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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

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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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