A new technique enables scientists to isolate, and chart gene expression in, tens of thousands of cells at once.

Watch the complete replay of Mark Bear discussing the latest research on treatments for fragile X syndrome.

Children with autism who carry mutations in the chromosomal region 16p11.2 or the gene CHD8 — two of the leading risk factors for autism — show distinct patterns of chemical tags on their DNA.

As prenatal testing improves, it presents a host of thorny issues — from what to test and how to interpret the results, to what to do about them.

A novel approach to microscopy reveals the sequences and spatial arrangement of DNA within cells.

Brain tissues from people with autism of unknown cause and from people with either of two genetic forms of the condition all show similar patterns of methyl groups on DNA.

A blood test can accurately detect whether a fetus carries large mutations of the kind linked to autism, according to pilot-study results.

Mice with extra copies of UBE3A, a gene linked to autism and related conditions, are susceptible to death from seizures.

About 81 percent of autism risk comes from inherited genetic factors, according to an analysis of more than 2 million children from five countries.

Mutations in the autism gene NLGN3 may alter the gut nervous system of mice.