Fragile X Syndrome – UCEDD – UW–Madison

Is FMR1 CGG repeat number polymorphism associated with phenotypic variation in the general population?

Mild neurological signs in FMR1 premutation women in an unselected community-based cohort.

Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndrome.

Change in behavior problems from childhood through adolescence for children with fragile X syndrome.

Artificial intelligence-assisted phenotype discovery of fragile X syndrome in a population-based sample.

Change in the Behavioral Phenotype of Adolescents and Adults with FXS: Role of the Family Environment

Trajectory and Predictors of Depression and Anxiety Disorders in Mothers with the FMR1 Premutation

Brief Report: Autism Symptoms in Infants with Fragile X Syndrome

Infant Development in Fragile X Syndrome: Cross-Syndrome Comparisons

Language development in infants and toddlers with fragile X syndrome: change over time and the role of attention