Tse-Ching Chen

1.1k total citations
21 papers, 629 citations indexed

About

Tse-Ching Chen is a scholar working on Oncology, Surgery and Cancer Research. According to data from OpenAlex, Tse-Ching Chen has authored 21 papers receiving a total of 629 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Oncology, 5 papers in Surgery and 5 papers in Cancer Research. Recurrent topics in Tse-Ching Chen's work include Liver Disease Diagnosis and Treatment (3 papers), Genetic factors in colorectal cancer (3 papers) and Cancer Genomics and Diagnostics (3 papers). Tse-Ching Chen is often cited by papers focused on Liver Disease Diagnosis and Treatment (3 papers), Genetic factors in colorectal cancer (3 papers) and Cancer Genomics and Diagnostics (3 papers). Tse-Ching Chen collaborates with scholars based in Taiwan, United States and India. Tse-Ching Chen's co-authors include Tseng-tong Kuo, Long‐Bin Jeng, Ann‐Joy Cheng, Yung‐Jen Chuang, Tzu‐Chen Yen, Chuan-Yi Tang, Jau‐Min Lien, Yin‐Ju Chen, Wen‐Ping Hsieh and Chun-Ta Liao and has published in prestigious journals such as PLoS ONE, Clinical Cancer Research and Journal of Catalysis.

In The Last Decade

Tse-Ching Chen

21 papers receiving 620 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tse-Ching Chen Taiwan 15 217 204 160 131 98 21 629
Carlos Barranco Spain 16 174 0.8× 273 1.3× 98 0.6× 179 1.4× 60 0.6× 40 793
Ji Eun Kwon South Korea 17 198 0.9× 188 0.9× 221 1.4× 172 1.3× 85 0.9× 61 786
Yasumasa Monobe Japan 13 199 0.9× 188 0.9× 294 1.8× 154 1.2× 118 1.2× 75 856
Takahiro Yasoshima Japan 17 338 1.6× 292 1.4× 186 1.2× 67 0.5× 114 1.2× 45 740
Sadako Nishimura Japan 15 237 1.1× 211 1.0× 168 1.1× 167 1.3× 102 1.0× 26 853
Makoto Emoto Japan 19 316 1.5× 428 2.1× 148 0.9× 150 1.1× 107 1.1× 55 1.1k
Hwa Jung Sung South Korea 16 216 1.0× 213 1.0× 95 0.6× 81 0.6× 94 1.0× 73 668
Joshua Z. Press Canada 17 230 1.1× 218 1.1× 183 1.1× 105 0.8× 119 1.2× 27 985
Marion Marty France 12 209 1.0× 217 1.1× 137 0.9× 136 1.0× 163 1.7× 40 561
Aijun Li China 12 155 0.7× 107 0.5× 306 1.9× 129 1.0× 75 0.8× 34 743

Countries citing papers authored by Tse-Ching Chen

Since Specialization
Citations

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

Fields of papers citing papers by Tse-Ching Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tse-Ching Chen. 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 Tse-Ching Chen. The network helps show where Tse-Ching Chen may publish in the future.

Co-authorship network of co-authors of Tse-Ching Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Tse-Ching Chen. A scholar is included among the top collaborators of Tse-Ching Chen 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 Tse-Ching Chen. Tse-Ching Chen 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.
Huang, Shih‐Chiang, Ian Yi‐Feng Chang, Tse-Ching Chen, et al.. (2024). Redefining aberrant P53 expression of gastric cancer and its distinct clinical significance among molecular-histologic subtypes. Asian Journal of Surgery. 47(11). 4699–4705. 3 indexed citations
2.
3.
Chang, Kung‐Chao, Jen‐Chieh Lee, Yu-Chu Wang, et al.. (2016). Polyclonality in Sclerosing Angiomatoid Nodular Transformation of the Spleen. The American Journal of Surgical Pathology. 40(10). 1343–1351. 25 indexed citations
4.
Chang, Sam S., Chia‐Wei Li, Yi‐Hsin Elsa Hsu, et al.. (2015). Severe Hepatitis Promotes Hepatocellular Carcinoma Recurrence via NF-κB Pathway-Mediated Epithelial–Mesenchymal Transition after Resection. Clinical Cancer Research. 22(7). 1800–1812. 25 indexed citations
5.
Huang, Shih‐Chiang, Ronald Ghossein, Justin A. Bishop, et al.. (2015). Novel PAX3-NCOA1 Fusions in Biphenotypic Sinonasal Sarcoma With Focal Rhabdomyoblastic Differentiation. The American Journal of Surgical Pathology. 40(1). 51–59. 77 indexed citations
6.
Chou, Wen‐Chi, Tai‐Di Chen, Tse-Ching Chen, et al.. (2014). Prognostic Factors in Adult Patients with Solid Cancers and Bone Marrow Metastases. Asian Pacific Journal of Cancer Prevention. 15(1). 61–67. 22 indexed citations
7.
Lai, Chyong‐Huey, Hung‐Hsueh Chou, Chee‐Jen Chang, et al.. (2012). Clinical implications of human papillomavirus genotype in cervical adeno-adenosquamous carcinoma. European Journal of Cancer. 49(3). 633–641. 17 indexed citations
8.
Chen, Tse-Ching, et al.. (2012). Large Fragment Pre-S Deletion and High Viral Load Independently Predict Hepatitis B Relapse after Liver Transplantation. PLoS ONE. 7(2). e32189–e32189. 7 indexed citations
9.
10.
Liao, Chun-Ta, Yin‐Ju Chen, Ann‐Joy Cheng, et al.. (2011). A Novel Molecular Signature Identified by Systems Genetics Approach Predicts Prognosis in Oral Squamous Cell Carcinoma. PLoS ONE. 6(8). e23452–e23452. 138 indexed citations
11.
Wang, Chih‐Wei, Tzu-I Wu, Chih-Teng Yu, et al.. (2009). Usefulness of p16 for Differentiating Primary Pulmonary Squamous Cell Carcinoma From Cervical Squamous Cell Carcinoma Metastatic to the Lung. American Journal of Clinical Pathology. 131(5). 715–722. 21 indexed citations
12.
Waldmann, Herman, Tse-Ching Chen, Luís Graça, et al.. (2006). Regulatory T cells in transplantation. Seminars in Immunology. 18(2). 111–119. 56 indexed citations
13.
Chuang, Wen‐Yu, et al.. (2002). Liver cell adenoma with concomitant hepatocellular carcinoma: report of two cases.. PubMed. 101(11). 798–802. 10 indexed citations
14.
Chen, Tse-Ching, et al.. (2001). Follicular Dendritic Cell Tumor of the Liver: A Clinicopathologic and Epstein-Barr Virus Study of Two Cases. Modern Pathology. 14(4). 354–360. 57 indexed citations
15.
Chen, Tse-Ching, et al.. (2000). Mutational analysis of the p27kip1 gene in hepatocellular carcinoma. Cancer Letters. 153(1-2). 169–173. 16 indexed citations
16.
Yeh, Ta-Sen, Ann‐Joy Cheng, Tse-Ching Chen, et al.. (1999). Telomerase Activity Is a Useful Marker to Distinguish Malignant Pancreatic Cystic Tumors from Benign Neoplasms and Pseudocysts. Journal of Surgical Research. 87(2). 171–177. 24 indexed citations
17.
Chen, Tse-Ching, et al.. (1999). Multiple pyogenic granulomas in sigmoid colon. Gastrointestinal Endoscopy. 49(2). 257–259. 10 indexed citations
18.
Chen, Tse-Ching, et al.. (1998). Absence of APC gene mutation in the mutation cluster region in hepatocellular carcinoma. Cancer Letters. 134(1). 23–28. 24 indexed citations
19.
Chen, Tse-Ching, et al.. (1998). Solitary extramedullary plasmacytoma in the retroperitoneum. American Journal of Hematology. 58(3). 235–238. 15 indexed citations
20.
Jeng, Long‐Bin, et al.. (1998). Frequent allelic loss on chromosomes 4q and 16q associated with human hepatocellular carcinoma in Taiwan. Cancer Letters. 123(1). 1–6. 29 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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