Camilo Toro

1.6k total citations
17 papers, 898 citations indexed

About

Camilo Toro is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Neurology. According to data from OpenAlex, Camilo Toro has authored 17 papers receiving a total of 898 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 6 papers in Cognitive Neuroscience and 6 papers in Neurology. Recurrent topics in Camilo Toro's work include Hereditary Neurological Disorders (6 papers), EEG and Brain-Computer Interfaces (4 papers) and Motor Control and Adaptation (3 papers). Camilo Toro is often cited by papers focused on Hereditary Neurological Disorders (6 papers), EEG and Brain-Computer Interfaces (4 papers) and Motor Control and Adaptation (3 papers). Camilo Toro collaborates with scholars based in United States, France and Italy. Camilo Toro's co-authors include Mark Hallett, Letizia Leocani, Ping Zhuang, Paolo Manganotti, Christian Gerloff, Hideto Katsuta, Norihiro Sadato, Thomas A. Zeffiro, A. Pascual–Leone and Eric M. Wassermann and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Camilo Toro

15 papers receiving 879 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Camilo Toro United States 12 612 280 191 162 102 17 898
K. Matsunami Japan 16 443 0.7× 290 1.0× 208 1.1× 181 1.1× 70 0.7× 30 849
Ana Pekanovic Switzerland 6 326 0.5× 208 0.7× 279 1.5× 78 0.5× 135 1.3× 8 678
Robert N. Holdefer United States 17 427 0.7× 214 0.8× 275 1.4× 173 1.1× 114 1.1× 34 897
Jean-Alban Rathelot United States 7 657 1.1× 271 1.0× 200 1.0× 289 1.8× 86 0.8× 9 915
Katiuska Molina-Luna Germany 8 299 0.5× 197 0.7× 258 1.4× 78 0.5× 109 1.1× 8 537
Steve G. Massaquoi United States 9 262 0.4× 224 0.8× 168 0.9× 82 0.5× 93 0.9× 12 582
Laurentiu S. Popa United States 18 516 0.8× 467 1.7× 280 1.5× 50 0.3× 87 0.9× 25 868
Riccardo Zucca Spain 13 400 0.7× 233 0.8× 171 0.9× 44 0.3× 104 1.0× 35 738
Javier J. González-Rosa Spain 21 546 0.9× 374 1.3× 146 0.8× 117 0.7× 157 1.5× 55 1.0k
Stephan Quessy Canada 15 535 0.9× 216 0.8× 141 0.7× 110 0.7× 52 0.5× 23 848

Countries citing papers authored by Camilo Toro

Since Specialization
Citations

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

Fields of papers citing papers by Camilo Toro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Camilo Toro. 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 Camilo Toro. The network helps show where Camilo Toro may publish in the future.

Co-authorship network of co-authors of Camilo Toro

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

All Works

17 of 17 papers shown
1.
Monfrini, Edoardo, Paola Rinchetti, Mathieu Anheim, et al.. (2025). RRP12 Variants Are Associated With Autosomal Recessive Brain Calcifications. Movement Disorders. 40(12). 2792–2803.
2.
Ramachandran, Prashanth, Bryan Smith, Greer Waldrop, et al.. (2024). Fanconi Anemia Associated Neurological Syndrome – Phenotyping and Immune Profiling of a Novel Condition (P8-4.004). Neurology. 102(7_supplement_1).
3.
Mo, Alisa, Afshin Saffari, Catherine Jordan, et al.. (2022). Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST. Movement Disorders. 37(12). 2440–2446. 6 indexed citations
4.
Fazal, Sarah, Matt C. Danzi, André B. P. Kuilenburg, et al.. (2022). Repeat expansions nested within tandem CNVs: a unique structural change in GLS exemplifies the diagnostic challenges of non-coding pathogenic variation. Human Molecular Genetics. 32(1). 46–54. 2 indexed citations
5.
Mazza, Davide, Franca Codazzi, Tyler Mark Pierson, et al.. (2019). Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation. Journal of Medical Genetics. 56(8). 499–511. 19 indexed citations
6.
Pascual, Belén, Susanne T. de Bot, Marcondes C. França, et al.. (2019). “Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia. American Journal of Neuroradiology. 40(1). 199–203. 39 indexed citations
7.
Valkanas, Elise, Katherine E. Schaffer, Christopher Dunham, et al.. (2016). Phenotypic evolution of UNC80 loss of function. American Journal of Medical Genetics Part A. 170(12). 3106–3114. 14 indexed citations
8.
Masdeu, Joseph C., Belén Pascual, Marcondes C. França, et al.. (2015). Sensitivity and Specificity of the “Ears of the Lynx” MRI Sign in Spastic Paraparesis with SPG Mutations (P2.038). Neurology. 84(14_supplement). 2 indexed citations
9.
Sambuughin, Nyamkhishig, Lev G. Goldfarb, Anna Sundborger, et al.. (2015). Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2. BMC Neurology. 15(1). 223–223. 38 indexed citations
10.
Wu, Yvonne W., Christopher P. Hess, Nilika S. Singhal, Catherine Groden, & Camilo Toro. (2013). Idiopathic Basal Ganglia Calcifications: An Atypical Presentation of PKAN. Pediatric Neurology. 49(5). 351–354. 18 indexed citations
11.
Manganotti, Paolo, Christian Gerloff, Camilo Toro, et al.. (1998). Task-related coherence and task-related spectral power changes during sequential finger movements. Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control. 109(1). 50–62. 199 indexed citations
12.
Gerloff, Christian, et al.. (1997). Steady-state movement-related cortical potentials: a new approach to assessing cortical activity associated with fast repetitive finger movements. Electroencephalography and Clinical Neurophysiology. 102(2). 106–113. 57 indexed citations
13.
Leocani, Letizia, Camilo Toro, Paolo Manganotti, Ping Zhuang, & Mark Hallett. (1997). Event-related coherence and event-related desynchronization/synchronization in the 10 Hz and 20 Hz EEG during self-paced movements. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section. 104(3). 199–206. 268 indexed citations
14.
Deuschl, Günther, Camilo Toro, Thomas A. Zeffiro, S. Massaquoi, & Mark Hallett. (1996). Adaptation motor learning of arm movements in patients with cerebellar disease.. Journal of Neurology Neurosurgery & Psychiatry. 60(5). 515–519. 57 indexed citations
15.
Toro, Camilo, et al.. (1994). Cortical magnetic and electric fields associated with voluntary finger movements. Brain Topography. 6(3). 175–183. 40 indexed citations
16.
Toro, Camilo, et al.. (1994). Head surface digitization and registration: A method for mapping positions on the head onto magnetic resonance images. Brain Topography. 6(3). 185–192. 32 indexed citations
17.
Wassermann, Eric M., et al.. (1993). Topography of the inhibitory and excitatory responses to transcranial magnetic stimulation in a hand muscle. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section. 89(6). 424–433. 107 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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