FOXP1 and autism spectrum disorder: A follow-up report to the 2013 PGC study estimated genetic correlation between the two diseases to be 23%, with shared risk loci including several genes involved in neurodevelopment, such as forkhead box P1 (FOXP1), exostosin glycosyltransferase 1 (EXT1), astrotactin 2 (ASTN2), mono-ADP ribosylase 2 (MACROD2), and histone deacetylase 4 (HDAC4) (The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium, 2017).