Jer‐Tsong Hsieh

16.4k total citations · 2 hit papers
267 papers, 12.9k citations indexed

About

Jer‐Tsong Hsieh is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Oncology. According to data from OpenAlex, Jer‐Tsong Hsieh has authored 267 papers receiving a total of 12.9k indexed citations (citations by other indexed papers that have themselves been cited), including 158 papers in Molecular Biology, 82 papers in Pulmonary and Respiratory Medicine and 78 papers in Oncology. Recurrent topics in Jer‐Tsong Hsieh's work include Prostate Cancer Treatment and Research (59 papers), Epigenetics and DNA Methylation (29 papers) and Virus-based gene therapy research (23 papers). Jer‐Tsong Hsieh is often cited by papers focused on Prostate Cancer Treatment and Research (59 papers), Epigenetics and DNA Methylation (29 papers) and Virus-based gene therapy research (23 papers). Jer‐Tsong Hsieh collaborates with scholars based in United States, Taiwan and China. Jer‐Tsong Hsieh's co-authors include Rey-Chen Pong, Takatsugu Okegawa, Leland W.K. Chung, Jeffrey M. Bergelson, Martin Gleave, Andrew C. von Eschenbach, Arthur I. Sagalowsky, Christopher J. Logothetis, Ching‐Ping Tseng and Patricia Troncoso and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Jer‐Tsong Hsieh

266 papers receiving 12.7k citations

Hit Papers

Expression of the protooncogene bcl-2 in the prostate and... 1992 2026 2003 2014 1992 2001 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jer‐Tsong Hsieh United States 63 7.5k 3.4k 2.6k 2.3k 2.0k 267 12.9k
Herman Yeger Canada 56 7.6k 1.0× 2.8k 0.8× 2.5k 0.9× 1.7k 0.8× 1.2k 0.6× 213 13.1k
Nadia Zaffaroni Italy 57 8.0k 1.1× 3.8k 1.1× 1.8k 0.7× 2.8k 1.2× 608 0.3× 351 13.0k
Jonathan W. Simons United States 51 9.4k 1.3× 4.9k 1.4× 2.8k 1.0× 6.1k 2.7× 2.8k 1.4× 116 17.9k
Dean W. Felsher United States 59 9.7k 1.3× 4.6k 1.4× 1.5k 0.6× 3.6k 1.6× 856 0.4× 176 15.9k
William P. Schiemann United States 59 6.8k 0.9× 3.5k 1.0× 1.3k 0.5× 2.4k 1.1× 791 0.4× 132 11.1k
Roy Bicknell United Kingdom 72 10.2k 1.4× 3.7k 1.1× 1.4k 0.5× 4.2k 1.9× 978 0.5× 232 16.1k
Bruce R. Zetter United States 61 7.9k 1.1× 2.5k 0.7× 1.1k 0.4× 2.7k 1.2× 803 0.4× 154 13.5k
Rolf A. Brekken United States 73 9.3k 1.2× 6.4k 1.9× 1.7k 0.6× 4.4k 2.0× 1.3k 0.6× 271 19.5k
Arne Östman Sweden 63 9.8k 1.3× 4.6k 1.4× 1.8k 0.7× 2.9k 1.3× 585 0.3× 165 16.8k
Marsha A. Moses United States 65 7.8k 1.1× 3.5k 1.0× 1.6k 0.6× 4.8k 2.1× 586 0.3× 212 15.3k

Countries citing papers authored by Jer‐Tsong Hsieh

Since Specialization
Citations

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

Fields of papers citing papers by Jer‐Tsong Hsieh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jer‐Tsong Hsieh. 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 Jer‐Tsong Hsieh. The network helps show where Jer‐Tsong Hsieh may publish in the future.

Co-authorship network of co-authors of Jer‐Tsong Hsieh

This figure shows the co-authorship network connecting the top 25 collaborators of Jer‐Tsong Hsieh. A scholar is included among the top collaborators of Jer‐Tsong Hsieh 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 Jer‐Tsong Hsieh. Jer‐Tsong Hsieh 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.
Debnath, Sashi, Yuan Chen, Elizabeth Hernández, et al.. (2023). A Theranostic Small-Molecule Prodrug Conjugate for Neuroendocrine Prostate Cancer. Pharmaceutics. 15(2). 481–481. 10 indexed citations
2.
Yi, Meihui, Fengbin Wang, Weiyi Tan, et al.. (2022). Enzyme Responsive Rigid-Rod Aromatics Target “Undruggable” Phosphatases to Kill Cancer Cells in a Mimetic Bone Microenvironment. Journal of the American Chemical Society. 144(29). 13055–13059. 46 indexed citations
3.
Chen, Yuan, David T.W. Tzeng, Yi‐Ping Huang, et al.. (2018). Antrocin Sensitizes Prostate Cancer Cells to Radiotherapy through Inhibiting PI3K/AKT and MAPK Signaling Pathways. Cancers. 11(1). 34–34. 45 indexed citations
4.
Lu, Miao, Lin Yang, Rui Li, et al.. (2017). Disrupting Androgen Receptor Signaling Induces Snail-Mediated Epithelial–Mesenchymal Plasticity in Prostate Cancer. Cancer Research. 77(11). 3101–3112. 66 indexed citations
5.
Chen, Yuan, Chun‐Jung Lin, Hwai‐Jeng Lin, et al.. (2016). Molecular Mechanisms and Potential Clinical Applications of Campylobacter jejuni Cytolethal Distending Toxin. Frontiers in Cellular and Infection Microbiology. 6. 9–9. 36 indexed citations
6.
Chen, Mei-Chih, Chih‐Hsiang Chang, Chih‐Ho Lai, et al.. (2016). Cdk5 Directly Targets Nuclear p21CIP1 and Promotes Cancer Cell Growth. Cancer Research. 76(23). 6888–6900. 32 indexed citations
7.
Yun, Eun-Jin, Jiancheng Zhou, Chun‐Jung Lin, et al.. (2015). Targeting Cancer Stem Cells in Castration-Resistant Prostate Cancer. Clinical Cancer Research. 22(3). 670–679. 76 indexed citations
8.
Zhou, Jiancheng, Kaijie Wu, Guodong Zhu, et al.. (2014). Reciprocal Regulation of Hypoxia-Inducible Factor 2α and GLI1 Expression Associated With the Radioresistance of Renal Cell Carcinoma. International Journal of Radiation Oncology*Biology*Physics. 90(4). 942–951. 34 indexed citations
9.
Wu, Kaijie, Daxing Xie, Yonglong Zou, et al.. (2013). The Mechanism of DAB2IP in Chemoresistance of Prostate Cancer Cells. Clinical Cancer Research. 19(17). 4740–4749. 55 indexed citations
10.
Dong, Ying, Erik A. Bey, Long-Shan Li, et al.. (2010). Prostate Cancer Radiosensitization through Poly(ADP-Ribose) Polymerase-1 Hyperactivation. Cancer Research. 70(20). 8088–8096. 75 indexed citations
11.
Xie, Daxing, Thomas Boike, Sandeep Burma, et al.. (2010). Downregulation of Human DAB2IP Gene Expression in Prostate Cancer Cells Results in Resistance to Ionizing Radiation. Cancer Research. 70(7). 2829–2839. 69 indexed citations
12.
Li, Yingming, et al.. (2009). Conditionally replicating adenovirus therapy utilizing bone sialoprotein promoter (Ad-BSP-E1a) in an in vivo study of treating androgen-independent intraosseous prostate cancer. Urologic Oncology Seminars and Original Investigations. 29(6). 624–633. 5 indexed citations
13.
Fan, Jinhai, Jennifer Stanfield, Yi Guo, et al.. (2008). Effect of Trans -2,3-Dimethoxycinnamoyl Azide on Enhancing Antitumor Activity of Romidepsin on Human Bladder Cancer. Clinical Cancer Research. 14(4). 1200–1207. 11 indexed citations
16.
Walsh, Lance P., Jennifer Stanfield, Kenneth Forster, et al.. (2006). Efficacy of Ablative High-Dose-per-Fraction Radiation for Implanted Human Renal Cell Cancer in a Nude Mouse Model. European Urology. 50(4). 795–800. 56 indexed citations
19.
Zhou, Jian & Jer‐Tsong Hsieh. (2001). The Inhibitory Role of DOC-2/DAB2 in Growth Factor Receptor-mediated Signal Cascade. Journal of Biological Chemistry. 276(30). 27793–27798. 93 indexed citations
20.
Hsieh, Jer‐Tsong & Ajit Kumar Verma. (1988). Involvement of protein kinase C in the transcriptional regulation of ornithine decarboxylase gene expression by 12-O-tetradecanoylphorbol-13-acetate in T24 human bladder carcinoma cells. Archives of Biochemistry and Biophysics. 262(1). 326–336. 30 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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