YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction
Michele Gabriele(European Institute of Oncology), Giuseppe Testa(Human Technopole), Arie van Haeringen(Leiden University), Jozef Gécz(The University of Adelaide), Rolph Pfundt(Radboud University Nijmegen), Zöe Powis(Quest Diagnostics (United Kingdom)), Peter J. Anderson(Women's and Children's Hospital), David A. Koolen(Radboud University Nijmegen), David Rodriguez‐Buritica(The University of Texas Health Science Center at Houston), Christian P. Schaaf(University of Cologne), Christian Gilissen(Radboud University Nijmegen), Alessandro Vitriolo(European Institute of Oncology), Sophie Patrier(Université de Rouen Normandie), Eirik Frengen(Oslo University Hospital), Petter Strømme(Oslo University Hospital), Pernille Mathiesen Tørring(Odense University Hospital), Katharina Steindl(University of Zurich), Lisenka E.L.M. Vissers(Radboud University Nijmegen), Anita Rauch(University of Zurich), Kimberly Nugent(Baylor College of Medicine), Eric Haan(The University of Adelaide), Stefan H. Lelieveld(Radboud University Nijmegen), Jill A. Rosenfeld(Baylor College of Medicine), Christeen Ramane J. Pedurupillay(Neurology, Inc), Perla Thulin(University of Utah), Toshiki Takenouchi(Keio University), Pascal Chambon(Université de Pau et des Pays de l'Adour), Asbjørg Stray‐Pedersen(Baylor College of Medicine), Laura S. Farach(The University of Texas Health Science Center), Anneke T. Vulto‐van Silfhout(Radboud University Nijmegen), Doriana Misceo(Oslo University Hospital), Jennifer Friedman(Rady Children's Hospital-San Diego), Janneke Schuurs-Hoeijmakers(Radboud University Nijmegen), Yunru Shao(Boston Children's Hospital), Sally Ann Lynch(University College Dublin), Pierre‐Luc Germain(University of Zurich), Evelyn Douglas(South Australia Pathology), Kenjiro Kosaki(Keio University), Charlotte Brasch‐Andersen(University of Southern Denmark), Susanne Kjærgaard(Rigshospitalet), Scott McLean(School of the Art Institute of Chicago), Han G. Brunner(Radboud University Nijmegen), Jenny Morton(Birmingham Women's Hospital), Raman Kumar(The University of Adelaide), Willy M. Nillesen(Radboud University Nijmegen), Joris Andrieux(Hôpital Jeanne de Flandre), Jillian Nicholl(South Australia Pathology), Bregje W.M. van Bon(Radboud University Nijmegen), William J. Craigen(Baylor College of Medicine), Anne Ronan(Hunter Genetics)
Cited by 173
Related Papers
Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation
|New England Journal of Medicine|2016|774
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations
|Pediatric Neurology|2021|727