| Year |
Citation |
Score |
| 2023 |
Bowler A, Arichi T, Fearon P, Meaburn E, Begum-Ali J, Pascoe G, Johnson MH, Jones EJH, Ronald A. PHENOTYPIC AND GENETIC ASSOCIATIONS BETWEEN PRESCHOOL FINE MOTOR SKILLS AND LATER NEURODEVELOPMENT, PSYCHOPATHOLOGY, AND EDUCATIONAL ACHIEVEMENT. Biological Psychiatry. PMID 38043695 DOI: 10.1016/j.biopsych.2023.11.017 |
0.545 |
|
| 2021 |
Donati G, Dumontheil I, Pain O, Asbury K, Meaburn EL. Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence. Scientific Reports. 11: 3851. PMID 33594131 DOI: 10.1038/s41598-021-82877-y |
0.42 |
|
| 2020 |
Gui A, Jones EJH, Wong CCY, Meaburn E, Xia B, Pasco G, Lloyd-Fox S, Charman T, Bolton P, Johnson MH. Leveraging epigenetics to examine differences in developmental trajectories of social attention: A proof-of-principle study of DNA methylation in infants with older siblings with autism. Infant Behavior & Development. 60: 101409. PMID 32623100 DOI: 10.1016/J.Infbeh.2019.101409 |
0.401 |
|
| 2019 |
Saffari A, Arno M, Nasser E, Ronald A, Wong CCY, Schalkwyk LC, Mill J, Dudbridge F, Meaburn EL. RNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation. Molecular Autism. 10: 38. PMID 31719968 DOI: 10.1186/S13229-019-0285-1 |
0.604 |
|
| 2019 |
Donati G, Dumontheil I, Meaburn EL. Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education. Mind, Brain and Education : the Official Journal of the International Mind, Brain, and Education Society. 13: 224-233. PMID 31598132 DOI: 10.1111/Mbe.12198 |
0.504 |
|
| 2019 |
Donati G, Meaburn EL, Dumontheil I. The specificity of associations between cognition and attainment in English, maths and science during adolescence Learning and Individual Differences. 69: 84-93. DOI: 10.1016/J.Lindif.2018.11.012 |
0.336 |
|
| 2017 |
Saffari A, Silver MJ, Zavattari P, Moi L, Columbano A, Meaburn EL, Dudbridge F. Estimation of a significance threshold for epigenome-wide association studies. Genetic Epidemiology. PMID 29034560 DOI: 10.1002/Gepi.22086 |
0.4 |
|
| 2016 |
Pourcain BS, Haworth CM, Davis OS, Wang K, Timpson NJ, Evans DM, Kemp JP, Ronald A, Price T, Meaburn E, Ring SM, Golding J, Hakonarson H, Plomin R, Smith GD. Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence. Human Genetics. PMID 27299648 DOI: 10.1007/s00439-016-1695-1 |
0.629 |
|
| 2016 |
Marzi SJ, Meaburn EL, Dempster EL, Lunnon K, Paya-Cano JL, Smith RG, Volta M, Troakes C, Schalkwyk LC, Mill J. Tissue-specific patterns of allelically-skewed DNA methylation. Epigenetics. 0. PMID 26786711 DOI: 10.1080/15592294.2015.1127479 |
0.392 |
|
| 2015 |
Spain SL, Pedroso I, Kadeva N, Miller MB, Iacono WG, McGue M, Stergiakouli E, Smith GD, Putallaz M, Lubinski D, Meaburn EL, Plomin R, Simpson MA. A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence. Molecular Psychiatry. PMID 26239293 DOI: 10.1038/Mp.2015.108 |
0.617 |
|
| 2015 |
St Pourcain B, Haworth CM, Davis OS, Wang K, Timpson NJ, Evans DM, Kemp JP, Ronald A, Price T, Meaburn E, Ring SM, Golding J, Hakonarson H, Plomin R, Davey Smith G. Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence. Human Genetics. 134: 539-51. PMID 25515860 DOI: 10.1007/S00439-014-1514-5 |
0.762 |
|
| 2015 |
Thomas MSC, Kovas Y, Meaburn EL, Tolmie A. What Can the Study of Genetics Offer to Educators? Mind, Brain, and Education. 9: 72-80. DOI: 10.1111/Mbe.12077 |
0.365 |
|
| 2015 |
Spain SL, Pedroso I, Kadeva N, Miller MB, Iacono WG, McGue M, Stergiakouli E, Smith GD, Putallaz M, Lubinski D, Meaburn EL, Plomin R, Simpson MA. A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence Molecular Psychiatry. DOI: 10.1038/mp.2015.145 |
0.487 |
|
| 2015 |
Spain SL, Pedroso I, Kadeva N, Miller MB, Iacono WG, McGue M, Stergiakouli E, Smith GD, Putallaz M, Lubinski D, Meaburn EL, Plomin R, Simpson MA. A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence Molecular Psychiatry. DOI: 10.1038/mp.2015.108 |
0.487 |
|
| 2014 |
St Pourcain B, Cents RA, Whitehouse AJ, Haworth CM, Davis OS, O'Reilly PF, Roulstone S, Wren Y, Ang QW, Velders FP, Evans DM, Kemp JP, Warrington NM, Miller L, Timpson NJ, ... ... Meaburn EL, et al. Common variation near ROBO2 is associated with expressive vocabulary in infancy. Nature Communications. 5: 4831. PMID 25226531 DOI: 10.1038/Ncomms5831 |
0.735 |
|
| 2014 |
Broadbent H, Farran EK, Chin E, Metcalfe K, Tassabehji M, Turnpenny P, Sansbury F, Meaburn E, Karmiloff-Smith A. Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients. Journal of Neurodevelopmental Disorders. 6: 18. PMID 25057328 DOI: 10.1186/1866-1955-6-18 |
0.577 |
|
| 2014 |
Davis OS, Band G, Pirinen M, Haworth CM, Meaburn EL, Kovas Y, Harlaar N, Docherty SJ, Hanscombe KB, Trzaskowski M, Curtis CJ, Strange A, Freeman C, Bellenguez C, Su Z, et al. The correlation between reading and mathematics ability at age twelve has a substantial genetic component. Nature Communications. 5: 4204. PMID 25003214 DOI: 10.1038/Ncomms5204 |
0.756 |
|
| 2014 |
Sieradzka D, Power RA, Freeman D, Cardno AG, McGuire P, Plomin R, Meaburn EL, Dudbridge F, Ronald A. Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence? Plos One. 9: e94398. PMID 24718684 DOI: 10.1371/Journal.Pone.0094398 |
0.679 |
|
| 2014 |
Harlaar N, Meaburn EL, Hayiou-Thomas ME, Davis OS, Docherty S, Hanscombe KB, Haworth CM, Price TS, Trzaskowski M, Dale PS, Plomin R. Genome-wide association study of receptive language ability of 12-year-olds. Journal of Speech, Language, and Hearing Research : Jslhr. 57: 96-105. PMID 24687471 DOI: 10.1044/1092-4388(2013/12-0303) |
0.743 |
|
| 2014 |
Wong CC, Meaburn EL, Ronald A, Price TS, Jeffries AR, Schalkwyk LC, Plomin R, Mill J. Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits. Molecular Psychiatry. 19: 495-503. PMID 23608919 DOI: 10.1038/Mp.2013.41 |
0.76 |
|
| 2014 |
Benyamin B, Pourcain B, Davis OS, Davies G, Hansell NK, Brion MJ, Kirkpatrick RM, Cents RA, Franić S, Miller MB, Haworth CM, Meaburn E, Price TS, Evans DM, Timpson N, et al. Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry. 19: 253-8. PMID 23358156 DOI: 10.1038/Mp.2012.184 |
0.752 |
|
| 2014 |
Sieradzka D, Power RA, Freeman D, Cardno A, McGuire P, Plomin R, Meaburn E, Dudbridge F, Ronald A. Poster #M139 INVESTIGATION INTO AN ASSOCIATION BETWEEN GENETIC RISK FACTORS FOR SCHIZOPHRENIA AND BIPOLAR DISORDER AND DIMENSION-SPECIFIC PSYCHOTIC EXPERIENCES IN ADOLESCENCE Schizophrenia Research. 153: S240. DOI: 10.1016/S0920-9964(14)70689-9 |
0.644 |
|
| 2013 |
Viding E, Price TS, Jaffee SR, Trzaskowski M, Davis OS, Meaburn EL, Haworth CM, Plomin R. Genetics of callous-unemotional behavior in children. Plos One. 8: e65789. PMID 23874384 DOI: 10.1371/Journal.Pone.0065789 |
0.72 |
|
| 2013 |
Trzaskowski M, Eley TC, Davis OS, Doherty SJ, Hanscombe KB, Meaburn EL, Haworth CM, Price T, Plomin R. First genome-wide association study on anxiety-related behaviours in childhood. Plos One. 8: e58676. PMID 23565138 DOI: 10.1371/Journal.Pone.0058676 |
0.761 |
|
| 2013 |
Plomin R, Haworth CM, Meaburn EL, Price TS, Davis OS. Common DNA markers can account for more than half of the genetic influence on cognitive abilities. Psychological Science. 24: 562-8. PMID 23501967 DOI: 10.1177/0956797612457952 |
0.721 |
|
| 2013 |
Trzaskowski M, Eley TC, Davis OSP, Docherty SJ, Hanscombe KB, Meaburn EL, Haworth CMA, Price T, Plomin R. Correction: First genome-wide association study on anxiety-related behaviours in childhood (PLoS ONE (2013) 8, 4 (e58676) DOI: 10.1371/journal. pone.0058676) Plos One. 8. DOI: 10.1371/Annotation/D320E3Eb-Ab8F-43Ce-B341-3Da36Cd7Ff99 |
0.667 |
|
| 2013 |
Viding E, Price TS, Jaffee SR, Trzaskowski M, Davis OSP, Meaburn EL, Haworth CMA, Plomin R. Correction: Genetics of Callous-Unemotional Behavior in Children Plos One. 8. DOI: 10.1371/Annotation/0B16418F-Ceb5-41B2-Be2A-A20F0C56F9A6 |
0.662 |
|
| 2012 |
Meaburn E, Schulz R. Next generation sequencing in epigenetics: insights and challenges. Seminars in Cell & Developmental Biology. 23: 192-9. PMID 22027613 DOI: 10.1016/J.Semcdb.2011.10.010 |
0.375 |
|
| 2010 |
Schosser A, Pirlo K, Gaysina D, Cohen-Woods S, Schalkwyk LC, Elkin A, Korszun A, Gunasinghe C, Gray J, Jones L, Meaburn E, Farmer AE, Craig IW, McGuffin P. Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays. Bmc Research Notes. 3: 274. PMID 21040578 DOI: 10.1186/1756-0500-3-274 |
0.461 |
|
| 2010 |
Meaburn EL, Schalkwyk LC, Mill J. Allele-specific methylation in the human genome: implications for genetic studies of complex disease. Epigenetics. 5: 578-82. PMID 20716955 DOI: 10.4161/Epi.5.7.12960 |
0.487 |
|
| 2010 |
Viding E, Hanscombe KB, Curtis CJ, Davis OS, Meaburn EL, Plomin R. In search of genes associated with risk for psychopathic tendencies in children: a two-stage genome-wide association study of pooled DNA. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 51: 780-8. PMID 20345837 DOI: 10.1111/J.1469-7610.2010.02236.X |
0.621 |
|
| 2010 |
Davis OS, Butcher LM, Docherty SJ, Meaburn EL, Curtis CJ, Simpson MA, Schalkwyk LC, Plomin R. A three-stage genome-wide association study of general cognitive ability: hunting the small effects. Behavior Genetics. 40: 759-67. PMID 20306291 DOI: 10.1007/S10519-010-9350-4 |
0.636 |
|
| 2010 |
Schalkwyk LC, Meaburn EL, Smith R, Dempster EL, Jeffries AR, Davies MN, Plomin R, Mill J. Allelic skewing of DNA methylation is widespread across the genome. American Journal of Human Genetics. 86: 196-212. PMID 20159110 DOI: 10.1016/J.Ajhg.2010.01.014 |
0.581 |
|
| 2010 |
Docherty SJ, Davis OS, Kovas Y, Meaburn EL, Dale PS, Petrill SA, Schalkwyk LC, Plomin R. A genome-wide association study identifies multiple loci associated with mathematics ability and disability. Genes, Brain, and Behavior. 9: 234-47. PMID 20039944 DOI: 10.1111/J.1601-183X.2009.00553.X |
0.735 |
|
| 2009 |
Meaburn EL, Fernandes C, Craig IW, Plomin R, Schalkwyk LC. Assessing individual differences in genome-wide gene expression in human whole blood: reliability over four hours and stability over 10 months. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 12: 372-80. PMID 19653838 DOI: 10.1375/Twin.12.4.372 |
0.468 |
|
| 2008 |
Haworth CM, Carnell S, Meaburn EL, Davis OS, Plomin R, Wardle J. Increasing heritability of BMI and stronger associations with the FTO gene over childhood. Obesity (Silver Spring, Md.). 16: 2663-8. PMID 18846049 DOI: 10.1038/Oby.2008.434 |
0.527 |
|
| 2008 |
Meaburn EL, Harlaar N, Craig IW, Schalkwyk LC, Plomin R. Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children. Molecular Psychiatry. 13: 729-40. PMID 17684495 DOI: 10.1038/Sj.Mp.4002063 |
0.614 |
|
| 2007 |
Haworth CM, Meaburn EL, Harlaar N, Plomin R. Reading and Generalist Genes. Mind, Brain and Education : the Official Journal of the International Mind, Brain, and Education Society. 1: 173-180. PMID 20383260 DOI: 10.1111/J.1751-228X.2007.00018.X |
0.591 |
|
| 2006 |
Meaburn E, Butcher LM, Schalkwyk LC, Plomin R. Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans. Nucleic Acids Research. 34: e27. PMID 16478714 DOI: 10.1093/Nar/Gnj027 |
0.558 |
|
| 2006 |
Meaburn E, Butcher LM, Harlaar N, Curtis C, Craig IW, Schalkwyk LC, Plomin R. An association scan using pooled DNA and 100k SNPS identifies a 'SNP set' for early reading American Journal of Medical Genetics. 703-704. DOI: 10.1002/Ajmg.B.30408 |
0.53 |
|
| 2005 |
Harlaar N, Butcher LM, Meaburn E, Sham P, Craig IW, Plomin R. A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 46: 1097-107. PMID 16178934 DOI: 10.1111/J.1469-7610.2005.01515.X |
0.581 |
|
| 2005 |
Craig I, Meaburn E, Butcher L, Hill L, Plomin R. Single-nucleotide polymorphism genotyping in DNA pools. Methods in Molecular Biology (Clifton, N.J.). 311: 147-64. PMID 16100406 DOI: 10.1385/1-59259-957-5:147 |
0.567 |
|
| 2005 |
Meaburn E, Butcher LM, Liu L, Fernandes C, Hansen V, Al-Chalabi A, Plomin R, Craig I, Schalkwyk LC. Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs. Bmc Genomics. 6: 52. PMID 15811185 DOI: 10.1186/1471-2164-6-52 |
0.575 |
|
| 2005 |
Butcher LM, Meaburn E, Knight J, Sham PC, Schalkwyk LC, Craig IW, Plomin R. SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children. Human Molecular Genetics. 14: 1315-25. PMID 15800012 DOI: 10.1093/Hmg/Ddi142 |
0.605 |
|
| 2005 |
Simpson CL, Knight J, Butcher LM, Hansen VK, Meaburn E, Schalkwyk LC, Craig IW, Powell JF, Sham PC, Al-Chalabi A. A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays. Nucleic Acids Research. 33: e25. PMID 15701753 DOI: 10.1093/Nar/Gni028 |
0.431 |
|
| 2005 |
Butcher LM, Meaburn E, Dale PS, Sham P, Schalkwyk LC, Craig IW, Plomin R. Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms. Molecular Psychiatry. 10: 384-92. PMID 15452586 DOI: 10.1038/Sj.Mp.4001589 |
0.585 |
|
| 2004 |
Butcher LM, Meaburn E, Liu L, Fernandes C, Hill L, Al-Chalabi A, Plomin R, Schalkwyk L, Craig IW. Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits. Behavior Genetics. 34: 549-55. PMID 15319578 DOI: 10.1023/B:Bege.0000038493.26202.D3 |
0.596 |
|
| 2003 |
Meaburn E, Schalkwyk L, Craig I, Plomin R. A genome wide scan using 400 non-synonymous SNP markers in DNA pools identifies genes associated with language impairment in children American Journal of Medical Genetics. 178-178. DOI: 10.1002/Ajmg.B.20095 |
0.585 |
|
| 2002 |
Meaburn E, Dale PS, Craig IW, Plomin R. Language-impaired children: No sign of the FOXP2 mutation. Neuroreport. 13: 1075-7. PMID 12060812 DOI: 10.1097/00001756-200206120-00020 |
0.47 |
|
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