Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndrome
Artificial intelligence-assisted phenotype discovery of fragile X syndrome in a population-based sample
Astroglial FMRP deficiency cell-autonomously up-regulates miR-128 and disrupts developmental astroglial mGluR5 signaling
Trajectories of Change in the Behavioral and Health Phenotype of Adolescents and Adults with Fragile X Syndrome and Intellectual Disability: Longitudinal Trends Over a Decade
Advances in Human Stem Cells and Genome Editing to Understand and Develop Treatment for Fragile X Syndrome
Comparing Tense and Agreement Productivity in Boys With Fragile X Syndrome, Children With Developmental Language Disorder, and Children With Typical Development
Expressive language sampling as a source of outcome measures for treatment studies in fragile X syndrome: feasibility, practice effects, test-retest reliability, and construct validity
