about
FOXP2Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorderDCDC2, KIAA0319 and CMIP are associated with reading-related traitsMultidisciplinary investigation links backward-speech trait and working memory through genetic mutation.Recent advances in the genetics of language impairmentInvestigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.Reading and language disorders: the importance of both quantity and quality.Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.Genome-wide screening for DNA variants associated with reading and language traitsGenetic influences on language impairment and phonological short-term memory.The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaTalking genes - the molecular basis of language impairment.Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean populationCopy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language ImpairmentSixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.Genome-Wide Studies of Specific Language Impairment.Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesisMulti-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomesCandidate gene variant effects on language disorders in Robinson Crusoe IslandCopy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomyPlay and prosociality are associated with fewer externalizing problems in children with developmental language disorder: The role of early language and communication environment
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description
researcher
@en
wetenschapper
@nl
name
Dianne F Newbury
@en
Dianne F Newbury
@nl
type
label
Dianne F Newbury
@en
Dianne F Newbury
@nl
prefLabel
Dianne F Newbury
@en
Dianne F Newbury
@nl
P106
P31
P496
0000-0002-9557-268X