List of works - Dianne F Newbury

Candidate gene variant effects on language disorders in Robinson Crusoe Island

scientific article published on 01 March 2019

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment

scientific article

Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy

scientific article published on 26 May 2020

DCDC2, KIAA0319 and CMIP are associated with reading-related traits

scientific article

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

scientific article published in April 2013

FOXP2

scientific article

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.

scientific article published on 14 June 2016

Genetic Advances in the Study of Speech and Language Disorders ⬇️

scientific article published on October 21, 2010

Genetic influences on language impairment and phonological short-term memory.

scientific article

Genome-Wide Studies of Specific Language Impairment

scientific article published in January 2014

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population ⬇️

scientific article

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

scientific article

Genome-wide screening for DNA variants associated with reading and language traits

scientific article

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

scientific article

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

scientific article

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.

scientific article published in February 2009

Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes

scientific article published on 20 April 2020

Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation

scientific article

Play and prosociality are associated with fewer externalizing problems in children with developmental language disorder: The role of early language and communication environment

scientific article published on 04 June 2020

Reading and language disorders: the importance of both quantity and quality.

scientific article published on 4, Apr, 2014

Recent advances in the genetics of language impairment

scientific article (publication date: 26 January 2010)

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.

scientific article published on January 2010

Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.

scientific article

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis

scientific article published on 10 October 2018

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis

scientific article published on 01 June 2021

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis

scientific article published on 07 September 2020

Talking genes - the molecular basis of language impairment.

scientific article

The Development of Mental Health Difficulties in Young People With and Without Developmental Language Disorder: A Gene–Environment Interplay Study Using Polygenic Scores

scientific article published in 2023

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.

scientific article

List of works by Dianne F Newbury

Candidate gene variant effects on language disorders in Robinson Crusoe Island

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment

Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy

DCDC2, KIAA0319 and CMIP are associated with reading-related traits

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

FOXP2

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.

Genetic Advances in the Study of Speech and Language Disorders ⬇️

Genetic influences on language impairment and phonological short-term memory.

Genome-Wide Studies of Specific Language Impairment

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population ⬇️

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 traits

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.

Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes

Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation

Play and prosociality are associated with fewer externalizing problems in children with developmental language disorder: The role of early language and communication environment

Reading and language disorders: the importance of both quantity and quality.

Recent advances in the genetics of language impairment

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.

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 hypothesis

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis

Talking genes - the molecular basis of language impairment.

The Development of Mental Health Difficulties in Young People With and Without Developmental Language Disorder: A Gene–Environment Interplay Study Using Polygenic Scores

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.