about
Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPsGenotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans.A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarraysCommon variation near ROBO2 is associated with expressive vocabulary in infancy.Allelic skewing of DNA methylation is widespread across the genome.Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays.Reading and Generalist GenesThe correlation between reading and mathematics ability at age twelve has a substantial genetic component.Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patientsChildhood intelligence is heritable, highly polygenic and associated with FNBP1LCommon DNA markers can account for more than half of the genetic influence on cognitive abilities.Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits.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.First genome-wide association study on anxiety-related behaviours in childhood.Gene set enrichment; a problem of pathways.Genetics of callous-unemotional behavior in children.Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence?Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence.Tissue-specific patterns of allelically-skewed DNA methylation.Assessing individual differences in genome-wide gene expression in human whole blood: reliability over four hours and stability over 10 monthsGenome-wide association study of receptive language ability of 12-year-olds.Next generation sequencing in epigenetics: insights and challenges.Correction: First Genome-Wide Association Study on Anxiety-Related Behaviours in Childhood.Correction: Genetics of Callous-Unemotional Behavior in Children.Estimation of a significance threshold for epigenome-wide association studies.Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms.Increasing heritability of BMI and stronger associations with the FTO gene over childhood.A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds.Language-impaired children: No sign of the FOXP2 mutation.Single-nucleotide polymorphism genotyping in DNA pools.Erratum: A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligenceGenome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and EducationRNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation
P50
Q21266602-1FE959C3-7D57-4C29-B18F-DED692FE0BAAQ24538972-54003668-F550-44B8-B50D-2E8A32486430Q24791896-95EA7DA8-86D6-483F-98F6-E19FAE52E162Q30587939-90453082-B9FC-46F1-BC5E-D6E710AA2D82Q33645884-C519C5FA-8EF7-427B-9DE2-741964B5F15EQ33735365-1ACA58D0-FCCA-4758-89D9-36B4803FC4C8Q33760110-AF3E05D6-5546-4D27-BA16-87650AEF1B6BQ33915041-B343511C-63AA-4B79-86E1-A640B6CF2B05Q33936913-CEA6AB60-34A1-437B-8EA5-D3B6F04FB9CFQ34324903-379C6D2E-FF4D-4308-A7C3-ED6E7D4CC331Q34333443-6CF5B274-0E71-4537-990E-BECDEFF4FAEEQ34342233-CD15A407-F36D-49E4-AA07-E99C3AABC87EQ34355762-7D135DB3-615B-4E1B-8CD6-C007B4996308Q34643291-B364AC71-B1A8-4C07-9A9E-4DC130660422Q34657860-64C92D8B-74E2-4716-89DF-F202F2882369Q34831645-B2CD0CC6-694F-4C77-9A70-60991EE751FEQ34846313-712ECD84-DF2B-41F5-9D81-DF23AC8DC04DQ35144308-B4AB3D6C-E792-47B2-BB78-684DC35C06BCQ35583245-F3674DB2-D749-4C7D-ADB1-50B9EB30DC8EQ36292641-34ADF5B4-7C62-48BE-B989-D574FA7BABD7Q36838971-D89D2F05-6050-4DF9-AB9A-8BA03601BF24Q37285359-A9A0B7D8-A1A0-4A27-9CFB-6C1D2DA04DDEQ37681915-359FB451-644D-40F9-8F38-866A5A971ECCQ37949510-44FE315F-3E60-4E16-ABAC-63C7A23F449DQ45748327-5EA89B46-2618-4066-B584-77A40BBB412DQ46026826-5187B00E-C7F2-4608-A7A4-9AB443F447F5Q46263944-AAB3CFB9-8DBA-41CC-8B31-A94E0869671BQ46393501-335A0AED-3A67-4A44-9533-3F78BB3492C7Q51931684-C3AD6CFD-DCA3-44EC-9439-210BFC0C9DC8Q51937027-4E9484B4-8B23-44CA-B542-E1B894A7768BQ51948138-36C63FA6-D15B-4C43-B26A-22BB75FAED0AQ51963904-D32C5201-6F1F-45EA-A6F4-0391038EECA2Q52118754-A1BCAD81-0379-461C-96DA-9A844B6B322DQ54648775-D7FF27B2-57ED-456C-968C-57F5166D4BECQ57277970-7D80BE0E-4C84-4267-90B2-D5160A62B8C3Q90618568-B83B76C8-8D05-4B2B-838E-0B485B59843BQ91261410-AD63FF88-12E8-456F-A39C-6084D1E1C9FB
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
E Meaburn
@ast
E Meaburn
@en
E Meaburn
@es
E Meaburn
@nl
type
label
E Meaburn
@ast
E Meaburn
@en
E Meaburn
@es
E Meaburn
@nl
prefLabel
E Meaburn
@ast
E Meaburn
@en
E Meaburn
@es
E Meaburn
@nl
P106
P31
P496
0000-0001-8096-9089