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Last Updated: 10/31/2025

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Found 61 publications

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.

Journal: bioRxiv : the preprint server for biology
Published: October 03, 2025

Natural history of epilepsy in FOXG1 Syndrome.

Natural history of epilepsy in FOXG1 Syndrome.

Journal: Epilepsy research
Published: July 07, 2025

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

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.

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.

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

PLP1-Targeting Antisense Oligonucleotides Improve FOXG1 Syndrome Mice.

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.

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

Journal: Molecular psychiatry
Published: March 13, 2024

Rett and Rett-related disorders: Common mechanisms for shared symptoms?

Rett and Rett-related disorders: Common mechanisms for shared symptoms?

Journal: Experimental biology and medicine (Maywood, N.J.)
Published: December 07, 2023

Menin Deficiency Induces Autism-Like Behaviors by Regulating Foxg1 Transcription and Participates in Foxg1-Related Encephalopathy.

Menin Deficiency Induces Autism-Like Behaviors by Regulating Foxg1 Transcription and Participates in Foxg1-Related Encephalopathy.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: October 23, 2023

Conditional Deletion of Foxg1 Delayed Myelination during Early Postnatal Brain Development.

Conditional Deletion of Foxg1 Delayed Myelination during Early Postnatal Brain Development.

Journal: International journal of molecular sciences
Published: August 12, 2023

Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders.

Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders.

Journal: Cytogenetic and genome research
Published: July 19, 2023

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

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

Journal: Research square
Published: July 03, 2023
Showing 1-12 of 61

Last Updated: 10/31/2025