Jeffrey Clothier Institution-verified
Sourced from institutional research profiles (UAMS TRI or ARA).
Researcher
faculty
Research Areas
Biography and Research Information
OverviewAI-generated summary
Jeffrey Clothier's research focuses on the genetic underpinnings of neurodevelopmental disorders, particularly autism spectrum disorder and intellectual disability. He has investigated molecular dysregulation in these conditions and identified candidate genes, such as DCAF1, through advanced sequencing and methylation analysis techniques. His work also extends to the implementation of pharmacogenomics testing within clinical settings, as demonstrated by his experience at Arkansas Children’s Hospital. Clothier has published 18 papers, accumulating 246 citations, and maintains a collegial network with researchers at the University of Arkansas for Medical Sciences, including Pritmohinder S. Gill and Jeffery L. Clothier, with whom he has co-authored multiple publications. His current scholarly activity indicates ongoing engagement in his research areas.
Metrics
- h-index: 6
- Publications: 19
- Citations: 247
Selected Publications
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165. Bridging Genetics and Psychiatry: ARID1B Haploinsufficiency in Autism Spectrum Disorder and Its Implications for C-L Psychiatry (2025)
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Lessons from an MD PhD – From SLC13A5 to Neurology (2023)
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Successful Treatment with High-Dose Immunoglobulin of a Complicated Patient with Catatonia and Central Nervous System Autoantibodies (2023)
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Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report (2022)
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Molecular Dysregulation in Autism Spectrum Disorder (2021)
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Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children’s Hospital (2021)
Grants & Funding
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