Search

What are you looking for?

  1. Phenotypically driven subgroups of ASD display distinct metabolomic profiles.

    Publication

  2. A genetics-first approach to dissecting the heterogeneity of autism: Phenotypic comparison of autism risk copy number variants.

    Publication

  3. Language characterization in 16p11.2 deletion and duplication syndromes.

    Publication

  4. Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.

    Publication

  5. Psychiatric disorders in children with 16p11.2 deletion and duplication.

    Publication

  6. Developmental trajectories for young children with 16p11.2 copy number variation.

    Publication

  7. Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplication.

    Publication

  8. The number of genomic copies at the 16p11.2 locus modulates language, verbal memory, and inhibition.

    Publication

  9. Clinical phenotype of the recurrent 1q21.1 copy-number variant.

    Publication

  10. Behavior and sensory interests questionnaire: Validation in a sample of children with autism spectrum disorder and other developmental disability.

    Publication

  11. Defining the effect of the 16p11.2 duplication on cognition, behavior, and medical comorbidities.

    Publication

  12. The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.

    Publication

  13. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.

    Publication

  14. Brief report: Prevalence of attention deficit/hyperactivity disorder among individuals with an autism spectrum disorder.

    Publication

  15. Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.

    Publication

  16. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

    Publication

  17. A multisite study of the clinical diagnosis of different autism spectrum disorders.

    Publication

  18. A pilot study to improve venipuncture compliance in children and adolescents with autism spectrum disorders.

    Publication

  19. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.

    Publication