K G Meilleur

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. 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
  2. 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
  3. 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
  • Jie Zhou
  • Ayo P Doumatey
  • Hanxia Huang
  • Charles N Rotimi
  • Alan Herbert
  • Guanjie Chen
  • Amy R Bentley
  • Daniel Shriner
  • Norman P Gerry
  • Michael F Christman

Detail Information

Publications3

  1. 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
    ....
  2. 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
    ....
  3. 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...