Epigenomic and phenotypic characterization of DEGCAGS syndrome
Karim Karimi(London Health Sciences Centre), Sofia Douzgou(University of Manchester), Peter Krawitz(University of Bonn), Roberto Mendoza‐Londono(University of Toronto), Neveen A. Soliman(Cairo University), Sandip Bartakke(Aditya Birla Memorial Hospital), Mateusz Biela(Wroclaw Medical University), Henrik Døllner(Norwegian University of Science and Technology), Julie Paulsen(St Olav's University Hospital), Denisa Weis(Johannes Kepler University of Linz), Lynn Pais(MACOM (United States)), David Murphy(National Hospital for Neurology and Neurosurgery), Abdulrahman Aldeeri(Boston Children's Hospital), Jennifer Kerkhof(London Health Sciences Centre), Bassam Musa Sadik Al-Musawi(University of Baghdad), Małgorzata Rydzanicz(Medical University of Warsaw), Tracy Lau(National Hospital for Neurology and Neurosurgery), Franco Laccone(Medical University of Vienna), Raissa Relator(London Health Sciences Centre), Ingvild Aukrust(Haukeland University Hospital), Lucie Dupuis(University of Toronto), Tzung‐Chien Hsieh(University of Bonn), Timothy W. Yu(Broad Institute), Shirlee Shril(MACOM (United States)), Bekim Sadiković(Western University), Hellen Lesmann(University of Bonn), Friedhelm Hildebrandt(Boston Children's Hospital), Andrea Šoltýsová(Slovak Academy of Sciences), Henry Houlden(University College London), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Ruqayah G. Y. Al‐Obaidi(University of Baghdad), Khalid Hama Salih(University of Sulaimani), Michael S. Santos(Hospitais da Universidade de Coimbra), Jessica Rzasa(London Health Sciences Centre), Sérgio B. Sousa, Hanna T. Gazda(Boston Children's Hospital), Michael A. Levy(London Health Sciences Centre), Thomas M. Kitzler(McGill University), Gabriela V. Pilshofer, Tilman Jobst‐Schwan(Harvard University)
Cited by 6
Related Papers
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
The 2017 international classification of the Ehlers–Danlos syndromes
|American Journal of Medical Genetics Part C Seminars in Medical Genetics|2017|1.9k
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
Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease
|New England Journal of Medicine|2019|803