Advancing knowledge of human development, developmental disabilities, and neurodegenerative diseases.
Becca Stroschein realized while volunteering as an undergraduate student at a non-profit for autistic adults, that she held a deep passion for helping others find a form of communication that works for them so that they can have access to their community.
Alexander disease (AxD) is a rare neurological disorder caused by dominant gain-of-function mutations in the gene for glial acidic fibrillary protein (GFAP).
A new Waisman study found that adverse childhood experiences (ACEs)—such as abuse, neglect, or exposure to household challenges—can have lasting effects on adults with Down syndrome, including their mental health and ability to cope with life changes. While ACES are known to impact the general population, this research is among the first to show similar—and in some cases heightened—effects in individuals with Down syndrome.
TI-Toolbox: An Open-Source Software for Temporal Interference Stimulation Research
Researchers at the Waisman Center’s University Center for Excellence in Developmental Disabilities (UCEDD) were recently awarded a grant from the Health Resources & Services Administration (HRSA) to support research to improve the health and well-being of children and youth with autism.
Paul Rathouz, PhD, former Chair of the Department of Biostatistics and Medical Informatics, passed away from complications of multiple myeloma on Wednesday afternoon, December 10, 2025. Paul served with distinction as the chair of the Department of Biostatistics and Medical Informatics from 2010-2017. He will be missed by those who knew him.
Tuberous Sclerosis Complex (TSC) is an autosomal dominant neurodevelopmental disorder caused by a monogenic mutation to either TSC1 or TSC2. Nearly one-half of TSC patients have mild to profound intellectual disabilities and autism, with the majority developing seizures and neuropsychiatric conditions.
Temple Grandin, PhD, is likely the most well-known living autistic individual, both nationally and internationally.
In Wisconsin, a new initiative is transforming the landscape of neonatal care by making genetic testing more accessible for critically-ill newborns.
Elevated intracranial pressure (ICP) is a complication of severe traumatic brain injury (TBI) that carries a risk of secondary brain injury.
