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Paper Details

High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCs.
bioRxiv
2
2023
ASTN2 proteins, CNVs, DNTBP1, JARID2, KOLF2, haploinsufficiencies, iPSC, iPSC lines, iPSCs, neural cell lineages, neural progenitors, neurodegenerative disease, neurodevelopmental disorders, neurological, neurological disorders, stem cell
Author NameAffiliation
Ophir ShalemRaymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia
Ophir ShalemUniversity of Pennsylvania
Deborah L FrenchRaymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia
Deborah L FrenchUniversity of Pennsylvania
Joseph T GlessnerCenter for Applied Genomics, The Children's Hospital of Philadelphia
Naiara AkizuRaymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia
Naiara AkizuUniversity of Pennsylvania
Naiara Akizu
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