Christopher W Bartlett

Summary

Affiliation: Rutgers University
Country: USA

Publications

  1. pmc A major susceptibility locus for specific language impairment is located on 13q21
    Christopher W Bartlett
    Center for Molecular and Behavioral Neuroscience, Rutgers University, Piscataway, NJ 08854 8095, USA
    Am J Hum Genet 71:45-55. 2002
  2. pmc Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment
    Christopher W Bartlett
    Center for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA
    Hum Hered 57:10-20. 2004
  3. ncbi request reprint Specific language impairment in families: evidence for co-occurrence with reading impairments
    Judy F Flax
    Center for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, Newark 07102, USA
    J Speech Lang Hear Res 46:530-43. 2003
  4. ncbi request reprint Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage
    Christopher W Bartlett
    Center for Statistical Genetics Research, College of Public Health and Roy J and Lucille A Carver College of Medicine, University of Iowa, Iowa City, IA, USA
    Genet Epidemiol 31:91-102. 2007
  5. ncbi request reprint Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene
    Thomas H Wassink
    Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, 52242, USA
    Am J Med Genet B Neuropsychiatr Genet 136:36-44. 2005
  6. doi request reprint Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16
    Thomas H Wassink
    Department of Psychiatry, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA
    Psychiatr Genet 18:85-91. 2008
  7. ncbi request reprint The search for autism disease genes
    Thomas H Wassink
    Department of Psychiatry, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA
    Ment Retard Dev Disabil Res Rev 10:272-83. 2004
  8. pmc Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set
    Christopher W Bartlett
    Center for Statistical Genetics Research, College of Public Health, and Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA
    Am J Hum Genet 76:688-95. 2005
  9. ncbi request reprint Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky
    Christopher W Bartlett
    Center for Quantitative and Computational Biology and Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, OH, USA
    Genet Epidemiol 31:S61-7. 2007
  10. ncbi request reprint Three autism candidate genes: a synthesis of human genetic analysis with other disciplines
    Christopher W Bartlett
    Center for Statistical Genetics Research, University of Iowa, Iowa City, IA, USA
    Int J Dev Neurosci 23:221-34. 2005

Detail Information

Publications10

  1. pmc A major susceptibility locus for specific language impairment is located on 13q21
    Christopher W Bartlett
    Center for Molecular and Behavioral Neuroscience, Rutgers University, Piscataway, NJ 08854 8095, USA
    Am J Hum Genet 71:45-55. 2002
    ..86, genomic P value <.06 under the recessive language impairment model). Our findings underscore the utility of traditional LOD-score-based methods in finding genes for complex diseases, specifically, SLI...
  2. pmc Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment
    Christopher W Bartlett
    Center for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA
    Hum Hered 57:10-20. 2004
    ..2003). Our results indicate that using samples selected for components of the autism phenotype may be a useful adjunct to autism genetics...
  3. ncbi request reprint Specific language impairment in families: evidence for co-occurrence with reading impairments
    Judy F Flax
    Center for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, Newark 07102, USA
    J Speech Lang Hear Res 46:530-43. 2003
    ..Results demonstrate that when LIs occur within families of SLI probands, these impairments generally co-occur with RIs. Our data are also consistent with prior findings that males show impairments more often than females...
  4. ncbi request reprint Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage
    Christopher W Bartlett
    Center for Statistical Genetics Research, College of Public Health and Roy J and Lucille A Carver College of Medicine, University of Iowa, Iowa City, IA, USA
    Genet Epidemiol 31:91-102. 2007
    ....
  5. ncbi request reprint Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene
    Thomas H Wassink
    Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, 52242, USA
    Am J Med Genet B Neuropsychiatr Genet 136:36-44. 2005
    ..We conclude, therefore, that 2q37.3 continues to be a region of interest for autism susceptibility, and that CENTG2 is an intriguing candidate gene that merits further scrutiny for its role in autism...
  6. doi request reprint Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16
    Thomas H Wassink
    Department of Psychiatry, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA
    Psychiatr Genet 18:85-91. 2008
    ..To apply phenotypic and statistical methods designed to account for heterogeneity to linkage analyses of the autism Collaborative Linkage Study of Autism (CLSA) affected sibling pair families...
  7. ncbi request reprint The search for autism disease genes
    Thomas H Wassink
    Department of Psychiatry, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA
    Ment Retard Dev Disabil Res Rev 10:272-83. 2004
    ....
  8. pmc Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set
    Christopher W Bartlett
    Center for Statistical Genetics Research, College of Public Health, and Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA
    Am J Hum Genet 76:688-95. 2005
    ..This analysis illustrates that the way in which heterogeneity is addressed in linkage analysis can dramatically affect the overall conclusions of a linkage study...
  9. ncbi request reprint Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky
    Christopher W Bartlett
    Center for Quantitative and Computational Biology and Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, OH, USA
    Genet Epidemiol 31:S61-7. 2007
    ..The difficulty of using (primarily) affected sib pair data in a gene x gene interaction analysis is explored...
  10. ncbi request reprint Three autism candidate genes: a synthesis of human genetic analysis with other disciplines
    Christopher W Bartlett
    Center for Statistical Genetics Research, University of Iowa, Iowa City, IA, USA
    Int J Dev Neurosci 23:221-34. 2005
    ..Integrating results from several scientific frameworks provides new hypotheses and alternative data collection strategies for future work...