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Christopher A. Walsh

Researcher at Howard Hughes Medical Institute

Publications -  470
Citations -  62520

Christopher A. Walsh is an academic researcher from Howard Hughes Medical Institute. The author has contributed to research in topics: Cerebral cortex & Microcephaly. The author has an hindex of 123, co-authored 455 publications receiving 55874 citations. Previous affiliations of Christopher A. Walsh include University of Liverpool & Newcastle University.

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Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

TL;DR: Analysis of a patient with hemimegalencephaly due to a somatic CNV of chromosome 1q found unexpected tetrasomy 1q in ~20% of neurons, suggesting that CNVs in a minority of cells can cause widespread brain dysfunction.
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Single-cell analysis reveals transcriptional heterogeneity of neural progenitors in human cortex

TL;DR: Single-cell transcriptional profiling in human, ferret and mouse revealed more cells coexpressing proneural neurogenin targets in human than in other species, suggesting greater neuronal lineage commitment and differentiation of self-renewing progenitors.
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Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior

TL;DR: Using chromatin interaction sequencing, massively parallel reporter assays, and transgenic mice, genetic evidence is provided that specific HARs are essential for normal development, consistent with suggestions that their evolutionary changes may have altered social and/or cognitive behavior.
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Cux1 and Cux2 regulate dendritic branching, spine morphology and synapses of the upper layer neurons of the cortex

TL;DR: Using knockout and knockdown studies combined with morphological, molecular, and electrophysiological analysis, it is shown that the homeobox Cux1 and Cux2 are intrinsic and complementary regulators of dendrite branching, spine development, and synapse formation in layer II-III neurons of the cortex.
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Systematic widespread clonal organization in cerebral cortex

TL;DR: The data suggest that migratory multipotential progenitors divide asymmetrically at intervals defined by cell cycle length, producing single cells or clusters of cells in different cortical regions, which may correspond to changes in migratory behavior.