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

Noelle R. Danylchuk

Researcher

Also affiliated: Arkansas Children's Hospital (2015–2018); Children's Hospital of Philadelphia (2019); Surdna Foundation (2019)

Faculty Researcher

8 h-index 13 pubs 360 cited

  • Humans
  • Female
  • Genetic Counseling
  • Child
  • Male
  • Developmental Disabilities
  • Adult
  • Intellectual Disability
  • Child, Preschool
  • United States
  • Telemedicine
  • Transforming Growth Factor beta
  • Infant
  • Mutation
  • Adolescent

Biography and Research Information

OverviewAI-generated summary

Noelle R. Danylchuk's research focuses on genetic counseling and related healthcare practices. She has investigated the utilization of genetic testing, examining 4,499 prior authorization requests for molecular genetic tests across four U.S. regional health plans. Danylchuk also conducted a systematic evidence review on the use of telehealth in genetic counseling. Her work has explored the experiences and career aspirations of genetic counseling assistants and examined factors influencing pediatric genetic counselors' practices regarding bullying screening.

Further research includes a comparison of hypermobile Ehlers-Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD) in a pediatric population. Danylchuk has also studied host perspectives on international fieldwork placements for U.S.-based genetic counseling students. Her scholarship metrics include an h-index of 8, with 13 total publications and 355 citations. She has collaborated with researchers from the University of Arkansas for Medical Sciences, including James P. Selig, Tiffany Lepard, Susan Steelman, and Jing Jin.

Metrics

  • h-index: 8
  • Publications: 13
  • Citations: 360

Selected Publications

  • Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students (2024)
    Journal of Genetic Counseling 1 citation DOI OpenAlex
  • P350: Comparison of hEDS and HSD in a pediatric population (2024)
    Genetics in Medicine Open 1 citation DOI OpenAlex
  • Clinical and laboratory genetic counseling assistants: Comparing background experiences, responsibilities, satisfaction, and career goals (2023)
    Journal of Genetic Counseling 6 citations DOI OpenAlex
  • Factors associated with pediatric genetic counselors' practices related to bullying screening (2022)
    Journal of Genetic Counseling 2 citations DOI OpenAlex
  • Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans (2021)
    Journal of Genetic Counseling 18 citations DOI OpenAlex
  • Telehealth for genetic counseling: A systematic evidence review (2021)
    Journal of Genetic Counseling 78 citations DOI OpenAlex
  • Eliciting culturally and medically informative family health histories from Marshallese patients living in the United States (2020)
    Journal of Genetic Counseling 10 citations DOI OpenAlex
  • A TALE OF 480 GENES CLINICAL UTILITY AND APPLICATION OF CARDIOVASCULAR GENETIC TESTING (2019)
    Journal of the American College of Cardiology DOI OpenAlex
  • <i>KCTD7</i> deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect (2018)
    Annals of Neurology 61 citations DOI OpenAlex
  • Advanced cardiovascular imaging in Williams syndrome: Abnormalities, usefulness, and strategy for use (2017)
    American Journal of Medical Genetics Part A 12 citations DOI OpenAlex
  • Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors (2015)
    Molecular Genetics and Metabolism 48 citations DOI OpenAlex

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Collaboration Network

26 Collaborators 13 Institutions 1 Country

Top Collaborators

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