Dianne F Newbury

Ontology type: schema:Person     

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Dianne F



Publications in SciGraph latest 50 shown

  • 2018-05 Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders in MOLECULAR PSYCHIATRY
  • 2017-12 Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment in SCIENTIFIC REPORTS
  • 2016-12 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2016-04 Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation in SCIENTIFIC REPORTS
  • 2015-12 Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2 in MOLECULAR CYTOGENETICS
  • 2015-10 Genome-wide analysis identifies a role for common copy number variants in specific language impairment in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-09 Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis’ in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2014-12 Associations of HLA alleles with specific language impairment in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2014-12 Genome-Wide Studies of Specific Language Impairment in CURRENT BEHAVIORAL NEUROSCIENCE REPORTS
  • 2014-10 Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-04 Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-06 Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-01 Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects in BEHAVIOR GENETICS
  • 2010-01 Recent advances in the genetics of language impairment in GENOME MEDICINE
  • 2002-01 Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia in NATURE GENETICS
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