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Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders
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Editorial: Advancing neurodevelopmental disorder models with human iPSC and multi-omics integration

Wardiya Afshar-Saber1,2, Vanya Metodieva3, Angelica D'Amore1,2

  • 1Department of Neurology, F.M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.

Frontiers in Neuroscience
|November 28, 2025
PubMed
Summary

No abstract available in PubMed .

Keywords:
disease modelinginduced pluripotent stem cells (iPSCs)multi-omicsneurodevelopmental disordersoptogenetics

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iPS Cell Differentiation01:22

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The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
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EPS and iPS Cells in Disease Research

Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...

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