Hung‐Chieh Lee

534 total citations
19 papers, 427 citations indexed

About

Hung‐Chieh Lee is a scholar working on Molecular Biology, Cell Biology and Cancer Research. According to data from OpenAlex, Hung‐Chieh Lee has authored 19 papers receiving a total of 427 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Cell Biology and 3 papers in Cancer Research. Recurrent topics in Hung‐Chieh Lee's work include Developmental Biology and Gene Regulation (8 papers), Congenital heart defects research (6 papers) and Zebrafish Biomedical Research Applications (4 papers). Hung‐Chieh Lee is often cited by papers focused on Developmental Biology and Gene Regulation (8 papers), Congenital heart defects research (6 papers) and Zebrafish Biomedical Research Applications (4 papers). Hung‐Chieh Lee collaborates with scholars based in Taiwan. Hung‐Chieh Lee's co-authors include Huai‐Jen Tsai, Cheng‐Yung Lin, Yau‐Hung Chen, Wei‐Ta Chen, Ming-Hsuan Lee, Tzu‐Ming Liu, Huai‐Jen Tsai, Chao‐Hsien Chu, Hongping Li and Yi‐Jiun Chen and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and The EMBO Journal.

In The Last Decade

Hung‐Chieh Lee

19 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hung‐Chieh Lee Taiwan 13 320 119 69 68 24 19 427
Shu Tu United States 9 308 1.0× 173 1.5× 45 0.7× 38 0.6× 63 2.6× 12 508
Valérie Bello France 13 270 0.8× 100 0.8× 45 0.7× 44 0.6× 38 1.6× 17 410
Michael A. Pickart United States 10 312 1.0× 159 1.3× 35 0.5× 89 1.3× 36 1.5× 18 471
Jennifer A. Schumacher United States 12 345 1.1× 154 1.3× 37 0.5× 32 0.5× 45 1.9× 17 466
Airon A. Wills United States 7 560 1.8× 161 1.4× 59 0.9× 56 0.8× 13 0.5× 8 668
Zhangji Dong China 14 338 1.1× 107 0.9× 52 0.8× 148 2.2× 67 2.8× 39 532
Rosa A. Uribe United States 14 348 1.1× 148 1.2× 49 0.7× 55 0.8× 28 1.2× 24 492
Matthew W. Grow United States 8 337 1.1× 64 0.5× 30 0.4× 106 1.6× 27 1.1× 11 459
Brigitte L. Arduini United States 11 405 1.3× 140 1.2× 85 1.2× 72 1.1× 25 1.0× 15 650
Ujwal J. Pyati United States 11 415 1.3× 210 1.8× 49 0.7× 50 0.7× 64 2.7× 11 583

Countries citing papers authored by Hung‐Chieh Lee

Since Specialization
Citations

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

Fields of papers citing papers by Hung‐Chieh Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hung‐Chieh Lee. 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 Hung‐Chieh Lee. The network helps show where Hung‐Chieh Lee may publish in the future.

Co-authorship network of co-authors of Hung‐Chieh Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Hung‐Chieh Lee. A scholar is included among the top collaborators of Hung‐Chieh Lee 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 Hung‐Chieh Lee. Hung‐Chieh Lee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
2.
Lee, Hung‐Chieh, et al.. (2022). Anp32a Promotes Neuronal Regeneration after Spinal Cord Injury of Zebrafish Embryos. International Journal of Molecular Sciences. 23(24). 15921–15921. 7 indexed citations
3.
Lee, Hung‐Chieh, Cheng‐Yung Lin, Ting‐Ying Huang, et al.. (2021). Poly(U)‐specific endoribonuclease ENDOU promotes translation of human CHOP mRNA by releasing uORF element‐mediated inhibition. The EMBO Journal. 40(11). e104123–e104123. 12 indexed citations
4.
Lee, Hung‐Chieh, Cheng‐Yung Lin, & Huai‐Jen Tsai. (2021). Zebrafish, an In Vivo Platform to Screen Drugs and Proteins for Biomedical Use. Pharmaceuticals. 14(6). 500–500. 26 indexed citations
5.
Lee, Hung‐Chieh, et al.. (2017). Embryonic expression patterns of Eukaryotic EndoU ribonuclease family gene endouC in zebrafish. Gene Expression Patterns. 25-26. 66–70. 8 indexed citations
6.
Lee, Hung‐Chieh, Chin‐Chieh Wu, Sheng‐Nan Chang, et al.. (2015). Amiodarone Induces Overexpression of Similar to Versican b to Repress the EGFR/Gsk3b/Snail Signaling Axis during Cardiac Valve Formation of Zebrafish Embryos. PLoS ONE. 10(12). e0144751–e0144751. 5 indexed citations
7.
Lee, Hung‐Chieh, et al.. (2015). Purple Chromoprotein Gene Serves as a New Selection Marker for Transgenesis of the Microalga Nannochloropsis oculata. PLoS ONE. 10(3). e0120780–e0120780. 14 indexed citations
8.
Lee, Hung‐Chieh, et al.. (2014). Zebrafish Transgenic Line huORFZ Is an Effective Living Bioindicator for Detecting Environmental Toxicants. PLoS ONE. 9(3). e90160–e90160. 25 indexed citations
9.
Lee, Hung‐Chieh, et al.. (2014). Glycogen synthase kinase 3 beta in somites plays a role during the angiogenesis of zebrafish embryos. FEBS Journal. 281(19). 4367–4383. 14 indexed citations
10.
Lin, Cheng‐Yung, et al.. (2013). Normal Function of Myf5 During Gastrulation Is Required for Pharyngeal Arch Cartilage Development in Zebrafish Embryos. Zebrafish. 10(4). 486–499. 10 indexed citations
11.
Lin, Cheng‐Yung, et al.. (2013). miR-1 and miR-206 target different genes to have opposing roles during angiogenesis in zebrafish embryos. Nature Communications. 4(1). 2829–2829. 57 indexed citations
12.
Lee, Hung‐Chieh, Yi‐Jiun Chen, Yuwei Liu, et al.. (2011). Transgenic zebrafish model to study translational control mediated by upstream open reading frame of human chop gene. Nucleic Acids Research. 39(20). e139–e139. 27 indexed citations
13.
Lee, Hung‐Chieh, et al.. (2009). FoxD5 mediates anterior–posterior polarity through upstream modulator Fgf signaling during zebrafish somitogenesis. Developmental Biology. 336(2). 232–245. 32 indexed citations
14.
Lin, Cheng‐Yung, et al.. (2009). The transcription factor Six1a plays an essential role in the craniofacial myogenesis of zebrafish. Developmental Biology. 331(2). 152–166. 32 indexed citations
15.
Lee, Hung‐Chieh, et al.. (2009). The molecular structures and expression patterns of zebrafish troponin I genes. Gene Expression Patterns. 9(5). 348–356. 20 indexed citations
16.
Lee, Hung‐Chieh, et al.. (2006). Foxd3 mediates zebrafish myf5 expression during early somitogenesis. Developmental Biology. 290(2). 359–372. 37 indexed citations
17.
Lin, Cheng‐Yung, et al.. (2006). Myogenic regulatory factors Myf5 and Myod function distinctly during craniofacial myogenesis of zebrafish. Developmental Biology. 299(2). 594–608. 67 indexed citations
18.
Lin, Cheng‐Yung, Yau‐Hung Chen, Hung‐Chieh Lee, & Huai‐Jen Tsai. (2004). Novel cis-element in intron 1 represses somite expression of zebrafish myf-5. Gene. 334. 63–72. 23 indexed citations
19.
Chen, Yau‐Hung, Hung‐Chieh Lee, Chia‐Feng Liu, Cheng‐Yung Lin, & Huai‐Jen Tsai. (2003). Novel regulatory sequence −82/−62 functions as a key element to drive the somite‐specificity of zebrafish myf‐5. Developmental Dynamics. 228(1). 41–50. 10 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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