D. Newbury

发表

A genomewide scan identifies two novel loci involved in specific language impairment.

G. Baird, P. Bolton, A. Pickles, 2002, American journal of human genetics.

A functional genetic link between distinct developmental language disorders.

D. Geschwind, B. Abrahams, A. Monaco, 2008, The New England journal of medicine.

Next-generation sequencing identifies novel gene variants and pathways involved in specific language impairment

A. Hoischen, C. Francks, J. Veltman, 2016, bioRxiv.

Genetic Advances in the Study of Speech and Language Disorders

A. Monaco, D. Newbury, 2010, Neuron.

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

Laura E. Covill, A. Monaco, J. Talcott, 2016, Human molecular genetics.

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

Dušica Filipović Đurđević, Laura E. Covill, D. Newbury, 2016, Scientific Reports.

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

Lon R. Cardon, Richard K. Olson, John C. DeFries, 2002, Nature Genetics.

The Genetic and Molecular Basis of Developmental Language Disorder: A Review

D. Newbury, A. Morgan, H. Mountford, 2022, Children.

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

D. Bishop, D. Newbury, N. H. Simpson, 2018, Wellcome open research.

Genetic and phenotypic effects of phonological short‐term memory and grammatical morphology in specific language impairment

A. Pickles, A. Pickles, A. Monaco, 2008, Genes, brain, and behavior.

Generalized Structured Component Analysis in candidate gene association studies: applications and limitations

D. Bishop, S. Fisher, D. Newbury, 2019, Wellcome open research.

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Rebecca C. Spillmann, N. Guex, J. Rosenfeld, 2020, bioRxiv.

Explorer CMIP and ATP 2 C 2 Modulate Phonological Short-Term Memory in Language Impairment

Dorothy V. M. Bishop, Gillian Baird, Dianne F. Newbury, 2009 .

Title: Finding Functional Disease-associated Non-coding Variation Using Next-generation Sequencing

C. Francks, S. Fisher, S. Vernes, 2016 .

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

S. Humphray, D. Newbury, G. Lunter, 2020, Communications Biology.

Finding functional disease-associated non-coding variation using next-generation sequencing

C. Francks, S. Fisher, S. Vernes, 2016, bioRxiv.

The Genetic Population Structure of Robinson Crusoe Island, Chile

D. Newbury, L. Carvajal-Carmona, J. Cazier, 2020, Frontiers in Genetics.

The effects of prenatal smoke exposure on language development ‐ a systematic review

D. Newbury, H. Mountford, Jessica Peixinho, 2022, Infant and Child Development.

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2

E. Volpi, D. Newbury, R. Nudel, 2015, Molecular Cytogenetics.

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

B. V. van Bon, E. Bongers, D. Newbury, 2011, Molecular Syndromology.

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Timothy C. Bates, Till F. M. Andlauer, C. Francks, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Timothy C. Bates, Till F. M. Andlauer, C. Francks, 2022, Translational Psychiatry.

Pathways from the early language and communication environment to literacy outcomes at the end of primary school; the roles of language development and social development

A. Pickles, D. Newbury, G. Conti-Ramsden, 2020, Oxford Review of Education.

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

G. Baird, P. Bolton, J. Knight, 2013, Developmental Medicine & Child Neurology.

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

D. Bishop, D. Newbury, H. Mountford, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

A. Hoischen, C. Francks, J. Veltman, 2017, Scientific Reports.

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders

C. Francks, S. Fisher, S. Vernes, 2017, Molecular Psychiatry.

Reading and Language Disorders: The Importance of Both Quantity and Quality

A. Monaco, D. Newbury, S. Paracchini, 2014, Genes.

FOXP2 is not a major susceptibility gene for autism or specific language impairment.

G Baird, A. Bailey, G. Baird, 2002, American journal of human genetics.

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures

J. Talcott, C. Hulme, M. Rice, 2021, medRxiv.

The Genetics of Specific Language Impairment

D. Newbury, R. Nudel, F. Ceroni, 2018 .

The Genetics of Specific Language Impairment (SLI)

D. Newbury, R. Nudel, F. Ceroni, 2015 .

The genomic landscape of language: Insights into evolution

D. Newbury, H. Mountford, 2018 .

FOXP2

D. Newbury, R. Nudel, 2013, Wiley interdisciplinary reviews. Cognitive science.

Recent advances in the genetics of language impairment

A. Monaco, S. Fisher, D. Newbury, 2010, Genome Medicine.

Advanced Review Foxp2

D. Newbury, R. Nudel, 2022 .

Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

A. Hoischen, C. Francks, G. Baird, 2015, PLoS genetics.

Genome-Wide Association Study of Motor Coordination

D. Newbury, A. Barnett, H. Mountford, 2021, Frontiers in Human Neuroscience.

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Timothy C. Bates, Till F. M. Andlauer, C. Francks, 2021 .

Using Polygenic Profiles to Predict Variation in Language and Psychosocial Outcomes in Early and Middle Childhood

A. Pickles, D. Newbury, G. Conti-Ramsden, 2019, Journal of speech, language, and hearing research : JSLHR.

Genome-wide analysis identifies a role for common copy number variants in specific language impairment

William W. Cohen, Gillian Baird, A Pickles, 2015, European Journal of Human Genetics.

Genome-wide analysis identi fi es a role for common copy number variants in speci fi c language impairment

G. Baird, P. Bolton, J. Knight, 2015 .

Associations of HLA alleles with specific language impairment

G. Baird, P. Bolton, A. Monaco, 2014, Journal of Neurodevelopmental Disorders.

Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays

J. Ragoussis, A. Monaco, D. Newbury, 2009, Cytogenetic and Genome Research.

Candidate gene variant effects on language disorders in Robinson Crusoe Island

D. Newbury, J. Cazier, H. Mountford, 2019, Annals of human biology.

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

D. Bishop, D. Newbury, P. Thompson, 2021, Wellcome open research.

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

D. Bishop, D. Newbury, P. Thompson, 2018, Wellcome open research.

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing

D. Bishop, D. Newbury, P. Thompson, 2018 .

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

Dorothy V M Bishop, D. Bishop, D. Newbury, 2018, Wellcome open research.

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

A. Monaco, J. Talcott, C. Hulme, 2016, Journal of Neurodevelopmental Disorders.

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

G Baird, C. Francks, G. Baird, 2014, Genes, brain, and behavior.

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

J. B. Talcott, A. Monaco, J. Talcott, 2010, Behavior genetics.

A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3

A. Monaco, S. Pääbo, A. Friederici, 2010, Genes, brain, and behavior.

Molecular genetics of speech and language disorders.

A. Monaco, D. Newbury, 2002, Current opinion in pediatrics.

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

Alessandra Renieri, Simon E Fisher, A. Monaco, 2012, European Journal of Human Genetics.

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.

C. Francks, S. Nelson, A. Monaco, 2002, American journal of human genetics.

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

C. Hulme, D. Newbury, M. Snowling, 2015, PloS one.

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment

Peter Donnelly, Gillian Baird, Simon E Fisher, 2014, European Journal of Human Genetics.

Genome-Wide Studies of Specific Language Impairment

D. Newbury, R. Nudel, Rose H. Reader, 2014, Current Behavioral Neuroscience Reports.

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

Timothy C. Bates, C. Francks, B. Pennington, 2014, Genes, brain, and behavior.

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

Dorothy V.M. Bishop, Gillian Baird, Dianne F. Newbury, 2009, American journal of human genetics.

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

E. Bacchelli, G. Baird, J. Lamb, 2009, American journal of medical genetics. Part A.

DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits

Dorothy V.M. Bishop, Dianne F. Newbury, Anthony P. Monaco, 2011, Biological Psychiatry.

Genetic influences on language impairment and phonological short-term memory

Dorothy V. M. Bishop, Dianne F. Newbury, Anthony P. Monaco, 2005, Trends in Cognitive Sciences.

FOXP 2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment

A. Bailey, G. Baird, P. Bolton, 2002 .

A genome wide screen for loci involved in specific language impairment

D. Newbury, 2002 .

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts

S. Ring, P. Thompson, S. Fisher, 2015, Genes, brain, and behavior.

The effects of reading and language intervention on literacy skills in children in a remote community: An exploratory randomized controlled trial

Paula J. Clarke, C. Hulme, D. Newbury, 2020, International Journal of Educational Research.

Evaluation of elements in hair samples of children with developmental language disorder (DLD)

D. Newbury, F. Al-Tamimi, Mazin Alqhazo, 2022, Nutritional neuroscience.

Language and reading impairments are associated with increased prevalence of non-right-handedness.

J. Talcott, D. Boomsma, J. Michaelson, 2023, Child development.

Scaling up early language intervention in educational settings: First steps matter

C. Hulme, D. Newbury, M. Snowling, 2022, Oxford Review of Education.

A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma

D. Pinto, A. Pagnamenta, E. Maestrini, 2014, Autism research : official journal of the International Society for Autism Research.

Peripheral Anomalies in USH2A Cause Central Auditory Anomalies in a Mouse Model of Usher Syndrome and CAPD

D. Newbury, R. Fitch, P. Perrino, 2021, Genes.

Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways

D. Newbury, U. Kini, Kate Wilson, 2023, Human molecular genetics.

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure

Dianne F. Newbury, Torkel Klingberg, Fahimeh Darki, 2012, PloS one.

Logical and Methodological Issues Affecting Genetic Studies of Humans Reported in Top Neuroscience Journals

Paul A. Thompson, Dorothy V. M. Bishop, Dianne F. Newbury, 2018, Journal of Cognitive Neuroscience.

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

G. Mirza, A. Monaco, D. Newbury, 2011, European Journal of Human Genetics.

Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'

P. Donnelly, C. Francks, A. Pagnamenta, 2014, European Journal of Human Genetics.

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

A. Pickles, D. Newbury, G. Conti-Ramsden, 2020, International journal of language & communication disorders.

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

D. Skuse, D. Bishop, D. Newbury, 2018, Wellcome open research.

Family aggregation of language impairment in an isolated Chilean population from Robinson Crusoe Island.

D. Newbury, Pía Villanueva, M. A. Fernández, 2018, International journal of language & communication disorders.