Lewis CM - Search Results

1

From SNPs to genes: disease association at the gene level.

Lehne B, Lewis CM, Schlitt T. Lehne B, et al. Among authors: lewis cm. PLoS One. 2011;6(6):e20133. doi: 10.1371/journal.pone.0020133. Epub 2011 Jun 30. PLoS One. 2011. PMID: 21738570 Free PMC article.

2

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.

Cuthbert AP, Fisher SA, Mirza MM, King K, Hampe J, Croucher PJ, Mascheretti S, Sanderson J, Forbes A, Mansfield J, Schreiber S, Lewis CM, Mathew CG. Cuthbert AP, et al. Among authors: lewis cm. Gastroenterology. 2002 Apr;122(4):867-74. doi: 10.1053/gast.2002.32415. Gastroenterology. 2002. PMID: 11910337

3

Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.

Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG. Fisher SA, et al. Among authors: lewis cm. Hum Mutat. 2006 Aug;27(8):778-85. doi: 10.1002/humu.20358. Hum Mutat. 2006. PMID: 16835882

4

Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.

Pearce AV, Fisher SA, Prescott NJ, Onnie CM, Pattni R, Green P, Forbes A, Mansfield J, Sanderson J, Schreiber S, Lewis CM, Mathew CG. Pearce AV, et al. Among authors: lewis cm. Int J Colorectal Dis. 2007 Apr;22(4):419-24. doi: 10.1007/s00384-006-0151-4. Epub 2006 May 31. Int J Colorectal Dis. 2007. PMID: 16944184

5

A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.

Prescott NJ, Fisher SA, Franke A, Hampe J, Onnie CM, Soars D, Bagnall R, Mirza MM, Sanderson J, Forbes A, Mansfield JC, Lewis CM, Schreiber S, Mathew CG. Prescott NJ, et al. Among authors: lewis cm. Gastroenterology. 2007 May;132(5):1665-71. doi: 10.1053/j.gastro.2007.03.034. Epub 2007 Mar 24. Gastroenterology. 2007. PMID: 17484864

6

Power of genetic association studies in the presence of linkage disequilibrium and allelic heterogeneity.

Fisher SA, Lewis CM. Fisher SA, et al. Among authors: lewis cm. Hum Hered. 2008;66(4):210-22. doi: 10.1159/000143404. Epub 2008 Jul 9. Hum Hered. 2008. PMID: 18612206 Free PMC article.

7

Meta-analysis of genome-wide linkage studies across autoimmune diseases.

Forabosco P, Bouzigon E, Ng MY, Hermanowski J, Fisher SA, Criswell LA, Lewis CM. Forabosco P, et al. Among authors: lewis cm. Eur J Hum Genet. 2009 Feb;17(2):236-43. doi: 10.1038/ejhg.2008.163. Epub 2008 Sep 10. Eur J Hum Genet. 2009. PMID: 18781189 Free PMC article.

8

Meta-analysis of genome-wide linkage studies in celiac disease.

Forabosco P, Neuhausen SL, Greco L, Naluai AT, Wijmenga C, Saavalainen P, Houlston RS, Ciclitira PJ, Babron MC, Lewis CM. Forabosco P, et al. Among authors: lewis cm. Hum Hered. 2009;68(4):223-30. doi: 10.1159/000228920. Epub 2009 Jul 22. Hum Hered. 2009. PMID: 19622889 Free PMC article.

9

Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.

Prescott NJ, Dominy KM, Kubo M, Lewis CM, Fisher SA, Redon R, Huang N, Stranger BE, Blaszczyk K, Hudspith B, Parkes G, Hosono N, Yamazaki K, Onnie CM, Forbes A, Dermitzakis ET, Nakamura Y, Mansfield JC, Sanderson J, Hurles ME, Roberts RG, Mathew CG. Prescott NJ, et al. Among authors: lewis cm. Hum Mol Genet. 2010 May 1;19(9):1828-39. doi: 10.1093/hmg/ddq041. Epub 2010 Jan 27. Hum Mol Genet. 2010. PMID: 20106866 Free PMC article.

10

Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.

Uher R, Perroud N, Ng MY, Hauser J, Henigsberg N, Maier W, Mors O, Placentino A, Rietschel M, Souery D, Zagar T, Czerski PM, Jerman B, Larsen ER, Schulze TG, Zobel A, Cohen-Woods S, Pirlo K, Butler AW, Muglia P, Barnes MR, Lathrop M, Farmer A, Breen G, Aitchison KJ, Craig I, Lewis CM, McGuffin P. Uher R, et al. Among authors: lewis cm. Am J Psychiatry. 2010 May;167(5):555-64. doi: 10.1176/appi.ajp.2009.09070932. Epub 2010 Apr 1. Am J Psychiatry. 2010. PMID: 20360315

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