Author: Daniel H. Geschwind

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Preprints

Single-cell in situ transcriptomic map of astrocyte cortical layer diversity

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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Global changes in patterning, splicing and primate specific lncRNAs in autism brain

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Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

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A single cell transcriptomic analysis of human neocortical development

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De novo mutations in regulatory elements cause neurodevelopmental disorders

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Genetic control of gene expression and splicing in the developing human brain

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Atypical neurogenesis in induced pluripotent stem cell (iPSC) from autistic individuals

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Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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Transcriptional reprogramming of distinct peripheral sensory neuron subtypes after axonal injury

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Transcriptomic and Cellular Decoding of Regional Brain Vulnerability to Neurodevelopmental Disorders

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Inducible And Reversible Phenotypes In A Novel Mouse Model Of Friedreich's Ataxia

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Correspondence between resting state activity and brain gene expression

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Cell-type specific effects of genetic variation on chromatin accessibility during human neuronal differentiation

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Genetic overlap between educational attainment, schizophrenia and autism

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Widespread RNA editing dysregulation in Autism Spectrum Disorders

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Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism

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Neuronal and glial 3D chromatin architecture illustrates cellular etiology of brain disorders

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Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 CNV Mediated Risk for Neuropsychiatric Disorders

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Evolutionary conservation and divergence of human brain co-expression networks

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Alterations in retrotransposition, synaptic connectivity, and myelination implicated by transcriptomic changes following maternal immune activation in non-human primates

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