Preprints

Dissociable cellular and genetic mechanisms of cortical thinning at different life stages.

Mobile elements in human population-specific genome and phenotype divergence.

Glial dysregulation in human brain in fragile X-related disorders.

Somatic mutations reveal hypermutable brains and are associated with neuropsychiatric disorders.

Enhancing the discriminatory power of ADHD and autism spectrum disorder polygenic scores in clinical and non-clinical samples.

Pax6 limits the competence of developing cerebral cortical cells.

Molecular and connectomic vulnerability shape cross-disorder cortical abnormalities.

Variability in sampling of cortex-wide neural dynamics explains individual differences in functional connectivity and behavioral phenotype.

Environmental carcinogens disproportionally mutate genes implicated in neurodevelopmental disorders.

Connectome-wide mega-analysis reveals robust patterns of atypical functional connectivity in autism.