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PRISMA Research

Our research at the University of Alberta is structured around genetics-first and phenotype-first frameworks that go beyond traditional diagnostic categories in autism and related neurodevelopmental conditions.

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Our Four Areas:

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Genetic Testing in Autism

Research focused on exploring the experiences and perspectives of children, adults, and physicians regarding genetic testing in autism.

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17q12 CNVs

Research focused on advancing precision medicine for individuals with 17q12 deletions and duplications

15q13.3
Deletion

Research focused on understanding the clinical and neurodevelopmental impact of the 15q13.3 deletion.

Implementation
Science

Research focused on developing and applying strategies to integrate evidence-based practices in genomics into real-world clinical care and community settings.

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Research

Territorial Acknowledgement 

PRISMA respectfully acknowledges that Alberta is located on Treaty 4, 6, 7, and 8 Territory traditional lands - a traditional gathering place for diverse Indigenous peoples, including the Cree, Blackfoot, Métis, Dene, Stoney-Nakoda Sioux, Saulteaux, Siksika, the Pikuni, the Kainai, the Tsuut’ina, the Stoney-Nakoda First Nations and many others whose histories, languages and cultures continue to influence our vibrant community.

Our Collaborators

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© 2026 PRISMA – Precision Medicine in Autism. All Rights Reserved. | In affiliation with the University of Alberta | Privacy Policy | Terms of Use

Contact us:

prisma@ualberta.ca

11361 87th Ave - Suite 5-020K

University of Alberta

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