Joseph T. Tseng

1.9k total citations
52 papers, 1.6k citations indexed

About

Joseph T. Tseng is a scholar working on Molecular Biology, Cancer Research and Immunology. According to data from OpenAlex, Joseph T. Tseng has authored 52 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 13 papers in Cancer Research and 10 papers in Immunology. Recurrent topics in Joseph T. Tseng's work include RNA modifications and cancer (13 papers), RNA Research and Splicing (9 papers) and RNA and protein synthesis mechanisms (7 papers). Joseph T. Tseng is often cited by papers focused on RNA modifications and cancer (13 papers), RNA Research and Splicing (9 papers) and RNA and protein synthesis mechanisms (7 papers). Joseph T. Tseng collaborates with scholars based in Taiwan, United States and Japan. Joseph T. Tseng's co-authors include Wen‐Chang Chang, Tang K. Tang, Liang‐Yi Hung, Yun‐Pung P. Hsu, Yi‐Chao Lee, Ju-Ming Wang, Chien‐Feng Li, Ying‐Nai Wang, Weiya Xia and Ju‐Ming Wang and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Joseph T. Tseng

51 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joseph T. Tseng Taiwan 26 1.0k 326 291 277 276 52 1.6k
Arūnas Kazlauskas Lithuania 19 827 0.8× 236 0.7× 127 0.4× 374 1.4× 96 0.3× 34 1.6k
Toru Fukushima Japan 21 1.6k 1.5× 267 0.8× 633 2.2× 373 1.3× 136 0.5× 35 2.1k
Zhiyong Ding China 20 1.3k 1.2× 194 0.6× 454 1.6× 450 1.6× 254 0.9× 44 2.0k
Pradeep Sathyanarayana United States 22 1.1k 1.1× 222 0.7× 194 0.7× 493 1.8× 127 0.5× 36 1.6k
Joshua N. Finger United States 15 1.4k 1.4× 719 2.2× 149 0.5× 315 1.1× 164 0.6× 18 2.1k
Clifford W. Schweinfest United States 26 1.7k 1.6× 173 0.5× 337 1.2× 220 0.8× 133 0.5× 47 2.3k
Qin Yang China 23 870 0.9× 323 1.0× 396 1.4× 498 1.8× 144 0.5× 70 1.7k
Wufang Fan China 18 1.1k 1.1× 187 0.6× 402 1.4× 312 1.1× 98 0.4× 28 1.6k
Clifford Liongue Australia 19 517 0.5× 763 2.3× 616 2.1× 219 0.8× 295 1.1× 49 1.7k
Béla Z. Schmidt United States 17 504 0.5× 247 0.8× 141 0.5× 198 0.7× 435 1.6× 32 1.3k

Countries citing papers authored by Joseph T. Tseng

Since Specialization
Citations

This map shows the geographic impact of Joseph T. Tseng'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 Joseph T. Tseng with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joseph T. Tseng more than expected).

Fields of papers citing papers by Joseph T. Tseng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph T. Tseng. 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 Joseph T. Tseng. The network helps show where Joseph T. Tseng may publish in the future.

Co-authorship network of co-authors of Joseph T. Tseng

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph T. Tseng. A scholar is included among the top collaborators of Joseph T. Tseng 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 Joseph T. Tseng. Joseph T. Tseng 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.
Yang, Yao‐Jong, et al.. (2025). Probiotics ameliorate H. pylori-associated gastric β-catenin and COX-2 carcinogenesis signaling by regulating miR-185. Journal of Biomedical Science. 32(1). 55–55. 4 indexed citations
2.
3.
Wu, Wei-Sheng, et al.. (2021). A tool for analyzing and visualizing ribo-seq data at the isoform level. BMC Bioinformatics. 22(S10). 271–271. 1 indexed citations
4.
Zhang, Yitong, et al.. (2020). mRNAsi Index: Machine Learning in Mining Lung Adenocarcinoma Stem Cell Biomarkers. Genes. 11(3). 257–257. 70 indexed citations
5.
Lin, Yu‐Hung, Yi-Lin Chen, Cheng‐Han Lin, et al.. (2020). Dissecting efficiency of a 5’ rapid amplification of cDNA ends (5’-RACE) approach for profiling T-cell receptor beta repertoire. PLoS ONE. 15(7). e0236366–e0236366. 9 indexed citations
6.
7.
Tseng, Joseph T., et al.. (2017). Medroxyprogesterone acetate drives M2 macrophage differentiation toward a phenotype of decidual macrophage. Molecular and Cellular Endocrinology. 452. 74–83. 37 indexed citations
8.
Tseng, Joseph T., et al.. (2015). Characterization and distribution of repetitive elements in association with genes in the human genome. Computational Biology and Chemistry. 57. 29–38. 12 indexed citations
9.
Wang, Yu-Chu, et al.. (2014). Overexpression of Aurora-C interferes with the spindle checkpoint by promoting the degradation of Aurora-B. Cell Death and Disease. 5(3). e1106–e1106. 10 indexed citations
10.
Liou, Jing‐Ping, Ching‐Chuan Kuo, Chi-Yen Chang, et al.. (2013). MPT0B098, a Novel Microtubule Inhibitor That Destabilizes the Hypoxia-Inducible Factor-1α mRNA through Decreasing Nuclear–Cytoplasmic Translocation of RNA-Binding Protein HuR. Molecular Cancer Therapeutics. 12(7). 1202–1212. 32 indexed citations
11.
Chen, Tsung-Ming, et al.. (2013). Overexpression of FGF9 in colon cancer cells is mediated by hypoxia-induced translational activation. Nucleic Acids Research. 42(5). 2932–2944. 48 indexed citations
12.
Chang, Cheng-Wei, Victor C. Kok, Joseph T. Tseng, Jorng‐Tzong Horng, & Chun-Eng Liu. (2012). Diabetic Patients with Severe Sepsis Admitted to Intensive Care Unit Do Not Fare Worse than Non-Diabetic Patients: A Nationwide Population-Based Cohort Study. PLoS ONE. 7(12). e50729–e50729. 32 indexed citations
13.
Li, Chien‐Feng, Chiung‐Yuan Ko, Min‐Hsiung Pan, et al.. (2010). CEBPD Reverses RB/E2F1-Mediated Gene Repression and Participates in HMDB-Induced Apoptosis of Cancer Cells. Clinical Cancer Research. 16(23). 5770–5780. 40 indexed citations
14.
Hsu, Chao‐Chin, et al.. (2010). Quantitative trait analysis suggests human DAZL may be involved in regulating sperm counts and motility. Reproductive BioMedicine Online. 21(1). 77–83. 11 indexed citations
15.
Chen, Chien‐Yen, Chien‐Yen Chen, Joseph T. Tseng, et al.. (2009). orf4 of the Bacillus cereus sigB Gene Cluster Encodes a General Stress-Inducible Dps-Like Bacterioferritin. Journal of Bacteriology. 191(14). 4522–4533. 14 indexed citations
16.
Li, Chien‐Feng, Tian‐Lu Cheng, Meng‐Ru Shen, et al.. (2009). ZBRK1 Acts as a Metastatic Suppressor by Directly Regulating MMP9 in Cervical Cancer. Cancer Research. 70(1). 192–201. 47 indexed citations
17.
Chiou, Chien‐Shun, Chien‐Yen Chen, Chien‐Yen Chen, et al.. (2009). Identification of prophage gene z2389 in Escherichia coli EDL933 encoding a DNA cytosine methyltransferase for full protection of NotI sites. International Journal of Medical Microbiology. 300(5). 296–303. 2 indexed citations
18.
Chang, Kuang-Yi, et al.. (2007). Nucleolin regulates c-Jun/Sp1-dependent transcriptional activation of cPLA2  in phorbol ester-treated non-small cell lung cancer A549 cells. Nucleic Acids Research. 36(1). 217–227. 36 indexed citations
19.
Tseng, Joseph T., Shirin M. Marfatia, Peter J. Bryant, et al.. (2001). VAM-1: a new member of the MAGUK family binds to human Veli-1 through a conserved domain. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1518(3). 249–259. 32 indexed citations
20.
Hu, Huimei, Chin-Kai Chuang, Meng‐Jen Lee, Joseph T. Tseng, & Tang K. Tang. (2000). Genomic Organization, Expression, and Chromosome Localization of a Third Aurora-Related Kinase Gene, Aie1. DNA and Cell Biology. 19(11). 679–688. 59 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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