Additional file 3 of Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
We report on results from whole-exome sequencing (WES) of 1,039 subjects diagnosed with autism spectrum disorders (ASD) and 870 controls selected from the NIMH repository to be of similar ancestry to
1)PolyPhen2 scores close to 1 are likely to be pathogenic (highlighted in bold). HumDiv-trained Polyphen-2 assumes even mildly deleterious alleles as damaging to evaluate rare alleles potentially invo
Objectives: Autism is a pervasive neurodevelopmental disorder with high heritability. Genetic factors play crucial roles in the aetiology of autism. Dual specificity phosphatase 15 (DUSP15) has been r
ap-value adjusted using Benjamini-Hochberg False Discovery Rate method; bBonferroni-adjusted p-value. *CNV located in Chromosomal band as reported by Pinto et al. [15].