Douglas M. Swank

1.7k total citations
58 papers, 1.4k citations indexed

About

Douglas M. Swank is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Douglas M. Swank has authored 58 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cardiology and Cardiovascular Medicine, 42 papers in Molecular Biology and 12 papers in Biomedical Engineering. Recurrent topics in Douglas M. Swank's work include Cardiomyopathy and Myosin Studies (46 papers), Muscle Physiology and Disorders (40 papers) and Cardiovascular Effects of Exercise (17 papers). Douglas M. Swank is often cited by papers focused on Cardiomyopathy and Myosin Studies (46 papers), Muscle Physiology and Disorders (40 papers) and Cardiovascular Effects of Exercise (17 papers). Douglas M. Swank collaborates with scholars based in United States, United Kingdom and Czechia. Douglas M. Swank's co-authors include Lawrence C. Rome, Sanford I. Bernstein, David W. Maughan, William A. Kronert, Aileen F. Knowles, Vivek K. Vishnudas, David J. Coughlin, Guixin Zhang, L. Wells and Seemanti Ramanath and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Douglas M. Swank

57 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Douglas M. Swank United States 22 709 685 331 251 191 58 1.4k
Douglas A. Syme Canada 20 248 0.3× 238 0.3× 465 1.4× 182 0.7× 330 1.7× 49 1.3k
H.A. Akster Netherlands 12 327 0.5× 133 0.2× 286 0.9× 108 0.4× 157 0.8× 23 738
Arian S. Forouhar United States 8 956 1.3× 455 0.7× 90 0.3× 16 0.1× 53 0.3× 10 1.5k
Kan Kobayashi Japan 32 750 1.1× 43 0.1× 558 1.7× 459 1.8× 86 0.5× 156 2.8k
Timothy G. West United Kingdom 20 259 0.4× 201 0.3× 555 1.7× 18 0.1× 209 1.1× 38 1.2k
Everett Bandman United States 30 1.6k 2.3× 786 1.1× 143 0.4× 32 0.1× 12 0.1× 66 2.2k
Darrell R. Stokes United States 15 145 0.2× 181 0.3× 135 0.4× 132 0.5× 27 0.1× 27 736
Silke Berger Australia 25 1.0k 1.5× 138 0.2× 272 0.8× 9 0.0× 83 0.4× 36 1.7k
David J. Coughlin United States 23 220 0.3× 105 0.2× 605 1.8× 246 1.0× 492 2.6× 53 1.1k
Krzysztof Jagla France 28 1.9k 2.6× 143 0.2× 136 0.4× 18 0.1× 59 0.3× 75 2.4k

Countries citing papers authored by Douglas M. Swank

Since Specialization
Citations

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

Fields of papers citing papers by Douglas M. Swank

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Douglas M. Swank

This figure shows the co-authorship network connecting the top 25 collaborators of Douglas M. Swank. A scholar is included among the top collaborators of Douglas M. Swank 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 Douglas M. Swank. Douglas M. Swank 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.
Huang, Alice H., et al.. (2021). Prolonged myosin binding increases muscle stiffness in Drosophila models of Freeman-Sheldon syndrome. Biophysical Journal. 120(5). 844–854. 1 indexed citations
3.
Viswanathan, Meera, William M. Schmidt, Peter Franz, et al.. (2020). A role for actin flexibility in thin filament-mediated contractile regulation and myopathy. Nature Communications. 11(1). 2417–2417. 19 indexed citations
4.
Palmer, Bradley M., Douglas M. Swank, Mark S. Miller, et al.. (2020). Enhancing diastolic function by strain-dependent detachment of cardiac myosin crossbridges. The Journal of General Physiology. 152(4). 3 indexed citations
5.
Guo, Yiming, William A. Kronert, Alice H. Huang, et al.. (2020). Drosophila myosin mutants model the disparate severity of type 1 and type 2B distal arthrogryposis and indicate an enhanced actin affinity mechanism. Skeletal Muscle. 10(1). 24–24. 4 indexed citations
6.
Kronert, William A., et al.. (2019). The R249Q hypertrophic cardiomyopathy myosin mutation decreases contractility in Drosophila by impeding force production. The Journal of Physiology. 597(9). 2403–2420. 9 indexed citations
7.
Straight, Chad R., et al.. (2019). A myosin-based mechanism for stretch activation and its possible role revealed by varying phosphate concentration in fast and slow mouse skeletal muscle fibers. American Journal of Physiology-Cell Physiology. 317(6). C1143–C1152. 12 indexed citations
8.
Kronert, William A., Meera Viswanathan, Girish C. Melkani, et al.. (2018). Prolonged cross-bridge binding triggers muscle dysfunction in a Drosophila model of myosin-based hypertrophic cardiomyopathy. eLife. 7. 23 indexed citations
9.
Glasheen, Bernadette M., et al.. (2018). Five Alternative Myosin Converter Domains Influence Muscle Power, Stretch Activation, and Kinetics. Biophysical Journal. 114(5). 1142–1152. 8 indexed citations
10.
Trujillo, Adriana S., Girish C. Melkani, Gerrie P. Farman, et al.. (2016). A Restrictive Cardiomyopathy Mutation in an Invariant Proline at the Myosin Head/Rod Junction Enhances Head Flexibility and Function, Yielding Muscle Defects in Drosophila. Journal of Molecular Biology. 428(11). 2446–2461. 9 indexed citations
11.
Koppes, Ryan A., Douglas M. Swank, & David T. Corr. (2014). A new experimental model to study force depression: theDrosophilajump muscle. Journal of Applied Physiology. 116(12). 1543–1550. 4 indexed citations
12.
Wang, Qian, Cuiping Zhao, & Douglas M. Swank. (2011). Calcium and Stretch Activation Modulate Power Generation in Drosophila Flight Muscle. Biophysical Journal. 101(9). 2207–2213. 23 indexed citations
13.
Ramanath, Seemanti, Qian Wang, Sanford I. Bernstein, & Douglas M. Swank. (2011). Disrupting the Myosin Converter-Relay Interface Impairs Drosophila Indirect Flight Muscle Performance. Biophysical Journal. 101(5). 1114–1122. 22 indexed citations
14.
Clark, Kathleen A., et al.. (2011). Deletion of Drosophila muscle LIM protein decreases flight muscle stiffness and power generation. American Journal of Physiology-Cell Physiology. 301(2). C373–C382. 7 indexed citations
15.
Simeonov, Dimitre R., et al.. (2010). The Mechanical Properties of Drosophila Jump Muscle Expressing Wild-Type and Embryonic Myosin Isoforms. Biophysical Journal. 98(7). 1218–1226. 20 indexed citations
16.
Purcell, Thomas J., Nariman Naber, Alexander R. Dunn, et al.. (2010). Nucleotide Pocket Thermodynamics Measured by EPR Reveal How Energy Partitioning Relates Myosin Speed to Efficiency. Journal of Molecular Biology. 407(1). 79–91. 18 indexed citations
17.
Koppes, Ryan A., Nathan R. Schiele, Douglas M. Swank, Douglas B. Chrisey, & David T. Corr. (2009). Passive Mechanical Analysis of Engineered Myotube Fibers. 1155–1156. 1 indexed citations
18.
Miller, Mark S., Douglas M. Swank, Hongjun Liu, et al.. (2006). Passive Stiffness in Drosophila Indirect Flight Muscle Reduced by Disrupting Paramyosin Phosphorylation, but Not by Embryonic Myosin S2 Hinge Substitution. Biophysical Journal. 91(12). 4500–4506. 14 indexed citations
19.
Swank, Douglas M., William A. Kronert, Sanford I. Bernstein, & David W. Maughan. (2004). Alternative N-Terminal Regions of Drosophila Myosin Heavy Chain Tune Muscle Kinetics for Optimal Power Output. Biophysical Journal. 87(3). 1805–1814. 41 indexed citations
20.
Swank, Douglas M., et al.. (2003). Variable N-terminal Regions of Muscle Myosin Heavy Chain Modulate ATPase Rate and Actin Sliding Velocity. Journal of Biological Chemistry. 278(19). 17475–17482. 26 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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