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  1. Comparison of autism domains across thirty rare variant genotypes.

    Publication

  2. Effects of gene dosage and development on subcortical nuclei volumes in individuals with 22q11.2 copy number variations.

    Publication

  3. Subcortical brain alterations in carriers of genomic copy number variants.

    Publication

  4. Multi-ancestry phenome-wide association of complement component 4 variation with psychiatric and brain phenotypes in youth.

    Publication

  5. Subcortical brain alterations in carriers of genomic copy number variants.

    Publication

  6. Multi-site normative modeling of diffusion tensor imaging metrics using hierarchical Bayesian regression.

    Publication

  7. Copy number variation at the 22q11.2 locus influences prevalence, severity, and psychiatric impact of sleep disturbance.

    Publication

  8. Rare CNVs and phenome-wide profiling: A tale of brain-structural divergence and phenotypical convergence.

    Publication

  9. Molecular and connectomic vulnerability shape cross-disorder cortical abnormalities.

    Publication

  10. ENIGMA-DTI: Translating reproducible white matter deficits into personalized vulnerability metrics in cross-diagnostic psychiatric research.

    Publication

  11. Effects of eight neuropsychiatric copy number variants on human brain structure.

    Publication

  12. Structural and functional brain alterations revealed by neuroimaging in CNV carriers.

    Publication

  13. Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions.

    Publication

  14. Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders.

    Publication

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

    Publication

  16. Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.

    Publication

  17. Reciprocal copy number variations at 22q11.2 produce distinct and convergent neurobehavioral impairments relevant for schizophrenia and autism spectrum disorder.

    Publication

  18. The general impact of haploinsufficiency on brain connectivity underlies the pleiotropic effect of neuropsychiatric CNVs.

    Publication

  19. Mapping 22q11.2 gene dosage effects on brain morphometry.

    Publication

  20. Reverse pathway genetic approach identifies epistasis in autism spectrum disorders.

    Publication

  21. Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.

    Publication

  22. Autism traits in the RASopathies.

    Publication