Toni S. Pearson

2.7k total citations
39 papers, 909 citations indexed

About

Toni S. Pearson is a scholar working on Neurology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Toni S. Pearson has authored 39 papers receiving a total of 909 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Neurology, 13 papers in Molecular Biology and 12 papers in Clinical Biochemistry. Recurrent topics in Toni S. Pearson's work include Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (11 papers) and Cerebral Palsy and Movement Disorders (10 papers). Toni S. Pearson is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (11 papers) and Cerebral Palsy and Movement Disorders (10 papers). Toni S. Pearson collaborates with scholars based in United States, Greece and Canada. Toni S. Pearson's co-authors include Darryl C. De Vivo, Kristin Engelstad, Cigdem I. Akman, Veronica J. Hinton, Roser Pons, Roula Ghaoui, Carolyn M. Sue, Kathrin Jeltsch, Manju A. Kurian and Thomas Opladen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Toni S. Pearson

37 papers receiving 892 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toni S. Pearson United States 15 354 303 213 201 182 39 909
Pierre Castelnau France 16 61 0.2× 283 0.9× 79 0.4× 160 0.8× 94 0.5× 50 826
Rebecca C. Ahrens‐Nicklas United States 17 139 0.4× 406 1.3× 184 0.9× 86 0.4× 108 0.6× 68 744
Peter P. De Deyn Belgium 21 52 0.1× 480 1.6× 618 2.9× 163 0.8× 240 1.3× 36 1.7k
Cécilia Marelli France 18 74 0.2× 378 1.2× 85 0.4× 327 1.6× 56 0.3× 35 682
Anna Maio Italy 15 57 0.2× 198 0.7× 84 0.4× 185 0.9× 60 0.3× 45 621
Daisy Rinaldi France 13 74 0.2× 273 0.9× 116 0.5× 294 1.5× 25 0.1× 23 602
R. Marconi Italy 14 166 0.5× 652 2.2× 167 0.8× 660 3.3× 61 0.3× 16 1.5k
Luigia Atorino Italy 7 59 0.2× 598 2.0× 277 1.3× 320 1.6× 43 0.2× 8 1.4k
Lucie Guyant‐Maréchal France 15 20 0.1× 398 1.3× 289 1.4× 282 1.4× 107 0.6× 31 1.0k
Mikko Kärppä Finland 14 343 1.0× 651 2.1× 70 0.3× 133 0.7× 55 0.3× 38 951

Countries citing papers authored by Toni S. Pearson

Since Specialization
Citations

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

Fields of papers citing papers by Toni S. Pearson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Toni S. Pearson. 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 Toni S. Pearson. The network helps show where Toni S. Pearson may publish in the future.

Co-authorship network of co-authors of Toni S. Pearson

This figure shows the co-authorship network connecting the top 25 collaborators of Toni S. Pearson. A scholar is included among the top collaborators of Toni S. Pearson 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 Toni S. Pearson. Toni S. Pearson 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.
Pons, Roser, Toni S. Pearson, Belén Pérez‐Dueñas, et al.. (2025). Development and Preliminary Validation of a Parkinsonism‐Dystonia Scale for Infants and Young Children. Movement Disorders. 40(8). 1669–1679. 1 indexed citations
2.
Hübschmann, Oya Kuseyri, Roser Pons, Toni S. Pearson, et al.. (2025). Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase ( TH ) Deficiency. Journal of Inherited Metabolic Disease. 48(6). e70106–e70106.
3.
Pearson, Toni S., et al.. (2024). Caregiver descriptions of dystonia in cerebral palsy. Annals of Clinical and Translational Neurology. 11(2). 242–250. 1 indexed citations
4.
Abela, Lucia, Erica Tagliatti, Kimberley M. Reid, et al.. (2024). Neurodevelopmental and synaptic defects in DNAJC6 parkinsonism, amenable to gene therapy. Brain. 147(6). 2023–2037. 7 indexed citations
5.
Pearson, Toni S., et al.. (2023). Emerging Subspecialties: Pediatric Movement Disorders Neurology. Neurology. 102(2). e208050–e208050.
6.
Pearson, Toni S., et al.. (2023). Brain Region Size Differences Associated With Dystonia in People With Cerebral Palsy Born Premature. Pediatric Neurology. 148. 8–13. 1 indexed citations
7.
Roubertie, Agathe, Thomas Opladen, Heiko Brennenstuhl, et al.. (2023). Gene therapy for aromatic L‐amino acid decarboxylase deficiency: Requirements for safe application and knowledge‐generating follow‐up. Journal of Inherited Metabolic Disease. 47(3). 463–475. 10 indexed citations
8.
Aravamuthan, Bhooma R., et al.. (2023). Determinants of gait dystonia severity in cerebral palsy. Developmental Medicine & Child Neurology. 65(7). 968–977. 8 indexed citations
9.
Lee, Michelle M., Darryl C. De Vivo, Daniel Friedman, et al.. (2022). The clinical spectrum of SMA‐PME and in vitro normalization of its cellular ceramide profile. Annals of Clinical and Translational Neurology. 9(12). 1941–1952. 5 indexed citations
10.
MacPherson, Amanda, et al.. (2022). Quantifying Patient Investment in Novel Neurological Drug Development. Neurotherapeutics. 19(5). 1507–1513. 4 indexed citations
11.
Thompson, Kyle, Emanuele Bellacchio, Courtney E. French, et al.. (2021). Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease. Human Molecular Genetics. 31(4). 523–534. 13 indexed citations
12.
Abreu, Damien, Stephen Stone, Toni S. Pearson, et al.. (2021). A phase 1b/2a clinical trial of dantrolene sodium in patients with Wolfram syndrome. JCI Insight. 6(15). 26 indexed citations
13.
Kennedy, Adam D., Kirk L. Pappan, Taraka Donti, et al.. (2019). 2-Pyrrolidinone and Succinimide as Clinical Screening Biomarkers for GABA-Transaminase Deficiency: Anti-seizure Medications Impact Accurate Diagnosis. Frontiers in Neuroscience. 13. 1344–1344. 29 indexed citations
14.
Meijer, Inge A. & Toni S. Pearson. (2018). The Twists of Pediatric Dystonia: Phenomenology, Classification, and Genetics. Seminars in Pediatric Neurology. 25. 65–74. 11 indexed citations
15.
Wassenberg, Tessa, Marta Molero-Luís, Kathrin Jeltsch, et al.. (2017). Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency. Orphanet Journal of Rare Diseases. 12(1). 12–12. 156 indexed citations
16.
Opladen, Thomas, Elisenda Cortès‐Saladelafont, Mario Mastrangelo, et al.. (2016). The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders. Molecular Genetics and Metabolism Reports. 9. 61–66. 39 indexed citations
17.
Gigante, Paul R., Michael M. McDowell, Samuel S. Bruce, et al.. (2013). Reduction in upper-extremity tone after lumbar selective dorsal rhizotomy in children with spastic cerebral palsy. Journal of Neurosurgery Pediatrics. 12(6). 588–594. 20 indexed citations
18.
Pearson, Toni S., Cigdem I. Akman, Veronica J. Hinton, Kristin Engelstad, & Darryl C. De Vivo. (2013). Phenotypic Spectrum of Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS). Current Neurology and Neuroscience Reports. 13(4). 342–342. 155 indexed citations
19.
Pearson, Toni S., John W. Krakauer, & Pietro Mazzoni. (2010). Learning Not to Generalize: Modular Adaptation of Visuomotor Gain. Journal of Neurophysiology. 103(6). 2938–2952. 37 indexed citations
20.
Pearson, Toni S., Ayman Al‐Eyadhy, Salem Al‐Tamemi, et al.. (2008). An intronic mutation in DKC1 in an infant with Høyeraal–Hreidarsson syndrome. American Journal of Medical Genetics Part A. 146A(16). 2159–2161. 14 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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