List of works - Emma Meaburn

A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds.

scientific article published in October 2005

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

scientific article

A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence.

scientific article

A three-stage genome-wide association study of general cognitive ability: hunting the small effects.

scientific article

Allele-specific methylation in the human genome: implications for genetic studies of complex disease

scientific article

Allelic skewing of DNA methylation is widespread across the genome

scientific article

Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence? ⬇️

scientific article

Assessing individual differences in genome-wide gene expression in human whole blood: reliability over four hours and stability over 10 months

scientific article published on August 2009

Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms.

scientific article published in April 2005

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

scientific article

Common DNA markers can account for more than half of the genetic influence on cognitive abilities

scientific article

Common variation near ROBO2 is associated with expressive vocabulary in infancy.

scientific article

Correction: First Genome-Wide Association Study on Anxiety-Related Behaviours in Childhood.

scientific article published on 27 June 2013

Correction: Genetics of Callous-Unemotional Behavior in Children.

scientific article published on 16 July 2013

Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.

scientific article

Erratum: A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence

article

Estimation of a significance threshold for epigenome-wide association studies

scientific article

First genome-wide association study on anxiety-related behaviours in childhood

scientific article

Gene set enrichment; a problem of pathways

scientific article

Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients

scientific article

Genetics of callous-unemotional behavior in children

scientific article

Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education

scientific article published on 30 June 2019

Genome-wide association study of receptive language ability of 12-year-olds

scientific article published on February 2014

Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs

scientific article

Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits.

scientific article

Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans

scientific article

Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

scientific article published on 17 December 2014

Increasing heritability of BMI and stronger associations with the FTO gene over childhood.

scientific article published on 9 October 2008

Language-impaired children: No sign of the FOXP2 mutation.

scientific article published in June 2002

Next generation sequencing in epigenetics: insights and challenges.

scientific article published on 19 October 2011

RNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation

scientific article published on 07 November 2019

Reading and Generalist Genes

scientific article

SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.

scientific article published on 30 March 2005

Single-nucleotide polymorphism genotyping in DNA pools.

scientific article

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

scientific article

Tissue-specific patterns of allelically-skewed DNA methylation

scientific article published on 19 January 2016

Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays

scientific article

List of works by Emma Meaburn

A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds.

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence.

A three-stage genome-wide association study of general cognitive ability: hunting the small effects.

Allele-specific methylation in the human genome: implications for genetic studies of complex disease

Allelic skewing of DNA methylation is widespread across the genome

Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence? ⬇️

Assessing individual differences in genome-wide gene expression in human whole blood: reliability over four hours and stability over 10 months

Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms.

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

Common DNA markers can account for more than half of the genetic influence on cognitive abilities

Common variation near ROBO2 is associated with expressive vocabulary in infancy.

Correction: First Genome-Wide Association Study on Anxiety-Related Behaviours in Childhood.

Correction: Genetics of Callous-Unemotional Behavior in Children.

Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.

Erratum: A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence

Estimation of a significance threshold for epigenome-wide association studies

First genome-wide association study on anxiety-related behaviours in childhood

Gene set enrichment; a problem of pathways

Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients

Genetics of callous-unemotional behavior in children

Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education

Genome-wide association study of receptive language ability of 12-year-olds

Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs

Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits.

Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans

Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

Increasing heritability of BMI and stronger associations with the FTO gene over childhood.

Language-impaired children: No sign of the FOXP2 mutation.

Next generation sequencing in epigenetics: insights and challenges.

RNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation

Reading and Generalist Genes

SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.

Single-nucleotide polymorphism genotyping in DNA pools.

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

Tissue-specific patterns of allelically-skewed DNA methylation

Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays