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  1. Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.

    Publication

  2. Chromosome X-wide common variant association study in autism spectrum disorder.

    Publication

  3. Specific EEG resting state biomarkers in FXS and ASD.

    Publication

  4. The phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples.

    Publication

  5. Genomic architecture of autism from comprehensive whole-genome sequence annotation.

    Publication

  6. Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.

    Publication

  7. A recurrent SHANK3 frameshift variant in autism spectrum disorder.

    Publication

  8. A phase II randomized, double-blind, placebo-controlled study of the efficacy, safety, and tolerability of arbaclofen administered for the treatment of social function in children and adolescents with autism spectrum disorders: Study protocol for AIMS-2-TRIALS-CT1.

    Publication

  9. An epigenetically distinct subset of children with autism spectrum disorder resulting from differences in blood cell composition.

    Publication

  10. Genome-wide detection of tandem DNA repeats that are expanded in autism.

    Publication

  11. Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.

    Publication

  12. Language ability predicts cortical structure and covariance in boys with autism spectrum disorder.

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  13. Structural gray matter differences during childhood development in autism spectrum disorder: A multimetric approach.

    Publication

  14. Clustering autism: Using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity.

    Publication