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Search results (43)

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nalysis of expression Quantitative Trait Loci for NLGN4X in relation to language and neurodevelopmental function: an exploratory analysis using FUSION and GTEx workflows

Simpson N. et al, (2021)

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

Newbury D. et al, (2021)

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

Newbury D. et al, (2020)

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

Mountford HS. et al, (2020), Am J Med Genet C Semin Med Genet, 184, 256 - 266

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

Newbury D. et al, (2018)

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

Newbury D. et al, (2018)

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

Newbury D. et al, (2018)

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

Newbury DF. et al, (2018), Wellcome Open Res, 3

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

Newbury DF. et al, (2018), Wellcome Open Res, 3

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

Chen XS. et al, (2017), Sci Rep, 7

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

Simpson NH. et al, (2015), Eur J Hum Genet, 23, 1370 - 1377

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

Ceroni F. et al, (2015), Eur J Hum Genet, 23, 1113 - 1115

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

Villanueva P. et al, (2015), PLoS Genet, 11

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

Pettigrew KA. et al, (2015), Genes Brain Behav, 14, 369 - 376

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

Villanueva P. et al, (2015), PLoS Genet, 11

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