Raymond Caylor

4PUBLICATIONS
10CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Flight dynamics
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Publications (4)

|Jul 16, 2025
Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizures.

Michelle Hua, Mohamad-Reza Aghanoori, Melissa MacPherson

|Sep 28, 2023
Parental age effects and Rett syndrome.

Xiaolan Fang, Lauren M Baggett, Raymond C Caylor

|Jun 01, 2023
Clinical case report: mosaic ANK3 pathogenic variant in a patient with autism spectrum disorder and neurodevelopmental delay.

Xiaolan Fang, Timothy Fee, Jessica Davis

|Mar 23, 2022
Analysis of X-inactivation status in a Rett syndrome natural history study cohort.

Xiaolan Fang, Kameryn M Butler, Fatima Abidi

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