Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.

Journal: American Journal of Human Genetics

Published: 2020-02-26

DOI: 10.1016/j.ajhg.2020.01.019

Affiliations: 40

Authors: 69

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Institutions Share
Greenwood Genetic Center (GGC), United States of America (USA) 0.10
London Health Sciences Centre (LHSC), Canada 0.09
Genetics of Development Disorders Team (GAD), France 0.07
AP-HP Pitié-Salpêtrière Hospital - Charles-Foix, France 0.06
Amsterdam Reproduction and Development, Netherlands 0.04
Maladies Rares: Génétique et Métabolisme (MRGM), France 0.04
Lyon University Hospital (HCL), France 0.04
IRCCS Bambino Gesù Children's Hospital, Italy 0.04
Epigenetics and Cell Fate Centre (EDC), France 0.04
Department of Pediatrics, McMaster University, Canada 0.03
Department of Pathology and Laboratory Medicine, UWO, Canada 0.03
Hôpital Armand-Trousseau, France 0.03
Department of Pediatrics, UdeM, Canada 0.03
Montpellier University Hospital, UM, France 0.03
Imagine Institute, France 0.03
Department of Pediatrics, UvA, Netherlands 0.01
Imaging and Brain, France 0.01
Donders Centre for Neuroscience, RU, Netherlands 0.01
St. Joseph's Health Care London, Canada 0.01
Centre Hospitalier Régional Universitaire de TOURS (CHRU de Tours), France 0.01
Cellules Souches, Plasticité Cellulaire, Régénération Tissulaire et Immunothérapie des Maladies Inflammatoires, France 0.01
French Rare Disease Network, France 0.01
Genetics of Learning and Disability Service (GOLD), Hunter Genetics, Australia 0.01
Department of Human Genetics, RU, Netherlands 0.01
Shinshu University Hospital, Japan 0.01
Pathology and Laboratory Medicine (PaLM), Canada 0.01
Department of Paediatrics, UWO, Canada 0.01
Institute of Molecular Genetics of Montpellier (IGMM), France 0.01
Schulich School of Medicine and Dentistry, UWO, Canada 0.01
Cochin Hospital, France 0.01
Laboratoire de Génétique Moléculaire et Génomique Médicale, CHU de Rennes, France 0.01
Centre de Génétique - Centre de Référence des Maladies Rares, Anomalies du Développement et Syndromes Malformatifs et Déficiences Intellectuelles de Causes Rares, Dijon University Hospital, France 0.01
Adelaide Medical School, Adelaide Uni, Australia 0.01
Robinson Research Institute (RRI), Adelaide Uni, Australia 0.01
Children's Health Research Institute (CHRI), Canada 0.01
Dijon University Hospital, France 0.01
Department of Biochemistry, UWO, Canada 0.01
South Australian Health and Medical Research Institute (SAHMRI), Australia 0

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