Chemical Society. 34(3). 946–948. 12 indexed citations
7.
Kim, Kyungjong, Hansoo Lee, Sanghwa Han, et al.. (2009). Celastrol binds to ERK and inhibits FcεRI signaling to exert an anti-allergic effect. European Journal of Pharmacology. 612(1-3). 131–142. 55 indexed citations
8.
Kim, Ji‐Hee, Young-Lai Cho, CK Kim, et al.. (2008). Desmethylanhydroicaritin inhibits NF-κB-regulated inflammatory gene expression by modulating the redox-sensitive PI3K/PTEN/Akt pathway. European Journal of Pharmacology. 602(2-3). 422–431. 32 indexed citations
9.
Han, Sanghwa. (2008). Force field parameters for S -nitrosocysteine and molecular dynamics simulations of S -nitrosated thioredoxin. Biochemical and Biophysical Research Communications. 377(2). 612–616. 24 indexed citations
10.
Min, Jeong‐Ki, Tae‐Yoon Kim, Shin‐Jeong Lee, et al.. (2005). [6]-Gingerol, a pungent ingredient of ginger, inhibits angiogenesis in vitro and in vivo. Biochemical and Biophysical Research Communications. 335(2). 300–308. 239 indexed citations
11.
Jung, Jae Hyung, et al.. (2004). Indirect oxidation of 6-tetrahydrobiopterin by tyrosinase. Biochemical and Biophysical Research Communications. 314(4). 937–942. 5 indexed citations
12.
Han, Sanghwa, et al.. (2003). Polyphenolic Compounds and Superoxide Radical Scavenging Activity of Moru-Ju. Food Science and Biotechnology. 12(3). 290–297. 5 indexed citations
13.
Han, Sanghwa, et al.. (2003). Ozone-induced inactivation of antioxidant enzymes. Biochimie. 85(10). 947–952. 17 indexed citations
14.
Han, Sanghwa, et al.. (2003). Tyrosinase scavenges tyrosyl radical. Biochemical and Biophysical Research Communications. 312(3). 642–649. 3 indexed citations
15.
Han, Sanghwa, et al.. (2000). Nitric oxide protects Cu,Zn‐superoxide dismutase from hydrogen peroxide‐induced inactivation. FEBS Letters. 479(1-2). 25–28. 15 indexed citations
16.
Han, Sanghwa, Satoshi Takahashi, & Denis L. Rousseau. (2000). Time Dependence of the Catalytic Intermediates in Cytochromec Oxidase. Journal of Biological Chemistry. 275(3). 1910–1919. 81 indexed citations
17.
Suh, Junghun, et al.. (1998). Activation and stabilization of chymotrypsin in Microdomains of poly(ethylenimine) derivatives. A model of in vivo environment. Bioorganic & Medicinal Chemistry Letters. 8(11). 1331–1336. 7 indexed citations
18.
Park, Hee‐Young, et al.. (1996). EPR Spectra of Spin-Labeled Cytochrome c Bound to Acidic Membranes: Implications for the Binding Site and Reversibility. BMB Reports. 29(2). 169–174.
19.
Kim, Young‐Myeong, et al.. (1995). Decay Studies of Dmpo-Spin Adducts of Free Radicals Produced by Reactions of Metmyoglobin and Methemoglobin with Hydrogen Peroxide. Free Radical Research. 22(1). 11–21. 11 indexed citations
20.
Rheingold, Arnold L., Donna L. Staley, Sanghwa Han, & Gregory L. Geoffroy. (1988). Di-μ-carbonyl-nonacarbonyl-μ4-(α–α'-η-diphenylacetylene)-(μ4-diphenylnitrene)-tetraruthenium(4 Ru–Ru). Acta Crystallographica Section C Crystal Structure Communications. 44(3). 570–572. 5 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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