K G Meilleur

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. doi request reprint Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies
    Katherine G Meilleur
    National Institute of Nursing Research, NIH, Bethesda, MD, USA Electronic address
    Neuromuscul Disord 25:43-54. 2015
  2. pmc Transferability and fine mapping of genome-wide associated loci for lipids in African Americans
    Adebowale Adeyemo
    Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA
    BMC Med Genet 13:88. 2012
  3. pmc Interventions to improve patient education regarding multifactorial genetic conditions: a systematic review
    Katherine G Meilleur
    Johns Hopkins University, School of Nursing, Bethesda, Maryland, USA
    Am J Med Genet A 149:819-30. 2009
  4. pmc Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19
    K G Meilleur
    Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    Neurogenetics 11:313-8. 2010

Collaborators

  • F Mochel
  • Adebowale Adeyemo
  • Ayo P Doumatey
  • Amy R Bentley
  • Hanxia Huang
  • Charles N Rotimi
  • Michael F Christman
  • Guanjie Chen
  • Daniel Shriner
  • Norman P Gerry
  • Alan Herbert
  • Jie Zhou

Detail Information

Publications4

  1. doi request reprint Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies
    Katherine G Meilleur
    National Institute of Nursing Research, NIH, Bethesda, MD, USA Electronic address
    Neuromuscul Disord 25:43-54. 2015
    ..The NSAA is useful as a complementary outcome measure in ambulatory individuals. Preliminary concurrent validity of several other clinical outcome measures was also demonstrated for these subtypes. ..
  2. pmc Transferability and fine mapping of genome-wide associated loci for lipids in African Americans
    Adebowale Adeyemo
    Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA
    BMC Med Genet 13:88. 2012
    ....
  3. pmc Interventions to improve patient education regarding multifactorial genetic conditions: a systematic review
    Katherine G Meilleur
    Johns Hopkins University, School of Nursing, Bethesda, Maryland, USA
    Am J Med Genet A 149:819-30. 2009
    ....
  4. pmc Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19
    K G Meilleur
    Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    Neurogenetics 11:313-8. 2010
    ..11-q12 that was not shared by controls. These findings indicate a clinically and genetically distinct form of hereditary spastic paraplegia with amyotrophy, designated SPG43...