Chi-Wu Chiang

1.3k total citations
20 papers, 1.1k citations indexed

About

Chi-Wu Chiang is a scholar working on Molecular Biology, Oncology and Epidemiology. According to data from OpenAlex, Chi-Wu Chiang has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Oncology and 3 papers in Epidemiology. Recurrent topics in Chi-Wu Chiang's work include Ubiquitin and proteasome pathways (7 papers), Cell death mechanisms and regulation (4 papers) and Cancer-related Molecular Pathways (3 papers). Chi-Wu Chiang is often cited by papers focused on Ubiquitin and proteasome pathways (7 papers), Cell death mechanisms and regulation (4 papers) and Cancer-related Molecular Pathways (3 papers). Chi-Wu Chiang collaborates with scholars based in Taiwan, United States and India. Chi-Wu Chiang's co-authors include Yu-San Yang, Elizabeth Yang, Chung‐Hsiang Yang, Yi-Chun Kuo, Chia‐Ling Chen, Chiou‐Feng Lin, Ming‐Shiou Jan, Yee-Shin Lin, Wei‐Ching Huang and Shirish Shenolikar and has published in prestigious journals such as Journal of Biological Chemistry, Blood and PLoS ONE.

In The Last Decade

Chi-Wu Chiang

20 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chi-Wu Chiang Taiwan 14 846 206 169 139 105 20 1.1k
Chul‐Woong Chung South Korea 12 829 1.0× 306 1.5× 170 1.0× 112 0.8× 159 1.5× 20 1.1k
Chae Young Hwang South Korea 17 710 0.8× 161 0.8× 212 1.3× 72 0.5× 106 1.0× 27 946
Zee‐Fen Chang Taiwan 17 553 0.7× 144 0.7× 140 0.8× 78 0.6× 130 1.2× 26 857
Nicholas M. George United States 14 541 0.6× 178 0.9× 167 1.0× 146 1.1× 72 0.7× 21 902
Almut Dufner Switzerland 10 1.4k 1.6× 219 1.1× 208 1.2× 107 0.8× 215 2.0× 11 1.7k
Constantinos Demetriades Germany 17 606 0.7× 144 0.7× 258 1.5× 170 1.2× 114 1.1× 25 1.0k
L. S. P. Davidson United Kingdom 24 1.1k 1.4× 169 0.8× 166 1.0× 76 0.5× 155 1.5× 50 1.6k
Janos Steffen United States 10 913 1.1× 127 0.6× 309 1.8× 239 1.7× 172 1.6× 10 1.1k
Valentina Iadevaia United Kingdom 19 879 1.0× 85 0.4× 124 0.7× 90 0.6× 90 0.9× 31 1.2k

Countries citing papers authored by Chi-Wu Chiang

Since Specialization
Citations

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

Fields of papers citing papers by Chi-Wu Chiang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chi-Wu Chiang. 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 Chi-Wu Chiang. The network helps show where Chi-Wu Chiang may publish in the future.

Co-authorship network of co-authors of Chi-Wu Chiang

This figure shows the co-authorship network connecting the top 25 collaborators of Chi-Wu Chiang. A scholar is included among the top collaborators of Chi-Wu Chiang 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 Chi-Wu Chiang. Chi-Wu Chiang 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.
Wang, Mengxiong, Mary E. Law, Bradley J. Davis, et al.. (2019). Disulfide bond-disrupting agents activate the tumor necrosis family-related apoptosis-inducing ligand/death receptor 5 pathway. Cell Death Discovery. 5(1). 153–153. 9 indexed citations
2.
Wang, Mengxiong, Renan B. Ferreira, Mary E. Law, et al.. (2019). A novel proteotoxic combination therapy for EGFR+ and HER2+ cancers. Oncogene. 38(22). 4264–4282. 8 indexed citations
3.
Wang, Chi‐Hsien, Chi-Wu Chiang, Marc Lombès, et al.. (2019). Identification of two independent SUMO-interacting motifs in Fas-associated factor 1 (FAF1): Implications for mineralocorticoid receptor (MR)-mediated transcriptional regulation. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1866(8). 1282–1297. 15 indexed citations
4.
Tang, Yen-An, et al.. (2017). Phosphorylation of Rab37 by protein kinase C alpha inhibits the exocytosis function and metastasis suppression activity of Rab37. Oncotarget. 8(65). 108556–108570. 13 indexed citations
5.
Lee, Yi‐Chao, Kuen‐Haur Lee, Chi-Wu Chiang, et al.. (2016). RINT-1 interacts with MSP58 within nucleoli and plays a role in ribosomal gene transcription. Biochemical and Biophysical Research Communications. 478(2). 873–880. 4 indexed citations
6.
Chiang, Chi-Wu, Chang-Han Chen, Yi‐Chao Lee, et al.. (2015). Identification and characterization of nuclear and nucleolar localization signals in 58-kDa microspherule protein (MSP58). Journal of Biomedical Science. 22(1). 33–33. 8 indexed citations
8.
Yen, Chia-Jui, Hung-Wen Tsai, Ting‐Fen Tsai, et al.. (2012). Hepatitis B Virus X Protein Upregulates mTOR Signaling through IKKβ to Increase Cell Proliferation and VEGF Production in Hepatocellular Carcinoma. PLoS ONE. 7(7). e41931–e41931. 61 indexed citations
9.
Yang, Yu-San, et al.. (2010). The B56γ3 Regulatory Subunit of Protein Phosphatase 2A (PP2A) Regulates S Phase-specific Nuclear Accumulation of PP2A and the G1 to S Transition. Journal of Biological Chemistry. 285(28). 21567–21580. 33 indexed citations
11.
Chiang, Chi-Wu, Yan Ling, & Elizabeth Yang. (2008). Chapter 14 Phosphatases and Regulation of Cell Death. Methods in enzymology on CD-ROM/Methods in enzymology. 446. 237–257. 13 indexed citations
13.
Chiang, Chi-Wu, et al.. (2007). Gypenosides Induce Apoptosis in Human Hepatoma Huh-7 Cells through a Calcium/Reactive Oxygen Species-Dependent Mitochondrial Pathway. Planta Medica. 73(6). 535–544. 32 indexed citations
14.
Lin, Chiou‐Feng, Chia‐Ling Chen, Chi-Wu Chiang, et al.. (2007). GSK-3β acts downstream of PP2A and the PI 3-kinase-Akt pathway, and upstream of caspase-2 in ceramide-induced mitochondrial apoptosis. Journal of Cell Science. 120(16). 2935–2943. 129 indexed citations
15.
Chen, Chia‐Ling, Chiou‐Feng Lin, Chi-Wu Chiang, Ming‐Shiou Jan, & Yee-Shin Lin. (2006). Lithium Inhibits Ceramide- and Etoposide-Induced Protein Phosphatase 2A Methylation, Bcl-2 Dephosphorylation, Caspase-2 Activation, and Apoptosis. Molecular Pharmacology. 70(2). 510–517. 55 indexed citations
16.
Chiang, Chi-Wu, et al.. (2003). Protein Phosphatase 2A Dephosphorylation of Phosphoserine 112 Plays the Gatekeeper Role for BAD-Mediated Apoptosis. Molecular and Cellular Biology. 23(18). 6350–6362. 123 indexed citations
17.
Hsu, Shih-Lan, et al.. (2001). Proteolysis of integrin α5 and β1 subunits involved in retinoic acid-induced apoptosis in human hepatoma Hep3B cells. Cancer Letters. 167(2). 193–204. 32 indexed citations
18.
Chiang, Chi-Wu, et al.. (2001). BAD/BCL-xL heterodimerization leads to bypass of G0/G1 arrest. Oncogene. 20(33). 4507–4518. 55 indexed citations
19.
Chiang, Chi-Wu, Shane C. Masters, Romesh R. Subramanian, et al.. (2001). Protein phosphatase 2A activates the proapoptotic function of BAD in interleukin- 3–dependent lymphoid cells by a mechanism requiring 14-3-3 dissociation. Blood. 97(5). 1289–1297. 131 indexed citations
20.
Chiang, Chi-Wu, William J. Sullivan, Robert G. K. Donald, et al.. (1999). The Adenosine Transporter of Toxoplasma gondii. Journal of Biological Chemistry. 274(49). 35255–35261. 57 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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