Genetics and Autism Research
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Blasi F, Bacchelli E, et al. SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. Eur J Hum Genet 14(1): 123-6, 2006.
Boris M, Goldblatt A, Galanko J, James J. Association of MTHFR gene variants with autism. J Am Phys Surg. 2004;9(4)106-8.
Brimacombe M, Xue Ming, Parikh A. Familial risk factors in autism. J Child Neurol. 2007 May;22(5):593-7.
Campbell DB, et al. A genetic variant that disrupts MET transcription is associated with autism. Proc Natl Acad Sci U S A. 2006 Oct 19.
Comi AM, Zimmerman AW, Frye VH, Law PA, Peeden JN. Familial clustering of autoimmune disorders and evaluation of medical risk factors in autism. J Child Neurol. 1999 Jun;14(6):388-94.
Folstein, S. and M. Rutter (1977). Genetic influences and infantile autism. Nature 265(5596): 726-8.
Gregg JP et al. Gene expression changes in children with autism. Genomics. 2008 Jan;91(1):22-29.
Herbert MR, Russo JP, Yang S et al. Autism and environmental genomics. Neurotoxicology 2006; 27(5):671-84.
Korvatska E, et al. Genetic and immunologic considerations in autism. Neurobiol Dis. 2002 Mar;9(2):107-25.
Molloy CA, et al. Familial autoimmune thyroid disease as a risk factor for regression in children with Autism Spectrum Disorder: a CPEA Study. J Autism Dev Disord. 2006 Apr;36(3):317-24.
Pasca SP, Dronca E, Kaucsar T, et al. One Carbon Metabolism Disturbances and the C667T MTHFR Gene Polymorphism in Children with Autism Spectrum Disorders. J Cell Molec Med. Aug 2008.
Persico AM, et al. Adenosine deaminase alleles and autistic disorder: case-control and family-based association studies. Am J Med Genet 2000 Dec 4;96(6):784-90.
Szatmari P. Heterogeneity and the genetics of autism. J Psychiatry Neurosci. 1999 Mar;24(2):159-65.
Torres AR, et al. The association and linkage of the HLA-A2 class I allele with autism. Hum Immunol. 2006 Apr-May;67(4-5):346-1.
Ueland PM, Hustad S, Schneede J, Refsum H, Vollset SE. Biological and clinical implications of the MTHFR C677T polymorphism. Trends Pharmacol Sci. 2001 Apr;22(4):195-201.
Williams TA, Mars AE, et al. Risk of autistic disorder in affected offspring of mothers with a glutathione S-transferase P1 haplotype. Arch Pediatr Adolesc Med 2007: 161(4): 356-61.