Last Updated: 09/26/2026
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Found 13 publications
Monogenic epilepsies exhibit distinct sleep endophenotypes.
Journal: medRxiv : the preprint server for health sciences
Published: July 10, 2026
Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
Journal: Nature genetics
Published: May 18, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
Journal: Nature genetics
Published: August 18, 2025
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
Journal: Nature genetics
Published: August 18, 2025
Neurodevelopmental Phenotyping and Genotyping in the Pediatric National Institute of Health Undiagnosed Disease Program.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: March 27, 2025
A Novel MACF1 Gene Mutation: Expanding the Fetal and Neonatal Phenotype.
Journal: Pediatric neurology
Published: October 27, 2024
Sleep and activity patterns in older patients discharged from the hospital.
Journal: Sleep
Published: December 04, 2018
Prospective longitudinal overnight video-EEG evaluation in Phelan-McDermid Syndrome.
Journal: Epilepsy & behavior : E&B
Published: August 17, 2017
Longitudinal outcomes of children with pediatric autoimmune neuropsychiatric disorder associated with streptococcal infections (PANDAS).
Journal: European child & adolescent psychiatry
Published: March 14, 2017
Electroencephalogram Coherence Patterns in Autism: An Updated Review.
Journal: Pediatric neurology
Published: February 26, 2016
Last Updated: 09/26/2026