Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions
Qin Qin Huang, Emilie M. Wigdor, Patrick H. Campbell, Daniel Shiloh Malawsky, Kaitlin E. Samocha, V. Kartik Chundru, Petr Danecek, Sarah Lindsay, Thomas Marchant, Mahmoud Koko, Sana Amanat, Davide Bonifanti, Eamonn G. Sheridan, Elizabeth J. Radford, Jeffrey C. Barrett, , Hilary C. Martin
This study investigates how common genetic variants contribute to risk for rare neurodevelopmental conditions and examines indirect genetic effects through parental non-transmitted alleles.
medRxiv · Mar 5, 2024 · PreprintGenetic & Genomic Medicine