Meaburn E - Search Results

1

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

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. St Pourcain B, et al. Among authors: meaburn e. Hum Genet. 2015 Jun;134(6):539-51. doi: 10.1007/s00439-014-1514-5. Epub 2014 Dec 17. Hum Genet. 2015. PMID: 25515860 Free PMC article. Clinical Trial.

2

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

Meaburn E, Dale PS, Craig IW, Plomin R. Meaburn E, et al. Neuroreport. 2002 Jun 12;13(8):1075-7. doi: 10.1097/00001756-200206120-00020. Neuroreport. 2002. PMID: 12060812

3

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

Butcher LM, Meaburn E, Liu L, Fernandes C, Hill L, Al-Chalabi A, Plomin R, Schalkwyk L, Craig IW. Butcher LM, et al. Among authors: meaburn e. Behav Genet. 2004 Sep;34(5):549-55. doi: 10.1023/B:BEGE.0000038493.26202.d3. Behav Genet. 2004. PMID: 15319578

4

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

Butcher LM, Meaburn E, Dale PS, Sham P, Schalkwyk LC, Craig IW, Plomin R. Butcher LM, et al. Among authors: meaburn e. Mol Psychiatry. 2005 Apr;10(4):384-92. doi: 10.1038/sj.mp.4001589. Mol Psychiatry. 2005. PMID: 15452586 Clinical Trial.

5

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

Butcher LM, Meaburn E, Knight J, Sham PC, Schalkwyk LC, Craig IW, Plomin R. Butcher LM, et al. Among authors: meaburn e. Hum Mol Genet. 2005 May 15;14(10):1315-25. doi: 10.1093/hmg/ddi142. Epub 2005 Mar 30. Hum Mol Genet. 2005. PMID: 15800012

6

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

Harlaar N, Butcher LM, Meaburn E, Sham P, Craig IW, Plomin R. Harlaar N, et al. Among authors: meaburn e. J Child Psychol Psychiatry. 2005 Oct;46(10):1097-107. doi: 10.1111/j.1469-7610.2005.01515.x. J Child Psychol Psychiatry. 2005. PMID: 16178934

7

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

Meaburn E, Butcher LM, Schalkwyk LC, Plomin R. Meaburn E, et al. Nucleic Acids Res. 2006 Feb 14;34(4):e27. doi: 10.1093/nar/gnj027. Nucleic Acids Res. 2006. PMID: 16478714 Free PMC article.

8

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children.

Meaburn EL, Harlaar N, Craig IW, Schalkwyk LC, Plomin R. Meaburn EL, et al. Mol Psychiatry. 2008 Jul;13(7):729-40. doi: 10.1038/sj.mp.4002063. Epub 2007 Aug 7. Mol Psychiatry. 2008. PMID: 17684495

9

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

Haworth CM, Carnell S, Meaburn EL, Davis OS, Plomin R, Wardle J. Haworth CM, et al. Obesity (Silver Spring). 2008 Dec;16(12):2663-8. doi: 10.1038/oby.2008.434. Epub 2008 Oct 9. Obesity (Silver Spring). 2008. PMID: 18846049 Free article.

10

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

Meaburn EL, Fernandes C, Craig IW, Plomin R, Schalkwyk LC. Meaburn EL, et al. Twin Res Hum Genet. 2009 Aug;12(4):372-80. doi: 10.1375/twin.12.4.372. Twin Res Hum Genet. 2009. PMID: 19653838 Free PMC article.

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