Nan‐Shan Chang

4.2k total citations
114 papers, 3.5k citations indexed

About

Nan‐Shan Chang is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Nan‐Shan Chang has authored 114 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 43 papers in Genetics and 24 papers in Cellular and Molecular Neuroscience. Recurrent topics in Nan‐Shan Chang's work include Genetics and Neurodevelopmental Disorders (42 papers), Ubiquitin and proteasome pathways (24 papers) and Nuclear Receptors and Signaling (23 papers). Nan‐Shan Chang is often cited by papers focused on Genetics and Neurodevelopmental Disorders (42 papers), Ubiquitin and proteasome pathways (24 papers) and Nuclear Receptors and Signaling (23 papers). Nan‐Shan Chang collaborates with scholars based in United States, Taiwan and India. Nan‐Shan Chang's co-authors include Li‐Jin Hsu, Lori Schultz, Gordon L. Sussman, Gary M. Liss, Donald H. Beezhold, Chun‐I Sze, John K. Heath, Qunying Hong, Shean-Jen Chen and Shenq‐Shyang Huang and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Biochemistry.

In The Last Decade

Nan‐Shan Chang

112 papers receiving 3.4k citations

Peers

Nan‐Shan Chang

GENET

CMN

ONCOL

Nigel J. Brand United Kingdom

Henry J. Kaplan United States

Chester A. Meyers United States

Colin Jamora United States

Paolo Macchi Italy

Dianqing Wu United States

Heidi Hahn Germany

Minoru Kimura Japan

Akio Masuda Japan

Seung‐Taek Lee South Korea

Nigel J. Brand United Kingdom

Nan‐Shan Chang

4.4k ×2.4

1.9k ×1.4

GENET

371 ×0.5

CMN

387 ×0.8

291 ×0.8

ONCOL

Citations per year, relative to Nan‐Shan Chang Nan‐Shan Chang (= 1×) peers Nigel J. Brand

Countries citing papers authored by Nan‐Shan Chang

Since Specialization

Citations

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

Fields of papers citing papers by Nan‐Shan Chang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nan‐Shan Chang

This figure shows the co-authorship network connecting the top 25 collaborators of Nan‐Shan Chang. A scholar is included among the top collaborators of Nan‐Shan 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 Nan‐Shan Chang. Nan‐Shan Chang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Huang, Shenq‐Shyang, et al.. (2018). Chasing the signaling run by tri-molecular time-lapse FRET microscopy. Cell Death Discovery. 4(1). 45–45. 11 indexed citations

Huang, Shenq‐Shyang, et al.. (2016). Role of WW Domain-containing Oxidoreductase WWOX in Driving T Cell Acute Lymphoblastic Leukemia Maturation. Journal of Biological Chemistry. 291(33). 17319–17331. 22 indexed citations

Chang, Nan‐Shan. (2015). In Memoriam: Shur-Tzu (Su) Chen, a pioneer in tumor suppressor WWOX for neuroscience. Journal of Biomedical Science. 22(1). 39–39. 1 indexed citations

Lee, Gang‐Hui, et al.. (2014). Folate deficiency-induced oxidative stress contributes to neuropathy in young and aged zebrafish — Implication in neural tube defects and Alzheimer's diseases. Neurobiology of Disease. 71. 234–244. 49 indexed citations

Chiang, Ming‐Fu, et al.. (2012). Overexpression of WW domain-containing oxidoreductase WOX1 preferentially induces apoptosis in human glioblastoma cells harboring mutant p53. Biomedicine & Pharmacotherapy. 66(6). 433–438. 20 indexed citations

Cheng, Li-Chung, Chia-Yuan Chang, Chun‐Yu Lin, et al.. (2012). Spatiotemporal focusing-based widefield multiphoton microscopy for fast optical sectioning. Optics Express. 20(8). 8939–8939. 71 indexed citations

Lee, Mi‐Hyun, et al.. (2011). Identification of an In Vivo MEK/WOX1 Complex as a Master Switch for Apoptosis in T Cell Leukemia. Genes & Cancer. 2(5). 550–562. 33 indexed citations

Su, Yuan-Deng, Kuo-Chih Chiu, Nan‐Shan Chang, Hua‐Lin Wu, & Shean-Jen Chen. (2010). Study of cell-biosubstrate contacts via surface plasmon polariton phase microscopy. Optics Express. 18(19). 20125–20125. 14 indexed citations

Hong, Qunying, et al.. (2007). Conformationally altered hyaluronan restricts complement classical pathway activation by binding to C1q, C1r, C1s, C2, C5 and C9, and suppresses WOX1 expression in prostate DU145 cells. International Journal of Molecular Medicine. 19(1). 173–9. 9 indexed citations

10.

Chang, Nan‐Shan, et al.. (2006). WW domain-containing oxidoreductase: a candidate tumor suppressor. Trends in Molecular Medicine. 13(1). 12–22. 109 indexed citations

11.

Chang, Nan‐Shan, et al.. (2005). WOX1 Is Essential for Tumor Necrosis Factor-, UV Light-, Staurosporine-, and p53-mediated Cell Death, and Its Tyrosine 33-phosphorylated Form Binds and Stabilizes Serine 46-phosphorylated p53. Journal of Biological Chemistry. 280(52). 43100–43108. 108 indexed citations

12.

Schultz, Lori, et al.. (2004). TIAF1 and p53 Functionally Interact in Mediating Apoptosis and Silencing of TIAF1 Abolishes Nuclear Translocation of Serine 15-Phosphorylated p53. DNA and Cell Biology. 23(1). 67–74. 16 indexed citations

13.

Chang, Nan‐Shan, Lori Schultz, Li‐Jin Hsu, et al.. (2004). 17β-Estradiol upregulates and activates WOX1/WWOXv1 and WOX2/WWOXv2 in vitro: potential role in cancerous progression of breast and prostate to a premetastatic state in vivo. Oncogene. 24(4). 714–723. 79 indexed citations

14.

Lee, Tzong‐Huei, Mong‐Wei Lin, Tsui‐Fen Chou, Chia‐Ti Tsai, & Nan‐Shan Chang. (2004). Adjunctive 17β-estradiol administration reduces infarct size by altered expression of canine myocardial connexin43 protein. Cardiovascular Research. 63(1). 109–117. 56 indexed citations

15.

Hsu, Li‐Jin, et al.. (2004). Cloning and characterization of a small-size peptide Zfra that regulates the cytotoxic function of tumor necrosis factor by interacting with JNK1. Biochemical and Biophysical Research Communications. 327(2). 415–423. 14 indexed citations

16.

Chuang, Jih‐Ing, et al.. (2004). Light-induced retinal damage involves tyrosine 33 phosphorylation, mitochondrial and nuclear translocation of WW domain-containing oxidoreductase in vivo. Neuroscience. 130(2). 397–407. 48 indexed citations

17.

Chang, Nan‐Shan, Jennifer Lewis, John K. Heath, et al.. (2003). Molecular mechanisms underlying WOX1 activation during apoptotic and stress responses. Biochemical Pharmacology. 66(8). 1347–1354. 69 indexed citations

18.

Chang, Nan‐Shan, et al.. (2001). Hyaluronidase Induction of a WW Domain-containing Oxidoreductase That Enhances Tumor Necrosis Factor Cytotoxicity. Journal of Biological Chemistry. 276(5). 3361–3370. 191 indexed citations

19.

Chang, Nan‐Shan. (2000). TGF-β-Induced Matrix Proteins Inhibit p42/44 MAPK and JNK Activation and Suppress TNF-Mediated IκBα Degradation and NF-κB Nuclear Translocation in L929 Fibroblasts. Biochemical and Biophysical Research Communications. 267(1). 194–200. 19 indexed citations

20.

Chang, Nan‐Shan, et al.. (1997). Characterization of serum adhesive proteins that block tumor necrosis factor-mediated cell death. Cell Death and Differentiation. 4(8). 779–786. 10 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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