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https://ahro.austin.org.au/austinjspui/handle/1/25212
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Trevis, Krysta J | - |
dc.contributor.author | Brown, Natasha J | - |
dc.contributor.author | Green, Cherie C | - |
dc.contributor.author | Lockhart, Paul J | - |
dc.contributor.author | Desai, Tarishi | - |
dc.contributor.author | Vick, Tanya | - |
dc.contributor.author | Anderson, Vicki | - |
dc.contributor.author | Pua, Emmanuel P K | - |
dc.contributor.author | Bahlo, Melanie | - |
dc.contributor.author | Delatycki, Martin B | - |
dc.contributor.author | Scheffer, Ingrid E | - |
dc.contributor.author | Wilson, Sarah J | - |
dc.date | 2020-10-27 | - |
dc.date.accessioned | 2020-11-05T03:48:48Z | - |
dc.date.available | 2020-11-05T03:48:48Z | - |
dc.date.issued | 2020-10-27 | - |
dc.identifier.citation | International Journal of Molecular Sciences 2020; 21(21): 7965 | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/25212 | - |
dc.description.abstract | Families comprising many individuals with Autism Spectrum Disorders (ASD) may carry a dominant predisposing mutation. We implemented rigorous phenotyping of the "Broader Autism Phenotype" (BAP) in large multiplex ASD families using a novel endophenotype approach for the identification and characterisation of distinct BAP endophenotypes. We evaluated ASD/BAP features using standardised tests and a semi-structured interview to assess social, intellectual, executive and adaptive functioning in 110 individuals, including two large multiplex families (Family A: 30; Family B: 35) and an independent sample of small families (n = 45). Our protocol identified four distinct psychological endophenotypes of the BAP that were evident across these independent samples, and showed high sensitivity (97%) and specificity (82%) for individuals classified with the BAP. Patterns of inheritance of identified endophenotypes varied between the two large multiplex families, supporting their utility for identifying genes in ASD. | en |
dc.language.iso | eng | |
dc.subject | Broader Autism Phenotype | en |
dc.subject | autism spectrum disorder | en |
dc.subject | genetic | en |
dc.subject | multiplex family | en |
dc.title | Tracing Autism Traits in Large Multiplex Families to Identify Endophenotypes of the Broader Autism Phenotype. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | International Journal of Molecular Sciences | en |
dc.identifier.affiliation | Department of Psychology and Counselling, School of Psychology and Public Health, La Trobe University, Bundoora, VIC 3086, Australia | en |
dc.identifier.affiliation | Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia | en |
dc.identifier.affiliation | Department of Paediatrics, The University of Melbourne, Parkville, VIC 3010, Australia | en |
dc.identifier.affiliation | Population Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia | en |
dc.identifier.affiliation | Department of Medical Biology, The University of Melbourne, Parkville, VIC 3010, Australia | en |
dc.identifier.affiliation | Psychological Service, The Royal Children's Hospital, Parkville, VIC 3052, Australia | en |
dc.identifier.affiliation | Barwon Health, Geelong, VIC 3220, Australia | en |
dc.identifier.affiliation | Medicine (University of Melbourne) | en |
dc.identifier.affiliation | Melbourne School of Psychological Sciences, The University of Melbourne, Parkville, VIC 3010, Australia | en |
dc.identifier.affiliation | The Florey Institute of Neuroscience and Mental Health, Parkville, VIC 3052, Australia | en |
dc.identifier.affiliation | Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia | en |
dc.identifier.affiliation | Clinical Sciences Research, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia | en |
dc.identifier.doi | 10.3390/ijms21217965 | en |
dc.type.content | Text | en |
dc.identifier.orcid | 0000-0003-3572-1839 | en |
dc.identifier.orcid | 0000-0003-2531-8413 | en |
dc.identifier.orcid | 0000-0001-9519-2495 | en |
dc.identifier.orcid | 0000-0001-5132-0774 | en |
dc.identifier.pubmedid | 33120939 | |
local.name.researcher | Delatycki, Martin B | |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Clinical Genetics | - |
crisitem.author.dept | Epilepsy Research Centre | - |
Appears in Collections: | Journal articles |
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