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  1. Brain mapping across 16 autism mouse models reveals a spectrum of functional connectivity subtypes.

    Publication

  2. Placental endocrine function shapes cerebellar development and social behavior.

    Publication

  3. Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling.

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  4. Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development.

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

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  6. Common functional networks in the mouse brain revealed by multi-centre resting-state fMRI analysis.

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  7. Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus.

    Publication

  8. Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions.

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  9. Altered neocortical gene expression, brain overgrowth and functional over-connectivity in Chd8 haploinsufficient mice.

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  10. Foxp1 in forebrain pyramidal neurons controls gene expression required for spatial learning and synaptic plasticity.

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  11. Foxp1 regulation of neonatal vocalizations via cortical development.

    Publication

  12. Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome.

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  13. Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.

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

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  15. Prenatal beta-catenin/BRN2/TBR2 transcriptional cascade regulates adult social and stereotypic behaviors.

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

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

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  18. Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.

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  19. Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.

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