Andrew T - Search Results

1

The association between polymorphisms in RLIP76 and drug response in epilepsy.

Leschziner GD, Jorgensen AL, Andrew T, Williamson PR, Marson AG, Coffey AJ, Middleditch C, Balding DJ, Rogers J, Bentley DR, Chadwick D, Johnson MR, Pirmohamed M. Leschziner GD, et al. Among authors: andrew t. Pharmacogenomics. 2007 Dec;8(12):1715-22. doi: 10.2217/14622416.8.12.1715. Pharmacogenomics. 2007. PMID: 18086001

2

ABCB1 genotype and PGP expression, function and therapeutic drug response: a critical review and recommendations for future research.

Leschziner GD, Andrew T, Pirmohamed M, Johnson MR. Leschziner GD, et al. Among authors: andrew t. Pharmacogenomics J. 2007 Jun;7(3):154-79. doi: 10.1038/sj.tpj.6500413. Epub 2006 Sep 12. Pharmacogenomics J. 2007. PMID: 16969364 Review.

3

Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study.

Leschziner G, Jorgensen AL, Andrew T, Pirmohamed M, Williamson PR, Marson AG, Coffey AJ, Middleditch C, Rogers J, Bentley DR, Chadwick DW, Balding DJ, Johnson MR. Leschziner G, et al. Among authors: andrew t. Lancet Neurol. 2006 Aug;5(8):668-76. doi: 10.1016/S1474-4422(06)70500-2. Lancet Neurol. 2006. PMID: 16857572

4

Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach.

Leschziner GD, Andrew T, Leach JP, Chadwick D, Coffey AJ, Balding DJ, Bentley DR, Pirmohamed M, Johnson MR. Leschziner GD, et al. Among authors: andrew t. Pharmacogenet Genomics. 2007 Mar;17(3):217-20. doi: 10.1097/01.fpc.0000230408.23146.b1. Pharmacogenet Genomics. 2007. PMID: 17460550

5

Bayesian survival analysis in genetic association studies.

Tachmazidou I, Andrew T, Verzilli CJ, Johnson MR, De Iorio M. Tachmazidou I, et al. Among authors: andrew t. Bioinformatics. 2008 Sep 15;24(18):2030-6. doi: 10.1093/bioinformatics/btn351. Epub 2008 Jul 9. Bioinformatics. 2008. PMID: 18617538 Free PMC article.

6

Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS).

Leschziner GD, Coffey AJ, Andrew T, Gregorio SP, Dias-Neto E, Calafato M, Bentley DR, Kinton L, Sander JW, Johnson MR. Leschziner GD, et al. Among authors: andrew t. Epilepsy Res. 2011 Sep;96(1-2):109-15. doi: 10.1016/j.eplepsyres.2011.05.010. Epub 2011 Jun 11. Epilepsy Res. 2011. PMID: 21658913

7

Functional constraint and small insertions and deletions in the ENCODE regions of the human genome.

Clark TG, Andrew T, Cooper GM, Margulies EH, Mullikin JC, Balding DJ. Clark TG, et al. Among authors: andrew t. Genome Biol. 2007;8(9):R180. doi: 10.1186/gb-2007-8-9-r180. Genome Biol. 2007. PMID: 17784950 Free PMC article.

8

Heritability of left ventricular mass in a large cohort of twins.

Sharma P, Middelberg RP, Andrew T, Johnson MR, Christley H, Brown MJ. Sharma P, et al. Among authors: andrew t. J Hypertens. 2006 Feb;24(2):321-4. doi: 10.1097/01.hjh.0000202815.18083.03. J Hypertens. 2006. PMID: 16508579

9

Joint linkage and association of six single-nucleotide polymorphisms in the factor XIII-A subunit gene point to V34L as the main functional locus.

de Lange M, Andrew T, Snieder H, Ge D, Futers TS, Standeven K, Spector TD, Grant PJ, Ariëns RA. de Lange M, et al. Among authors: andrew t. Arterioscler Thromb Vasc Biol. 2006 Aug;26(8):1914-9. doi: 10.1161/01.ATV.0000231538.60223.92. Epub 2006 Jun 8. Arterioscler Thromb Vasc Biol. 2006. PMID: 16763156

10

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

Richards JB, Rivadeneira F, Inouye M, Pastinen TM, Soranzo N, Wilson SG, Andrew T, Falchi M, Gwilliam R, Ahmadi KR, Valdes AM, Arp P, Whittaker P, Verlaan DJ, Jhamai M, Kumanduri V, Moorhouse M, van Meurs JB, Hofman A, Pols HA, Hart D, Zhai G, Kato BS, Mullin BH, Zhang F, Deloukas P, Uitterlinden AG, Spector TD. Richards JB, et al. Among authors: andrew t. Lancet. 2008 May 3;371(9623):1505-12. doi: 10.1016/S0140-6736(08)60599-1. Lancet. 2008. PMID: 18455228 Free PMC article.

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