Match tier Likely match
Presence Current · Arkansas
Last published 2024
Sources OpenAlex · ORCID
Refreshed 2026-08-08

John Dehnel

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

Unknown Researcher

1 h-index 4 pubs 23 cited

  • Eye Diseases
  • Genetic Testing
  • Humans
  • Phenotype
  • Retrospective Studies

Biography and Research Information

OverviewAI-generated summary

John Dehnel's research focuses on genetic factors contributing to eye diseases. His recent publication, "Intrafamilial Phenotypic Variability in PRPH2-Related Retinopathy," published in 2024, investigates how genetic mutations in the PRPH2 gene can manifest differently within the same family. This work contributes to understanding the complex relationship between genotype and phenotype in inherited retinal disorders. Dehnel collaborates with researchers at the University of Arkansas for Medical Sciences, including Sami H. Uwaydat, Anna B. Sharabura, and Sairi Zhang, with whom he has co-authored publications. His scholarship metrics include an h-index of 1, with a total of 4 publications and 23 citations.

Metrics

  • h-index: 1
  • Publications: 4
  • Citations: 23

Selected Publications

  • Intrafamilial Phenotypic Variability in PRPH2-Related Retinopathy (2024)
    Cureus 1 citation DOI OpenAlex
  • Rates of diagnostic genetic testing in a tertiary ocular genetics clinic (2020)
    Ophthalmic Genetics 1 citation DOI OpenAlex

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Collaboration Network

4 Collaborators 1 Institution 1 Country

Top Collaborators

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