Ultra-rare variants point to new autism candidate genes
A large, whole-genome sequencing study of families yields insights into ultra-rare genetic variants that contribute to autism.
A large, whole-genome sequencing study of families yields insights into ultra-rare genetic variants that contribute to autism.
The double empathy theory challenges the idea that social difficulties are specific to autism and suggests that problems arise from a mismatch in perspective between autistic and non-autistic people.
When probing the circuits underlying social behavior in animal models of autism, researchers should consider potentially confounding variables, use multiple behavioral assays and report results in a descriptive and unbiased manner.
In this edition of Null and Noteworthy, researchers open the case on acetaminophen and close it on oxytocin.
Researchers can roughly project what autistic children’s lives will look like years down the road. But how good is their crystal ball — and what are its benefits?
A new method to track autism prevalence in 11 U.S. states is twice as fast as the old approach — and yields similar results.
Mosaic mutations, which affect only some of the body’s cells, play a small but meaningful role in autism. Though they are difficult to study, researchers are working to master their complexity.
The U.S. government today announced the latest iteration of the Interagency Autism Coordinating Committee, the body of scientists and advocates that helps set priorities for federally funded autism research and services.
Many of the genes strongly linked to autism are involved in the remodeling of chromatin, the complex of DNA and proteins that makes up chromosomes. Scientists are just beginning to understand why.
Young autistic children with sleep troubles tend to have difficulty regulating their behavior later in childhood.