Match tier Likely match
Presence Current · Arkansas
Last published 2025
Sources OpenAlex · ORCID
Refreshed 2026-08-08

Hannah Barkley

This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.

Researcher

Graduate Student Researcher

2 pubs

  • Porphobilinogen Synthase
  • Muscle Hypotonia
  • Porphyrias
  • Humans
  • Infant, Newborn
  • Male
  • Mutation, Missense

Biography and Research Information

OverviewAI-generated summary

Hannah Barkley's research has focused on medical case studies and health sciences education. She has co-authored publications addressing profound hypotonia in infants with δ-aminolevulinic acid dehydratase deficient porphyria. Barkley has also contributed to research on quality improvement training within pediatric residency programs and the implementation of evaluation systems in a single institution.

Her scholarly work includes two publications, with her most recent appearing in 2025. Barkley collaborates with researchers at the University of Arkansas for Medical Sciences, including Carissa Rodriquez, Abhay A. Shukla, T. Burrow, and Alexis N. Roach, with whom she shares three co-authored publications.

Metrics

  • Publications: 2

Selected Publications

  • Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program (2025)
    Academic Pediatrics DOI OpenAlex
  • Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria (2025)
    European Journal of Human Genetics DOI OpenAlex
  • Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria (2024)
    European Journal of Human Genetics 2 citations DOI OpenAlex
  • 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations (2024)

View all publications on OpenAlex →

Collaboration Network

14 Collaborators 3 Institutions 1 Country

Top Collaborators

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