Miranda J. Jankovic

This study identifies gene regulatory programs and cell type-specific molecular mechanisms underlying inferior colliculus development and auditory function.

This study shows that deleting EGR3 in Kcna1-null mice rescues seizures, behavior, and brain pathology, linking early seizures to long-term transcriptional changes.

This study investigates the cell type-specific roles of FOXP1 in mouse neocortical development, revealing its impact on neurogenesis, gene expression, and cortical layering, with implications for ASD and FOXP1 syndrome.

The paper investigates the molecular and cellular mechanisms of KCNQ2 encephalopathy through structural analysis, functional assays, and an animal model, revealing multiple pathogenic effects of the G256W variant.

This study examines the effects of valproic acid on mouse behavior and development using home-cage monitoring and pup open field assays, identifying behavioral changes linked to psychiatric and developmental outcomes.

This study uses home-cage monitoring to identify ictal and interictal behavioral changes in mouse seizure models, revealing distinct behavioral and convulsive severity profiles.