Armin Raznahan

Summary

Affiliation: King's College London
Country: UK

Publications

  1. ncbi Biological markers of intellectual disability in tuberous sclerosis
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King s College London, UK
    Psychol Med 37:1293-304. 2007
  2. doi Serotonin transporter genotype and neuroanatomy in autism spectrum disorders
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry, KCL, UK
    Psychiatr Genet 19:147-50. 2009
  3. doi Cortical anatomy in autism spectrum disorder: an in vivo MRI study on the effect of age
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King s College London, London, UK
    Cereb Cortex 20:1332-40. 2010
  4. pmc A functional polymorphism of the brain derived neurotrophic factor gene and cortical anatomy in autism spectrum disorder
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry IOP, Kings College London KCL, 16 De Crespigny Park, London, SE5 8AF, UK
    J Neurodev Disord 1:215-23. 2009
  5. pmc Cortical anatomy in human X monosomy
    Armin Raznahan
    Department of Child Psychiatry, Institute of Psychiatry, King s College London, UK
    Neuroimage 49:2915-23. 2010
  6. pmc Allelic variation within the putative autism spectrum disorder risk gene homeobox A1 and cerebellar maturation in typically developing children and adolescents
    Armin Raznahan
    Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA
    Autism Res 5:93-100. 2012

Detail Information

Publications6

  1. ncbi Biological markers of intellectual disability in tuberous sclerosis
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King s College London, UK
    Psychol Med 37:1293-304. 2007
    ..We have used univariate and multivariate analyses, including both CT and epilepsy measures as predictors, in an attempt to clarify the pattern of cross-sectional associations between these variables and ID in TS...
  2. doi Serotonin transporter genotype and neuroanatomy in autism spectrum disorders
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry, KCL, UK
    Psychiatr Genet 19:147-50. 2009
    ....
  3. doi Cortical anatomy in autism spectrum disorder: an in vivo MRI study on the effect of age
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King s College London, London, UK
    Cereb Cortex 20:1332-40. 2010
    ..This may reflect primary abnormalities in cortical plasticity and/or be secondary to disturbed interactions between individuals with ASD and their environment...
  4. pmc A functional polymorphism of the brain derived neurotrophic factor gene and cortical anatomy in autism spectrum disorder
    Armin Raznahan
    Department of Child and Adolescent Psychiatry, Institute of Psychiatry IOP, Kings College London KCL, 16 De Crespigny Park, London, SE5 8AF, UK
    J Neurodev Disord 1:215-23. 2009
    ..If correct, this suggests ASD is associated with a distorted relationship between BDNF val66met genotype and the determinants of regional cortical surface area - gyrification and/or sulcal positioning...
  5. pmc Cortical anatomy in human X monosomy
    Armin Raznahan
    Department of Child Psychiatry, Institute of Psychiatry, King s College London, UK
    Neuroimage 49:2915-23. 2010
    ..g. cortical folding) and CT (e.g. dendritic arborization/pruning). CT disruptions are maximal within and between cortical regions previously implicated in the TS cognitive phenotype...
  6. pmc Allelic variation within the putative autism spectrum disorder risk gene homeobox A1 and cerebellar maturation in typically developing children and adolescents
    Armin Raznahan
    Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA
    Autism Res 5:93-100. 2012
    ..002). Our results suggest that common genetic variation within this putative ASD risk gene has the capacity to modify the development of cerebellar systems implicated in ASD neurobiology...