Journal article
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees
Abstract
Autism spectrum disorder (ASD) is a relatively common childhood onset neurodevelopmental disorder with a complex genetic etiology. While progress has been made in identifying the de novo mutational landscape of ASD, the genetic factors that underpin the ASD's tendency to run in families are not well understood. In this study, nine extended pedigrees each with three or more individuals with ASD, and others with a lesser autism phenotype, were …
Authors
Woodbury‐Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL
Journal
American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Vol. 183, No. 5, pp. 268–276
Publisher
Wiley
Publication Date
July 2020
DOI
10.1002/ajmg.b.32785
ISSN
1552-4841
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Autism Spectrum DisorderAutistic DisorderChildChild, PreschoolDNA Copy Number VariationsDNA Mutational AnalysisFemaleGene DosageGenetic LinkageGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansInfantMaleMutationNerve Tissue ProteinsPedigreePhenotypeRisk FactorsSynapsesWhole Genome Sequencing