Dalia Kasperaviciute

Summary

Affiliation: University College London
Country: UK

Publications

  1. ncbi request reprint Large-scale pathways-based association study in amyotrophic lateral sclerosis
    Dalia Kasperaviciute
    Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, UK
    Brain 130:2292-301. 2007
  2. doi request reprint Analysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosis
    Catherine J E Ingram
    The Centre for Genetic Anthropology, University College London Genetics Institute, Research Department of Genetics, Evolution and Environment, University College London, London WC1E 6BT, UK
    Amyotroph Lateral Scler 13:341-6. 2012
  3. pmc Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
    Dalia Kasperaviciute
    1 NIHR University College London Hospitals Biomedical Research Centre, Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK
    Brain 136:3140-50. 2013
  4. pmc Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
    Dalia Kasperaviciute
    Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK
    Brain 133:2136-47. 2010
  5. ncbi request reprint Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
    Jennifer C Schymick
    Laboratory of Neurogenetics, National Institute on Aging, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA
    Lancet Neurol 6:322-8. 2007

Collaborators

Detail Information

Publications5

  1. ncbi request reprint Large-scale pathways-based association study in amyotrophic lateral sclerosis
    Dalia Kasperaviciute
    Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, UK
    Brain 130:2292-301. 2007
    ..It is reliable for large scale genotyping studies of diseases such as ALS, where DNA sample collections are limited because of low disease prevalence and short survival time...
  2. doi request reprint Analysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosis
    Catherine J E Ingram
    The Centre for Genetic Anthropology, University College London Genetics Institute, Research Department of Genetics, Evolution and Environment, University College London, London WC1E 6BT, UK
    Amyotroph Lateral Scler 13:341-6. 2012
    ..Combining the data with other studies will allow meta-analysis to look for variants with modest effect sizes. The sequencing of complete mitochondrial genomes will be required to assess the role of rare mutations...
  3. pmc Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
    Dalia Kasperaviciute
    1 NIHR University College London Hospitals Biomedical Research Centre, Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK
    Brain 136:3140-50. 2013
    ....
  4. pmc Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
    Dalia Kasperaviciute
    Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK
    Brain 133:2136-47. 2010
    ..Data emerging from genome-wide association-studies will be valuable during the next serious challenge of interpreting all the genetic variation emerging from whole-genome sequencing studies...
  5. ncbi request reprint Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
    Jennifer C Schymick
    Laboratory of Neurogenetics, National Institute on Aging, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA
    Lancet Neurol 6:322-8. 2007
    ..We sought to identify genetic variants associated with an increased or decreased risk for developing ALS in a cohort of American sporadic cases...