Match tier
Listed
Presence
Current · Arkansas
Last published
2025
Sources
OpenAlex · ORCID
Refreshed
2026-08-08
A
Alexandrea Wadley
Assistant Professor
Also affiliated: Mayo Clinic in Florida (2020); University of Oklahoma Health Sciences Center (2017–2023); University of Oklahoma (2016–2019)
Faculty Researcher
CHP | Genetic Counseling
7 h-index
14 pubs
394 cited
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Alexandrea Wadley's research focuses on identifying genetic variants associated with neurodevelopmental disorders in children. Her work includes the study of de novo missense variants in genes such as ZBTB47, which have been linked to phenotypes including developmental delays, hypotonia, seizures, and movement abnormalities. She has also contributed to the understanding of de novo variants in SNAP25, associated with early-onset developmental and epileptic encephalopathy. Wadley's research network includes collaborators from the University of Arkansas for Medical Sciences, with whom she has co-authored publications. She has authored 14 publications with 379 citations and an h-index of 7, with recent activity indicated by publications in 2023 and 2025.
Metrics
- h-index: 7
- Publications: 14
- Citations: 394
Selected Publications
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Assessing the perspectives of genetic counselors with oncology patients at the end of life (2025)
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De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities (2023)
Collaboration Network
Top Collaborators
Scott Ward
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Chun-Hui Tsai
University of Oklahoma Health Sciences Center (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Paul J. Benke
Joe DiMaggio Children's Hospital (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Lisa Emrick
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Kristen Fisher
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Kimberly Houck
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Hongzheng Dai
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
María J. Guillen Sacoto
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
William Craigen
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Kimberly Glaser
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
David R. Murdock
Brooke Army Medical Center (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Luis Rohena
Brooke Army Medical Center (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Karin E. M. Diderich
Erasmus MC (NL)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Hennie T. Brüggenwirth
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Brendan Lee
Baylor College of Medicine (US)
1 shared publication
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
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