Richard E. Cheney

10.5k total citations · 4 hit papers
77 papers, 8.1k citations indexed

About

Richard E. Cheney is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Richard E. Cheney has authored 77 papers receiving a total of 8.1k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 34 papers in Cardiology and Cardiovascular Medicine and 34 papers in Cell Biology. Recurrent topics in Richard E. Cheney's work include Cardiomyopathy and Myosin Studies (34 papers), Muscle Physiology and Disorders (21 papers) and Cellular Mechanics and Interactions (21 papers). Richard E. Cheney is often cited by papers focused on Cardiomyopathy and Myosin Studies (34 papers), Muscle Physiology and Disorders (21 papers) and Cellular Mechanics and Interactions (21 papers). Richard E. Cheney collaborates with scholars based in United States, Brazil and Italy. Richard E. Cheney's co-authors include Jonathan S. Berg, Mark S. Mooseker, Mark S. Mooseker, Bradford C. Powell, Deanna Kuhn, Michael Weinstock, Ronald S. Rock, Matthias Rief, James A. Spudich and Amit Mehta and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Richard E. Cheney

72 papers receiving 7.9k citations

Hit Papers

Myosin-V is a processive actin-based motor 1999 2026 2008 2017 1999 2001 2000 2001 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richard E. Cheney United States 43 4.8k 3.6k 2.3k 665 658 77 8.1k
Clare M. Waterman United States 79 8.0k 1.7× 13.7k 3.8× 648 0.3× 2.0k 3.1× 1.3k 2.0× 149 20.3k
Lawrence Shapiro United States 69 9.8k 2.0× 3.9k 1.1× 481 0.2× 456 0.7× 2.3k 3.5× 189 16.1k
Michael W. Klymkowsky United States 46 4.2k 0.9× 1.7k 0.5× 238 0.1× 60 0.1× 531 0.8× 122 6.9k
Maddy Parsons United Kingdom 56 5.4k 1.1× 4.6k 1.3× 384 0.2× 521 0.8× 1.1k 1.7× 244 12.0k
Tama Hasson United States 35 3.1k 0.7× 1.5k 0.4× 1.2k 0.5× 170 0.3× 350 0.5× 48 4.8k
David Stephens United Kingdom 42 3.3k 0.7× 3.2k 0.9× 88 0.0× 179 0.3× 385 0.6× 128 6.4k
Thomas B. Friedman United States 57 5.7k 1.2× 1.1k 0.3× 455 0.2× 52 0.1× 327 0.5× 181 9.8k
M. Abercrombie United Kingdom 39 2.8k 0.6× 2.8k 0.8× 88 0.0× 166 0.2× 542 0.8× 97 7.0k
Charles Ferguson Australia 45 5.5k 1.1× 3.3k 0.9× 517 0.2× 123 0.2× 299 0.5× 76 7.9k
Abigail Williams United Kingdom 59 5.5k 1.1× 867 0.2× 207 0.1× 40 0.1× 737 1.1× 147 13.3k

Countries citing papers authored by Richard E. Cheney

Since Specialization
Citations

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

Fields of papers citing papers by Richard E. Cheney

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Richard E. Cheney

This figure shows the co-authorship network connecting the top 25 collaborators of Richard E. Cheney. A scholar is included among the top collaborators of Richard E. Cheney 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 Richard E. Cheney. Richard E. Cheney 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.
Xu, Jing, Yize Li, Aidan McGinnis, et al.. (2026). Mitochondrial transfer from glia to neurons protects against peripheral neuropathy. Nature. 650(8103). 951–960.
2.
Dillard, Miriam E., Daniel P. Stewart, Yan Zhang, et al.. (2021). Cytoneme delivery of Sonic Hedgehog from ligand-producing cells requires Myosin 10 and a Dispatched-BOC/CDON co-receptor complex. eLife. 10. 46 indexed citations
3.
Hammers, David W., Michael K. Matheny, Ernest G. Heimsath, et al.. (2021). Filopodia powered by class x myosin promote fusion of mammalian myoblasts. eLife. 10. 9 indexed citations
4.
Bultema, Jarred J., et al.. (2014). Myosin Vc Interacts with Rab32 and Rab38 Proteins and Works in the Biogenesis and Secretion of Melanosomes. Journal of Biological Chemistry. 289(48). 33513–33528. 55 indexed citations
6.
Sidhu, Gurjit, Wei Li, Aparna B. Bohil, et al.. (2012). Myosin-X facilitatesShigella-induced membrane protrusions and cell-to-cell spread. Cellular Microbiology. 15(3). 353–367. 38 indexed citations
7.
Cheney, Richard E., et al.. (2010). Myosin X Regulates Sealing Zone Patterning in Osteoclasts through Linkage of Podosomes and Microtubules. Journal of Biological Chemistry. 285(13). 9506–9515. 49 indexed citations
8.
Marchelletta, Ronald R., Damon T. Jacobs, Joel Schechter, Richard E. Cheney, & Sarah F. Hamm‐Alvarez. (2008). The class V myosin motor, myosin 5c, localizes to mature secretory vesicles and facilitates exocytosis in lacrimal acini. American Journal of Physiology-Cell Physiology. 295(1). C13–C28. 27 indexed citations
9.
Pi, Xinchun, et al.. (2006). Abstract 817: Myo10 is a Sensor for Endothelial Migration Induced by BMP6 via Regulation of Filopodia. Circulation. 114(1). 233–4. 1 indexed citations
10.
Sousa, Aurea D., Jonathan S. Berg, Brian W. Robertson, Rick B. Meeker, & Richard E. Cheney. (2005). Myo10 in brain: developmental regulation, identification of a headless isoform and dynamics in neurons. Journal of Cell Science. 119(1). 184–194. 67 indexed citations
11.
Sousa, Aurea D. & Richard E. Cheney. (2005). Myosin-X: a molecular motor at the cell's fingertips. Trends in Cell Biology. 15(10). 533–539. 99 indexed citations
12.
Zhang, Hongquan, Jonathan S. Berg, Zhilun Li, et al.. (2004). Myosin-X provides a motor-based link between integrins and the cytoskeleton. Nature Cell Biology. 6(6). 523–531. 275 indexed citations
13.
Hales, Chadwick M., et al.. (2003). Dynamics of the Apical Plasma Membrane Recycling System During Cell Division. Traffic. 4(10). 681–693. 31 indexed citations
14.
Berg, Jonathan S. & Richard E. Cheney. (2002). Myosin-X is an unconventional myosin that undergoes intrafilopodial motility. Nature Cell Biology. 4(3). 246–250. 278 indexed citations
15.
Puthalakath, Hamsa, Andreas Villunger, Lorraine A. O’Reilly, et al.. (2001). Bmf: A Proapoptotic BH3-Only Protein Regulated by Interaction with the Myosin V Actin Motor Complex, Activated by Anoikis. Science. 293(5536). 1829–1832. 502 indexed citations breakdown →
16.
Kuhn, Deanna, Richard E. Cheney, & Michael Weinstock. (2000). The development of epistemological understanding. Cognitive Development. 15(3). 309–328. 520 indexed citations breakdown →
17.
Mehta, Amit, Ronald S. Rock, Matthias Rief, et al.. (1999). Myosin-V is a processive actin-based motor. Nature. 400(6744). 590–593. 631 indexed citations breakdown →
18.
Cheney, Richard E.. (1998). [1] Purification and assay of myosin V. Methods in enzymology on CD-ROM/Methods in enzymology. 298. 3–18. 51 indexed citations
19.
Luna, Elizabeth J., Kersi Pestonjamasp, Richard E. Cheney, et al.. (1997). Actin-binding membrane proteins identified by F-actin blot overlays.. PubMed. 52. 3–18. 18 indexed citations
20.
Schatten, Heide, Richard E. Cheney, Ron Balczon, et al.. (1986). Localization of fodrin during fertilization and early development of sea urchins and mice. Developmental Biology. 118(2). 457–466. 72 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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