Gene List:
ADNP, ADSL, ALDH5A1, ANKRD11, ARID1B, ARX, AUTS2, BCL11A, BRAF, CACNA1C, CC2D1A, CDKL5, CHD2, CHD7, CHD8, CNTN6, CNTNAP2, CREBBP, CSNK2A1, CTNND2, DHCR7, DYRK1A, EHMT1, FMR1, FOLR1, FOXG1, FOXP1, GABRB3, GAMT, GRIN2B, GRIP1, HDAC8, HOXA1, HPRT1, KATNAL2, KMT5B, MAGEL2, MBD5, MECP2, MED12, MEF2C, MID1, NHS, NIPBL, NLGN3, NLGN4X, NRXN1, NSD1, PCDH19, POGZ, PQBP1, PTCHD1, PTEN, PTPN11, RAB39B, RAD21, RAI1, RELN, RPL10, SCN1A, SCN2A, SHANK2, SHANK3, SLC6A1, SLC6A8, SLC9A6, SMC1A, SMC3, SPAST, SYNGAP1, TBR1, TCF20, TCF4, TSC1, TSC2, UBE3A, UPF3B, VPS13B, ZEB2

References:
Lauritsen et al. Effects of familial risk factors and place of birth on the risk of autism: a nationwide register-based study. J Child Psychol Psychiatry. 2005;46:963–971.

Saunders et al. Comprehensive ZEB2 gene analysis for Mowat-Wilson syndrome in a North American cohort: a suggested approach to molecular diagnostics. Am J Med Genet A. 2009;149A:2527–31.

Shen et al. Clinical Genetic Testing for Patients With Autism Spectrum Disorders. Pediatrics. 2010 Apr; 125(4): e727–e735.

Fernell et al. Early diagnosis of autism and impact on prognosis: a narrative review. Clin Epidemiol. 2013; 5: 33–43.

Zoghbi HY, Bear MF. Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities. Cold Spring Harb Perspect Biol. 2012 Mar; 4(3): a009886.