Match tier Listed
Presence Current · Arkansas
Last published 2025
Sources OpenAlex · ORCID
Refreshed 2026-08-15

Katie Bosanko

Researcher

Also affiliated: Arkansas Children's Hospital (2025)

Unknown Researcher

2 h-index 3 pubs 43 cited

  • Neurodevelopmental Disorders
  • Adolescent
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Male
  • Nerve Tissue Proteins
  • Young Adult
  • Adult
  • Seizures, Febrile
  • Epilepsy
  • Middle Aged
  • Phenotype
  • Exome Sequencing

Biography and Research Information

OverviewAI-generated summary

Katie Bosanko investigates genetic variants associated with neurodevelopmental disorders. Her recent work focuses on variants in the *BSN* gene, which encodes the presynaptic protein Bassoon. Mutations in this gene have been linked to a distinct neurodevelopmental disorder that presents with a wide range of symptoms. Bosanko's research contributes to understanding the molecular basis of these disorders and their clinical manifestations. She has authored 3 publications and has a current h-index of 2, with 40 total citations. Bosanko collaborates with T. Burrow at the University of Arkansas for Medical Sciences, with whom she has co-authored 2 publications.

Metrics

  • h-index: 2
  • Publications: 3
  • Citations: 43

Selected Publications

  • Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range (2025)
    The American Journal of Human Genetics 4 citations DOI OpenAlex
  • Variants in <i>BSN</i> , encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range (2025)
    medRxiv DOI OpenAlex
  • De novo variants in <i>EBF3</i> are associated with hypotonia, developmental delay, intellectual disability, and autism (2017)
    Molecular Case Studies 38 citations DOI OpenAlex

View all publications on OpenAlex →

Collaboration Network

26 Collaborators 15 Institutions 3 Countries

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