UC Davis MIND Institute researchers Randi and Paul Hagerman are calling for increased awareness and screening for fragile X-associated conditions. In a new paper published in the New England Journal ...

Mutations in FMR1, the gene encoding fragile X messenger ribonucleoprotein 1 (FMRP), located at Xq27.3 and discovered in 1991, are the leading single-gene causes of autism and intellectual disability.

Nearly a year and a half ago, I penned my final “From the Editor” column for Lowcountry Parent, sharing publicly for the first time about my son Archer’s diagnosis of Fragile X syndrome at 3 years old ...

Joel Richter receives funding from NIH and FRAXA. Sneha Shah receives funding from the FRAXA Research Foundation. Fragile X syndrome is a genetic disorder caused by a mutation in a gene that lies at ...