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Paper Details

Coexpression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders.
Genome Res
9
2020
ASD, NDD, NDDs, autism spectrum disorder, brain cell types, epilepsy, intermediate progenitor cell, neural progenitor cells, neurodevelopmental disorders, single
Author NameAffiliation
Chao ChengBaylor College of Medicine
Chao ChengInstitute for Clinical and Translational Research, Baylor College of Medicine
Chao ChengBaylor College of Medicine
Chao ChengInstitute for Clinical and Translational Research, Baylor College of Medicine
Zhandong LiuBaylor College of Medicine
Zhandong LiuJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital
Zhandong LiuComputational and Integrative Biomedical Research Center, Baylor College of Medicine
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Datasets

Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink