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