Match tier Listed
Presence Current · Arkansas
Last published 2023
Sources OpenAlex · ORCID
Refreshed 2026-08-18

Aaron Hiegert

Researcher

Graduate Student Researcher

1 h-index 2 pubs 5 cited

  • Developmental Disabilities
  • Phenotype
  • Transcription Factors
  • Matrix Attachment Region Binding Proteins
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Male
  • Severity of Illness Index
  • Syndrome
  • Genetic Association Studies

Biography and Research Information

OverviewAI-generated summary

Aaron Hiegert's research focuses on the genotype-phenotype correlations within SATB2-associated syndrome. He has contributed to publications detailing quantitative phenotype morbidity descriptions and the development of a severity score for this syndrome, incorporating genotype-phenotype correlations and a dedicated SATB2 portal. His work involves analyzing specific genetic and phenotypic characteristics to better understand the spectrum and severity of SATB2-associated syndrome. Hiegert collaborates with researchers at the University of Arkansas for Medical Sciences, including Yuri A. Zárate, Larry D. Hartzell, and Kirk Simmons, with whom he has co-authored multiple publications. His scholarship metrics include an h-index of 1, with 2 total publications and 5 total citations.

Metrics

  • h-index: 1
  • Publications: 2
  • Citations: 5

Selected Publications

  • Quantitative Phenotype Morbidity Description of SATB2-Associated Syndrome (2023)
    Human Mutation 5 citations DOI OpenAlex
  • P369: SATB2-associated syndrome severity score: Genotype/phenotype correlations and the SATB2 portal (2023)
    Genetics in Medicine Open DOI OpenAlex

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Collaboration Network

18 Collaborators 11 Institutions 3 Countries

Top Collaborators

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