Toni S. Pearson
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
72
Citations
2,835
Est. group size
—
Recurring co-author estimate
Active years
25
Publishing since 2001
Toni S. Pearson's research focuses on movement disorders in children, especially dystonia and parkinsonism related to cerebral palsy and rare inherited metabolic and neurodevelopmental conditions. This work combines clinical characterization, assessment tool development, and evaluation of emerging treatments including gene therapy for rare genetic disorders. The research is clinically oriented, often involving collaborative, multi-institutional studies and consensus guidelines.
Publication output has fluctuated over the past decade with a peak around 2020, followed by a somewhat slower but steady pace in recent years, averaging about 4 publications per year over the last five years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase ( <scp>TH</scp> ) Deficiency
Journal of Inherited Metabolic Disease · 2025
- Tasks for Assessing Dystonia in Young People With Cerebral Palsy
Pediatric Neurology · 2025
- Development and Preliminary Validation of a Parkinsonism‐Dystonia Scale for Infants and Young Children
Movement Disorders · 2025
- Tasks for assessing dystonia in young people with cerebral palsy
medRxiv · 2025
- IMPROVING FELLOW CONTINUITY CLINIC IN THE SETTING OF MULTIPLE SUBSPECIALTY CLINICS: RESULTS OF A QUALITY IMPROVEMENT INITIATIVE
Academic Pediatrics · 2025
- Neurodevelopmental and synaptic defects in <i>DNAJC6</i> parkinsonism, amenable to gene therapy
Brain · 2024
- Selective Serotonin Reuptake Inhibitor Treatment Post Gene Therapy for an Ultrarare Neurometabolic Disorder (AADC Deficiency)
Journal of the American Academy of Child & Adolescent Psychiatry · 2024
- Caregiver descriptions of dystonia in cerebral palsy
Annals of Clinical and Translational Neurology · 2024
- Gene therapy for aromatic L‐amino acid decarboxylase deficiency: Requirements for safe application and knowledge‐generating follow‐up
Journal of Inherited Metabolic Disease · 2023
- Determinants of gait dystonia severity in cerebral palsy
Developmental Medicine & Child Neurology · 2023
- Under‐recognition of leg dystonia in people with cerebral palsy
Annals of the Child Neurology Society · 2023
- Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder
Genetics in Medicine · 2023
- Upper Extremity Dystonia Features in People With Spastic Cerebral Palsy
Neurology Clinical Practice · 2023
- Emerging Subspecialties: Pediatric Movement Disorders Neurology
Neurology · 2023
- Brain Region Size Differences Associated With Dystonia in People With Cerebral Palsy Born Premature
Pediatric Neurology · 2023
- Neurology×6
- Journal of Inherited Metabolic Disease×4
- medRxiv×4
- Figshare×4
- Orphanet Journal of Rare Diseases×3
- H. Schmidt
Biochemistry, Genetics and Molecular Biology · Indiana University
- Melissa Lah
Biochemistry, Genetics and Molecular Biology · Indiana University
- Beth Heuer
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Miller Ll
Biochemistry, Genetics and Molecular Biology · Indiana University
- Paul M. Coates
Biochemistry, Genetics and Molecular Biology · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
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