Megan Abbott

5PUBLICATIONS
35CO-AUTHORS
Cellular nervous systemNeurology and neuromuscular diseasesInfant and child healthEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Jul 30, 2026
Epilepsy-associated SCN2A-L1342P mutation drives network hyperexcitability and widespread transcriptomic changes in human cortical organoids.

|Jul 14, 2026
A prospective natural history study protocol for clinical trial readiness in synaptic disorders.

|Aug 06, 2025
Cortical Visual Impairment Across a Range of Neurodevelopmental Disorders: Clinical Characterization, Diagnostic Tool Evaluation, and Association with Developmental Outcomes.

Megan Abbott, Katie Angione, Megan Stringfellow

|Jun 19, 2025
Evaluation, Diagnosis, and Treatment of Concomitant Movement Disorders in Genetic Epilepsies.

Jordan Garris, Megan Abbott, Erika Axeen

|May 22, 2024
Rett syndrome diagnostic odyssey: Limitations of NextGen sequencing.

Megan Abbott, Katie Angione, Emily Forbes

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Frequent Collaborators

2 joint publications

Scott Demarest

1 joint publications

Laura Tochen

1 joint publications

John M Schreiber

1 joint publications

Kristina Malik