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PRISMA Research

Our research at the University of Alberta explores how genetics and neurodevelopment influence autism and related conditions. Using genetics-first and phenotype-first approaches, we aim to better understand individual experiences and support more personalized healthcare.

Our Four Areas:

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Autism & Genetic Testing

Research exploring the experiences and perspectives of autistic individuals, families, and healthcare providers regarding genetic testing.

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17q12 Research

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

15q13.3
Deletion

Research focused on understanding how the 15q13.3 deletion affects health and neurodevelopment.

Implementation
Science

Research focused on improving how genomics and evidence-based care are integrated into clinical and community settings.

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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