• A novel frameshift mutation of FOXG1-induced congenital variant of Rett syndrome: A case report
• Behavioral and brain anatomical analysis of Foxg1 heterozygous mice
• Behavioral Phenotypes of Foxg1 Heterozygous Mice
• Caregiver Perspective of Benefits and Side Effects of Anti-Seizure Medications in CDKL5 Deficiency Disorder from an International Database
• Comparison of evoked potentials across four related developmental encephalopathies
• Comprehensive Transcriptomic Investigation of Rett Syndrome Reveals Increasing Complexity Trends from Induced Pluripotent Stem Cells to Neurons with Implications for Enriched Pathways
• Conditional Deletion of <em>Foxg1</em> Delayed Myelination during Early Postnatal Brain Development
• Conditional Deletion of Foxg1 Delayed Myelination during Early Postnatal Brain Development
• De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India
• Developmental trajectories of GABAergic cortical interneurons are sequentially modulated by dynamic FoxG1 expression levels
• Drug repurposing in Rett and Rett-like syndromes: a promising yet underrated opportunity?
• Effects of ganaxolone on non-seizure outcomes in CDKL5 Deficiency Disorder: Double-blind placebo-controlled randomized trial
• Epileptic spasms in CDKL5 deficiency disorder: Delayed treatment and poor response to first-line therapies
• Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study
• Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
• Expanding genotype-phenotype correlations in FOXG1 syndrome: results from a patient registry
• Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders
• FOXG1 drives transcriptomic networks to specify principal neuron subtypes during the development of the medial pallium
• FOXG1 Syndrome
• FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development
• Genetic Diagnosis Impacts Medical Management for Pediatric Epilepsies
• Identification of a <em>de novo</em> mutation of the <em>FOXG1</em> gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathies
• International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency Disorder
• Involvement of Mitochondrial Dysfunction in <em>FOXG1</em> Syndrome
• Involvement of Mitochondrial Dysfunction in FOXG1 Syndrome
• Letter to the editor on "A novel frameshift mutation of FOXG1-induced congenital variant of Rett syndrome: A case report"
• Menin Deficiency Induces Autism-Like Behaviors by Regulating Foxg1 Transcription and Participates in Foxg1-Related Encephalopathy
• Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome
• Prevalence of Endocrinopathies in a Cohort of Patients with Rett Syndrome: A Two-Center Observational Study
• Rett and Rett-related disorders: Common mechanisms for shared symptoms?
• The clinical and sleep manifestations in children with FOXG1 syndrome
• The development, content and response process validation of a caregiver-reported severity measure for CDKL5 deficiency disorder
• The Heart of Rett Syndrome: A Quantitative Analysis of Cardiac Repolarization
• The patient-specific mouse model with Foxg1 frameshift mutation uncovers the pathophysiology of FOXG1 syndrome
• The postnatal injection of AAV9-FOXG1 rescues corpus callosum agenesis and other brain deficits in the mouse model of FOXG1 syndrome
• Timing the clinical onset of epileptic spasms in infantile epileptic spasms syndrome: A tertiary health center's experience
• Top Caregiver Concerns in Rett syndrome and related disorders: data from the US Natural History Study
• Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study
• ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function
• Zika virus induces FOXG1 nuclear displacement and downregulation in human neural progenitors