Molecular Mechanisms

Boosting myelination as a therapeutic strategy in autism

Molecular and cellular dynamics of the developing human neocortex at single-cell resolution.

Astrocyte mitochondria are a sensitive target of PCB52 and its human-relevant metabolites.

Pathogenic gating pore current conducted by autism-related mutations in the NaV1.2 brain sodium channel.

Early developmental origins of cortical disorders modeled in human neural stem cells.

Cell type specific roles of FOXP1 during early neocortical murine development.

Cell-type-specific effects of autism-associated 15q duplication syndrome in the human brain.

A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus.

Unveiling the role of IGF1R in autism spectrum disorder: a multi-omics approach to decipher common pathogenic mechanisms in the IGF signaling pathway.

Reactivating FMR1 to treat fragile X syndrome

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