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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
2015
332 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
15.09
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling | Researchclopedia
Céline Helsmoortel
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University of Antwerp
Megan T. Cho
Alexander Hoischen
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Radboud University Nijmegen
Lisenka E.L.M. Vissers
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Radboud University Medical Center
Tom S. Koemans
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Radboud University Nijmegen
W.M. Wissink-Lindhout
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Radboud University Medical Center
Evan E. Eichler
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University of Washington
Corrado Romano
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Oasi Maria SS
Hilde Van Esch
Connie T. R. M. Stumpel
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Maastricht University Medical Centre
Maaike Vreeburg
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Maastricht University Medical Centre
Eric Smeets
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Maastricht University Medical Centre
Karin Oberndorff
Bregje W.M. van Bon
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Radboud University Medical Center
Marie Shaw
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University of Adelaide
Jozef Gécz
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University of Adelaide
Eric Haan
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South Australia Pathology
Melanie Bienek
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Max Planck Institute for Molecular Genetics
Corinna Jensen
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Max Planck Institute for Molecular Genetics
Bart Loeys
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Antwerp University Hospital
Anke Van Dijck
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University of Antwerp
A. Micheil Innes
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Alberta Children's Hospital
Hilary Racher
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University of Calgary
Sascha Vermeer
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University Medical Center Groningen
Nataliya Di Donato
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University Hospital Carl Gustav Carus
Andreas Rump
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TU Dresden
Katrina Tatton‐Brown
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St George's, University of London
Michael Parker
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Sheffield Children's Hospital
Alex Henderson
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Newcastle upon Tyne Hospitals NHS Foundation Trust
Sally Ann Lynch
Alan Fryer
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University of Liverpool
Alison Ross
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Wessex Regional Genetics Laboratory
Pradeep Vasudevan
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Leicester Royal Infirmary
Usha Kini
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Oxford University Hospitals NHS Trust
Ruth Newbury‐Ecob
Kate Chandler
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Manchester Academic Health Science Centre
Alison Male
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Great Ormond Street Hospital
Sybe Dijkstra
Jolanda Schieving
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Radboud University Medical Center
Jacques C. Giltay
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University Medical Center Utrecht
Koen L.I. van Gassen
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University Medical Center Utrecht
Janneke Schuurs-Hoeijmakers
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Radboud University Medical Center
Perciliz L. Tan
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Duke Medical Center
Igor Pediaditakis
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Duke University
Stefan A. Haas
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Max Planck Institute for Molecular Genetics
Kyle Retterer
Patrick Reed
Kristin G. Monaghan
Eden Haverfield
Marvin R. Natowicz
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Cleveland Clinic
Angela Myers
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Sanford Children's Specialty Clinic
Michael C. Kruer
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Barrow Neurological Institute
Quinn Stein
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Phoenix Children's Hospital
Kevin A. Strauss
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Franklin & Marshall College
Karlla W. Brigatti
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Clinic for Special Children
Katherine E. Keating
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Lurie Children's Hospital
Barbara K. Burton
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Lurie Children's Hospital
Katherine H. Kim
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Lurie Children's Hospital
Joel Charrow
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Lurie Children's Hospital
Jennifer Norman
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Integris Health
Audrey Foster‐Barber
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UCSF Benioff Children's Hospital
Antonie D. Kline
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Greater Baltimore Medical Center
Amy Kimball
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Greater Baltimore Medical Center
Elaine H. Zackai
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Children's Hospital of Philadelphia
Margaret Harr
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Children's Hospital of Philadelphia
Joyce E. Fox
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Cohen Children's Medical Center
Julie McLaughlin
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Cohen Children's Medical Center
Kristin Lindstrom
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Phoenix Children's Hospital
Katrina Haude
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University of Rochester Medical Center
Kees van Roozendaal
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Maastricht University Medical Centre
Han G. Brunner
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Maastricht University Medical Centre
Wendy K. Chung
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Columbia University Irving Medical Center
R. Frank Kooy
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Antwerp University Hospital
Rolph Pfundt
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Radboud University Nijmegen
Vera M. Kalscheuer
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Max Planck Institute for Molecular Genetics
Sarju Mehta
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Addenbrooke's Hospital
Nicholas Katsanis
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Duke University Hospital
Tjitske Kleefstra
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Radboud University Nijmegen