Common Genetic Variants in Autism Spectrum Disorders
Author:
Publisher
Elsevier
Reference126 articles.
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2. A genome-wide scan for common alleles affecting risk for Autism;Anney;Human Molecular Genetics,2010
3. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of Autism;Arking;American Journal of Human Genetics,2008
4. Investigation of potential gene-gene interactions between APOE and RELN contributing to Autism risk;Ashley-Koch;Psychiatric Genetics,2007
5. An analysis paradigm for investigating multi-locus effects in complex disease: Examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder;Ashley-Koch;Annals of Human Genetics,2006
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