Ashley M. Driver

This study shows Ttc21b ablation in Bergmann glia causes ectopic granule cells and reduced Shh signaling in the cerebellum, suggesting Ttc21b's role in regulating Shh signaling in these cells.

The paper identifies a de novo TUBA1A mutation linked to cortical dysgenesis and shows it impairs neural progenitor survival and differentiation using iPSCs.

The paper identifies COPB2 mutations as a cause of human microcephaly and shows that Copb2 is essential for embryogenesis and corticogenesis in mice.