Studies pinpoint key gene in region linked to autism
A single gene, OTUD7A, may account for most of the features seen in people missing a segment of chromosome 15 known as 15q13.3.
A single gene, OTUD7A, may account for most of the features seen in people missing a segment of chromosome 15 known as 15q13.3.
A semirural Colombian town called Ricaurte is home to the largest recorded genetic cluster of people with mutations linked to fragile X syndrome.
People with autism who are admitted to the hospital for self-injury tend to have low intelligence quotients and severe repetitive behaviors.
Spontaneous mutations that impair proteins may lead to motor problems in children with autism.
An algorithm combs through genetic data to identify variants involved in autism and four other brain conditions.
Existing genome scans do not detect many of the DNA variants that underlie behavioral problems.
Researchers find a surprising link between certain pollutants and reduced autism risk, the world welcomes — and fears — the first primate clones, and new U.S. clinical trial rules reverberate globally.
Black parents are less likely than white parents to report concerns about autism features in their children, human brain organoids in rodent bodies raise ethical concerns, and science graduate programs in the United States have few American students.
Two new gadgets join the gene-editing toolbox, many children with autism get smarter with age, and a survey points to a research reset for Autism Speaks.
People with autism who have rare, damaging mutations tend to have low scores on intelligence tests.