Match tier
Listed
Presence
Current · Arkansas
Last published
2024
Sources
OpenAlex · ORCID
Refreshed
2026-10-08
N
Noelle R. Danylchuk
Associate Professor and Department Chair / Program Director
Also affiliated: Arkansas Children's Hospital (2015–2018); Children's Hospital of Philadelphia (2019)
8 h-index
13 pubs
364 cited
Research Areas
Biomedical Subjects
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: 364
Positions
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Associate Professor and Department Chair / Program Director publications 2015–2024University of Arkansas for Medical Sciences Institution web page
Selected Publications
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Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students (2024)
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P350: Comparison of hEDS and HSD in a pediatric population (2024)
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Clinical and laboratory genetic counseling assistants: Comparing background experiences, responsibilities, satisfaction, and career goals (2023)
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Factors associated with pediatric genetic counselors' practices related to bullying screening (2022)
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Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans (2021)
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Telehealth for genetic counseling: A systematic evidence review (2021)
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Eliciting culturally and medically informative family health histories from Marshallese patients living in the United States (2020)
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A TALE OF 480 GENES CLINICAL UTILITY AND APPLICATION OF CARDIOVASCULAR GENETIC TESTING (2019)
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KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect (2018)
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Advanced cardiovascular imaging in Williams syndrome: Abnormalities, usefulness, and strategy for use (2017)
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Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors (2015)
Collaboration Network
Top Collaborators
Thomas C. Markello
National Institutes of Health (US)
2 shared publications
- KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
Adolfo D. Garnica
Arkansas Children's Hospital
2 shared publications
In database
- KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
G. Bradley Schaefer
Surdna Foundation (US)
2 shared publications
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
- A TALE OF 480 GENES CLINICAL UTILITY AND APPLICATION OF CARDIOVASCULAR GENETIC TESTING
Tiffany Lepard
University of Arkansas for Medical Sciences
2 shared publications
In database
- Advanced cardiovascular imaging in Williams syndrome: Abnormalities, usefulness, and strategy for use
- Factors associated with pediatric genetic counselors' practices related to bullying screening
Julie Kaylor
Surdna Foundation (US)
2 shared publications
- Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans
- A TALE OF 480 GENES CLINICAL UTILITY AND APPLICATION OF CARDIOVASCULAR GENETIC TESTING
Rebecca Sutphen
Surdna Foundation (US)
2 shared publications
- Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans
- A TALE OF 480 GENES CLINICAL UTILITY AND APPLICATION OF CARDIOVASCULAR GENETIC TESTING
Lori Williamson Dean
University of Arkansas for Medical Sciences
2 shared publications
In database
- Eliciting culturally and medically informative family health histories from Marshallese patients living in the United States
- Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students
James P. Selig
University of Arkansas for Medical Sciences
2 shared publications
In database
- Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans
- Factors associated with pediatric genetic counselors' practices related to bullying screening
Christina Lam
National Human Genome Research Institute (US)
1 shared publication
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
Gretchen Golas
National Human Genome Research Institute (US)
1 shared publication
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
Mariska Davids
National Human Genome Research Institute (US)
1 shared publication
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
Marjan Huizing
National Human Genome Research Institute (US)
1 shared publication
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
Megan Kane
National Human Genome Research Institute (US)
1 shared publication
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
Donna M. Krasnewich
National Institute of General Medical Sciences (US)
1 shared publication
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
May Christine V. Malicdan
National Human Genome Research Institute (US)
1 shared publication
- Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors
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