Tom Van Agtmael

Summary

Affiliation: University of Edinburgh
Country: UK

Publications

  1. ncbi Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy
    Tom Van Agtmael
    Molecular Physiology, Centre for Cardiovascular Science, University of Edinburgh, UK
    Hum Mol Genet 14:3161-8. 2005
  2. ncbi Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Parkville, Melbourne, Australia
    Eur J Hum Genet 10:623-30. 2002
  3. ncbi Parametric and nonparametric genome scan analyses for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Melbourne, Australia
    Eur J Hum Genet 11:779-83. 2003
  4. ncbi COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps
    Emmanuelle Plaisier
    INSERM Unité 702, Universite Pierre et Marie Curie, Paris 6, Unités Mixtes de Recherche Scientifique 702, Assistance Publique Hopitaux de Paris, Hopital Tenon, France
    N Engl J Med 357:2687-95. 2007

Detail Information

Publications4

  1. ncbi Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy
    Tom Van Agtmael
    Molecular Physiology, Centre for Cardiovascular Science, University of Edinburgh, UK
    Hum Mol Genet 14:3161-8. 2005
    ....
  2. ncbi Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Parkville, Melbourne, Australia
    Eur J Hum Genet 10:623-30. 2002
    ..This demonstrates the power to identify the genes specifying handedness by the conduct of extended genetic studies on these and similar cohorts...
  3. ncbi Parametric and nonparametric genome scan analyses for human handedness
    Tom Van Agtmael
    Murdoch Childrens Research Institute, Royal Children s Hospital, Melbourne, Australia
    Eur J Hum Genet 11:779-83. 2003
    ..These results suggest that handedness is a human quantitative trait locus and that the proposed non-Mendelian monogenic models are incorrect...
  4. ncbi COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps
    Emmanuelle Plaisier
    INSERM Unité 702, Universite Pierre et Marie Curie, Paris 6, Unités Mixtes de Recherche Scientifique 702, Assistance Publique Hopitaux de Paris, Hopital Tenon, France
    N Engl J Med 357:2687-95. 2007
    ..However, the causative genes for a number of hereditary multicystic kidney diseases, myopathies with cramps, and heritable intracranial aneurysms remain unknown...