Aislinn Joanmarie Williams

This study examines cerebellar development in mouse models with SCN2A premature termination codon variants, finding age- and position-dependent effects on cerebellar structure and function.

This study shows that different SCN2A premature stop codons have distinct effects on neuronal function and behavior in mice, challenging the assumption of uniform haploinsufficiency.

This study shows that deleting the CaV1.3 gene in mice reduces Purkinje cell dendritic complexity but does not affect cerebellar-mediated eyeblink conditioning or MLI numbers.

This study identifies lobule VI-specific structural and functional cerebellar abnormalities in 16p11.2 microduplication mice, linking them to learning impairments and neuropsychiatric disorder symptoms.

This study examines functional connectivity of the cerebellar vermis in bipolar disorder and its association with mood states, finding altered connectivity patterns linked to depression and mania.

This study finds smaller cerebellar cortex volumes in bipolar disorder type I patients, with medication use potentially influencing cerebellar structure.

This study shows that CaV1.3 knockout mice have motor learning deficits and impaired gait adaptation but normal anxiety, depression, and social behaviors.