Morris A - Search Results

1

Bayesian refinement of association signals for 14 loci in 3 common diseases.

Wellcome Trust Case Control Consortium; Maller JB, McVean G, Byrnes J, Vukcevic D, Palin K, Su Z, Howson JM, Auton A, Myers S, Morris A, Pirinen M, Brown MA, Burton PR, Caulfield MJ, Compston A, Farrall M, Hall AS, Hattersley AT, Hill AV, Mathew CG, Pembrey M, Satsangi J, Stratton MR, Worthington J, Craddock N, Hurles M, Ouwehand W, Parkes M, Rahman N, Duncanson A, Todd JA, Kwiatkowski DP, Samani NJ, Gough SC, McCarthy MI, Deloukas P, Donnelly P. Wellcome Trust Case Control Consortium, et al. Among authors: morris a. Nat Genet. 2012 Dec;44(12):1294-301. doi: 10.1038/ng.2435. Epub 2012 Oct 28. Nat Genet. 2012. PMID: 23104008 Free PMC article.

2

The impact of SNP density on fine-scale patterns of linkage disequilibrium.

Ke X, Hunt S, Tapper W, Lawrence R, Stavrides G, Ghori J, Whittaker P, Collins A, Morris AP, Bentley D, Cardon LR, Deloukas P. Ke X, et al. Among authors: morris ap. Hum Mol Genet. 2004 Mar 15;13(6):577-88. doi: 10.1093/hmg/ddh060. Epub 2004 Jan 20. Hum Mol Genet. 2004. PMID: 14734624

3

Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.

Durrant C, Zondervan KT, Cardon LR, Hunt S, Deloukas P, Morris AP. Durrant C, et al. Am J Hum Genet. 2004 Jul;75(1):35-43. doi: 10.1086/422174. Epub 2004 May 13. Am J Hum Genet. 2004. PMID: 15148658 Free PMC article.

4

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

Ke X, Durrant C, Morris AP, Hunt S, Bentley DR, Deloukas P, Cardon LR. Ke X, et al. Hum Mol Genet. 2004 Nov 1;13(21):2557-65. doi: 10.1093/hmg/ddh294. Epub 2004 Sep 14. Hum Mol Genet. 2004. PMID: 15367493

5

How useful is the fine-scale mapping of complex trait linkage peaks? Evaluating the impact of additional microsatellite genotyping on the posterior probability of linkage.

Wiltshire S, Morris AP, McCarthy MI, Cardon LR. Wiltshire S, et al. Genet Epidemiol. 2005 Jan;28(1):1-10. doi: 10.1002/gepi.20023. Genet Epidemiol. 2005. PMID: 15493062

6

Genotype prediction using a dense map of SNPs.

Evans DM, Cardon LR, Morris AP. Evans DM, et al. Genet Epidemiol. 2004 Dec;27(4):375-84. doi: 10.1002/gepi.20045. Genet Epidemiol. 2004. PMID: 15543641

7

Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes.

Morris AP. Morris AP. Genet Epidemiol. 2005 Sep;29(2):91-107. doi: 10.1002/gepi.20080. Genet Epidemiol. 2005. PMID: 15940704

8

Gearing up for genome-wide gene-association studies.

Farrall M, Morris AP. Farrall M, et al. Hum Mol Genet. 2005 Oct 15;14 Spec No. 2:R157-62. doi: 10.1093/hmg/ddi273. Hum Mol Genet. 2005. PMID: 16244314 Review.

9

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants.

Lawrence R, Evans DM, Morris AP, Ke X, Hunt S, Paolucci M, Ragoussis J, Deloukas P, Bentley D, Cardon LR. Lawrence R, et al. Genome Res. 2005 Nov;15(11):1503-10. doi: 10.1101/gr.4217605. Genome Res. 2005. PMID: 16251460 Free PMC article.

10

An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets.

Zeggini E, Rayner W, Morris AP, Hattersley AT, Walker M, Hitman GA, Deloukas P, Cardon LR, McCarthy MI. Zeggini E, et al. Among authors: morris ap. Nat Genet. 2005 Dec;37(12):1320-2. doi: 10.1038/ng1670. Epub 2005 Oct 30. Nat Genet. 2005. PMID: 16258542

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