Webinar: The Future of SPARK and Autism Research
In this recorded webinar, Dr. Wendy Chung provides an overview of the SPARK study and where autism research is headed.
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Because of SPARK and other research studies throughout the world, we are rapidly learning how genes affect our biology and development. We are also learning how changes to some genes can lead to autism. Read about the latest research on autism genetics and visit with people who have learned about a genetic change associated with their autism.
Life with Autism, Times Five
The McBrides, one of the first families to join SPARK, have five family members with autism. SPARK found a genetic diagnosis for one of them.
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Webinar: Ask Me Anything – Dr. Wendy Chung
In this recorded webinar, Dr. Wendy Chung answers your questions about SPARK and autism.
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SPARK Data Reveals a Common Genetic Change Linked to Autism
A new study using data from 6,000 families in SPARK suggests that a gene called DDHD2 may play a role in autism.
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First a Cleft Lip, then Autism
More than three years after a genetic diagnosis, Brody Eidam has surpassed doctor’s expectations. But he and his family still face lots of challenges.
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Genetic Differences in Males and Females Diagnosed with Autism
A new study suggests that different genes can contribute to autism in biological males and females.
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Getting a Genetic Diagnosis from SPARK Answers a Family’s Questions
When Mercedes Riggs opened the email from SPARK, she texted her husband, “You won’t believe this.” Learn how SPARK provided answers to one family’s questions about their son’s autism.
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Webinar: Sex Bias and the Genetics of Autism
In this recorded webinar, learn about recent genetic research that may help explain why more males than females are diagnosed with autism.
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Self-Injury and Affection: In Rare Disorder, a Puzzling Collection of Symptoms
By participating in research, the Manning family hopes to connect with others with the same rare condition as their daughter.
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Extremely Rare Condition Linked to Autism
The King family learned their son had a change in a gene called CUL3.
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