Roberts RG - Search Results

1

Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expression.

Rosenstiel P, Huse K, Franke A, Hampe J, Reichwald K, Platzer C, Roberts RG, Mathew CG, Platzer M, Schreiber S. Rosenstiel P, et al. Among authors: roberts rg. BMC Genomics. 2007 Dec 20;8:472. doi: 10.1186/1471-2164-8-472. BMC Genomics. 2007. PMID: 18096043 Free PMC article.

2

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.

King K, Bagnall R, Fisher SA, Sheikh F, Cuthbert A, Tan S, Mundy NI, Rosenstiel P, Schreiber S, Mathew CG, Roberts RG. King K, et al. Among authors: roberts rg. Genomics. 2007 Oct;90(4):493-501. doi: 10.1016/j.ygeno.2007.07.009. Epub 2007 Aug 24. Genomics. 2007. PMID: 17719742 Free article.

3

Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.

Bagnall RD, Roberts RG, Mirza MM, Torigoe T, Prescott NJ, Mathew CG. Bagnall RD, et al. Among authors: roberts rg. Eur J Hum Genet. 2008 May;16(5):619-25. doi: 10.1038/sj.ejhg.5201996. Epub 2008 Jan 23. Eur J Hum Genet. 2008. PMID: 18212821 Free article.

4

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

King K, Sheikh MF, Cuthbert AP, Fisher SA, Onnie CM, Mirza MM, Pattni RC, Sanderson J, Forbes A, Mansfield J, Lewis CM, Roberts RG, Mathew CG. King K, et al. Among authors: roberts rg. Hum Mutat. 2006 Jan;27(1):44-54. doi: 10.1002/humu.20264. Hum Mutat. 2006. PMID: 16278823

5

Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.

Abbs S, Roberts RG, Mathew CG, Bentley DR, Bobrow M. Abbs S, et al. Among authors: roberts rg. Genomics. 1990 Aug;7(4):602-6. doi: 10.1016/0888-7543(90)90205-9. Genomics. 1990. PMID: 1974880

6

Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCR.

Gibson RA, Buchwald M, Roberts RG, Mathew CG. Gibson RA, et al. Among authors: roberts rg. Hum Mol Genet. 1993 Jan;2(1):35-8. doi: 10.1093/hmg/2.1.35. Hum Mol Genet. 1993. PMID: 8490620

7

Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31.

Onnie C, Fisher SA, King K, Mirza M, Roberts R, Forbes A, Sanderson J, Lewis CM, Mathew CG. Onnie C, et al. Genes Immun. 2006 Jul;7(5):359-65. doi: 10.1038/sj.gene.6364307. Epub 2006 May 18. Genes Immun. 2006. PMID: 16724073

8

A MseI polymorphism in exon 48 of the dystrophin gene.

Yau SC, Roberts RG, Bentley DR, Mathew CG, Bobrow M. Yau SC, et al. Among authors: roberts rg. Nucleic Acids Res. 1991 Oct 25;19(20):5803. doi: 10.1093/nar/19.20.5803-a. Nucleic Acids Res. 1991. PMID: 1682892 Free PMC article.

9

Dystrophin point mutation screening using a multiplexed protein truncation test.

Whittock NV, Roberts RG, Mathew CG, Abbs SJ. Whittock NV, et al. Among authors: roberts rg. Genet Test. 1997;1(2):115-23. doi: 10.1089/gte.1997.1.115. Genet Test. 1997. PMID: 10464635

10

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: roberts rg. 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.

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