Additional file 3 of Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
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].
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
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
Afreq, allele frequency; Families, number of informative families; S, test statistics for the observed number of transmitted alleles; E(S), expected value of S under the null hypothesis (i.e., no link