Jun‐Song Chen

1.4k total citations
49 papers, 995 citations indexed

About

Jun‐Song Chen is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Jun‐Song Chen has authored 49 papers receiving a total of 995 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 29 papers in Cell Biology and 7 papers in Plant Science. Recurrent topics in Jun‐Song Chen's work include Fungal and yeast genetics research (25 papers), Microtubule and mitosis dynamics (20 papers) and Protein Kinase Regulation and GTPase Signaling (10 papers). Jun‐Song Chen is often cited by papers focused on Fungal and yeast genetics research (25 papers), Microtubule and mitosis dynamics (20 papers) and Protein Kinase Regulation and GTPase Signaling (10 papers). Jun‐Song Chen collaborates with scholars based in United States, China and United Kingdom. Jun‐Song Chen's co-authors include Kathleen L. Gould, Anna Feoktistova, Rachel H. Roberts-Galbraith, John H. Exton, Jianqiu Wang, Dannel McCollum, Steven P. Gygi, Melanie D. Ohi, Ian X. McLeod and John R. Yates and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and The Journal of Cell Biology.

In The Last Decade

Jun‐Song Chen

44 papers receiving 990 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jun‐Song Chen United States 18 870 641 114 72 57 49 995
Mara C. Duncan United States 16 684 0.8× 535 0.8× 72 0.6× 34 0.5× 26 0.5× 28 888
Anna Feoktistova United States 24 1.3k 1.5× 911 1.4× 233 2.0× 90 1.3× 112 2.0× 35 1.5k
Hisashi Tatebe Japan 16 870 1.0× 416 0.6× 158 1.4× 52 0.7× 33 0.6× 23 985
Justin W. Chartron United States 17 1.0k 1.2× 371 0.6× 48 0.4× 48 0.7× 58 1.0× 23 1.2k
John Lippincott United States 9 917 1.1× 463 0.7× 100 0.9× 108 1.5× 110 1.9× 13 1.0k
Shirin Bahmanyar United States 18 1.0k 1.2× 692 1.1× 57 0.5× 27 0.4× 46 0.8× 28 1.2k
Teresa Żołądek Poland 16 742 0.9× 317 0.5× 40 0.4× 20 0.3× 47 0.8× 40 853
Angela Hach United States 9 864 1.0× 290 0.5× 66 0.6× 12 0.2× 45 0.8× 9 988
Susan Raths Switzerland 7 876 1.0× 673 1.0× 58 0.5× 16 0.2× 89 1.6× 8 989
Esther Zanin Germany 13 617 0.7× 382 0.6× 53 0.5× 12 0.2× 38 0.7× 24 819

Countries citing papers authored by Jun‐Song Chen

Since Specialization
Citations

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

Fields of papers citing papers by Jun‐Song Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jun‐Song 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 Jun‐Song Chen. The network helps show where Jun‐Song Chen may publish in the future.

Co-authorship network of co-authors of Jun‐Song Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Jun‐Song Chen. A scholar is included among the top collaborators of Jun‐Song 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 Jun‐Song Chen. Jun‐Song 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.
Chen, Jun‐Song, Liping Ren, Lesley Turner, et al.. (2024). The core spindle pole body scaffold Ppc89 links the pericentrin orthologue Pcp1 to the fission yeast spindle pole body via an evolutionarily conserved interface. Molecular Biology of the Cell. 35(8). ar112–ar112. 1 indexed citations
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Chen, Jun‐Song, et al.. (2024). Substrate displacement of CK1 C-termini regulates kinase specificity. Science Advances. 10(19). eadj5185–eadj5185. 3 indexed citations
4.
Chen, Jun‐Song, et al.. (2024). Abstract 1844 Substrate displacement of CK1 C-termini regulates kinase specificity. Journal of Biological Chemistry. 300(3). 106984–106984.
5.
Suárez, M. Belén, Jingjing Sun, Patrícia Salomão Garcia, et al.. (2024). The Greatwall-Endosulfine-PP2A/B55 pathway regulates entry into quiescence by enhancing translation of Elongator-tunable transcripts. Nature Communications. 15(1). 10603–10603.
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Chaikuad, A., Jun‐Song Chen, Jakob Gebel, et al.. (2022). Kinase domain autophosphorylation rewires the activity and substrate specificity of CK1 enzymes. Molecular Cell. 82(11). 2006–2020.e8. 17 indexed citations
9.
Bhattacharjee, Rahul, Jun‐Song Chen, Rachel H. Roberts-Galbraith, et al.. (2020). DYRK kinase Pom1 drives F-BAR protein Cdc15 from the membrane to promote medial division. Molecular Biology of the Cell. 31(9). 917–929. 17 indexed citations
10.
Chen, Jun‐Song, et al.. (2015). A Degenerate Cohort of Yeast Membrane Trafficking DUBs Mediates Cell Polarity and Survival*. Molecular & Cellular Proteomics. 14(12). 3132–3141. 15 indexed citations
11.
Ren, Liping, Alaina H. Willet, Rachel H. Roberts-Galbraith, et al.. (2014). The Cdc15 and Imp2 SH3 domains cooperatively scaffold a network of proteins that redundantly ensure efficient cell division in fission yeast. Molecular Biology of the Cell. 26(2). 256–269. 41 indexed citations
12.
Johnson, Alyssa E., Jun‐Song Chen, & Kathleen L. Gould. (2013). CK1 Is Required for a Mitotic Checkpoint that Delays Cytokinesis. Current Biology. 23(19). 1920–1926. 33 indexed citations
13.
Chen, Jun‐Song, et al.. (2013). Comprehensive Proteomics Analysis Reveals New Substrates and Regulators of the Fission Yeast Clp1/Cdc14 Phosphatase. Molecular & Cellular Proteomics. 12(5). 1074–1086. 40 indexed citations
14.
Bohnert, K. Adam, et al.. (2009). A Link between Aurora Kinase and Clp1/Cdc14 Regulation Uncovered by the Identification of a Fission Yeast Borealin-Like Protein. Molecular Biology of the Cell. 20(16). 3646–3659. 19 indexed citations
15.
Feoktistova, Anna, et al.. (2008). The SIN Kinase Sid2 Regulates Cytoplasmic Retention of the S. pombe Cdc14-like Phosphatase Clp1. Current Biology. 18(20). 1594–1599. 64 indexed citations
16.
Feoktistova, Anna, et al.. (2008). The Spindle Checkpoint Functions of Mad3 and Mad2 Depend on a Mad3 KEN Box-mediated Interaction with Cdc20-Anaphase-promoting Complex (APC/C). Journal of Biological Chemistry. 283(34). 23039–23047. 76 indexed citations
17.
Feoktistova, Anna, et al.. (2006). Role of Hcn1 and Its Phosphorylation in Fission Yeast Anaphase-promoting Complex/Cyclosome Function. Journal of Biological Chemistry. 281(43). 32284–32293. 16 indexed citations
18.
Chen, Jun‐Song & John H. Exton. (2005). Sites on phospholipase D2 phosphorylated by PKCα. Biochemical and Biophysical Research Communications. 333(4). 1322–1326. 4 indexed citations
19.
Chen, Jun‐Song & John H. Exton. (2004). Regulation of Phospholipase D2 Activity by Protein Kinase Cα. Journal of Biological Chemistry. 279(21). 22076–22083. 58 indexed citations
20.
Zhao, Sheng, Xiaoyan Du, Jun‐Song Chen, Yuan-Cong Zhou, & Jianguo Song. (2002). Secretory Phospholipase A2 Inhibits Epidermal Growth Factor-Induced Receptor Activation. Experimental Cell Research. 279(2). 354–364. 9 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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