Edna C. Hardeman

11.0k total citations · 2 hit papers
144 papers, 8.4k citations indexed

About

Edna C. Hardeman is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Edna C. Hardeman has authored 144 papers receiving a total of 8.4k indexed citations (citations by other indexed papers that have themselves been cited), including 108 papers in Molecular Biology, 72 papers in Cardiology and Cardiovascular Medicine and 50 papers in Cell Biology. Recurrent topics in Edna C. Hardeman's work include Cardiomyopathy and Myosin Studies (70 papers), Muscle Physiology and Disorders (69 papers) and Cellular Mechanics and Interactions (38 papers). Edna C. Hardeman is often cited by papers focused on Cardiomyopathy and Myosin Studies (70 papers), Muscle Physiology and Disorders (69 papers) and Cellular Mechanics and Interactions (38 papers). Edna C. Hardeman collaborates with scholars based in Australia, United States and United Kingdom. Edna C. Hardeman's co-authors include Peter W. Gunning, Anthony J. Kee, Geraldine M. O’Neill, Helen M. Blau, Galina Schevzov, Choy‐Pik Chiu, Jürgen Götz, Janet van Eersel, Matthias Staufenbiel and Billy Chieng and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Edna C. Hardeman

141 papers receiving 8.3k citations

Hit Papers

Dendritic Function of Tau Mediate... 1985 2026 1998 2012 2010 1985 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edna C. Hardeman Australia 45 5.3k 2.2k 2.0k 1.8k 1.3k 144 8.4k
Alexander Pfeifer Germany 60 6.8k 1.3× 1.4k 0.6× 826 0.4× 2.5k 1.4× 1.7k 1.4× 187 11.5k
Kristine E. Kamm United States 53 4.7k 0.9× 2.6k 1.2× 1.5k 0.8× 1.6k 0.9× 674 0.5× 112 7.7k
Robert Feil Germany 57 6.0k 1.1× 2.1k 1.0× 602 0.3× 2.5k 1.4× 1.7k 1.4× 160 10.6k
Kazushi Kimura Japan 28 5.3k 1.0× 734 0.3× 3.0k 1.5× 1.4k 0.8× 1.1k 0.9× 46 8.6k
Kazuki Nakao Japan 58 9.6k 1.8× 1.2k 0.6× 2.0k 1.0× 1.2k 0.7× 2.3k 1.9× 221 15.7k
Barbara E. Ehrlich United States 54 7.6k 1.4× 1.2k 0.5× 1.7k 0.9× 864 0.5× 2.8k 2.2× 177 11.2k
Bé Wieringa Netherlands 55 9.3k 1.8× 1.4k 0.6× 1.7k 0.8× 1.1k 0.6× 4.9k 3.9× 193 12.6k
Vincenzo Sorrentino Italy 53 6.7k 1.3× 2.5k 1.1× 754 0.4× 784 0.4× 1.9k 1.5× 203 9.1k
Toshimasa Ishizaki Japan 44 9.6k 1.8× 1.1k 0.5× 7.3k 3.7× 1.6k 0.9× 1.7k 1.4× 76 15.4k
Mutsuki Amano Japan 52 11.4k 2.2× 1.5k 0.7× 6.7k 3.4× 2.4k 1.3× 2.6k 2.1× 100 17.1k

Countries citing papers authored by Edna C. Hardeman

Since Specialization
Citations

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

Fields of papers citing papers by Edna C. Hardeman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edna C. Hardeman. 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 Edna C. Hardeman. The network helps show where Edna C. Hardeman may publish in the future.

Co-authorship network of co-authors of Edna C. Hardeman

This figure shows the co-authorship network connecting the top 25 collaborators of Edna C. Hardeman. A scholar is included among the top collaborators of Edna C. Hardeman 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 Edna C. Hardeman. Edna C. Hardeman 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, Tong, Miriam Teeuwssen, Wenjie Sun, et al.. (2024). Tropomyosin1 isoforms underlie epithelial to mesenchymal plasticity, metastatic dissemination, and resistance to chemotherapy in high-grade serous ovarian cancer. Cell Death and Differentiation. 31(3). 360–377. 5 indexed citations
2.
Masedunskas, Andrius, Muhibullah S. Tora, Seham Ebrahim, et al.. (2024). Coordination of force-generating actin-based modules stabilizes and remodels membranes in vivo. The Journal of Cell Biology. 223(11).
3.
Wang, Yao, Jeffrey H. Stear, Xing Xu, et al.. (2020). Drug Targeting the Actin Cytoskeleton Potentiates the Cytotoxicity of Low Dose Vincristine by Abrogating Actin-Mediated Repair of Spindle Defects. Molecular Cancer Research. 18(7). 1074–1087. 13 indexed citations
4.
Hardeman, Edna C., Nicole S. Bryce, & Peter W. Gunning. (2019). Impact of the actin cytoskeleton on cell development and function mediated via tropomyosin isoforms. Seminars in Cell and Developmental Biology. 102. 122–131. 25 indexed citations
5.
Meiring, Joyce C. M., Nicole S. Bryce, Yao Wang, et al.. (2018). Co-polymers of Actin and Tropomyosin Account for a Major Fraction of the Human Actin Cytoskeleton. Current Biology. 28(14). 2331–2337.e5. 47 indexed citations
6.
Currier, Mark A., Justine Stehn, Duo Chen, et al.. (2017). Identification of Cancer-Targeted Tropomyosin Inhibitors and Their Synergy with Microtubule Drugs. Molecular Cancer Therapeutics. 16(8). 1555–1565. 36 indexed citations
7.
Gunning, Peter W. & Edna C. Hardeman. (2017). Tropomyosins. Current Biology. 27(1). R8–R13. 20 indexed citations
8.
Carmona-Mora, Paulina, Jocelyn Widagdo, Florence Tomasetig, et al.. (2015). The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation. Human Genetics. 134(10). 1099–1115. 15 indexed citations
9.
Head, Stewart I., et al.. (2014). Properties of regenerated mouse extensor digitorum longus muscle following notexin injury. Experimental Physiology. 99(4). 664–674. 14 indexed citations
10.
Anderson, Judy E., Josephine E. Joya, Stewart I. Head, et al.. (2013). Aged skeletal muscle retains the ability to fully regenerate functional architecture. PubMed. 3(2). 25–37. 47 indexed citations
11.
Curthoys, Nikki M., Andrea R. Connor, Melissa Desouza, et al.. (2013). Tropomyosins induce neuritogenesis and determine neurite branching patterns in B35 neuroblastoma cells. Molecular and Cellular Neuroscience. 58. 11–21. 29 indexed citations
12.
Howard, Monique, Stephen J. Palmer, Matthew W. Spitzer, et al.. (2011). Mutation of Gtf2ird1 from the Williams–Beuren syndrome critical region results in facial dysplasia, motor dysfunction, and altered vocalisations. Neurobiology of Disease. 45(3). 913–922. 25 indexed citations
13.
Nguyen, Mai-Anh, Josephine E. Joya, Anthony J. Kee, et al.. (2011). Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy. Brain. 134(12). 3516–3529. 51 indexed citations
14.
Kee, Anthony J., Peter W. Gunning, & Edna C. Hardeman. (2009). Diverse roles of the actin cytoskeleton in striated muscle. Journal of Muscle Research and Cell Motility. 30(5-6). 187–197. 46 indexed citations
15.
MacArthur, Daniel G., Nan Yang, Jane T. Seto, et al.. (2006). A gene for speed: the ACTN3 R577X polymorphism influences muscle performance. Neuromuscular Disorders. 16. 1 indexed citations
16.
Corbett, Mark, P. Anthony Akkari, Ana Domazetovska, et al.. (2004). An αtropomyosin mutation alters dimer preference in nemaline myopathy. Annals of Neurology. 57(1). 42–49. 44 indexed citations
17.
Nair‐Shalliker, Visalini, et al.. (2004). Myofiber adaptational response to exercise in a mouse model of nemaline myopathy. Muscle & Nerve. 30(4). 470–480. 19 indexed citations
18.
Hardeman, Edna C., et al.. (2002). Atrichia with papular lesions resulting from compound heterozygous mutations in the hairless gene: A lesson for differential diagnosis of alopecia universalis. Journal of the American Academy of Dermatology. 47(4). 519–523. 25 indexed citations
19.
Ilkovski, Biljana, Sandra T. Cooper, Kristen L. Nowak, et al.. (2001). Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene. The American Journal of Human Genetics. 68(6). 1333–1343. 119 indexed citations
20.
Gunning, Peter W., Edna C. Hardeman, Robert Wade, et al.. (1987). Differential Patterns of Transcript Accumulation during Human Myogenesis. Molecular and Cellular Biology. 7(11). 4100–4114. 34 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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