Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology
Lingyu Zhan, Dongmei Yu, Franjo Ivankovic, Maria Niarchou, Laura Domènech, Cathy L. Barr, Fortu Benarroch, Cathy L. Budman, Daniëlle C. Cath, Nelson B. Freimer, Helena Garrido, Marco A. Grados, Varda Gross‐Tsur, Luis Diego Herrera-Amighetti, Robert A. King, , Roel A. Ophoff
This study identifies distinct rare de novo coding variants associated with Tourette Syndrome, highlighting loss-of-function mutations and novel candidate genes.
bioRxiv · Nov 4, 2025 · PreprintNeuroscience