Genetic analysis from the first 457 families to enroll in SPARK provides new support for several genes linked to autism.Read More
Get the latest autism updates from SPARK, including information about genes and ASD research, webinars, and personal stories from our community.
Our ‘genes’ page provides short, easy-to-understand descriptions of genes linked to autism. Under ‘research’, you’ll find the latest updates from SPARK and other autism studies. In our ‘stories’ section, families, scientists and others share their journeys. In our monthly webinars, speakers from the autism community provide useful information for families and people with autism. All are welcome–invitation links are issued in our monthly newsletter. If you have suggestions for webinar topics, please email us at email@example.com.
Their son’s genetic diagnosis revealed an undiagnosed heart condition.Read More
After enrolling in SPARK, the Meiles learned that their son has a change in the POGZ gene. The diagnosis helps explain a mysterious health issue.Read More
People with a disruption in the ASXL3 gene typically have severe intellectual disability, impaired speech and features of autism. They may also have low muscle tone, significant feeding difficulties and distinctive facial features, such as a prominent forehead and arched eyebrows. The condition is also known as Bainbridge-Ropers syndrome.Read More