Article open access publication

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Nature Genetics, Springer Nature, ISSN 1061-4036

Volume 45, 7, 2013

DOI:10.1038/ng.2646, Dimensions: pub.1008791569, PMC: PMC3704157, PMID: 23708187,



  1. (1) University of Washington, grid.34477.33
  2. (2) University of Melbourne, grid.1008.9
  3. (3) VA Puget Sound Health Care System, grid.413919.7
  4. (4) Neurosciences Children's Health Queensland, Royal and Mater Children's Hospitals, Brisbane, Queensland, Australia
  5. (5) University of Otago, grid.29980.3a
  6. (6) Department of Paediatric Neurology, University of New South Wales, Sydney Children's Hospital, Sydney, New South Wales, Australia
  7. (7) Department of Neurology, Westmead Hospital, University of Sydney, Sydney, New South Wales, Australia
  8. (8) Royal Children's Hospital, grid.416107.5
  9. (9) Schneider Children's Medical Center, grid.414231.1
  10. (10) Murdoch Children's Research Institute, grid.1058.c
  11. (11) Monash Medical Centre, grid.416060.5
  12. (12) Children's Hospital at Westmead, grid.413973.b
  13. (13) Tel Aviv University, grid.12136.37
  14. (14) Department of Pediatrics, Carmel Medical Center, Technion Faculty of Medicine, Haifa, Israel
  15. (15) Wolfson Medical Center, grid.414317.4
  16. (16) Filadelfia, grid.452376.1
  17. (17) University of Toronto, grid.17063.33
  18. (18) Florey Institute of Neuroscience and Mental Health, grid.418025.a


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Times Cited: 415

Field Citation Ratio (FCR): 42.37

Relative Citation ratio (RCR): 13.29

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Green, Accepted