Charles B. Shuster

1.7k total citations
43 papers, 1.3k citations indexed

About

Charles B. Shuster is a scholar working on Cell Biology, Molecular Biology and Organic Chemistry. According to data from OpenAlex, Charles B. Shuster has authored 43 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Cell Biology, 24 papers in Molecular Biology and 7 papers in Organic Chemistry. Recurrent topics in Charles B. Shuster's work include Microtubule and mitosis dynamics (19 papers), Cellular Mechanics and Interactions (13 papers) and Protist diversity and phylogeny (6 papers). Charles B. Shuster is often cited by papers focused on Microtubule and mitosis dynamics (19 papers), Cellular Mechanics and Interactions (13 papers) and Protist diversity and phylogeny (6 papers). Charles B. Shuster collaborates with scholars based in United States, South Africa and Germany. Charles B. Shuster's co-authors include David R. Burgess, Ira M. Herman, Angus L. Dawe, Michèle Shuster, Ralph W. Preszler, John H. Henson, Olivia George, Chinnasamy Ramesh, Jeffrey B. Arterburn and Menuka Karki and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nature Communications.

In The Last Decade

Charles B. Shuster

42 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charles B. Shuster United States 20 581 573 151 140 80 43 1.3k
Kathryn G. Miller United States 27 1.0k 1.7× 2.2k 3.9× 71 0.5× 141 1.0× 57 0.7× 51 2.9k
Björn Sjöblom Sweden 15 299 0.5× 662 1.2× 21 0.1× 66 0.5× 38 0.5× 35 1.3k
Ashley A. Rowland United States 6 639 1.1× 919 1.6× 69 0.5× 7 0.1× 8 0.1× 6 1.5k
Frank Solomon United States 32 1.5k 2.6× 2.1k 3.7× 24 0.2× 58 0.4× 149 1.9× 63 3.2k
James Rae Australia 20 611 1.1× 825 1.4× 10 0.1× 47 0.3× 38 0.5× 32 1.3k
Didem Vardar‐Ulu United States 14 186 0.3× 706 1.2× 12 0.1× 22 0.2× 64 0.8× 22 956
David A. Begg United States 17 441 0.8× 547 1.0× 24 0.2× 11 0.1× 32 0.4× 24 1.0k
B. Lakshmi India 17 128 0.2× 1.7k 3.0× 22 0.1× 174 1.2× 25 0.3× 49 3.3k
Jessica L. Feldman United States 18 1.1k 1.8× 1.4k 2.4× 16 0.1× 240 1.7× 11 0.1× 41 2.1k
Clare M. O’Connor United States 21 373 0.6× 1.0k 1.8× 32 0.2× 9 0.1× 13 0.2× 49 1.6k

Countries citing papers authored by Charles B. Shuster

Since Specialization
Citations

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

Fields of papers citing papers by Charles B. Shuster

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles B. Shuster. 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 Charles B. Shuster. The network helps show where Charles B. Shuster may publish in the future.

Co-authorship network of co-authors of Charles B. Shuster

This figure shows the co-authorship network connecting the top 25 collaborators of Charles B. Shuster. A scholar is included among the top collaborators of Charles B. Shuster 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 Charles B. Shuster. Charles B. Shuster 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.
2.
Swartz, S. Zachary, et al.. (2022). Use of Echinoderm Gametes and Early Embryos for Studying Meiosis and Mitosis. Methods in molecular biology. 2415. 1–17. 1 indexed citations
3.
4.
Henson, John H., et al.. (2020). Rac and Arp2/3-Nucleated Actin Networks Antagonize Rho During Mitotic and Meiotic Cleavages. Frontiers in Cell and Developmental Biology. 8. 591141–591141. 11 indexed citations
5.
Henson, John H., et al.. (2019). Cytoskeletal polarization and cytokinetic signaling drives polar lobe formation in spiralian embryos. Developmental Biology. 456(2). 201–211. 5 indexed citations
6.
Shuster, Charles B., et al.. (2019). Live-cell fluorescence imaging of echinoderm embryos. Methods in cell biology. 151. 379–397. 3 indexed citations
7.
Henson, John H., et al.. (2018). Cdc42 controls primary mesenchyme cell morphogenesis in the sea urchin embryo. Developmental Biology. 437(2). 140–151. 20 indexed citations
8.
Karki, Menuka, Neda Keyhaninejad, & Charles B. Shuster. (2017). Precocious centriole disengagement and centrosome fragmentation induced by mitotic delay. Nature Communications. 8(1). 15803–15803. 24 indexed citations
9.
Henson, John H., et al.. (2016). Central Spindle Self-Organization and Cytokinesis in Artificially Activated Sea Urchin Eggs. Biological Bulletin. 230(2). 85–95. 3 indexed citations
10.
Frolova, Liliya V., Igor V. Magedov, Anntherese E. Romero, et al.. (2013). Exploring Natural Product Chemistry and Biology with Multicomponent Reactions. 5. Discovery of a Novel Tubulin-Targeting Scaffold Derived from the Rigidin Family of Marine Alkaloids. Journal of Medicinal Chemistry. 56(17). 6886–6900. 43 indexed citations
11.
Shuster, Charles B., et al.. (2012). PRC1 controls spindle polarization and recruitment of cytokinetic factors during monopolar cytokinesis. Molecular Biology of the Cell. 23(7). 1196–1207. 34 indexed citations
12.
Magedov, Igor V., Nikolai M. Evdokimov, Menuka Karki, et al.. (2012). Reengineered epipodophyllotoxin. Chemical Communications. 48(84). 10416–10416. 7 indexed citations
13.
Foe, Victoria E., et al.. (2012). Centralspindlin and chromosomal passenger complex behavior during normal and Rappaport furrow specification in echinoderm embryos. Cytoskeleton. 69(10). 840–853. 19 indexed citations
14.
Magedov, Igor V., Liliya V. Frolova, Madhuri Manpadi, et al.. (2011). Anticancer Properties of an Important Drug Lead Podophyllotoxin Can Be Efficiently Mimicked by Diverse Heterocyclic Scaffolds Accessible via One-Step Synthesis. Journal of Medicinal Chemistry. 54(12). 4234–4246. 57 indexed citations
15.
Shuster, Charles B., et al.. (2009). Mutual Dependence of Mob1 and the Chromosomal Passenger Complex for Localization during Mitosis. Molecular Biology of the Cell. 21(3). 380–392. 16 indexed citations
16.
Henson, John H., et al.. (2009). Structure and dynamics of an Arp2/3 complex‐independent component of the lamellipodial actin network. Cell Motility and the Cytoskeleton. 66(9). 679–692. 5 indexed citations
17.
Stack, Christianna, et al.. (2006). A Global, Myosin Light Chain Kinase-dependent Increase in Myosin II Contractility Accompanies the Metaphase–Anaphase Transition in Sea Urchin Eggs. Molecular Biology of the Cell. 17(9). 4093–4104. 31 indexed citations
18.
Stack, Christianna, et al.. (2006). Calcium‐responsive contractility during fertilization in sea urchin eggs. Developmental Dynamics. 235(4). 1042–1052. 11 indexed citations
19.
George, Olivia, et al.. (2006). Aurora B Kinase Maintains Chromatin Organization During the MI to MII Transition in Surf Clam Oocytes. Cell Cycle. 5(22). 2648–2656. 18 indexed citations
20.
Shuster, Charles B. & David R. Burgess. (2002). Transitions Regulating the Timing of Cytokinesis in Embryonic Cells. Current Biology. 12(10). 854–858. 37 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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