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 Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder characterized
by core impairments in social communication as well as restricted, repetitive patterns of …

Abstract Fragile X Syndrome (FXS) is a monogenetic form of intellectual disability and
autism in which well-established knockout (KO) animal models point to neuronal …

There are no approved medicines for fragile X syndrome (FXS), a monogenic,
neurodevelopmental disorder. Electroencephalogram (EEG) studies show alterations in …

Fragile X syndrome (FXS) is one of the most common inherited causes of intellectual
disabilities. While there is currently no cure for FXS, EEG is considered an important method …

Introduction: Fragile X syndrome (FXS) is a genetic disorder caused by a mutation of the
fragile X mental retardation 1 gene (FMR1). FXS is associated with neurophysiological …

Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by a trinucleotide
expansion on the FMR1 gene and characterized by intellectual disability, sensory …

Abstract Objective Fragile X Syndrome (FXS) is the leading monogenic cause of intellectual
disability and autism spectrum disorder. Currently, there are no established biomarkers for …

Abstract Background Fragile X syndrome (FXS) is the most common inherited form of
neurodevelopmental disability. It is often characterized, especially in males, by intellectual …