J Mogensen

Summary

Affiliation: Aarhus Amtssygehus
Country: Denmark

Publications

  1. ncbi request reprint Assignment of the human cardiac troponin I gene (TNNI3) to chromosome 19q13.4 by radiation hybrid mapping
    J Mogensen
    Department of Cardiology, Skejby University Hospital, Aarhus, Denmark
    Cytogenet Cell Genet 79:272-3. 1997
  2. pmc Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
    J Mogensen
    Department of Cardiology, and Research Unit for Molecular Medicine, Skejby University Hospital, Brendstrupgaardsvej, DK 8200 Aarhus N, Denmark
    J Clin Invest 103:R39-43. 1999
  3. ncbi request reprint Refined localization of the human alpha-tropomyosin gene (TPM1) by genetic mapping
    J Mogensen
    Department of Cardiology and Research Unit for Molecular Medicine, Skejby University Hospital, Arhus N, Denmark
    Cytogenet Cell Genet 84:35-6. 1999
  4. ncbi request reprint Assignment of the human skeletal muscle [FC12]a-actin gene (ACTA1) to chromosome 1q42.13-->q42.2 by radiation hybrid mapping
    J Mogensen
    Department of Cardiology and Research Unit for Molecular Medicine, Skejby University Hospital, Denmark
    Cytogenet Cell Genet 83:224-5. 1998
  5. pmc Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations
    P S Andersen
    J Med Genet 38:E43. 2001
  6. pmc Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy
    J Mogensen
    J Med Genet 40:e59. 2003
  7. pmc Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy
    J Mogensen
    J Med Genet 41:e10. 2004
  8. pmc Myocardial late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy caused by mutations in troponin I
    J C Moon
    Centre for Advanced Magnetic Resonance in Cardiology, Royal Brompton Hospital, London, UK
    Heart 91:1036-40. 2005
  9. pmc Prevalence and clinical significance of systolic impairment in hypertrophic cardiomyopathy
    R Thaman
    The Heart Hospital, University College London, London, UK
    Heart 91:920-5. 2005

Collaborators

Detail Information

Publications9

  1. ncbi request reprint Assignment of the human cardiac troponin I gene (TNNI3) to chromosome 19q13.4 by radiation hybrid mapping
    J Mogensen
    Department of Cardiology, Skejby University Hospital, Aarhus, Denmark
    Cytogenet Cell Genet 79:272-3. 1997
  2. pmc Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
    J Mogensen
    Department of Cardiology, and Research Unit for Molecular Medicine, Skejby University Hospital, Brendstrupgaardsvej, DK 8200 Aarhus N, Denmark
    J Clin Invest 103:R39-43. 1999
    ..We hypothesize that ACTC mutations affecting sarcomere contraction lead to FHC and that mutations affecting force transmission from the sarcomere to the surrounding syncytium lead to IDC...
  3. ncbi request reprint Refined localization of the human alpha-tropomyosin gene (TPM1) by genetic mapping
    J Mogensen
    Department of Cardiology and Research Unit for Molecular Medicine, Skejby University Hospital, Arhus N, Denmark
    Cytogenet Cell Genet 84:35-6. 1999
  4. ncbi request reprint Assignment of the human skeletal muscle [FC12]a-actin gene (ACTA1) to chromosome 1q42.13-->q42.2 by radiation hybrid mapping
    J Mogensen
    Department of Cardiology and Research Unit for Molecular Medicine, Skejby University Hospital, Denmark
    Cytogenet Cell Genet 83:224-5. 1998
  5. pmc Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations
    P S Andersen
    J Med Genet 38:E43. 2001
  6. pmc Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy
    J Mogensen
    J Med Genet 40:e59. 2003
  7. pmc Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy
    J Mogensen
    J Med Genet 41:e10. 2004
  8. pmc Myocardial late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy caused by mutations in troponin I
    J C Moon
    Centre for Advanced Magnetic Resonance in Cardiology, Royal Brompton Hospital, London, UK
    Heart 91:1036-40. 2005
    ..To examine the influence of genotype on late gadolinium enhancement (LGE) and the potential of cardiovascular magnetic resonance (CMR) to detect preclinical hypertrophic cardiomyopathy...
  9. pmc Prevalence and clinical significance of systolic impairment in hypertrophic cardiomyopathy
    R Thaman
    The Heart Hospital, University College London, London, UK
    Heart 91:920-5. 2005
    ..To determine the frequency of systolic impairment (SI) and its impact on the natural history of hypertrophic cardiomyopathy (HCM)...