Dianne F Newbury

Summary

Affiliation: University of Oxford
Country: UK

Publications

  1. pmc Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment
    Dianne F Newbury
    Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Headington, Oxford, UK
    Am J Med Genet A 149:588-97. 2009
  2. ncbi request reprint Talking genes - the molecular basis of language impairment
    Dianne F Newbury
    University of Oxford, UK
    Biologist (London) 49:255-60. 2002
  3. ncbi request reprint Genetic influences on language impairment and phonological short-term memory
    Dianne F Newbury
    Wellcome Trust Centre for Human Genetics, Oxford University, Roosevelt Drive, Headington, Oxford, OX3 7BN, UK
    Trends Cogn Sci 9:528-34. 2005
  4. pmc Genetic advances in the study of speech and language disorders
    D F Newbury
    Wellcome Trust Centre for Human Genetics, Headington, Oxford, UK
    Neuron 68:309-20. 2010
  5. pmc Recent advances in the genetics of language impairment
    Dianne F Newbury
    Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford OX3 7BN, UK
    Genome Med 2:6. 2010
  6. pmc DCDC2, KIAA0319 and CMIP are associated with reading-related traits
    Tom S Scerri
    Wellcome Trust Centre for Human Genetics, University of Oxford, UK
    Biol Psychiatry 70:237-45. 2011
  7. pmc A genomewide scan for loci involved in attention-deficit/hyperactivity disorder
    Simon E Fisher
    Wellcome Trust Centre for Human Genetics, Oxford University, Oxford, United Kingdom
    Am J Hum Genet 70:1183-96. 2002
  8. ncbi request reprint Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
    Nuala H Simpson
    Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
    Dev Med Child Neurol 56:346-53. 2014
  9. pmc The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
    Thomas S Scerri
    Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
    PLoS ONE 7:e50321. 2012
  10. pmc A functional genetic link between distinct developmental language disorders
    Sonja C Vernes
    Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
    N Engl J Med 359:2337-45. 2008

Detail Information

Publications13

  1. pmc Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment
    Dianne F Newbury
    Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Headington, Oxford, UK
    Am J Med Genet A 149:588-97. 2009
    ..Nevertheless, it remains possible that variants in the flanking genes may underlie evidence of linkage at this locus...
  2. ncbi request reprint Talking genes - the molecular basis of language impairment
    Dianne F Newbury
    University of Oxford, UK
    Biologist (London) 49:255-60. 2002
    ..Many children acquire language so smoothly that it appears to be an innate ability. If this is true, then it should be possible to identify genes that underlie variations in linguistic abilities...
  3. ncbi request reprint Genetic influences on language impairment and phonological short-term memory
    Dianne F Newbury
    Wellcome Trust Centre for Human Genetics, Oxford University, Roosevelt Drive, Headington, Oxford, OX3 7BN, UK
    Trends Cogn Sci 9:528-34. 2005
    ..Identifying those cognitive deficits that work best as indices of heritable phenotypes will help us to uncover the aetiology of developmental disorders...
  4. pmc Genetic advances in the study of speech and language disorders
    D F Newbury
    Wellcome Trust Centre for Human Genetics, Headington, Oxford, UK
    Neuron 68:309-20. 2010
    ....
  5. pmc Recent advances in the genetics of language impairment
    Dianne F Newbury
    Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford OX3 7BN, UK
    Genome Med 2:6. 2010
    ..We discuss how characterization of these genes, and the pathways in which they are involved, may enhance our understanding of language disorders and improve our understanding of the biological foundations of language acquisition...
  6. pmc DCDC2, KIAA0319 and CMIP are associated with reading-related traits
    Tom S Scerri
    Wellcome Trust Centre for Human Genetics, University of Oxford, UK
    Biol Psychiatry 70:237-45. 2011
    ..Several susceptibility genes have been proposed for dyslexia (reading disability; RD) and specific language impairment (SLI). RD and SLI show comorbidity, but it is unclear whether a common genetic component is shared...
  7. pmc A genomewide scan for loci involved in attention-deficit/hyperactivity disorder
    Simon E Fisher
    Wellcome Trust Centre for Human Genetics, Oxford University, Oxford, United Kingdom
    Am J Hum Genet 70:1183-96. 2002
    ..Two of the regions highlighted in the present study, 2q24 and 16p13, coincided with the top linkage peaks reported by a recent genome-scan study of autistic sib pairs...
  8. ncbi request reprint Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
    Nuala H Simpson
    Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
    Dev Med Child Neurol 56:346-53. 2014
    ..We assess the frequency of sex chromosome aneuploidies in individuals with language impairment or dyslexia...
  9. pmc The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
    Thomas S Scerri
    Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
    PLoS ONE 7:e50321. 2012
    ....
  10. pmc A functional genetic link between distinct developmental language disorders
    Sonja C Vernes
    Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
    N Engl J Med 359:2337-45. 2008
    ..Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and language disorder. We hypothesized that neural pathways downstream of FOXP2 influence more common phenotypes, such as specific language impairment...
  11. pmc CMIP and ATP2C2 modulate phonological short-term memory in language impairment
    Dianne F Newbury
    Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
    Am J Hum Genet 85:264-72. 2009
    ..This work therefore implicates CMIP and ATP2C2 in the etiology of SLI and provides molecular evidence for the importance of phonological short-term memory in language acquisition...
  12. ncbi request reprint Molecular genetics of speech and language disorders
    Dianne F Newbury
    Welcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, United Kingdom
    Curr Opin Pediatr 14:696-701. 2002
    ..We also discuss recent molecular genetic advances made in the study of generalized specific language impairment...
  13. ncbi request reprint Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
    Simon E Fisher
    Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK
    Nat Genet 30:86-91. 2002
    ..This is the first report of QTL-based genome-wide scanning for a human cognitive trait...