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Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders.
Levy, Michael A; Relator, Raissa; McConkey, Haley; Pranckeviciene, Erinija; Kerkhof, Jennifer; Barat-Houari, Mouna; Bargiacchi, Sara; Biamino, Elisa; Palomares Bralo, María; Cappuccio, Gerarda; Ciolfi, Andrea; Clarke, Angus; DuPont, Barbara R; Elting, Mariet W; Faivre, Laurence; Fee, Timothy; Ferilli, Marco; Fletcher, Robin S; Cherick, Florian; Foroutan, Aidin; Friez, Michael J; Gervasini, Cristina; Haghshenas, Sadegheh; Hilton, Benjamin A; Jenkins, Zandra; Kaur, Simranpreet; Lewis, Suzanne; Louie, Raymond J; Maitz, Silvia; Milani, Donatella; Morgan, Angela T; Oegema, Renske; Østergaard, Elsebet; Pallares, Nathalie R; Piccione, Maria; Plomp, Astrid S; Poulton, Cathryn; Reilly, Jack; Rius, Rocio; Robertson, Stephen; Rooney, Kathleen; Rousseau, Justine; Santen, Gijs W E; Santos-Simarro, Fernando; Schijns, Josephine; Squeo, Gabriella M; John, Miya St; Thauvin-Robinet, Christel; Traficante, Giovanna; van der Sluijs, Pleuntje J.
Affiliation
  • Levy MA; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, Ontario, Canada.
  • Relator R; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, Ontario, Canada.
  • McConkey H; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, Ontario, Canada.
  • Pranckeviciene E; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, Ontario, Canada.
  • Kerkhof J; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, Ontario, Canada.
  • Barat-Houari M; Autoinflammatory and Rare Diseases Unit, Medical Genetic Department for Rare Diseases and Personalized Medicine, CHU Montpellier, Montpellier, France.
  • Bargiacchi S; Medical Genetics Unit, "A. Meyer" Children Hospital of Florence, Florence, Italy.
  • Biamino E; Department of Pediatrics, University of Turin, Turin, Italy.
  • Palomares Bralo M; Institute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  • Cappuccio G; Department of Translational Medicine, Federico II University of Naples, Naples, Italy.
  • Ciolfi A; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.
  • Clarke A; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.
  • DuPont BR; Cardiff University School of Medicine, Cardiff, UK.
  • Elting MW; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Faivre L; Amsterdam UMC, University of Amsterdam, Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam, The Netherlands.
  • Fee T; INSERM-Université de Bourgogne UMR1231 GAD, Génétique Des Anomalies du Développement, FHU-TRANSLAD, UFR Des Sciences de Santé, Dijon, France.
  • Ferilli M; Centre de Référence Maladies Rares, Anomalies du Développement et Syndromes Malformatifs, Centre de Génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
  • Fletcher RS; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Cherick F; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.
  • Foroutan A; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Friez MJ; Genetic Medical Center, CHU Clermont Ferrand, France.
  • Gervasini C; Montpellier University, Reference Center for Rare Disease, Medical Genetic Department for Rare Disease and Personalize Medicine, CHU Montpellier, Montpellier, France.
  • Haghshenas S; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.
  • Hilton BA; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Jenkins Z; Division of Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
  • Kaur S; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.
  • Lewis S; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Louie RJ; Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Maitz S; Brain and Mitochondrial Research Group, Murdoch Children s Research Institute and Department of Paediatrics, University of Melbourne, Melbourne, Australia.
  • Milani D; BC Children's and Women's Hospital and Department of Medical Genetics, Faculty of Medicine, University of British Columbia.
  • Morgan AT; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Oegema R; Clinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, Hospital San Gerardo, Monza, Italy.
  • Østergaard E; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Pallares NR; Murdoch Children's Research Institute and Department of Paediatrics, University of Melbourne, Melbourne, Australia.
  • Piccione M; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Plomp AS; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Poulton C; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Reilly J; Autoinflammatory and Rare Diseases Unit, Medical Genetic Department for Rare Diseases and Personalized Medicine, CHU Montpellier, Montpellier, France.
  • Rius R; Medical Genetics Unit Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Robertson S; Amsterdam UMC, University of Amsterdam, Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam, The Netherlands.
  • Rooney K; Undiagnosed Diseases Program, Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Australia.
  • Rousseau J; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.
  • Santen GWE; Brain and Mitochondrial Research Group, Murdoch Children's Research Institute, Melbourne, Australia.
  • Santos-Simarro F; Department of Paediatrics, University of Melbourne, Melbourne, Australia.
  • Schijns J; Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Squeo GM; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, Ontario, Canada.
  • John MS; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.
  • Thauvin-Robinet C; CHU Sainte-Justine Research Center, University of Montreal, Montreal, Quebec, Canada.
  • Traficante G; Department of Clinical Genetics, LUMC, Leiden, The Netherlands.
  • van der Sluijs PJ; Institute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
Hum Mutat ; 43(11): 1609-1628, 2022 11.
Article in En | MEDLINE | ID: mdl-35904121
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Methylation / Neurodevelopmental Disorders Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Type: Article Affiliation country: Canada
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Methylation / Neurodevelopmental Disorders Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Type: Article Affiliation country: Canada