Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus
Sheng Chih Jin(Yale University), Charles C. Duncan, Andrew T. Timberlake(IS practice), Tyrone DeSpenza(Duke University Hospital), Eric M. Jackson(Johns Hopkins University), Steven J. Schiff(McGill University), Helena Pérez‐Peña(University College London), Yaşar Bayri(Marmara University), Hannah Smith(Yale University), Bülent Güçlü(Dr Lütfi Kırdar Kartal Eğitim ve Araştırma Hastanesi), Edith Mbabazi Kabachelor(CURE Children’s Hospital of Uganda), Weilai Dong(Yale New Haven Hospital), June Goto(Brigham and Women's Hospital), Carol Nelson‐Williams(Howard Hughes Medical Institute), Rebecca L. Walker(Broad Institute), Christopher Castaldi(Yale University), Shozeb Haider(University College London), James R. Broach(Penn State Milton S. Hershey Medical Center), William E. Butler(Harvard University), Arnaud Marlier(Yale University), David D. Limbrick(Virginia Commonwealth University), Shrikant Mane(Yale Cancer Center), Shreyas Panchagnula(Yale University), Edward R. Smith(Boston Children's Hospital), James M. Johnston(Knoxville College), August Allocco(Yale University), Peter Ssenyonga(CURE Children’s Hospital of Uganda), Sierra Conine(Yale University), Adam J. Kundishora(Yale University), Bermans J. Iskandar(University of Wisconsin System), Jason K. Karimy(Yale University), Gregory G. Heuer(Children's Hospital of Philadelphia), Xue Zeng(Yale University), Ashley Dunbar(Yale University), Charuta G. Furey(Barrow Neurological Institute), Benjamin C. Reeves(Yale University), Christine Hehnly(Boston Children's Hospital), Andrés Moreno-De-Luca(Autism & Developmental Medicine Institute), Michael C. Sierant(Yale University), James Knight(Yale University), Qiongshi Lu(Yale University), Phan Q. Duy(Yale University), Francesco T. Mangano(Cincinnati Children's Hospital Medical Center), Boyang Li(Yale University), Ge Li(University of Wisconsin–Madison), William Sullivan(Yale University), Irina R. Tikhonova(Yale Cancer Center), Benjamin C. Warf(Boston Children's Hospital), Yener Şahin(Marmara University), Boris Keren(Sorbonne Université)
Cited by 162
Related Papers
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
|Neuron|2015|1.5k
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
|Neuron|2011|1.3k
Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel
|Cell|1994|1.3k