A
Alexandrea Wadley
Assistant Professor
faculty
CHP | Genetic Counseling
7 h-index
14 pubs
382 cited
Research Areas
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: 382
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)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Lindsay C. Burrage
Baylor College of Medicine (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Jill A. Rosenfeld
Baylor College of Medicine (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Carlos A. Bacino
Baylor College of Medicine (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Brendan Lee
Erasmus MC (NL)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Lisa Emrick
Baylor College of Medicine (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Kristen Fisher
Baylor College of Medicine (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Chun-Hui Tsai
University of Oklahoma Health Sciences Center (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Paul J. Benke
Joe DiMaggio Children's Hospital (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Kimberly Glaser
Baylor Genetics (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
David R. Murdock
Baylor College of Medicine (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Luis Rohena
The University of Texas Health Science Center at Houston (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Kimberly Houck
Baylor College of Medicine (US)
2 shared publications
- De novo missense variants in <i>ZBTB47</i> are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
- P348: De novo missense variants in ZBTB47 cause a neurodevelopmental phenotype of developmental delays, seizures, and possible movement abnormalities
Chiara Klöckner
Leipzig University (DE)
1 shared publication
- Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy
Heinrich Sticht
Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
1 shared publication
- Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy
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