JEFFREY NEUL

Summary

Affiliation: Texas Medical Center
Country: USA

Publications

  1. pmc Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome
    J L Neul
    Section of Neurology, Department of Pediatrics, Baylor College of Medicine, Room 319C, One Baylor Plaza, Houston, TX 77030, USA
    Neurology 70:1313-21. 2008
  2. pmc Rett syndrome: revised diagnostic criteria and nomenclature
    Jeffrey L Neul
    Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA
    Ann Neurol 68:944-50. 2010
  3. ncbi request reprint Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas
    Stephen M Maricich
    Section of Neurology, Department of Pediatrics, Texas Children s Hospital, Houston, Texas, USA
    Pediatrics 114:e626-33. 2004
  4. ncbi request reprint Rett syndrome: a prototypical neurodevelopmental disorder
    Jeffrey L Neul
    Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA
    Neuroscientist 10:118-28. 2004
  5. ncbi request reprint Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
    Daniela del Gaudio
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA
    Genet Med 8:784-92. 2006
  6. pmc A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
    Rodney C Samaco
    Department of Molecular and Human Genetics, Houston, TX 77030, USA
    Hum Mol Genet 17:1718-27. 2008

Collaborators

Detail Information

Publications6

  1. pmc Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome
    J L Neul
    Section of Neurology, Department of Pediatrics, Baylor College of Medicine, Room 319C, One Baylor Plaza, Houston, TX 77030, USA
    Neurology 70:1313-21. 2008
    ..To determine if a relationship exists between the clinical features of Rett syndrome, an X-linked dominant neurodevelopmental disorder, and specific mutations in MECP2...
  2. pmc Rett syndrome: revised diagnostic criteria and nomenclature
    Jeffrey L Neul
    Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA
    Ann Neurol 68:944-50. 2010
    ..The purpose of this work was to revise and clarify 2002 consensus criteria for the diagnosis of RTT in anticipation of treatment trials...
  3. ncbi request reprint Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas
    Stephen M Maricich
    Section of Neurology, Department of Pediatrics, Texas Children s Hospital, Houston, Texas, USA
    Pediatrics 114:e626-33. 2004
    ....
  4. ncbi request reprint Rett syndrome: a prototypical neurodevelopmental disorder
    Jeffrey L Neul
    Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA
    Neuroscientist 10:118-28. 2004
    ..Thus, Rett syndrome is a prototype for the genetic, molecular, and neurobiological analysis of neurodevelopmental disorders...
  5. ncbi request reprint Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
    Daniela del Gaudio
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA
    Genet Med 8:784-92. 2006
    ..Recent clinical testing for MECP2 gene rearrangements revealed that entire MECP2 gene duplication occurs in some males manifesting a progressive neurodevelopmental syndrome...
  6. pmc A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
    Rodney C Samaco
    Department of Molecular and Human Genetics, Houston, TX 77030, USA
    Hum Mol Genet 17:1718-27. 2008
    ..These results indicate that precise control of MeCP2 is critical for normal behavior and predict that human neurodevelopmental disorders will result from a subtle reduction in MeCP2 expression...

Research Grants3

  1. Analysis of the dopamine system in Rett syndrome
    JEFFREY NEUL; Fiscal Year: 2007
    ..This insight may pave the way for future therapeutic strategies for other movement disorders such as: Parkinson's disease or Huntington's disease. ..
  2. Characterization of autonomic dysfunction in Rett syndrome and other MECP2 disord
    Jeffrey L Neul; Fiscal Year: 2010
    ....