Alexandrea Wadley

Assistant Professor

University of Arkansas for Medical Sciences

faculty

CHP | Genetic Counseling

7 h-index 14 pubs 378 cited

Research Areas

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OverviewAI-generated summary

Alexandrea Wadley's research investigates the genetic underpinnings of neurodevelopmental disorders. Her work has identified de novo missense variants in the ZBTB47 gene as being associated with a range of conditions including developmental delays, hypotonia, seizures, and gait abnormalities. She has also contributed to research on SNAP25 variants causing early-onset developmental and epileptic encephalopathy. Wadley's scholarly output includes 14 publications with 378 citations and an h-index of 7. She collaborates with researchers at the University of Arkansas for Medical Sciences, including Yuri A. Zárate, Lori Williamson Dean, and Renita Brown, with whom she shares publications. Wadley is also exploring the perspectives of genetic counselors regarding end-of-life care for oncology patients.

Metrics

h-index: 7
Publications: 14
Citations: 378

Selected Publications

Assessing the perspectives of genetic counselors with oncology patients at the end of life (2025) DOI
De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities (2023) DOI