Eric C. Chang

2.6k total citations
38 papers, 1.7k citations indexed

About

Eric C. Chang is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Eric C. Chang has authored 38 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 19 papers in Cell Biology and 6 papers in Oncology. Recurrent topics in Eric C. Chang's work include Protein Kinase Regulation and GTPase Signaling (12 papers), Fungal and yeast genetics research (11 papers) and Microtubule and mitosis dynamics (9 papers). Eric C. Chang is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (12 papers), Fungal and yeast genetics research (11 papers) and Microtubule and mitosis dynamics (9 papers). Eric C. Chang collaborates with scholars based in United States, China and Russia. Eric C. Chang's co-authors include Michael Wigler, Hsueh-Chi S. Yen, Vincent Jung, Yan Wang, Haopeng Xu, Maureen M. Barr, Brian Onken, Mark R. Philips, Chia‐Chi Ho and George M. Whitesides and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Eric C. Chang

37 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric C. Chang United States 21 1.3k 712 191 185 165 38 1.7k
Shuling Guo United States 21 1.6k 1.2× 938 1.3× 89 0.5× 307 1.7× 149 0.9× 58 2.7k
Paul D. Andrews United Kingdom 22 2.0k 1.6× 1.8k 2.6× 350 1.8× 71 0.4× 368 2.2× 30 2.7k
Wendy R. Gordon United States 16 1.4k 1.1× 250 0.4× 71 0.4× 90 0.5× 248 1.5× 33 1.8k
Anirban Datta United States 19 1.7k 1.3× 1.5k 2.2× 96 0.5× 240 1.3× 347 2.1× 30 2.8k
Metello Innocenti Italy 21 1.4k 1.1× 1.2k 1.7× 69 0.4× 93 0.5× 228 1.4× 35 2.4k
Klaas W. Mulder Netherlands 20 1.7k 1.4× 252 0.4× 109 0.6× 43 0.2× 252 1.5× 34 2.3k
Keiichiro Tanaka Japan 15 676 0.5× 514 0.7× 163 0.9× 160 0.9× 135 0.8× 26 1.2k
C. Thomas United Kingdom 21 850 0.7× 464 0.7× 69 0.4× 62 0.3× 192 1.2× 43 1.7k
Alf Herzig Germany 15 1.3k 1.0× 257 0.4× 177 0.9× 33 0.2× 70 0.4× 18 2.1k
Paul D. Kassner United States 23 945 0.7× 528 0.7× 47 0.2× 97 0.5× 335 2.0× 46 2.6k

Countries citing papers authored by Eric C. Chang

Since Specialization
Citations

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

Fields of papers citing papers by Eric C. Chang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric C. 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 Eric C. Chang. The network helps show where Eric C. Chang may publish in the future.

Co-authorship network of co-authors of Eric C. Chang

This figure shows the co-authorship network connecting the top 25 collaborators of Eric C. Chang. A scholar is included among the top collaborators of Eric C. 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 Eric C. Chang. Eric C. 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.
Jaehnig, Eric J., Meenakshi Anurag, Jonathan T. Lei, et al.. (2025). NF1-depleted ER + breast cancers are differentially sensitive to CDK4/6 inhibitors. Science Translational Medicine. 17(813). eadq5492–eadq5492.
2.
Zheng, Ze‐Yi, Jonathan T. Lei, Hong Yan, et al.. (2022). Elevated NRAS expression during DCIS is a potential driver for progression to basal-like properties and local invasiveness. Breast Cancer Research. 24(1). 68–68. 3 indexed citations
3.
Calton, Melissa A., A A Jeffrey, Eric C. Chang, et al.. (2019). VE-4840, an oral plasma kallikrein inhibitor, decreases human plasma kallikrein and VEGF-induced retinal thickening and vascular permeability. Investigative Ophthalmology & Visual Science. 60(9). 2725–2725. 2 indexed citations
4.
Zheng, Ze‐Yi, Jing Li, Fuhai Li, et al.. (2018). Induction of N-Ras degradation by flunarizine-mediated autophagy. Scientific Reports. 8(1). 16932–16932. 12 indexed citations
5.
Medina, Daniel, Sabrina Herrera, Ze‐Yi Zheng, et al.. (2015). Int6 reduction activates stromal fibroblasts to enhance transforming activity in breast epithelial cells. Cell & Bioscience. 5(1). 10–10. 9 indexed citations
6.
Zheng, Ze‐Yi & Eric C. Chang. (2014). A Bimolecular Fluorescent Complementation Screen Reveals Complex Roles of Endosomes in Ras-Mediated Signaling. Methods in enzymology on CD-ROM/Methods in enzymology. 535. 25–38. 4 indexed citations
7.
Zheng, Ze‐Yi, et al.. (2012). Escorting Ras. Small GTPases. 3(4). 236–239. 5 indexed citations
9.
Otero, Joel, et al.. (2010). Int6 and Moe1 interact with Cdc48 to regulate ERAD and proper chromosome segregation. Cell Cycle. 9(1). 147–161. 8 indexed citations
10.
Sha, Zhe, Tegy J. Vadakkan, Joel Otero, et al.. (2010). Proteasome Nuclear Import Mediated by Arc3 Can Influence Efficient DNA Damage Repair and Mitosis in Schizosaccharomyces Pombe. Molecular Biology of the Cell. 21(18). 3125–3136. 15 indexed citations
11.
Sha, Zhe, Laurence M. Brill, Oded Kleifeld, et al.. (2009). The eIF3 Interactome Reveals the Translasome, a Supercomplex Linking Protein Synthesis and Degradation Machineries. Molecular Cell. 36(1). 141–152. 109 indexed citations
12.
Sha, Zhe, et al.. (2007). Isolation of the Schizosaccharomyces pombe Proteasome Subunit Rpn7 and a Structure-Function Study of the Proteasome-COP9-Initiation Factor Domain. Journal of Biological Chemistry. 282(44). 32414–32423. 14 indexed citations
13.
Chang, Eric C. & Mark R. Philips. (2006). Spatial Segregation of Ras Signaling—New Evidence from Fission Yeast. Cell Cycle. 5(17). 1936–1939. 20 indexed citations
14.
Dixit, Ram, Eric C. Chang, & Richard J. Cyr. (2005). Establishment of Polarity during Organization of the Acentrosomal Plant Cortical Microtubule Array. Molecular Biology of the Cell. 17(3). 1298–1305. 71 indexed citations
15.
Yen, Hsueh-Chi S., Christine Espiritu, & Eric C. Chang. (2003). Rpn5 Is a Conserved Proteasome Subunit and Required for Proper Proteasome Localization and Assembly. Journal of Biological Chemistry. 278(33). 30669–30676. 31 indexed citations
16.
Pizon, Véronique, et al.. (2002). Two Ras Pathways in Fission Yeast Are Differentially Regulated by Two Ras Guanine Nucleotide Exchange Factors. Molecular and Cellular Biology. 22(13). 4598–4606. 60 indexed citations
17.
Chen, Chang-Rung, Jing Chen, & Eric C. Chang. (2000). A Conserved Interaction between Moe1 and Mal3 Is Important for Proper Spindle Formation inSchizosaccharomyces pombe. Molecular Biology of the Cell. 11(12). 4067–4077. 28 indexed citations
18.
Chang, Eric C., Geoffrey Bartholomeusz, Ruth A. Pimental, et al.. (1999). Direct Binding and In Vivo Regulation of the Fission Yeast p21-Activated Kinase Shk1 by the SH3 Domain Protein Scd2. Molecular and Cellular Biology. 19(12). 8066–8074. 38 indexed citations
19.
Chang, Eric C., Maureen M. Barr, Yan Wang, et al.. (1994). Cooperative interaction of S. pombe proteins required for mating and morphogenesis. Cell. 79(1). 131–141. 260 indexed citations
20.
Andersen, Lone B., Roymarie Ballester, Douglas A. Marchuk, et al.. (1993). A Conserved Alternative Splice in the von Recklinghausen Neurofibromatosis ( NF1 ) Gene Produces Two Neurofibromin Isoforms, Both of Which Have GTPase-Activating Protein Activity. Molecular and Cellular Biology. 13(1). 487–495. 137 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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