Fragile X syndrome is caused by an expansion of CGG nucleotide repeats in the FMR1 gene at the end of the long arms of the X chromosome. To identify the mutation, researchers culture cells in media ...

The only way you can tell if someone has the condition is through a DNA test. “This process is easier if there is an ...

a study by MIT neuroscientists at The Picower Institute for Learning and Memory reports a new way to treat pathology and symptoms of fragile X syndrome, the most common genetically-caused autism ...

A new study suggests a potential molecular strategy for treating fragile X syndrome, an inherited neurodevelopmental disorder that causes autism spectrum disorder and intellectual disability.

Many couples consider lifestyle, nutrition, and timing when trying to conceive. Nevertheless, an important factor is frequently overlooked: genetics. Some genetic disorders can be passed from parents ...

The behavior of a person's genes doesn't just depend on the genes' DNA sequence - it's also affected by so-called epigenetic factors. Changes in these factors can play a critical role in disease.

Exclusive: A world-first Australian study could pave the way for all couples to have free genetic screening before starting a ...

People are more likely to have autism if they have related genetic disorders, such as fragile X syndrome, Rett syndrome, and tuberous sclerosis. Autism is also more likely due to a number of ...