U.S. authorizes rapid blood test for fragile X syndrome
A new blood test can identify within seven hours whether a person carries the genetic mutation underlying fragile X syndrome.
A new blood test can identify within seven hours whether a person carries the genetic mutation underlying fragile X syndrome.
A new technique allows researchers to analyze raw data across multiple studies that use electroencephalography.
A new technique detects rare mutations that occur in only a subset of the body’s cells.
A new jumpsuit is fitted with sensors that can track and classify an infant’s posture and movements.
Electronic neurons made from silicon mimic brain cells and could be used to treat conditions such as autism.
A new resource details the genetic diversity of people in Asia and may shed light on genetic conditions such as autism.
Mutations in a gene called ZNF292 lead to a variety of developmental conditions, including autism and intellectual disability.
A new database cross-checks study participants to avoid double-counting variants linked to autism genes.
Nearly one-third of autistic young people put themselves or others in danger in any given three-month period.
A mix of two drugs eases hypersensitivity to noise in mice missing an autism gene — offering the promise of a similar treatment for autistic people.