PMC:4067558 / 26352-26740 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4067558","sourcedb":"PMC","sourceid":"4067558","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4067558","text":"We tested whether multiple genes within a CNV or across unlinked genetic lesions in the same individual might act in concert to increase risk of ASD. In logit modeling, the number of genes overlapped by CNVs, the average brain-expression value for those genes, and the deletion or duplication status were used as predictors with the case-control status as the outcome (Figures 3C and 3D).","tracks":[]}