The Williams lab is interested in understanding the molecular and cellular mechanisms by which genetic risk factors contribute to psychiatric disease from a developmental perspective. Our current projects focus on voltage-gated calcium channel genes, which have been linked to the risk of developing bipolar disorder, schizophrenia, depression, and autism. We use induced pluripotent stem cells and transgenic mouse models to study how calcium channel gene SNPs alter neuronal development, neural circuit function, and affective behavior. We employ a wide range of approaches, including molecular biology, live cell imaging, neuropathology, and animal behavioral assessments, to try to unravel the developmental pathways involved in neuropsychiatric disease, in the hope of identifying novel treatment targets.
We are pleased to welcome postdoctoral fellow Deniz Madencioglu, PhD!
Krislen Tison was awarded a fellowship through the Genetics Program NIH T32 training grant