Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34424
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dc.contributor.authorPua, Emmanuel Peng Kiat-
dc.contributor.authorDesai, Tarishi-
dc.contributor.authorGreen, Cherie-
dc.contributor.authorTrevis, Krysta-
dc.contributor.authorBrown, Natasha-
dc.contributor.authorDelatycki, Martin B-
dc.contributor.authorScheffer, Ingrid E-
dc.contributor.authorWilson, Sarah-
dc.date2023-
dc.date.accessioned2023-12-13T05:24:48Z-
dc.date.available2023-12-13T05:24:48Z-
dc.date.issued2023-11-30-
dc.identifier.citationAutism Research : Official Journal of the International Society for Autism Research 2023-11-30en_US
dc.identifier.issn1939-3806-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34424-
dc.description.abstractRelatives of individuals with autism spectrum disorder (ASD) may display milder social traits of the broader autism phenotype (BAP) providing potential endophenotypic markers of genetic risk for ASD. We performed a case-control comparison to quantify social cognition and pragmatic language difficulties in the BAP (n = 25 cases; n = 33 controls) using the Faux Pas test (FPT) and the Goldman-Eisler Cartoon task. Using deep phenotyping we then examined patterns of inheritance of social cognition in two large multiplex families and the spectrum of performance in 32 additional families (159 members; n = 51 ASD, n = 87 BAP, n = 21 unaffected). BAP individuals showed significantly poorer FPT performance and reduced verbal fluency with the absence of a compression effect in social discourse compared to controls. In multiplex families, we observed reduced FPT performance in 89% of autistic family members, 63% of BAP relatives and 50% of unaffected relatives. Across all affected families, there was a graded spectrum of difficulties, with ASD individuals showing the most severe FPT difficulties, followed by the BAP and unaffected relatives compared to community controls. We conclude that relatives of probands show an inherited pattern of graded difficulties in social cognition with atypical faux pas detection in social discourse providing a novel candidate endophenotype for ASD.en_US
dc.language.isoeng-
dc.subjectautism spectrum disorderen_US
dc.subjectbehavioral geneticsen_US
dc.subjectbroader autism phenotypeen_US
dc.subjectlanguage pragmaticsen_US
dc.subjectsocial cognitionen_US
dc.titleEndophenotyping social cognition in the broader autism phenotype.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAutism Research : Official Journal of the International Society for Autism Researchen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationMelbourne School of Psychological Sciences, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Psychology, Counselling & Therapy, School of Psychology and Public Health, La Trobe University, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationMelbourne School of Psychological Sciences, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationVictorian Clinical Genetics Service, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.;Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.;Bruce Lefroy Centre, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationRadiologyen_US
dc.identifier.affiliationMelbourne School of Psychological Sciences, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.doi10.1002/aur.3057en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-9519-2495en_US
dc.identifier.orcid0009-0007-5648-6790en_US
dc.identifier.orcid0000-0002-3160-2106en_US
dc.identifier.orcid0000-0003-3572-1839en_US
dc.identifier.orcid0000-0002-1822-9191en_US
dc.identifier.orcid0000-0002-2311-2174en_US
dc.identifier.orcid0000-0002-2678-1576en_US
dc.identifier.pubmedid38037242-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptClinical Genetics-
crisitem.author.deptEpilepsy Research Centre-
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