Zee‐Fen Chang

1.0k total citations
26 papers, 857 citations indexed

About

Zee‐Fen Chang is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Zee‐Fen Chang has authored 26 papers receiving a total of 857 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 7 papers in Oncology and 7 papers in Cell Biology. Recurrent topics in Zee‐Fen Chang's work include Protein Kinase Regulation and GTPase Signaling (7 papers), Cellular Mechanics and Interactions (6 papers) and Cancer-related Molecular Pathways (5 papers). Zee‐Fen Chang is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (7 papers), Cellular Mechanics and Interactions (6 papers) and Cancer-related Molecular Pathways (5 papers). Zee‐Fen Chang collaborates with scholars based in Taiwan, United States and Sweden. Zee‐Fen Chang's co-authors include Hsiao‐Hui Lee, Yen‐Ling Chen, Jean‐Cheng Kuo, Hsiao-Chien Tsai, Won‐Jing Wang, Jia‐Ren Lin, Ruey‐Hwa Chen, Staffan Eriksson, Jin-Mei Lai and Chia‐Ling Hsieh and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and The Journal of Cell Biology.

In The Last Decade

Zee‐Fen Chang

26 papers receiving 844 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zee‐Fen Chang Taiwan 17 553 144 140 130 83 26 857
Tad Guszczynski United States 12 991 1.8× 210 1.5× 82 0.6× 175 1.3× 98 1.2× 15 1.3k
Noriaki Kitamura Japan 12 483 0.9× 127 0.9× 87 0.6× 86 0.7× 119 1.4× 21 688
Carlo Cosimo Campa Italy 14 748 1.4× 94 0.7× 290 2.1× 95 0.7× 49 0.6× 23 1.1k
Savithri Rangarajan Netherlands 12 696 1.3× 87 0.6× 123 0.9× 98 0.8× 93 1.1× 16 968
Yu‐Chi Juang United States 14 801 1.4× 176 1.2× 106 0.8× 154 1.2× 105 1.3× 16 922
Daiki Kobayashi Japan 18 820 1.5× 123 0.9× 184 1.3× 105 0.8× 121 1.5× 37 1.3k
Yasuyuki Nakamura Japan 18 701 1.3× 151 1.0× 62 0.4× 58 0.4× 156 1.9× 40 927
Arno Kalkuhl Germany 19 424 0.8× 103 0.7× 62 0.4× 163 1.3× 116 1.4× 34 948
Giulia Germena Germany 13 399 0.7× 73 0.5× 216 1.5× 199 1.5× 59 0.7× 21 739

Countries citing papers authored by Zee‐Fen Chang

Since Specialization
Citations

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

Fields of papers citing papers by Zee‐Fen Chang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zee‐Fen Chang. 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 Zee‐Fen Chang. The network helps show where Zee‐Fen Chang may publish in the future.

Co-authorship network of co-authors of Zee‐Fen Chang

This figure shows the co-authorship network connecting the top 25 collaborators of Zee‐Fen Chang. A scholar is included among the top collaborators of Zee‐Fen Chang 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 Zee‐Fen Chang. Zee‐Fen Chang 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.
Honsho, Masanori, Yuichi Abe, Yuuta Imoto, et al.. (2020). Mammalian Homologue NME3 of DYNAMO1 Regulates Peroxisome Division. International Journal of Molecular Sciences. 21(21). 8040–8040. 13 indexed citations
2.
Jane, Wann-Neng, et al.. (2018). Equilibrative Nucleoside Transporter 3 Regulates T Cell Homeostasis by Coordinating Lysosomal Function with Nucleoside Availability. Cell Reports. 23(8). 2330–2341. 26 indexed citations
3.
Lee, Hsiao‐Hui, et al.. (2016). The Shp2-induced epithelial disorganization defect is reversed by HDAC6 inhibition independent of Cdc42. Nature Communications. 7(1). 10420–10420. 6 indexed citations
4.
Chen, Chih‐Wei, Yun Yen, Xiyong Liu, et al.. (2016). The Impact of dUTPase on Ribonucleotide Reductase-Induced Genome Instability in Cancer Cells. Cell Reports. 16(5). 1287–1299. 22 indexed citations
5.
Kuo, Yuan‐Yeh, et al.. (2016). Epigenetic repression of ribosomal RNA transcription by ROCK-dependent aberrant cytoskeletal organization. Scientific Reports. 6(1). 28685–28685. 4 indexed citations
6.
Yang, Chih‐Yu, Zee‐Fen Chang, Yat‐Pang Chau, et al.. (2015). Uremia Induces Dental Pulp Ossification but Reciprocally Inhibits Adjacent Alveolar Bone Osteogenesis. Calcified Tissue International. 97(5). 466–475. 4 indexed citations
7.
Hsu, Chih‐Yi, Zee‐Fen Chang, & Hsiao‐Hui Lee. (2015). Immunohistochemical evaluation of ROCK activation in invasive breast cancer. BMC Cancer. 15(1). 943–943. 11 indexed citations
9.
Yang, Chih‐Yu, Zee‐Fen Chang, Yat‐Pang Chau, et al.. (2015). Circulating Wnt/β-catenin signalling inhibitors and uraemic vascular calcifications. Nephrology Dialysis Transplantation. 30(8). 1356–1363. 40 indexed citations
10.
Chuang, Hsiang-Hao, et al.. (2013). Ser1333 phosphorylation indicates ROCKI activation. Journal of Biomedical Science. 20(1). 83–83. 15 indexed citations
11.
Lee, Hsiao‐Hui, et al.. (2012). Protein tyrosine phosphatase SHP2 suppresses podosome rosette formation in Src-transformed fibroblasts. Journal of Cell Science. 126(2). 657–666. 18 indexed citations
12.
Chen, Chih‐Wei, Jim‐Min Fang, Sheh‐Yi Sheu, et al.. (2012). Tumor Cells Require Thymidylate Kinase to Prevent dUTP Incorporation during DNA Repair. Cancer Cell. 22(1). 36–50. 52 indexed citations
13.
Lee, Hsiao‐Hui, et al.. (2010). Src-dependent phosphorylation of ROCK participates in regulation of focal adhesion dynamics. Journal of Cell Science. 123(19). 3368–3377. 59 indexed citations
14.
Chen, Yen‐Ling, Staffan Eriksson, & Zee‐Fen Chang. (2010). Regulation and Functional Contribution of Thymidine Kinase 1 in Repair of DNA Damage. Journal of Biological Chemistry. 285(35). 27327–27335. 66 indexed citations
15.
Chen, Yen‐Ling, Dan‐Jae Lin, & Zee‐Fen Chang. (2008). Identification of a putative human mitochondrial thymidine monophosphate kinase associated with monocytic/macrophage terminal differentiation. Genes to Cells. 13(7). 679–689. 34 indexed citations
16.
Chang, Zee‐Fen & Hsiao‐Hui Lee. (2006). RhoA signaling in phorbol ester-induced apoptosis. Journal of Biomedical Science. 13(2). 173–180. 10 indexed citations
17.
Lee, Hsiao‐Hui, C. L. Chien, Hsin-Kai Liao, Yu‐Ju Chen, & Zee‐Fen Chang. (2004). Nuclear efflux of heterogeneous nuclear ribonucleoprotein C1/C2 in apoptotic cells: a novel nuclear export dependent on Rho-associated kinase activation. Journal of Cell Science. 117(23). 5579–5589. 24 indexed citations
18.
Wang, Won‐Jing, Jean‐Cheng Kuo, Hsiao-Chien Tsai, et al.. (2004). Bidirectional signals transduced by DAPK–ERK interaction promote the apoptotic effect of DAPK. The EMBO Journal. 24(2). 294–304. 193 indexed citations
19.
Chang, Yun-Shiang, Han‐Ching Wang, Zee‐Fen Chang, et al.. (2002). Ribonucleotide Reductase of Shrimp White Spot Syndrome Virus (WSSV): Expression and Enzymatic Activity in a Baculovirus/Insect Cell System and WSSV-Infected Shrimp. Virology. 304(2). 282–290. 27 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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