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Paper Details

Neuronal defects in a human cellular model of 22q11.2 deletion syndrome.
Nat Med
86
2020
22q11, 22q11DS, DGCR8, Neuronal, calcium, calcium abnormality, human, human cellular, induced pluripotent stem cells, neuronal excitability-related genes, neuropsychiatric disease, organoid, organoid- and 2D-derived cortical neurons, stem cell
Author NameAffiliation
Matthew H PorteusStanford University
Judith L RapoportNational Institute of Mental Health
Judith L RapoportNational Institute of Mental Health
Jonathan A BernsteinStanford University
Ruth O'HaraStanford University
Joachim HallmayerStanford University
Daniel H GeschwindUniversity of California Los Angeles
Daniel H GeschwindDavid Geffen School of Medicine, University of California Los Angeles
Daniel H GeschwindCenter for Autism Research and Treatment, Semel Institute, University of California Los Angeles
Daniel H GeschwindInstitute of Precision Health, University of California Los Angeles
Daniel H GeschwindUniversity of California Los Angeles
Daniel H GeschwindDavid Geffen School of Medicine, University of California Los Angeles
Daniel H GeschwindCenter for Autism Research and Treatment, Semel Institute, University of California Los Angeles
Daniel H GeschwindInstitute of Precision Health, University of California Los Angeles
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