Daniel B Campbell

Summary

Affiliation: University of Southern California
Country: USA

Publications

  1. ncbi Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder
    Daniel B Campbell
    Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90089, USA
    J Neurodev Disord 3:101-12. 2011
  2. ncbi Association of MET with social and communication phenotypes in individuals with autism spectrum disorder
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, Tennessee, USA
    Am J Med Genet B Neuropsychiatr Genet 153:438-46. 2010
  3. ncbi Association of RGS2 and RGS5 variants with schizophrenia symptom severity
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA
    Schizophr Res 101:67-75. 2008
  4. ncbi Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions
    Daniel B Campbell
    Vanderbilt University, 8114 MRB3, 465 21st Ave South, Nashville, TN 37232, USA
    Pediatrics 123:1018-24. 2009
  5. ncbi Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232, USA
    Autism Res 1:159-68. 2008
  6. ncbi Disruption of cerebral cortex MET signaling in autism spectrum disorder
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, TN 37203, USA
    Ann Neurol 62:243-50. 2007
  7. ncbi The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders
    Pat Levitt
    Vanderbilt Kennedy Center for Research on Human Development and Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee, USA
    J Clin Invest 119:747-54. 2009
  8. ncbi The autism risk genes MET and PLAUR differentially impact cortical development
    Kathie L Eagleson
    Zilkha Neurogenetic Institute, Keck School of Medicine at USC, Los Angeles, California 90033, USA
    Autism Res 4:68-83. 2011
  9. ncbi Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain
    Matthew C Judson
    Graduate Program in Neuroscience, Vanderbilt University Medical Center, Nashville, Tennessee 37203, USA
    J Comp Neurol 513:511-31. 2009
  10. ncbi A genetic variant that disrupts MET transcription is associated with autism
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, TN 37203, USA
    Proc Natl Acad Sci U S A 103:16834-9. 2006

Detail Information

Publications12

  1. ncbi Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder
    Daniel B Campbell
    Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90089, USA
    J Neurodev Disord 3:101-12. 2011
    ....
  2. ncbi Association of MET with social and communication phenotypes in individuals with autism spectrum disorder
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, Tennessee, USA
    Am J Med Genet B Neuropsychiatr Genet 153:438-46. 2010
    ..These data indicate that the MET C allele influences at least two of the three domains of the autism triad...
  3. ncbi Association of RGS2 and RGS5 variants with schizophrenia symptom severity
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA
    Schizophr Res 101:67-75. 2008
    ..3-1q31. Due to overlapping cellular functions and chromosomal proximity, we hypothesized that multiple RGS genes may contribute to schizophrenia severity and treatment responsiveness...
  4. ncbi Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions
    Daniel B Campbell
    Vanderbilt University, 8114 MRB3, 465 21st Ave South, Nashville, TN 37232, USA
    Pediatrics 123:1018-24. 2009
    ....
  5. ncbi Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232, USA
    Autism Res 1:159-68. 2008
    ..These data further support our hypothesis that genetic susceptibility impacting multiple components of the MET signaling pathway contributes to ASD risk...
  6. ncbi Disruption of cerebral cortex MET signaling in autism spectrum disorder
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, TN 37203, USA
    Ann Neurol 62:243-50. 2007
    ..Here we examined expression levels of MET and members of the MET signaling pathway in postmortem cerebral cortex from ASD cases and healthy control subjects...
  7. ncbi The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders
    Pat Levitt
    Vanderbilt Kennedy Center for Research on Human Development and Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee, USA
    J Clin Invest 119:747-54. 2009
    ....
  8. ncbi The autism risk genes MET and PLAUR differentially impact cortical development
    Kathie L Eagleson
    Zilkha Neurogenetic Institute, Keck School of Medicine at USC, Los Angeles, California 90033, USA
    Autism Res 4:68-83. 2011
    ..An altered balance between excitation and inhibition has been postulated as a biological mechanism for ASD; this imbalance could arise from different risk genes differentially affecting either or both elements...
  9. ncbi Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain
    Matthew C Judson
    Graduate Program in Neuroscience, Vanderbilt University Medical Center, Nashville, Tennessee 37203, USA
    J Comp Neurol 513:511-31. 2009
    ..Collectively, these data suggest that Met signaling may be necessary for the appropriate wiring of forebrain circuits, with particular relevance to the social and emotional dimensions of behavior...
  10. ncbi A genetic variant that disrupts MET transcription is associated with autism
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, TN 37203, USA
    Proc Natl Acad Sci U S A 103:16834-9. 2006
    ..These data implicate reduced MET gene expression in autism susceptibility, providing evidence of a previously undescribed pathophysiological basis for this behaviorally and medically complex disorder...
  11. ncbi Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia
    Daniel B Campbell
    Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232, USA
    Biol Psychiatry 63:32-41. 2008
    ..The central role of RGS4 in regulating signaling via Gi/o coupled neurotransmitter receptors led us to hypothesize that there may be RGS4 genotypes predictive of specific disease phenotypes and antipsychotic treatment responses...
  12. ncbi A noncoding RNA antisense to moesin at 5p14.1 in autism
    Tara Kerin
    Program in Biomedical and Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA
    Sci Transl Med 4:128ra40. 2012
    ..7-fold) in postmortem cerebral cortex of individuals with ASD, and could regulate levels of moesin protein in human cell lines. These data reveal a biologically functional element that may contribute to ASD risk...