Thomas E. Sladewski

563 total citations
18 papers, 401 citations indexed

About

Thomas E. Sladewski is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Thomas E. Sladewski has authored 18 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Cardiology and Cardiovascular Medicine and 6 papers in Cell Biology. Recurrent topics in Thomas E. Sladewski's work include Cardiomyopathy and Myosin Studies (10 papers), Genetic Neurodegenerative Diseases (4 papers) and Fungal and yeast genetics research (4 papers). Thomas E. Sladewski is often cited by papers focused on Cardiomyopathy and Myosin Studies (10 papers), Genetic Neurodegenerative Diseases (4 papers) and Fungal and yeast genetics research (4 papers). Thomas E. Sladewski collaborates with scholars based in United States, France and Germany. Thomas E. Sladewski's co-authors include Matthew Lord, Kathleen M. Trybus, Carol S. Bookwalter, Elena B. Krementsova, Luther W. Pollard, Alex R. Hodges, Michael J. Previs, Thomas D. Pollard, Patricia M. Fagnant and Neil Billington and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Thomas E. Sladewski

17 papers receiving 391 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas E. Sladewski United States 12 293 210 131 52 46 18 401
S. Pernigo United Kingdom 8 197 0.7× 203 1.0× 58 0.4× 22 0.4× 58 1.3× 8 349
Nicanor González‐Morales Canada 11 187 0.6× 92 0.4× 83 0.6× 7 0.1× 62 1.3× 17 323
Sathish Thiyagarajan United States 8 208 0.7× 199 0.9× 18 0.1× 8 0.2× 47 1.0× 14 272
Anup Padmanabhan Singapore 8 258 0.9× 227 1.1× 27 0.2× 4 0.1× 39 0.8× 12 378
Saravanan Palani United Kingdom 15 424 1.4× 298 1.4× 45 0.3× 8 0.2× 51 1.1× 28 528
Ting Gang Chew Singapore 12 386 1.3× 281 1.3× 32 0.2× 14 0.3× 27 0.6× 21 471
François Iv France 4 190 0.6× 157 0.7× 17 0.1× 10 0.2× 15 0.3× 7 279
Chikako Kitayama Japan 8 307 1.0× 304 1.4× 99 0.8× 3 0.1× 97 2.1× 9 456
Angela S. Otero United States 9 297 1.0× 31 0.1× 79 0.6× 21 0.4× 74 1.6× 13 395
Christopher Hoel United States 5 199 0.7× 109 0.5× 13 0.1× 28 0.5× 8 0.2× 5 299

Countries citing papers authored by Thomas E. Sladewski

Since Specialization
Citations

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

Fields of papers citing papers by Thomas E. Sladewski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas E. Sladewski. 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 Thomas E. Sladewski. The network helps show where Thomas E. Sladewski may publish in the future.

Co-authorship network of co-authors of Thomas E. Sladewski

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

All Works

18 of 18 papers shown
1.
Cao, Wenxiang, Thomas E. Sladewski, Aoife T. Heaslip, & Enrique M. De La Cruz. (2024). Bending stiffness of Toxoplasma gondii actin filaments. Journal of Biological Chemistry. 301(2). 108101–108101.
2.
Hvorecny, Kelli L., Thomas E. Sladewski, Enrique M. De La Cruz, Justin M. Kollman, & Aoife T. Heaslip. (2024). Toxoplasma gondii actin filaments are tuned for rapid disassembly and turnover. Nature Communications. 15(1). 1840–1840. 8 indexed citations
3.
Sladewski, Thomas E., et al.. (2023). Cytokinesis in Trypanosoma brucei relies on an orphan kinesin that dynamically crosslinks microtubules. Current Biology. 33(5). 899–911.e5. 4 indexed citations
4.
Sladewski, Thomas E., et al.. (2022). Revealing spatio-temporal dynamics with long-term trypanosomatid live-cell imaging. PLoS Pathogens. 18(1). e1010218–e1010218. 2 indexed citations
5.
Sladewski, Thomas E., et al.. (2021). The Trypanosoma brucei subpellicular microtubule array is organized into functionally discrete subdomains defined by microtubule associated proteins. PLoS Pathogens. 17(5). e1009588–e1009588. 12 indexed citations
6.
Sladewski, Thomas E., et al.. (2018). Identification of TOEFAZ1‐interacting proteins reveals key regulators of Trypanosoma brucei cytokinesis. Molecular Microbiology. 109(3). 306–326. 37 indexed citations
7.
Sladewski, Thomas E., Neil Billington, M. Yusuf Ali, et al.. (2018). Recruitment of two dyneins to an mRNA-dependent Bicaudal D transport complex. eLife. 7. 49 indexed citations
8.
Sladewski, Thomas E., Elena B. Krementsova, & Kathleen M. Trybus. (2016). Myosin Vc Is Specialized for Transport on a Secretory Superhighway. Current Biology. 26(16). 2202–2207. 10 indexed citations
9.
Sladewski, Thomas E. & Kathleen M. Trybus. (2014). A single molecule approach to mRNA transport by a class V myosin. RNA Biology. 11(8). 986–991. 5 indexed citations
10.
Sladewski, Thomas E., et al.. (2013). Single-molecule reconstitution of mRNA transport by a class V myosin. Nature Structural & Molecular Biology. 20(8). 952–957. 32 indexed citations
11.
Hodges, Alex R., Elena B. Krementsova, Carol S. Bookwalter, et al.. (2012). Tropomyosin Is Essential for Processive Movement of a Class V Myosin from Budding Yeast. Current Biology. 22(15). 1410–1416. 47 indexed citations
12.
Sladewski, Thomas E., et al.. (2011). Escherichia coli Rep DNA helicase and error‐prone DNA polymerase IV interact physically and functionally. Molecular Microbiology. 80(2). 524–541. 13 indexed citations
13.
James, Michael L., et al.. (2011). A calmodulin-related light chain from fission yeast that functions with myosin-I and PI 4-kinase. Journal of Cell Science. 124(14). 2466–2477. 15 indexed citations
14.
Krementsova, Elena B., Alex R. Hodges, Carol S. Bookwalter, et al.. (2011). Two single-headed myosin V motors bound to a tetrameric adapter protein form a processive complex. The Journal of Cell Biology. 195(4). 631–641. 29 indexed citations
15.
Sladewski, Thomas E., et al.. (2010). Tropomyosin and Myosin-II Cellular Levels Promote Actomyosin Ring Assembly in Fission Yeast. Molecular Biology of the Cell. 21(6). 989–1000. 64 indexed citations
16.
Sladewski, Thomas E., Michael J. Previs, & Matthew Lord. (2009). Regulation of Fission Yeast Myosin-II Function and Contractile Ring Dynamics by Regulatory Light-Chain and Heavy-Chain Phosphorylation. Molecular Biology of the Cell. 20(17). 3941–3952. 31 indexed citations
17.
Lord, Matthew, Thomas E. Sladewski, & Thomas D. Pollard. (2008). Yeast UCS proteins promote actomyosin interactions and limit myosin turnover in cells. Proceedings of the National Academy of Sciences. 105(23). 8014–8019. 27 indexed citations
18.
Sladewski, Thomas E., et al.. (2006). The effect of ionic strength on the UV–vis spectrum of congo red in aqueous solution. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 65(3-4). 985–987. 16 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by S. Pernigo Breakdown of academic impact, for papers by Nicanor González‐Morales Breakdown of academic impact, for papers by Sathish Thiyagarajan Breakdown of academic impact, for papers by Anup Padmanabhan Breakdown of academic impact, for papers by Saravanan Palani Breakdown of academic impact, for papers by Ting Gang Chew Breakdown of academic impact, for papers by François Iv Breakdown of academic impact, for papers by Chikako Kitayama Breakdown of academic impact, for papers by Angela S. Otero Breakdown of academic impact, for papers by Christopher Hoel
Rankless by CCL
2026