Constance L. Smith-Hicks - Publications

Biphasic sleep is a feature of sleep disturbance in SYNGAP1-RD.

Journal: Sleep medicine

Published: February 18, 2026

Detrended Fluctuation Analysis to Assess Long-Range Temporal Correlations in EEG from SYNGAP1-Related Disorder.

Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Published: December 03, 2025

Development and Adaptive Function in Individuals With SCN2A-Related Disorders.

Journal: Neurology

Published: July 22, 2025

Adult-onset drug-resistant progressive epilepsy in a patient with novel MECP2 mutation.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: July 17, 2025

Finding buried genetic test results in the electronic health record is inefficient and variable across institutions.

Journal: Therapeutic advances in rare disease

Published: November 15, 2024

Remote monitoring of social attention in neurogenetic syndromes and idiopathic neurodevelopmental disability.

Journal: Autism research : official journal of the International Society for Autism Research

Published: August 18, 2024

Quantifying neurobehavioral profiles across neurodevelopmental genetic syndromes and idiopathic neurodevelopmental disorders.

Journal: Developmental medicine and child neurology

Published: July 05, 2024

Recommendations for the management of gastrointestinal comorbidities with or without trofinetide use in Rett syndrome.

Journal: Expert review of gastroenterology & hepatology

Published: June 13, 2024

Cortical Vision Impairment (CVI)-informed assessment and treatment of challenging behavior in a child with SCN2A-related disorder.

Journal: Journal of neurodevelopmental disorders

Published: May 31, 2024

POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxia.

Journal: Epilepsia

Published: March 29, 2024

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations.

Journal: European journal of human genetics : EJHG

Published: January 24, 2024

Resolution of severe neurobehavioral difficulties in an individual with Primrose syndrome with sertraline.

Journal: American journal of medical genetics. Part A

Published: August 28, 2023