Common Variant Associations with Fragile X Syndrome
James J. Crowley, Jin Szatkiewicz, Anna K. Kähler, Paola Giusti‐Rodríguez, NaEshia Ancalade, Jessica K. Booker, Jennifer L. Carr, Greg E. Crawford, Molly C. Losh, Craig A. Stockmeier, Annette K. Taylor, Joseph Piven, Patrick F. Sullivan
This study identifies genome-wide significant associations near FMR1 with Fragile X Syndrome in males, highlighting the complexity of monogenetic disorders.
Molecular Psychiatry · Dec 7, 2018Peer-reviewedGenetics