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Abstract Neurodevelopmental disorders arise due to various risk factors that can perturb different stages of brain development, and a combinatorial impact of these risk factors programs the phenotype in adulthood. While modeling the complete phenotype of a neurodevelopmental disorder is challenging, individual developmental perturbations can be successfully modeled in vivo in animals and in vitro in human cellular models. Nevertheless, our limited knowledge of human brain development restricts modeling strategies and has raised questions of how well a model corresponds to human in vivo brain development. Recent progress in high-resolution analysis of human tissue with single-cell and spatial omics techniques has enhanced our understanding of the complex events that govern the development of the human brain in health and disease. This new knowledge can be utilized to improve modeling of neurodevelopmental disorders and pave the way to more accurately portraying the relevant developmental perturbations in disease models.
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Konstantin Khodosevich
University of Copenhagen
Carl M. Sellgren
Karolinska Institutet
Molecular Psychiatry
Karolinska Institutet
University of Copenhagen
Stockholm County Council
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Khodosevich et al. (Fri,) studied this question.
synapsesocial.com/papers/696f7c4d30899b4a561dd91c — DOI: https://doi.org/10.1038/s41380-022-01876-1