An integrative system biology approach to delineate complex genotype-phenotype associations in Autism Spectrum Disorder

Introduction: Autism Spectrum Disorder (ASD) is characterized by deficits in social interaction and communication, and by the presence of repetitive behavior and/or restricted interests. ASD manifests with heterogeneous phenotype and has an estimated global prevalence of ~1%;- ASD is difficult to di...

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Detalhes bibliográficos
Autor principal: Asif, M (author)
Outros Autores: Martiniano, Hugo F. (author), Rasga, Celia (author), Marques, Ana R. (author), Santos, Joao X. (author), O., Guiomar (author), Couto, Francisco M. (author), Vicente, Astrid M. (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2017
Assuntos:
Texto completo:http://hdl.handle.net/10400.18/4852
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/4852
Descrição
Resumo:Introduction: Autism Spectrum Disorder (ASD) is characterized by deficits in social interaction and communication, and by the presence of repetitive behavior and/or restricted interests. ASD manifests with heterogeneous phenotype and has an estimated global prevalence of ~1%;- ASD is difficult to diagnose in very young children. Delayed diagnosis leads to delay in applying behavioral therapies that may help to reduce symptoms, particularly when applied at young age; - Copy Number Variant (CNV) screening has been widely used for primary diagnosis purposes and is associated with phenotypic variability in ASD patients; - Large scale studies have identified hundreds of ASD implicated loci; however, mechanistic and clinical interpretation of these disease-causing variants remains elusive.