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Raymond Caylor

4PUBLICATIONS

10CO-AUTHORS

Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Flight dynamics

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Publications (4)

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|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 <i>ANK3</i> 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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Frequent Collaborators

3 joint publications

Xiaolan Fang

1 joint publications

Elliot S Stolerman

1 joint publications

Jeffrey L Neul

1 joint publications

Tim A Benke

1 joint publications

Eric D Marsh

1 joint publications

Steven A Skinner

1 joint publications

Antonio Vitobello

1 joint publications

Daniel Calame

1 joint publications

James Ellis

1 joint publications

Jonathan Epp

Frequent Collaborators

3 joint publications

Xiaolan Fang

1 joint publications

Elliot S Stolerman

1 joint publications

Jeffrey L Neul

1 joint publications

Tim A Benke

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