Last Updated: 09/26/2026
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Found 317 publications
Electroencephalographic Transient Beta Event Rates in Autism and Related Neurogenetic Conditions.
Journal: medRxiv : the preprint server for health sciences
Published: August 20, 2026
Genetic Counselor Utilization Across Non-Genetics Departments for Neurodevelopmental Disorders.
Journal: medRxiv : the preprint server for health sciences
Published: August 01, 2026
From Infancy to Early School Age: Longitudinal Developmental Outcomes and Autism Diagnostic Stability in Tuberous Sclerosis Complex.
Journal: Pediatric neurology
Published: May 07, 2026
Development of a human iPSC and patient phenotyping resource for preclinical investigations of neurodevelopmental disorders.
Journal: Stem cell research
Published: April 13, 2026
Postnatal gene restoration in succinic semialdehyde dehydrogenase deficiency (SSADHD) reveals phenotype reversibility.
Journal: bioRxiv : the preprint server for biology
Published: April 03, 2026
Collaboration as a Catalyst for Advancing Rare Disease Research: The Experience of the Rare Diseases Clinical Research Network.
Journal: Clinical and translational science
Published: January 29, 2026
Closing the Gap to Interventions for Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders (TAND): Protocol for a Longitudinal Study of TAND Severity, Predictors, and Caregiver Well-Being (TANDem-2).
Journal: JMIR research protocols
Published: January 22, 2026
Early Vigabatrin Treatment Before Seizure Onset Decreased Interictal Epileptiform Discharges Over the Duration of the PREVeNT Study.
Journal: Pediatric neurology
Published: December 29, 2025
A two-step temporal data augmentation and supervised learning framework for predicting autism diagnosis at 36 months in patients with tuberous sclerosis complex.
Journal: Computers in biology and medicine
Published: November 17, 2025
Last Updated: 09/26/2026