Publications

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Rare variants in axonogenesis genes connect three families with sound–color synesthesia

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Neural transcriptome of constitutional Pten dysfunction in mice and its relevance to human idiopathic autism spectrum disorder.

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Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.

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Balancing Proliferation and Connectivity in PTEN-associated Autism Spectrum Disorder.

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Germline disruption of Pten localization causes enhanced sex-dependent social motivation and increased glial production.

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