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  • Mice lacking full length Adgrb1 (Bai1) exhibit social deficits, increased seizure susceptibility, and altered brain development
  • Harnessing rare variants in neuropsychiatric and neurodevelopment disorders-a Keystone Symposia report
  • Stress-Sensitive Protein Rac1 and Its Involvement in Neurodevelopmental Disorders
  • Resting state EEG in youth with ASD: age, sex, and relation to phenotype
  • Maternal Plasma Metabolic Profile Demarcates a Role for Neuroinflammation in Non-Typical Development of Children
  • Pharmacologic Interventions for Irritability, Aggression, Agitation and Self-Injurious Behavior in Fragile X Syndrome: An Initial Cross-Sectional Analysis
  • Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts
  • Mapping brain asymmetry in health and disease through the ENIGMA consortium
  • A framework for the investigation of rare genetic disorders in neuropsychiatry
  • New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry