Lewis A. Wheaton

3.5k total citations · 1 hit paper
58 papers, 2.6k citations indexed

About

Lewis A. Wheaton is a scholar working on Cognitive Neuroscience, Social Psychology and Biomedical Engineering. According to data from OpenAlex, Lewis A. Wheaton has authored 58 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Cognitive Neuroscience, 26 papers in Social Psychology and 23 papers in Biomedical Engineering. Recurrent topics in Lewis A. Wheaton's work include Motor Control and Adaptation (35 papers), Action Observation and Synchronization (26 papers) and Muscle activation and electromyography studies (23 papers). Lewis A. Wheaton is often cited by papers focused on Motor Control and Adaptation (35 papers), Action Observation and Synchronization (26 papers) and Muscle activation and electromyography studies (23 papers). Lewis A. Wheaton collaborates with scholars based in United States, Italy and Japan. Lewis A. Wheaton's co-authors include Mark Hallett, Guido Nolte, Sherry Vorbach, Ou Bai, Zoltán Mari, J. C. Mizelle, Esteban A. Fridman, Stephan Bohlhalter, Anna M. Borghi and Nikhilesh Natraj and has published in prestigious journals such as Nature Neuroscience, PLoS ONE and NeuroImage.

In The Last Decade

Lewis A. Wheaton

56 papers receiving 2.6k citations

Hit Papers

Identifying true brain interaction from EEG data using th... 2004 2026 2011 2018 2004 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
Lewis A. Wheaton United States 23 2.1k 653 325 276 264 58 2.6k
Chantal Delon‐Martin France 22 1.7k 0.8× 519 0.8× 379 1.2× 214 0.8× 306 1.2× 52 2.7k
Elizabeth A. Franz New Zealand 29 1.6k 0.8× 544 0.8× 293 0.9× 95 0.3× 228 0.9× 92 2.4k
Tamar R. Makin United Kingdom 31 2.1k 1.0× 840 1.3× 580 1.8× 385 1.4× 643 2.4× 74 3.4k
Kenji Kansaku Japan 25 1.7k 0.8× 319 0.5× 216 0.7× 468 1.7× 190 0.7× 66 2.1k
Alexandra Battaglia‐Mayer Italy 33 2.5k 1.2× 709 1.1× 336 1.0× 207 0.8× 322 1.2× 54 2.8k
Joseph F. X. DeSouza Canada 24 2.3k 1.1× 590 0.9× 138 0.4× 175 0.6× 238 0.9× 62 2.7k
Hiroki C. Tanabe Japan 27 1.9k 0.9× 653 1.0× 462 1.4× 207 0.8× 188 0.7× 81 3.2k
Ilka Immisch Germany 17 1.0k 0.5× 364 0.6× 155 0.5× 262 0.9× 272 1.0× 27 1.7k
Bettina Pollok Germany 32 2.0k 0.9× 286 0.4× 310 1.0× 501 1.8× 766 2.9× 83 2.7k

Countries citing papers authored by Lewis A. Wheaton

Since Specialization
Citations

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

Fields of papers citing papers by Lewis A. Wheaton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lewis A. Wheaton. 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 Lewis A. Wheaton. The network helps show where Lewis A. Wheaton may publish in the future.

Co-authorship network of co-authors of Lewis A. Wheaton

This figure shows the co-authorship network connecting the top 25 collaborators of Lewis A. Wheaton. A scholar is included among the top collaborators of Lewis A. Wheaton 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 Lewis A. Wheaton. Lewis A. Wheaton 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.
2.
Hammond, Frank L., et al.. (2022). Alpha-band activity in parietofrontal cortex predicts future availability of vibrotactile feedback in prosthesis use. Experimental Brain Research. 240(5). 1387–1398. 1 indexed citations
3.
Natraj, Nikhilesh, et al.. (2021). Flexible constraint hierarchy during the visual encoding of tool‐object interactions. European Journal of Neuroscience. 54(7). 6520–6532. 1 indexed citations
4.
Wheaton, Lewis A.. (2021). Racial equity and inclusion still lacking in neuroscience meetings. Nature Neuroscience. 24(12). 1645–1647. 6 indexed citations
5.
Mitchell, Sarah, et al.. (2019). Implicit development of gaze strategies support motor improvements during action encoding training of prosthesis use. Neuropsychologia. 127. 75–83. 6 indexed citations
6.
Natraj, Nikhilesh, et al.. (2018). The Role of Attention and Saccades on Parietofrontal Encoding of Contextual and Grasp-specific Affordances of Tools: An ERP Study. Neuroscience. 394. 243–266. 8 indexed citations
7.
Wheaton, Lewis A., et al.. (2017). Novel behavioral indicator of explicit awareness reveals temporal course of frontoparietal neural network facilitation during motor learning. PLoS ONE. 12(4). e0175176–e0175176. 3 indexed citations
8.
Mizelle, J. C., et al.. (2016). Remodeling of cortical activity for motor control following upper limb loss. Clinical Neurophysiology. 127(9). 3128–3134. 14 indexed citations
9.
Borich, Michael R., Lewis A. Wheaton, Sonia M. Brodie, Bimal Lakhani, & Lara A. Boyd. (2016). Evaluating interhemispheric cortical responses to transcranial magnetic stimulation in chronic stroke: A TMS-EEG investigation. Neuroscience Letters. 618. 25–30. 49 indexed citations
10.
Mizelle, J. C., et al.. (2015). Reliability of Visual and Somatosensory Feedback in Skilled Movement: The Role of the Cerebellum. Brain Topography. 29(1). 27–41. 12 indexed citations
11.
Natraj, Nikhilesh, et al.. (2015). The visual encoding of tool–object affordances. Neuroscience. 310. 512–527. 22 indexed citations
12.
Patterson, Rebecca, et al.. (2014). Motor performance benefits of matched limb imitation in prosthesis users. Experimental Brain Research. 232(7). 2143–2154. 13 indexed citations
13.
Wheaton, Lewis A., et al.. (2012). Neural activation differences in amputees during imitation of intact versus amputee movements. Frontiers in Human Neuroscience. 6. 182–182. 17 indexed citations
14.
Natraj, Nikhilesh, Victoria N. Poole, J. C. Mizelle, et al.. (2012). Context and hand posture modulate the neural dynamics of tool–object perception. Neuropsychologia. 51(3). 506–519. 32 indexed citations
15.
Mizelle, J. C., Larry W. Forrester, Mark Hallett, & Lewis A. Wheaton. (2010). Electroencephalographic reactivity to unimodal and bimodal visual and proprioceptive demands in sensorimotor integration. Experimental Brain Research. 203(4). 659–670. 14 indexed citations
16.
Fridman, Esteban A., M. Crespo, Mirta F. Villarreal, et al.. (2009). Kinematic improvement following Botulinum Toxin-A injection in upper-limb spasticity due to stroke. Journal of Neurology Neurosurgery & Psychiatry. 81(4). 423–427. 5 indexed citations
17.
Wheaton, Lewis A., Esteban A. Fridman, Stephan Bohlhalter, Sherry Vorbach, & Mark Hallett. (2009). Left parietal activation related to planning, executing and suppressing praxis hand movements. Clinical Neurophysiology. 120(5). 980–986. 42 indexed citations
18.
Buxbaum, Laurel J., Kathleen Y. Haaland, Mark Hallett, et al.. (2008). Treatment of Limb Apraxia. American Journal of Physical Medicine & Rehabilitation. 87(2). 149–161. 63 indexed citations
19.
Wheaton, Lewis A., Guido Nolte, Stephan Bohlhalter, Esteban A. Fridman, & Mark Hallett. (2005). Synchronization of parietal and premotor areas during preparation and execution of praxis hand movements. Clinical Neurophysiology. 116(6). 1382–1390. 66 indexed citations
20.
Nolte, Guido, Ou Bai, Lewis A. Wheaton, et al.. (2004). Identifying true brain interaction from EEG data using the imaginary part of coherency. Clinical Neurophysiology. 115(10). 2292–2307. 1248 indexed citations breakdown →

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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