Our mission is to understand the neurobiology of age-related conditions affecting cognition, including Alzheimer's disease,
frontotemporal dementia, and cognitive aging, and to contribute to developing new treatments for these conditions.

Alzheimer's disease (AD) and frontotemporal dementia (FTD) are leading causes of dementia. Neither has highly effective treatments available. The microtubule-associated protein tau is a focus in the Roberson lab, as it accumulates with aging and plays important roles in both diseases. We also study progranulin, a common genetic cause of FTD. We are particularly interested in the how these molecules affect vulnerable brain networks the default mode network in AD and the salience network in FTD to cause neuronal dysfunction. We use mouse models and other approaches to address these questions.