Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder
Campbell D, Datta D, Jones S, Batey Lee E, Sutcliffe J, Hammock E, Levitt P. Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder. Journal Of Neurodevelopmental Disorders 2011, 3: 101-112. PMID: 21484202, PMCID: PMC3113442, DOI: 10.1007/s11689-010-9071-2.Peer-Reviewed Original ResearchAutism spectrum disorderASD susceptibilitySocial behaviorGenetic association analysisSpectrum disorderGenetic variationOxytocin receptor gene variantsGenetic polymorphismsGenetic markersAssociation analysisLines of evidenceCommon genetic polymorphismsPhenotype domainsCore deficitBehavioral flexibilityOXTR polymorphismsPolymorphismOXTR geneGene variantsASD phenotypeSubset of familiesASD riskCurrent findingsLarge independent cohortsFunctional polymorphisms