Irma E Järvelä

Summary

Affiliation: Helsinki University Central Hospital
Country: Finland

Publications

  1. pmc Subjective face recognition difficulties, aberrant sensibility, sleeping disturbances and aberrant eating habits in families with Asperger syndrome
    Taina Nieminen-von Wendt
    Department of Child Neurology, Hospital for Children and Adolescents, Helsinki University Central Hospital, Helsinki, Finland
    BMC Psychiatry 5:20. 2005
  2. ncbi request reprint Genome-wide scan for loci of Asperger syndrome
    T Ylisaukko-oja
    Department of Molecular Medicine, National Public Health Institute, Biomedicum, PO Box 104, 00251 Helsinki, Finland
    Mol Psychiatry 9:161-8. 2004
  3. ncbi request reprint Molecular genetics of adult-type hypolactasia
    Irma E Järvelä
    Laboratory of Molecular Genetics, Helsinki University Central Hospital, Finland
    Ann Med 37:179-85. 2005
  4. ncbi request reprint Molecular diagnosis of adult-type hypolactasia (lactase non-persistence)
    I E Jarvela
    Laboratory of Molecular Genetics, Helsinki University Central Hospital and Department of Medical Genetics, University of Helsinki, Helsinki, Finland
    Scand J Clin Lab Invest 65:535-9. 2005
  5. ncbi request reprint Molecularly defined adult-type hypolactasia among working age people with reference to milk consumption and gastrointestinal symptoms
    Sari R Anthoni
    Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland
    World J Gastroenterol 13:1230-5. 2007
  6. ncbi request reprint Sequence analysis of the genes encoding for H+/K+-ATPase in autoimmune gastritis
    Aino M Oksanen
    Herttoniemi Municipal Hospital, and Department of Medical Genetics, University of Helsinki, Finland
    Ann Med 38:287-93. 2006
  7. pmc Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration
    Sanna P Seitsonen
    Department of Ophthalmology, University of Helsinki, Helsinki, Finland
    PLoS ONE 3:e3833. 2008

Collaborators

Detail Information

Publications7

  1. pmc Subjective face recognition difficulties, aberrant sensibility, sleeping disturbances and aberrant eating habits in families with Asperger syndrome
    Taina Nieminen-von Wendt
    Department of Child Neurology, Hospital for Children and Adolescents, Helsinki University Central Hospital, Helsinki, Finland
    BMC Psychiatry 5:20. 2005
    ....
  2. ncbi request reprint Genome-wide scan for loci of Asperger syndrome
    T Ylisaukko-oja
    Department of Molecular Medicine, National Public Health Institute, Biomedicum, PO Box 104, 00251 Helsinki, Finland
    Mol Psychiatry 9:161-8. 2004
    ..The present study is the first genome-wide screen in AS and therefore replication data sets are needed to evaluate further the significance of the AS-loci identified here...
  3. ncbi request reprint Molecular genetics of adult-type hypolactasia
    Irma E Järvelä
    Laboratory of Molecular Genetics, Helsinki University Central Hospital, Finland
    Ann Med 37:179-85. 2005
    ..Identification of the genetic change has highlighted the role of non-coding variants in the regulation of common genes and created new tools to study the mechanism of lactase enzyme activation...
  4. ncbi request reprint Molecular diagnosis of adult-type hypolactasia (lactase non-persistence)
    I E Jarvela
    Laboratory of Molecular Genetics, Helsinki University Central Hospital and Department of Medical Genetics, University of Helsinki, Helsinki, Finland
    Scand J Clin Lab Invest 65:535-9. 2005
  5. ncbi request reprint Molecularly defined adult-type hypolactasia among working age people with reference to milk consumption and gastrointestinal symptoms
    Sari R Anthoni
    Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland
    World J Gastroenterol 13:1230-5. 2007
    ..To study milk consumption and subjective milk-related symptoms in adults genotyped for adult-type hypolactasia...
  6. ncbi request reprint Sequence analysis of the genes encoding for H+/K+-ATPase in autoimmune gastritis
    Aino M Oksanen
    Herttoniemi Municipal Hospital, and Department of Medical Genetics, University of Helsinki, Finland
    Ann Med 38:287-93. 2006
    ..H+/K+-ATPase is the target autoantigen in autoimmune gastritis (AIG), an organ-specific autoimmune disease with a strong hereditary component...
  7. pmc Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration
    Sanna P Seitsonen
    Department of Ophthalmology, University of Helsinki, Helsinki, Finland
    PLoS ONE 3:e3833. 2008
    ..Variants in the complement cascade genes and the LOC387715/HTRA1, have been widely reported to associate with age-related macular degeneration (AMD), the most common cause of visual impairment in industrialized countries...