Research Articles

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.

Expression of genes in the 16p11.2 locus during development of the human fetal cerebral cortex.

Imputing the number of responders from the mean and standard deviation of CGI-Improvement in clinical trials investigating medications for autism spectrum disorder.

Recording gene expression order in DNA by CRISPR addition of retron barcodes.

Improving the measurement of alexithymia in autistic adults: A psychometric investigation of the 20-item Toronto Alexithymia Scale and generation of a general alexithymia factor score using item response theory.

“Guilt by association” is not competitive with genetic association for identifying autism risk genes.

Genetic correlates of phenotypic heterogeneity in autism.

Psychological distress among caregivers raising a child with autism spectrum disorder during the COVID-19 pandemic.

Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances.

Autism symptoms in anorexia nervosa: A comparative study with females with autism spectrum disorder.