Neuropsychiatric disorders such as autism spectrum disorders and schizophrenia have a significant genetic component. More than 100 risk genes have been identified for each condition, and a number of these overlap across disorders. On which neurobiological pathways do these gene mutations converge? Conversely, how do single gene disruptions serve as a risk factor for multiple psychiatric disorders? We aim to answer these questions using an integrative research pipeline that combines molecular, cellular, and circuit approaches in animal models.