David M. Warshaw

10.2k total citations
158 papers, 7.9k citations indexed

About

David M. Warshaw is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cell Biology. According to data from OpenAlex, David M. Warshaw has authored 158 papers receiving a total of 7.9k indexed citations (citations by other indexed papers that have themselves been cited), including 120 papers in Cardiology and Cardiovascular Medicine, 80 papers in Molecular Biology and 48 papers in Cell Biology. Recurrent topics in David M. Warshaw's work include Cardiomyopathy and Myosin Studies (119 papers), Muscle Physiology and Disorders (61 papers) and Cardiovascular Effects of Exercise (50 papers). David M. Warshaw is often cited by papers focused on Cardiomyopathy and Myosin Studies (119 papers), Muscle Physiology and Disorders (61 papers) and Cardiovascular Effects of Exercise (50 papers). David M. Warshaw collaborates with scholars based in United States, United Kingdom and Canada. David M. Warshaw's co-authors include Kathleen M. Trybus, David Harris, Guy G. Kennedy, M. Yusuf Ali, Steven S. Work, Norman R. Alpert, Matthew J. Tyska, Michael J. Mulvany, Shane R. Nelson and Jeffrey Robbins and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

David M. Warshaw

156 papers receiving 7.7k citations

Peers

David M. Warshaw

CCM

AMPO

Susan Lowey United States

Kathleen M. Trybus United States

Dietmar J. Manstein Germany

Marion L. Greaser United States

John Trinick United Kingdom

Michael A. Geeves United Kingdom

Anne Houdusse France

William Lehman United States

Shin’ichi Ishiwata Japan

Roger Craig United States

Susan Lowey United States

David M. Warshaw

5.9k ×1.2

CCM

5.9k ×1.4

2.6k ×1.3

873 ×0.8

AMPO

568 ×0.8

Citations per year, relative to David M. Warshaw David M. Warshaw (= 1×) peers Susan Lowey

Countries citing papers authored by David M. Warshaw

Since Specialization

Citations

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

Fields of papers citing papers by David M. Warshaw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David M. Warshaw. 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 David M. Warshaw. The network helps show where David M. Warshaw may publish in the future.

Co-authorship network of co-authors of David M. Warshaw

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

All Works

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20 of 20 papers shown

Nelson, Shane R., et al.. (2024). Tail length and E525K dilated cardiomyopathy mutant alter human β-cardiac myosin super-relaxed state. The Journal of General Physiology. 156(6). 5 indexed citations

Mead, Andrew F., Shane R. Nelson, Bradley M. Palmer, et al.. (2024). Functional role of myosin-binding protein H in thick filaments of developing vertebrate fast-twitch skeletal muscle. The Journal of General Physiology. 156(12).

Previs, Samantha Beck, et al.. (2024). Kinesin-1-transported liposomes prefer to go straight in 3D microtubule intersections by a mechanism shared by other molecular motors. Proceedings of the National Academy of Sciences. 121(29). e2407330121–e2407330121. 1 indexed citations

Nelson, Shane R., Samantha Beck Previs, Sakthivel Sadayappan, Carl Tong, & David M. Warshaw. (2023). Myosin-binding protein C stabilizes, but is not the sole determinant of SRX myosin in cardiac muscle. The Journal of General Physiology. 155(4). 14 indexed citations

Nelson, Shane R., et al.. (2019). Myosin Va transport of liposomes in three-dimensional actin networks is modulated by actin filament density, position, and polarity. Proceedings of the National Academy of Sciences. 116(17). 8326–8335. 24 indexed citations

Li, Amy, Shane R. Nelson, Filip Braet, et al.. (2019). Skeletal MyBP-C isoforms tune the molecular contractility of divergent skeletal muscle systems. Proceedings of the National Academy of Sciences. 116(43). 21882–21892. 29 indexed citations

Mead, Andrew F., Guy G. Kennedy, Samantha Beck Previs, et al.. (2019). Zebrafish Embryos Enable Multi-Scale High-Throughput Muscle Mechanics. Biophysical Journal. 116(3). 405a–405a. 1 indexed citations

Michalek, Arthur J., Guy G. Kennedy, David M. Warshaw, & M. Yusuf Ali. (2015). Flexural Stiffness of Myosin Va Subdomains as Measured from Tethered Particle Motion. PubMed. 2015. 1–9. 2 indexed citations

Nelson, Shane R., et al.. (2014). Two glycosylase families diffusively scan DNA using a wedge residue to probe for and identify oxidatively damaged bases. Proceedings of the National Academy of Sciences. 111(20). E2091–9. 81 indexed citations

10.

Previs, Michael J., Arthur J. Michalek, & David M. Warshaw. (2014). Molecular modulation of actomyosin function by cardiac myosin-binding protein C. Pflügers Archiv - European Journal of Physiology. 466(3). 439–444. 19 indexed citations

11.

Previs, Michael J., et al.. (2013). Dephosphorylated Cardiac Myosin-Binding Protein C (cMyBP-C) Activates Native Cardiac Thin Filaments within the C-Zone of Native Cardiac Thick Filaments. Biophysical Journal. 104(2). 186a–186a. 2 indexed citations

12.

Heaslip, Aoife T., et al.. (2013). Involvement of Myova and Actin in Insulin Granule Trafficking. Biophysical Journal. 104(2). 651a–651a. 1 indexed citations

13.

Ali, M. Yusuf, Hailong Lu, Carol S. Bookwalter, David M. Warshaw, & Kathleen M. Trybus. (2008). Myosin V and Kinesin act as tethers to enhance each others' processivity. Proceedings of the National Academy of Sciences. 105(12). 4691–4696. 105 indexed citations

14.

Ali, M. Yusuf, Elena B. Krementsova, Guy G. Kennedy, et al.. (2007). Myosin Va maneuvers through actin intersections and diffuses along microtubules. Proceedings of the National Academy of Sciences. 104(11). 4332–4336. 122 indexed citations

15.

Palmiter, Kimberly A., et al.. (1999). Kinetic differences at the single molecule level account for the functional diversity of rabbit cardiac myosin isoforms. The Journal of Physiology. 519(3). 669–678. 101 indexed citations

16.

Harris, David, et al.. (1994). Smooth, cardiac and skeletal muscle myosin force and motion generation assessed by cross-bridge mechanical interactions in vitro. Journal of Muscle Research and Cell Motility. 15(1). 11–19. 159 indexed citations

17.

Harris, David & David M. Warshaw. (1990). Slowing of velocity during isotonic shortening in single isolated smooth muscle cells. Evidence for an internal load.. The Journal of General Physiology. 96(3). 581–601. 29 indexed citations

18.

Harris, David, et al.. (1990). Mechanical transients of single toad stomach smooth muscle cells. Effects of lowering temperature and extracellular calcium.. The Journal of General Physiology. 95(4). 697–715. 15 indexed citations

19.

Warshaw, David M., et al.. (1988). Characterization of cross-bridge elasticity and kinetics of cross-bridge cycling during force development in single smooth muscle cells.. The Journal of General Physiology. 91(6). 761–779. 29 indexed citations

20.

Warshaw, David M.. (1987). Force: velocity relationship in single isolated toad stomach smooth muscle cells.. The Journal of General Physiology. 89(5). 771–789. 30 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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