Collectively, neurodevelopmental disorders are highly prevalent, but more than a third of
neurodevelopmental disorders have an identifiable genetic etiology, each of which is …

The etiology of autism spectrum disorder (ASD) is genetic, environmental, and epigenetic. In
addition to sex differences in the prevalence of ASD, which is 3–4 times more common in …

Abstract Fragile X Syndrome (FXS) is a leading known genetic cause of intellectual disability
with symptoms that include increased anxiety and social and sensory processing deficits …

Fragile X syndrome (FXS) is a genetic neurodevelopmental disorder characterized by
intellectual disability and is related to autism. FXS is caused by mutations of the fragile X …

Nearly half of children with fragile X syndrome experience sleep problems including trouble
falling asleep and frequent nighttime awakenings. The goals here were to assess sleep …

Fragile X syndrome (FXS) is a rare genetic disease caused by mutations in the fifth
untranslated region of the FMRI gene situated on the Xq27. 3 site, resulting in an expansion …

Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by Fragile X
Messenger Ribonucleoprotein (FMRP) deficiency. Electroencephalogram (EEG) changes in …

Abstract Background Fragile X syndrome (FXS) is an X chromosome–linked genetic
disorder characterized by increased risk for behavioral, social, and neurocognitive deficits …

Sleep problems are a significant phenotype in children with fragile X syndrome. Our prior
work assessed sleep–wake cycles in Fmr1KO male mice and wild type (WT) littermate …

Introduction: Treatment studies in FMR1 knockout rodent models have found that
minocycline and lovastatin each improve synaptic, neurological, and behavioral functioning …