The Simons Simplex Collection is a bold new initiative to search for the causes of autism. Researchers at eleven sites in North America will collect DNA samples from families with just one child affected by an autism spectrum disorder. This valuable data will be available to the best scientific minds in the world to search for clues that will lead to important breakthroughs. The Simons Foundation, a New York-based philanthropic organization, has committed millions of dollars to the Simons Simplex Collection, and other cutting edge autism research.
The wide range of autistic symptoms presents a formidable challenge to researchers looking for risk factors, causes, and treatments. Earlier efforts studied multiplex families, or families with more than one child with autism.
This initiative is different. It is focused on families with just one child with autism, called simplex families, which will provide insight into the most common and unexplained form of autism. This comes at an exciting time in history, in which breakthroughs in gene mapping, advancement of high-tech tools and the latest brain research present a unique opportunity for progress.
Families will be welcomed as part of the local community and the larger team. We hope to follow the progress of patients and their families over time, offering ongoing support as well as access to the latest research results.
Eligibility Requirements Two thousand families from across North America will join our study group. Families eligible to participate consist of:
Three Research Components
Contact one of our sites across North America.
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