Ewa Próchniewicz

1.8k total citations
42 papers, 1.5k citations indexed

About

Ewa Próchniewicz is a scholar working on Cardiology and Cardiovascular Medicine, Cell Biology and Molecular Biology. According to data from OpenAlex, Ewa Próchniewicz has authored 42 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cardiology and Cardiovascular Medicine, 24 papers in Cell Biology and 17 papers in Molecular Biology. Recurrent topics in Ewa Próchniewicz's work include Cardiomyopathy and Myosin Studies (28 papers), Cellular Mechanics and Interactions (20 papers) and Muscle Physiology and Disorders (15 papers). Ewa Próchniewicz is often cited by papers focused on Cardiomyopathy and Myosin Studies (28 papers), Cellular Mechanics and Interactions (20 papers) and Muscle Physiology and Disorders (15 papers). Ewa Próchniewicz collaborates with scholars based in United States, Poland and Japan. Ewa Próchniewicz's co-authors include David D. Thomas, Hanna Strzelecka-Gołaszewska, Toshio Yanagida, W. Drabikowski, Albina Orlova, Edward H. Egelman, Enrique M. De La Cruz, LaDora V. Thompson, Paul A. Janmey and Timothy F. Walseth and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Molecular Biology.

In The Last Decade

Ewa Próchniewicz

42 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ewa Próchniewicz United States 23 811 788 698 355 213 42 1.5k
Birgit Brandmeier United Kingdom 12 322 0.4× 758 1.0× 901 1.3× 276 0.8× 98 0.5× 18 1.4k
Lewis C. Gershman United States 25 1.0k 1.2× 563 0.7× 778 1.1× 287 0.8× 301 1.4× 40 1.8k
Lynn A. Selden United States 22 884 1.1× 343 0.4× 451 0.6× 273 0.8× 244 1.1× 32 1.3k
Hirofumi Onishi Japan 21 891 1.1× 972 1.2× 1.3k 1.8× 107 0.3× 32 0.2× 58 2.0k
Joseph M. Chalovich United States 35 1.2k 1.5× 2.8k 3.6× 2.4k 3.5× 598 1.7× 86 0.4× 123 4.0k
John Sleep United Kingdom 24 505 0.6× 1.3k 1.6× 1.2k 1.7× 892 2.5× 80 0.4× 37 2.3k
Gábor Hild Hungary 16 442 0.5× 262 0.3× 275 0.4× 178 0.5× 133 0.6× 40 723
Yasuharu Takagi United States 22 439 0.5× 473 0.6× 596 0.9× 204 0.6× 74 0.3× 39 1.2k
E. Pate United States 20 358 0.4× 1.0k 1.3× 881 1.3× 208 0.6× 26 0.1× 28 1.7k
Sven Tågerud Sweden 22 340 0.4× 277 0.4× 548 0.8× 151 0.4× 25 0.1× 49 1.3k

Countries citing papers authored by Ewa Próchniewicz

Since Specialization
Citations

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

Fields of papers citing papers by Ewa Próchniewicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ewa Próchniewicz. 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 Ewa Próchniewicz. The network helps show where Ewa Próchniewicz may publish in the future.

Co-authorship network of co-authors of Ewa Próchniewicz

This figure shows the co-authorship network connecting the top 25 collaborators of Ewa Próchniewicz. A scholar is included among the top collaborators of Ewa Próchniewicz 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 Ewa Próchniewicz. Ewa Próchniewicz 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.
Próchniewicz, Ewa, et al.. (2020). Actin-binding compounds, previously discovered by FRET-based high-throughput screening, differentially affect skeletal and cardiac muscle. Journal of Biological Chemistry. 295(41). 14100–14110. 5 indexed citations
2.
Próchniewicz, Ewa, et al.. (2018). High-throughput screen, using time-resolved FRET, yields actin-binding compounds that modulate actin–myosin structure and function. Journal of Biological Chemistry. 293(31). 12288–12298. 16 indexed citations
3.
Elam, W. Austin, Wenxiang Cao, Hyeran Kang, et al.. (2017). Phosphomimetic S3D cofilin binds but only weakly severs actin filaments. Journal of Biological Chemistry. 292(48). 19565–19579. 35 indexed citations
4.
Próchniewicz, Ewa, et al.. (2017). A Cardiomyopathy Mutation in the Myosin Essential Light Chain Alters Actomyosin Structure. Biophysical Journal. 113(1). 91–100. 16 indexed citations
5.
Elam, W. Austin, et al.. (2015). Phosphomimic S3D Cofilin Binds Actin Filaments but does not Sever them. Biophysical Journal. 108(2). 300a–300a. 1 indexed citations
6.
Próchniewicz, Ewa, et al.. (2012). Impacts of Dystrophin and Utrophin Domains on Actin Structural Dynamics: Implications for Therapeutic Design. Journal of Molecular Biology. 420(1-2). 87–98. 17 indexed citations
7.
Próchniewicz, Ewa, et al.. (2012). Allosteric communication in Dictyostelium myosin II. Journal of Muscle Research and Cell Motility. 33(5). 305–312. 6 indexed citations
8.
Próchniewicz, Ewa, Anaëlle Pierre, Brannon R. McCullough, et al.. (2011). Actin Filament Dynamics in the Actomyosin VI Complex Is Regulated Allosterically by Calcium–Calmodulin Light Chain. Journal of Molecular Biology. 413(3). 584–592. 7 indexed citations
9.
Próchniewicz, Ewa, Harvey F. Chin, Arnon Henn, et al.. (2009). Myosin Isoform Determines the Conformational Dynamics and Cooperativity of Actin Filaments in the Strongly Bound Actomyosin Complex. Journal of Molecular Biology. 396(3). 501–509. 39 indexed citations
10.
Próchniewicz, Ewa, LaDora V. Thompson, & David D. Thomas. (2007). Age-related decline in actomyosin structure and function. Experimental Gerontology. 42(10). 931–938. 49 indexed citations
11.
Próchniewicz, Ewa, Dawn A. Lowe, Daniel Spakowicz, et al.. (2007). Functional, structural, and chemical changes in myosin associated with hydrogen peroxide treatment of skeletal muscle fibers. American Journal of Physiology-Cell Physiology. 294(2). C613–C626. 91 indexed citations
12.
Próchniewicz, Ewa, David D. Thomas, & LaDora V. Thompson. (2005). Age-Related Decline in Actomyosin Function. The Journals of Gerontology Series A. 60(4). 425–431. 39 indexed citations
13.
Korman, Vicci L., et al.. (2005). Structural Dynamics of the Actin–Myosin Interface by Site-directed Spectroscopy. Journal of Molecular Biology. 356(5). 1107–1117. 20 indexed citations
14.
Thomas, David D., Ewa Próchniewicz, & Osha Roopnarine. (2002). Changes in Actin and Myosin Structural Dynamics Due to Their Weak and Strong Interactions. Results and problems in cell differentiation. 36. 7–19. 26 indexed citations
15.
Orlova, Albina, Inna N. Rybakova, Ewa Próchniewicz, et al.. (2001). Binding of Dystrophin’s Tandem Calponin Homology Domain to F-Actin Is Modulated by Actin’s Structure. Biophysical Journal. 80(4). 1926–1931. 17 indexed citations
16.
Próchniewicz, Ewa, et al.. (1996). Microsecond Rotational Dynamics of Actin: Spectroscopic Detection and Theoretical Simulation. Journal of Molecular Biology. 255(3). 446–457. 57 indexed citations
17.
Próchniewicz, Ewa, et al.. (1995). Chemical Modification of Actin Restricts Microsecond Rotational Dynamics and Inhibits Sliding Movement.. Biophysical Journal. 68. 1 indexed citations
18.
Próchniewicz, Ewa, Eisaku Katayama, Toshio Yanagida, & David D. Thomas. (1993). Cooperativity in F-actin: chemical modifications of actin monomers affect the functional interactions of myosin with unmodified monomers in the same actin filament. Biophysical Journal. 65(1). 113–123. 51 indexed citations
19.
20.
Próchniewicz, Ewa & Toshio Yanagida. (1990). Inhibition of sliding movement of F-actin by crosslinking emphasizes the role of actin structure in the mechanism of motility. Journal of Molecular Biology. 216(3). 761–772. 94 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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