Aaron Woodall
Assistant Professor
Also affiliated: Arkansas Children's Hospital (2019–2021); The Bronx Defenders (2012)
Faculty Researcher
CHP | Physician Assistant Studies
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Aaron Woodall's research focuses on rare genetic disorders affecting neuromuscular function. His work includes investigating the genetic underpinnings of congenital myasthenic syndromes, a group of inherited disorders that impair neuromuscular transmission. In 2021, he co-authored a publication identifying a novel mutation in the CHAT gene associated with this condition. Woodall's research network includes collaborators at the University of Arkansas for Medical Sciences, with whom he has co-authored publications. His current scholarly metrics indicate a h-index of 1 across 5 total publications with 3 citations.
Metrics
- h-index: 1
- Publications: 5
- Citations: 3
Selected Publications
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Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene (2021)
Collaboration Network
Top Collaborators
- Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene
- Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene
- Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene
- Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene
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