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.

Mutations that disrupt binding sites in RNA molecules may play a role in autism and a variety of psychiatric conditions, according to a new study.

Genetic variants that contribute to autism may also be involved in attention deficit hyperactivity disorder and Tourette syndrome, according to a new study.

Researchers expand a massive repository of data on gene activity in people to show differences between males and females.

Lowered expression of a gene called DDHD2 may increase a person’s likelihood of having autism, according to a new analysis.

Some of the inherited variants implicated in autism also increase the odds of schizophrenia, bipolar disorder, depression or attention deficit hyperactivity disorder.

A new analysis of nearly 40,000 people pinpoints 48 genetic variants that may determine the volume of certain brain areas.