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Paper Details

Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.
Nat Med
76
2020
CH, CH genes, CSF) accumulation, Congenital hydrocephalus, enlarged, excessive cerebrospinal fluid (, genetic, genetic disruption, human, neural stem cell, neural stem cell biology, patients, sporadic congenital hydrocephalus, ventriculomegaly
Author NameAffiliation
Rebecca L WalkerCenter for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, University of California Los Angeles
Christopher CastaldiYale Center for Genome Analysis, Yale University
Irina R TikhonovaYale Center for Genome Analysis, Yale University
James M JohnstonUniversity of Alabama School of Medicine
Eric M JacksonJohns Hopkins School of Medicine
Shrikant ManeYale University School of Medicine
Shrikant ManeYale Center for Genome Analysis, Yale University
Shozeb HaiderDepartment of Pharmaceutical and Biological Chemistry, University College London School of Pharmacy
Nenad SestanDepartment of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine
Nenad SestanDepartment of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine
Seth L AlperDivision of Nephrology and Center for Vascular Biology Research, Beth Israel Deaconess Medical Center, Harvard Medical School
Kaya BilguvarYale University School of Medicine
Kaya BilguvarYale Center for Genome Analysis, Yale University
Daniel H GeschwindDavid Geffen School of Medicine, University of California Los Angeles
Daniel H GeschwindDavid Geffen School of Medicine, University of California Los Angeles
Murat GunelYale University School of Medicine
Murat GunelYale University School of Medicine
Richard P LiftonThe Rockefeller University
Richard P LiftonYale University School of Medicine
Richard P LiftonThe Rockefeller University
Richard P LiftonYale University School of Medicine
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