The mutations occur spontaneously in noncoding stretches of DNA that control gene expression.

Women who carry genetic variants tied to autism have an elevated chance of experiencing pregnancy-related events linked to the condition in their children.

Deletion of the 22q11.2 chromosomal region alters the expression of numerous autism- and schizophrenia-linked genes, most of which are not contained within the deleted region, a new study suggests.

Genetic factors could help explain why the ‘social hormone’ failed to benefit autistic people in a phase 3 clinical trial last year.

The inflammation associated with the disease, particularly in mothers, may contribute to autism traits in children.

Even the best data practices and technology drop key variants in attempts to predict autism likelihood.

Scientists have at last filled in the missing gaps — an advance likely to inform every aspect of autism genetics research, Eichler says.

The X chromosome holds stronger-than-expected genetic sway over the structure of several brain regions. The genes that may underlie this oversized influence have ties to autism.

Spontaneous mutations in parts of the genome that regulate gene EBF3 appear to contribute to autism risk.

The more scientists dig into DNA, the more intricate its contribution to autism seems to be. Here, we unravel the complex genetics of autism.