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Paper Details

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet
54
2017
Cas9, Congenital Kidney Malformations, GREB1L, Hoxb1, LOF, RHD, Renal agenesis, SLIT3, Shha, Slit3, alleles, chronic kidney disease, congenital heart defect, greb1l, human, humans, hypodysplasia, kidney malformations, mRNA, mouse, pronephric defects, wild-type human GREB1L mRNA, zebrafish
Author NameAffiliation
Hila Milo RasoulyColumbia University
Krzysztof KirylukColumbia University
Krzysztof KirylukColumbia University
Matthew G SampsonUniversity of Michigan School of Medicine ann arbor
Friedhelm HildebrandtBoston Children's Hospital, Harvard Medical School
Shrikant ManeYale University School of Medicine
David B GoldsteinInstitute for Genomic Medicine, Columbia University Medical Center
David B GoldsteinInstitute for Genomic Medicine, Columbia University Medical Center
Richard P LiftonYale University School of Medicine, USA Howard Hughes Medical Institute
Richard P LiftonYale University School of Medicine, USA Howard Hughes Medical Institute
Nicholas KatsanisCenter for Human Disease Modeling, Duke University
Nicholas KatsanisCenter for Human Disease Modeling, Duke University
Ali G GharaviColumbia University
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