Tero Ylisaukko-Oja

Summary

Affiliation: National Public Health Institute
Country: Finland

Publications

  1. ncbi Family-based association study of DYX1C1 variants in autism
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland
    Eur J Hum Genet 13:127-30. 2005
  2. ncbi MECP2 mutation analysis in patients with mental retardation
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland
    Am J Med Genet A 132:121-4. 2005
  3. ncbi Analysis of four neuroligin genes as candidates for autism
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland
    Eur J Hum Genet 13:1285-92. 2005
  4. pmc Allelic variants in HTR3C show association with autism
    Karola Rehnstrom
    Department of Molecular Medicine, National Public Health Institute and Institute for Molecular Medicine Finland, Helsinki, Finland
    Am J Med Genet B Neuropsychiatr Genet 150:741-6. 2009
  5. doi Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD)
    Katri Kantojärvi
    Department of Medical Genetics, Haartman Institute, University of Helsinki, Helsinki, Finland
    Autism Res 4:228-33. 2011
  6. pmc Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland
    Helena Kilpinen
    Department of Molecular Medicine, Institute for Molecular Medicine, Finland
    Hum Mol Genet 18:2912-21. 2009
  7. pmc A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27
    Mari Auranen
    Department of Molecular Medicine, National Public Health Institute, University of Helsinki, Finland
    Am J Hum Genet 71:777-90. 2002
  8. ncbi No association between common variants in glyoxalase 1 and autism spectrum disorders
    Karola Rehnstrom
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland karola
    Am J Med Genet B Neuropsychiatr Genet 147:124-7. 2008
  9. ncbi Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, University of Helsinki, 00251 Helsinki, Finland
    Ann Neurol 59:145-55. 2006
  10. 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

Detail Information

Publications15

  1. ncbi Family-based association study of DYX1C1 variants in autism
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland
    Eur J Hum Genet 13:127-30. 2005
    ..Thus it seems unlikely that DYX1C1 gene would be involved in the genetic etiology of autism in Finnish patients...
  2. ncbi MECP2 mutation analysis in patients with mental retardation
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland
    Am J Med Genet A 132:121-4. 2005
    ..None of these variants is likely to be causal. We conclude that the evidence across all the mutation screening studies implies that MECP2 mutations do not represent a major cause of nonspecific MR...
  3. ncbi Analysis of four neuroligin genes as candidates for autism
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland
    Eur J Hum Genet 13:1285-92. 2005
    ..014), and NLGN4 (DXS996, P=0.031). We conclude that neuroligin mutations most probably represent rare causes of autism and that it is unlikely that the allelic variants in these genes would be major risk factors for autism...
  4. pmc Allelic variants in HTR3C show association with autism
    Karola Rehnstrom
    Department of Molecular Medicine, National Public Health Institute and Institute for Molecular Medicine Finland, Helsinki, Finland
    Am J Med Genet B Neuropsychiatr Genet 150:741-6. 2009
    ..Based on the association analysis results in a previously identified linkage region, we propose that HTR3C represents a novel candidate locus for ASDs and should be tested in other populations...
  5. doi Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD)
    Katri Kantojärvi
    Department of Medical Genetics, Haartman Institute, University of Helsinki, Helsinki, Finland
    Autism Res 4:228-33. 2011
    ..A total of six novel and 11 known single nucleotide polymorphisms were identified. Further studies are warranted to analyze the candidate genes at Xq11.1-q21.33...
  6. pmc Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland
    Helena Kilpinen
    Department of Molecular Medicine, Institute for Molecular Medicine, Finland
    Hum Mol Genet 18:2912-21. 2009
    ..We identified a putative autism susceptibility locus at 19p13.3 and obtained further evidence for previously identified loci at 1q23 and 15q11-q13. Most promising candidate genes were TLE2 and TLE6 clustered at 19p13 and ATP1A2 at 1q23...
  7. pmc A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27
    Mari Auranen
    Department of Molecular Medicine, National Public Health Institute, University of Helsinki, Finland
    Am J Hum Genet 71:777-90. 2002
    ....
  8. ncbi No association between common variants in glyoxalase 1 and autism spectrum disorders
    Karola Rehnstrom
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland karola
    Am J Med Genet B Neuropsychiatr Genet 147:124-7. 2008
    ..We did not observe significant linkage or association between any SNP and ASDs. Therefore, we suggest that common variants in GLO1 are not significant susceptibility factors for ASDs in the Finnish population...
  9. ncbi Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families
    Tero Ylisaukko-Oja
    Department of Molecular Medicine, National Public Health Institute, University of Helsinki, 00251 Helsinki, Finland
    Ann Neurol 59:145-55. 2006
    ..The objective of this study was to search for potential susceptibility loci for autism, which are supported by two independent samples...
  10. 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
    ....
  11. pmc Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency
    Mikko Kuokkanen
    Department of Molecular Medicine, National Public Health Institute, Helsinki, Finland
    Am J Hum Genet 78:339-44. 2006
    ....
  12. ncbi PAK3 related mental disability: further characterization of the phenotype
    Maarit Peippo
    Department of Medical Genetics, Family Federation of Finland, Helsinki, Finland
    Am J Med Genet A 143:2406-16. 2007
    ....
  13. doi Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism
    Joni A Turunen
    Department of Molecular Medicine and Institute for Molecular Medicine, Finland, National Public Health Institute, Helsinki, Finland
    Autism Res 1:189-92. 2008
    ..By contrast, analysis of the AS sample yielded no evidence for association. This study shows further support that genetic variants within SLC25A12 gene contribute to the etiology of autism...
  14. ncbi Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation
    Tero Ylisaukko-Oja
    National Public Health Institute, Department of Molecular Medicine, P O Box 104, 00251 Helsinki, Finland
    Hum Genet 114:211-3. 2004
    ..The patients with AGTR2 sequence variants had severe/profound mental retardation, epileptic seizures, restlessness, hyperactivity, and disturbed development of speech...
  15. ncbi Exclusion of 14 candidate loci for primary open angle glaucoma in Finnish families
    Susanna Lemmelä
    Department of Medical Genetics, University of Helsinki, Helsinki, Finland
    Mol Vis 10:260-4. 2004
    ..In addition, we analysed loci for the MYOC gene on 1q23-24 and the OPTN gene on 10p14-15...