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  3. Exome-wide Rare Variant Genetic Load Is Associated With Cognition, Intellectual Disability and Psychiatric Disorders In Population-based Cohorts

Exome-wide rare variant genetic load is associated with cognition, intellectual disability and psychiatric disorders in population-based cohorts

Mohammad Ahangari, Spencer Moore, Justin Schleede, Jonathan Anomaly, Alexander Strudwick Young, Tobias Wolfram
medRxiv 2026.10.13.26365349; doi: https://doi.org/10.64898/2026.10.13.26365349
https://doi.org/10.64898/2026.10.13.26365349
Preprint
Oct 15, 2026
Consortium publication
No

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The University of Helsinki is the organization responsible for the FinnGen research project. The Finnish consortium partners include all Finnish public biobanks and their background organisations, so the project covers the whole of Finland. All partners are listed on this page.

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