Jui‐Chou Hsu

1.4k total citations
23 papers, 1.2k citations indexed

About

Jui‐Chou Hsu is a scholar working on Molecular Biology, Hepatology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jui‐Chou Hsu has authored 23 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Hepatology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jui‐Chou Hsu's work include Liver physiology and pathology (8 papers), Developmental Biology and Gene Regulation (8 papers) and Neurobiology and Insect Physiology Research (4 papers). Jui‐Chou Hsu is often cited by papers focused on Liver physiology and pathology (8 papers), Developmental Biology and Gene Regulation (8 papers) and Neurobiology and Insect Physiology Research (4 papers). Jui‐Chou Hsu collaborates with scholars based in Taiwan, United States and Spain. Jui‐Chou Hsu's co-authors include Rebecca Taub, R Bravo, Kenneth Mohn, Thomas M. Laz, Norbert Perrimon, Drew E. Cressman, Anna E. Melby, Shu‐Yi Wei, Li‐Hsun Chang and Paweł Dobrzański and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genes & Development and Molecular and Cellular Biology.

In The Last Decade

Jui‐Chou Hsu

23 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
Jui‐Chou Hsu Taiwan 17 724 332 216 186 179 23 1.2k
Yoshihiko Uehara Japan 15 835 1.2× 158 0.5× 176 0.8× 619 3.3× 179 1.0× 30 1.6k
Chantal Kress France 16 1.1k 1.5× 203 0.6× 132 0.6× 61 0.3× 52 0.3× 24 1.6k
Xiaobing Qian United States 19 1.0k 1.4× 80 0.2× 88 0.4× 78 0.4× 136 0.8× 47 1.5k
Rico Barsacchi Germany 11 665 0.9× 82 0.2× 144 0.7× 85 0.5× 38 0.2× 15 966
Lev M. Fedorov United States 12 823 1.1× 115 0.3× 72 0.3× 50 0.3× 73 0.4× 34 1.1k
Maria Kontogiannea Canada 13 853 1.2× 151 0.5× 140 0.6× 33 0.2× 235 1.3× 17 1.3k
Cyril Berthet United States 22 1.8k 2.5× 393 1.2× 187 0.9× 51 0.3× 57 0.3× 25 2.4k
Ingvar Ferby Germany 15 1.0k 1.4× 428 1.3× 128 0.6× 32 0.2× 49 0.3× 18 1.4k
Mary J. Stewart United States 9 973 1.3× 172 0.5× 132 0.6× 27 0.1× 175 1.0× 10 1.2k
Celeste Richardson United States 12 1.2k 1.7× 296 0.9× 146 0.7× 18 0.1× 57 0.3× 16 1.6k

Countries citing papers authored by Jui‐Chou Hsu

Since Specialization
Citations

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

Fields of papers citing papers by Jui‐Chou Hsu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jui‐Chou Hsu. 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 Jui‐Chou Hsu. The network helps show where Jui‐Chou Hsu may publish in the future.

Co-authorship network of co-authors of Jui‐Chou Hsu

This figure shows the co-authorship network connecting the top 25 collaborators of Jui‐Chou Hsu. A scholar is included among the top collaborators of Jui‐Chou Hsu 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 Jui‐Chou Hsu. Jui‐Chou Hsu 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.
Tang, Wei‐Chun, et al.. (2018). Adherens junction-associated pores mediate the intercellular transport of endosomes and cytoplasmic proteins. Biochemical and Biophysical Research Communications. 505(3). 664–670. 1 indexed citations
2.
Chen, Bi‐Chang, et al.. (2015). Novel transport function of adherens junction revealed by live imaging in Drosophila. Biochemical and Biophysical Research Communications. 463(4). 686–692. 4 indexed citations
3.
Hsu, Jui‐Chou, et al.. (2012). Capulet and Slingshot share overlapping functions during Drosophila eye morphogenesis. Journal of Biomedical Science. 19(1). 46–46. 6 indexed citations
4.
Chang, Li‐Hsun, et al.. (2011). Differential adhesion and actomyosin cable collaborate to drive Echinoid-mediated cell sorting. Development. 138(17). 3803–3812. 38 indexed citations
5.
Wei, Shu‐Yi, et al.. (2010). Echinoid regulates Flamingo endocytosis to control ommatidial rotation in theDrosophilaeye. Development. 137(5). 745–754. 20 indexed citations
6.
Lin, Hui‐Ping, Hui-Min Chen, Shu‐Yi Wei, et al.. (2007). Cell adhesion molecule Echinoid associates with unconventional myosin VI/Jaguar motor to regulate cell morphology during dorsal closure in Drosophila. Developmental Biology. 311(2). 423–433. 39 indexed citations
7.
Chen, Liying, et al.. (2006). Weckle Is a Zinc Finger Adaptor of the Toll Pathway in Dorsoventral Patterning of the Drosophila Embryo. Current Biology. 16(12). 1183–1193. 25 indexed citations
8.
Wei, Shu‐Yi, Luis M. Escudero, Fengwei Yu, et al.. (2005). Echinoid Is a Component of Adherens Junctions That Cooperates with DE-Cadherin to Mediate Cell Adhesion. Developmental Cell. 8(4). 493–504. 146 indexed citations
9.
Escudero, Luis M., et al.. (2003). Echinoid synergizes with the Notch signaling pathway inDrosophilamesothorax bristle patterning. Development. 130(25). 6305–6316. 21 indexed citations
10.
Perrimon, Norbert, et al.. (2001). The cell adhesion molecule Echinoid defines a new pathway that antagonizes the Drosophila EGF receptor signaling pathway. Development. 128(4). 591–601. 55 indexed citations
11.
Chen, Shyh‐Jye, et al.. (1997). Crossed ectopic left lung with fusion to the right lung: a variant of horseshoe lung?. American Journal of Roentgenology. 168(5). 1347–1348. 5 indexed citations
12.
Perrimon, Norbert, Xiangyi Lu, Xianyu Hou, et al.. (1995). Dissection of the Torso signal transduction pathway in Drosophila. Molecular Reproduction and Development. 42(4). 515–522. 24 indexed citations
13.
Hsu, Jui‐Chou & Norbert Perrimon. (1994). A temperature-sensitive MEK mutation demonstrates the conservation of the signaling pathways activated by receptor tyrosine kinases.. Genes & Development. 8(18). 2176–2187. 57 indexed citations
14.
Hsu, Jui‐Chou, et al.. (1993). Promoter-specific trans-activation and inhibition mediated by JunB.. PubMed. 53(16). 3789–94. 51 indexed citations
15.
Hsu, Jui‐Chou, Rodrigo Bravo, & Rebecca Taub. (1992). Interactions among LRF-1, JunB, c-Jun, and c-Fos Define a Regulatory Program in the G 1 Phase of Liver Regeneration. Molecular and Cellular Biology. 12(10). 4654–4665. 3 indexed citations
16.
Tewari, Manorama, Paweł Dobrzański, Kenneth Mohn, et al.. (1992). Rapid Induction in Regenerating Liver of RL/IF-1 (an ΙκΒ That Inhibits NF-κΒ, RelB-p50, and c-Rel-p50) and PHF, a Novel κΒ Site-Binding Complex. Molecular and Cellular Biology. 12(6). 2898–2908. 41 indexed citations
17.
Tewari, Manu, Paweł Dobrzański, Kenneth Mohn, et al.. (1992). Rapid induction in regenerating liver of RL/IF-1 (an I kappa B that inhibits NF-kappa B, RelB-p50, and c-Rel-p50) and PHF, a novel kappa B site-binding complex.. Molecular and Cellular Biology. 12(6). 2898–2908. 137 indexed citations
18.
Mohn, Kenneth, Thomas M. Laz, Jui‐Chou Hsu, et al.. (1991). The Immediate-Early Growth Response in Regenerating Liver and Insulin-Stimulated H-35 Cells: Comparison with Serum-Stimulated 3T3 Cells and Identification of 41 Novel Immediate-Early Genes. Molecular and Cellular Biology. 11(1). 381–390. 56 indexed citations
19.
Mohn, Kenneth, Thomas M. Laz, Jui‐Chou Hsu, et al.. (1991). The immediate-early growth response in regenerating liver and insulin-stimulated H-35 cells: comparison with serum-stimulated 3T3 cells and identification of 41 novel immediate-early genes.. Molecular and Cellular Biology. 11(1). 381–390. 189 indexed citations
20.
Hsu, Jui‐Chou, Thomas M. Laz, Kenneth Mohn, & Rebecca Taub. (1991). Identification of LRF-1, a leucine-zipper protein that is rapidly and highly induced in regenerating liver.. Proceedings of the National Academy of Sciences. 88(9). 3511–3515. 125 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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