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A genome-wide DNA methylation signature for SETD1B-related syndrome.
Krzyzewska, I M; Maas, S M; Henneman, P; Lip, K V D; Venema, A; Baranano, K; Chassevent, A; Aref-Eshghi, E; van Essen, A J; Fukuda, T; Ikeda, H; Jacquemont, M; Kim, H-G; Labalme, A; Lewis, S M E; Lesca, G; Madrigal, I; Mahida, S; Matsumoto, N; Rabionet, R; Rajcan-Separovic, E; Qiao, Y; Sadikovic, B; Saitsu, H; Sweetser, D A; Alders, M; Mannens, M M A M.
Affiliation
  • Krzyzewska IM; Amsterdam UMC, Department of Clinical Genetics, Genome Diagnostics laboratory Amsterdam, Reproduction & Development, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
  • Maas SM; Amsterdam UMC, Department of Pediatrics, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
  • Henneman P; Amsterdam UMC, Department of Clinical Genetics, Genome Diagnostics laboratory Amsterdam, Reproduction & Development, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
  • Lip KVD; Amsterdam UMC, Department of Clinical Genetics, Genome Diagnostics laboratory Amsterdam, Reproduction & Development, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
  • Venema A; Amsterdam UMC, Department of Clinical Genetics, Genome Diagnostics laboratory Amsterdam, Reproduction & Development, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
  • Baranano K; Kennedy Krieger Institute, Department of Neurogenetics, 801 N. Broadway, Rm 564, Baltimore, MD, 21205, USA.
  • Chassevent A; Kennedy Krieger Institute, Department of Neurogenetics, 801 N. Broadway, Rm 564, Baltimore, MD, 21205, USA.
  • Aref-Eshghi E; Department of Pathology and Laboratory Medicine, Western University, 800 Commissioner's Road E, London, ON, N6A 5W9, Canada.
  • van Essen AJ; University Medical Centre Groningen, University of Groningen, Department of Medical Genetics, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.
  • Fukuda T; Department of Pediatrics, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, 431-3192, Japan.
  • Ikeda H; National Epilepsy Centre, NHO, Shizuoka Institute of Epilepsy and Neurological Disorders, 886 Urushiyama, Aoi-ku, Shizuoka, 420-8688, Japan.
  • Jacquemont M; Department of medical genetics, CHU La Reunion-Groupe Hospitalier Sud Reunion, La Reunion, France.
  • Kim HG; Neurological Disorder Center Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
  • Labalme A; Department of medical genetics, Hospices Civils de Lyon, Bron, France.
  • Lewis SME; Department of Medical Genetics, Children's & Women's Health Centre of British Columbia University of British Columbia, C234-4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Lesca G; Department of medical genetics, Hospices Civils de Lyon, Bron, France.
  • Madrigal I; Biochemistry and Molecular Genetics Service, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Center for Biomedical Network Research on Rare Diseases (CIBERER), Barcelona, Spain.
  • Mahida S; Kennedy Krieger Institute, Department of Neurogenetics, 801 N. Broadway, Rm 564, Baltimore, MD, 21205, USA.
  • Matsumoto N; Department of Human Genetics, Graduate School of Medicine, Yokohama City University, Fukuura 3-9, Kanazawa-ku, Yokohama, 236-0004, Japan.
  • Rabionet R; Department of Genetics, Microbiology and Statistics, Faculty of Biology, University of Barcelona, av diagonal 643, 08028, Barcelona, Spain.
  • Rajcan-Separovic E; Department of Medical Genetics, Children's & Women's Health Centre of British Columbia University of British Columbia, C234-4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Qiao Y; Department of Medical Genetics, Children's & Women's Health Centre of British Columbia University of British Columbia, C234-4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Sadikovic B; Department of Pathology and Laboratory Medicine, Western University, 800 Commissioner's Road E, London, ON, N6A 5W9, Canada.
  • Saitsu H; Department of Biochemistry, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, 431-3192, Japan.
  • Sweetser DA; MassGeneral Hospital, Division of Medical Genetics and Metabolism, 175 Cambridge St, Suite 500, Boston, Massachusetts, 02114, USA.
  • Alders M; Amsterdam UMC, Department of Clinical Genetics, Genome Diagnostics laboratory Amsterdam, Reproduction & Development, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands. m.alders@amsterdamumc.nl.
  • Mannens MMAM; Amsterdam UMC, Department of Clinical Genetics, Genome Diagnostics laboratory Amsterdam, Reproduction & Development, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
Clin Epigenetics ; 11(1): 156, 2019 11 04.
Article in En | MEDLINE | ID: mdl-31685013
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Anxiety / Histone-Lysine N-Methyltransferase / DNA Methylation / Epilepsy / Autism Spectrum Disorder / Loss of Function Mutation / Intellectual Disability Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Newborn Language: En Journal: Clin Epigenetics Year: 2019 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Anxiety / Histone-Lysine N-Methyltransferase / DNA Methylation / Epilepsy / Autism Spectrum Disorder / Loss of Function Mutation / Intellectual Disability Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Newborn Language: En Journal: Clin Epigenetics Year: 2019 Document type: Article Affiliation country: