Owen CJ - Search Results

1

Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.

Sutherland A, Davies J, Owen CJ, Vaikkakara S, Walker C, Cheetham TD, James RA, Perros P, Donaldson PT, Cordell HJ, Quinton R, Pearce SH. Sutherland A, et al. Among authors: owen cj. J Clin Endocrinol Metab. 2007 Aug;92(8):3338-41. doi: 10.1210/jc.2007-0173. Epub 2007 May 29. J Clin Endocrinol Metab. 2007. PMID: 17535987 Free PMC article.

2

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, Donaldson PT, Ball SG, James RA, Quinton R, Perros P, Pearce SH. Velaga MR, et al. Among authors: owen cj. J Clin Endocrinol Metab. 2004 Nov;89(11):5862-5. doi: 10.1210/jc.2004-1108. J Clin Endocrinol Metab. 2004. PMID: 15531553

3

A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population.

Jennings CE, Owen CJ, Wilson V, Pearce SH. Jennings CE, et al. Among authors: owen cj. J Mol Endocrinol. 2005 Jun;34(3):859-63. doi: 10.1677/jme.1.01760. J Mol Endocrinol. 2005. PMID: 15956353

4

Role of the CD40 locus in Graves' disease.

Houston FA, Wilson V, Jennings CE, Owen CJ, Donaldson P, Perros P, Pearce SH. Houston FA, et al. Among authors: owen cj. Thyroid. 2004 Jul;14(7):506-9. doi: 10.1089/1050725041517039. Thyroid. 2004. PMID: 15307939

5

No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease.

Jennings CE, Owen CJ, Wilson V, Pearce SH. Jennings CE, et al. Among authors: owen cj. Clin Endocrinol (Oxf). 2005 Mar;62(3):362-5. doi: 10.1111/j.1365-2265.2005.02224.x. Clin Endocrinol (Oxf). 2005. PMID: 15730420

6

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.

Owen CJ, Eden JA, Jennings CE, Wilson V, Cheetham TD, Pearce SH. Owen CJ, et al. J Mol Endocrinol. 2006 Aug;37(1):97-104. doi: 10.1677/jme.1.02072. J Mol Endocrinol. 2006. PMID: 16901927

7

Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association.

Owen CJ, Kelly H, Eden JA, Merriman ME, Pearce SH, Merriman TR. Owen CJ, et al. J Clin Endocrinol Metab. 2007 Mar;92(3):1106-11. doi: 10.1210/jc.2006-2183. Epub 2007 Jan 2. J Clin Endocrinol Metab. 2007. PMID: 17200162

8

Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.

Owen CJ, Jennings CE, Imrie H, Lachaux A, Bridges NA, Cheetham TD, Pearce SH. Owen CJ, et al. J Clin Endocrinol Metab. 2003 Dec;88(12):6034-9. doi: 10.1210/jc.2003-031080. J Clin Endocrinol Metab. 2003. PMID: 14671208

9

Discordance for X-linked hypophosphataemic rickets in identical twin girls.

Owen CJ, Habeb A, Pearce SH, Wright M, Ichikawa S, Sorenson AH, Econs MJ, Cheetham TD. Owen CJ, et al. Horm Res. 2009;71(4):237-44. doi: 10.1159/000201113. Epub 2009 Mar 4. Horm Res. 2009. PMID: 19258716

10

Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1.

Gopal-Kothandapani JS, Doshi AB, Smith K, Christian M, Mushtaq T, Banerjee I, Padidela R, Ramakrishnan R, Owen C, Cheetham T, Dimitri P. Gopal-Kothandapani JS, et al. J Pediatr Endocrinol Metab. 2019 Sep 25;32(9):959-967. doi: 10.1515/jpem-2018-0538. J Pediatr Endocrinol Metab. 2019. PMID: 31301676

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