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Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.
Levy, Michael A; Beck, David B; Metcalfe, Kay; Douzgou, Sofia; Sithambaram, Sivagamy; Cottrell, Trudie; Ansar, Muhammad; Kerkhof, Jennifer; Mignot, Cyril; Nougues, Marie-Christine; Keren, Boris; Moore, Hannah W; Oegema, Renske; Giltay, Jacques C; Simon, Marleen; van Jaarsveld, Richard H; Bos, Jessica; van Haelst, Mieke; Motazacker, M Mahdi; Boon, Elles M J; Santen, Gijs W E; Ruivenkamp, Claudia A L; Alders, Marielle; Luperchio, Teresa Romeo; Boukas, Leandros; Ramsey, Keri; Narayanan, Vinodh; Schaefer, G Bradley; Bonasio, Roberto; Doheny, Kimberly F; Stevenson, Roger E; Banka, Siddharth; Sadikovic, Bekim; Fahrner, Jill A.
Afiliação
  • Levy MA; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON, N6A5W9, Canada.
  • Beck DB; National Human Genome Research Institute, Bethesda, MD, 20892, USA.
  • Metcalfe K; Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PL, UK.
  • Douzgou S; Manchester Centre for Genomic Medicine, St Mary's Hospital, Health Innovation Manchester, Manchester University NHS Foundation Trust, Manchester, M13 9WL, UK.
  • Sithambaram S; Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M13 9PL, UK.
  • Cottrell T; Manchester Centre for Genomic Medicine, St Mary's Hospital, Health Innovation Manchester, Manchester University NHS Foundation Trust, Manchester, M13 9WL, UK.
  • Ansar M; Manchester Centre for Genomic Medicine, St Mary's Hospital, Health Innovation Manchester, Manchester University NHS Foundation Trust, Manchester, M13 9WL, UK.
  • Kerkhof J; Manchester Centre for Genomic Medicine, St Mary's Hospital, Health Innovation Manchester, Manchester University NHS Foundation Trust, Manchester, M13 9WL, UK.
  • Mignot C; Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, 45320, Islamabad, Pakistan.
  • Nougues MC; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON, N6A5W9, Canada.
  • Keren B; Assistance Publique-Hopitaux de Paris, Sorbonne Université, Departement de Génétique, Groupe Hospitalier Pitie-Salpetriere et Hopital Trousseau, Paris, 75651, France.
  • Moore HW; Department of Neuropediatrics, Armand Trousseau Hospital, Assistance Publique-Hopitaux de Paris, Paris, 75012, France.
  • Oegema R; Laboratoire de génétique, Hôpital Pïtié-Salpêtrière, Assistance Publique-Hopitaux de Paris, Paris, 75013, France.
  • Giltay JC; Greenwood Genetic Center, Greenwood, SC, 29646, USA.
  • Simon M; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • van Jaarsveld RH; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Bos J; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • van Haelst M; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Motazacker MM; Section Clinical Genetics, Department Human Genetics, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
  • Boon EMJ; Section Clinical Genetics, Department Human Genetics, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
  • Santen GWE; Department of Human Genetics, Laboratory of Genome Diagnostics, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, Netherlands.
  • Ruivenkamp CAL; Department of Human Genetics, VU University Medical Center Amsterdam, Amsterdam UMC, van der Boechorststraat 7, 1081 BT, Amsterdam, The Netherlands.
  • Alders M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Luperchio TR; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Boukas L; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
  • Ramsey K; Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
  • Narayanan V; Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
  • Schaefer GB; Department of Biostatistics, Johns Hopkins University, Baltimore, MD, 21205, USA.
  • Bonasio R; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ, USA.
  • Doheny KF; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ, USA.
  • Stevenson RE; University of Arkansas for Medical Sciences, Springdale, AR, 72762, USA.
  • Banka S; Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
  • Sadikovic B; Epigenetics Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
  • Fahrner JA; Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
NPJ Genom Med ; 6(1): 100, 2021 Nov 24.
Article em En | MEDLINE | ID: mdl-34819528
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article