FOXG1 Syndrome Latest Advances

Integrating molecular studies and clinical disease models to provide mechanistic insight into neurodevelopment: guidance from FOXG1 syndrome.

Journal: Developmental biology

Published: January 29, 2026

AAV-mediated neuronal expression of FOXG1 restores oligodendrocyte maturation, myelination, and hippocampal structure in mouse models of FOXG1 syndrome.

Journal: bioRxiv : the preprint server for biology

Published: January 23, 2026

Human patient-specific FOXG1 syndrome mouse model revealed FOXG1-MYCN-mediated regulation of protein homeostasis in neurodevelopmental disorder.

Journal: bioRxiv : the preprint server for biology

Published: October 03, 2025

FOXG1 Hierarchically Shapes Synaptic Functions in Striatal iSPNs and Contributes to ASD Etiology.

Journal: Neuroscience bulletin

Published: July 16, 2025

Natural history of epilepsy in FOXG1 Syndrome.

Journal: Epilepsy research

Published: July 07, 2025

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

Journal: Nature communications

Published: March 25, 2025

Foxg1 gene mutation impairs auditory cortex response and reduces sound tolerance.

Journal: Cerebral cortex (New York, N.Y. : 1991)

Published: March 17, 2025

Considerations and procedures for acquiring EEG as part of multi-site studies for Rett syndrome and other genetic neurodevelopmental disorders.

Journal: Frontiers in integrative neuroscience

Published: February 11, 2025

The patient-specific mouse model with Foxg1 frameshift mutation provides insights into the pathophysiology of FOXG1 syndrome.

Journal: bioRxiv : the preprint server for biology

Published: February 03, 2025

Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome.

Journal: Journal of neurodevelopmental disorders

Published: December 05, 2024

PLP1-Targeting Antisense Oligonucleotides Improve FOXG1 Syndrome Mice.

Journal: International journal of molecular sciences

Published: September 18, 2024

Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndrome.

Journal: Molecular psychiatry

Published: March 13, 2024

FOXG1 Syndrome Latest Advances

Find the Latest Research About FOXG1 Syndrome

Integrating molecular studies and clinical disease models to provide mechanistic insight into neurodevelopment: guidance from FOXG1 syndrome.

Integrating molecular studies and clinical disease models to provide mechanistic insight into neurodevelopment: guidance from FOXG1 syndrome.

AAV-mediated neuronal expression of FOXG1 restores oligodendrocyte maturation, myelination, and hippocampal structure in mouse models of FOXG1 syndrome.

AAV-mediated neuronal expression of FOXG1 restores oligodendrocyte maturation, myelination, and hippocampal structure in mouse models of FOXG1 syndrome.

Human patient-specific FOXG1 syndrome mouse model revealed FOXG1-MYCN-mediated regulation of protein homeostasis in neurodevelopmental disorder.

Human patient-specific FOXG1 syndrome mouse model revealed FOXG1-MYCN-mediated regulation of protein homeostasis in neurodevelopmental disorder.

FOXG1 Hierarchically Shapes Synaptic Functions in Striatal iSPNs and Contributes to ASD Etiology.

FOXG1 Hierarchically Shapes Synaptic Functions in Striatal iSPNs and Contributes to ASD Etiology.

Natural history of epilepsy in FOXG1 Syndrome.

Natural history of epilepsy in FOXG1 Syndrome.

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

Foxg1 gene mutation impairs auditory cortex response and reduces sound tolerance.

Foxg1 gene mutation impairs auditory cortex response and reduces sound tolerance.

Considerations and procedures for acquiring EEG as part of multi-site studies for Rett syndrome and other genetic neurodevelopmental disorders.

Considerations and procedures for acquiring EEG as part of multi-site studies for Rett syndrome and other genetic neurodevelopmental disorders.

The patient-specific mouse model with Foxg1 frameshift mutation provides insights into the pathophysiology of FOXG1 syndrome.

The patient-specific mouse model with Foxg1 frameshift mutation provides insights into the pathophysiology of FOXG1 syndrome.

Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome.

Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome.

PLP1-Targeting Antisense Oligonucleotides Improve FOXG1 Syndrome Mice.

PLP1-Targeting Antisense Oligonucleotides Improve FOXG1 Syndrome Mice.

Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndrome.

Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndrome.