Imrie H - Search Results

1

Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population.

Imrie H, Vaidya B, Perros P, Kelly WF, Toft AD, Young ET, Kendall-Taylor P, Pearce SH. Imrie H, et al. J Clin Endocrinol Metab. 2001 Feb;86(2):626-30. doi: 10.1210/jcem.86.2.7191. J Clin Endocrinol Metab. 2001. PMID: 11158020

2

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. Among authors: imrie h. J Clin Endocrinol Metab. 2003 Dec;88(12):6034-9. doi: 10.1210/jc.2003-031080. J Clin Endocrinol Metab. 2003. PMID: 14671208

3

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.

Keavney B, Mayosi B, Gaukrodger N, Imrie H, Baker M, Fraser R, Ingram M, Watkins H, Farrall M, Davies E, Connell J. Keavney B, et al. Among authors: imrie h. J Clin Endocrinol Metab. 2005 Feb;90(2):1072-7. doi: 10.1210/jc.2004-0870. Epub 2004 Nov 2. J Clin Endocrinol Metab. 2005. PMID: 15522937

4

Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.

Imrie H, Freel M, Mayosi BM, Davies E, Fraser R, Ingram M, Cordell HJ, Farrall M, Avery PJ, Watkins H, Keavney B, Connell JM. Imrie H, et al. J Clin Endocrinol Metab. 2006 Dec;91(12):5051-6. doi: 10.1210/jc.2006-1481. Epub 2006 Sep 19. J Clin Endocrinol Metab. 2006. PMID: 16984984

5

Mutational analysis of the thyrotropin receptor gene in sporadic and familial feline thyrotoxicosis.

Pearce SH, Foster DJ, Imrie H, Myerscough N, Beckett GJ, Thoday KL, Kendall-Taylor P. Pearce SH, et al. Among authors: imrie h. Thyroid. 1997 Dec;7(6):923-7. doi: 10.1089/thy.1997.7.923. Thyroid. 1997. PMID: 9459639

6

A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1.

Pearce SH, Cheetham T, Imrie H, Vaidya B, Barnes ND, Bilous RW, Carr D, Meeran K, Shaw NJ, Smith CS, Toft AD, Williams G, Kendall-Taylor P. Pearce SH, et al. Among authors: imrie h. Am J Hum Genet. 1998 Dec;63(6):1675-84. doi: 10.1086/302145. Am J Hum Genet. 1998. PMID: 9837820 Free PMC article.

7

Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves disease.

Pearce SH, Vaidya B, Imrie H, Perros P, Kelly WF, Toft AD, McCarthy MI, Young ET, Kendall-Taylor P. Pearce SH, et al. Among authors: imrie h. Am J Hum Genet. 1999 Nov;65(5):1462-5. doi: 10.1086/302610. Am J Hum Genet. 1999. PMID: 10521315 Free PMC article. No abstract available.

8

Evidence for a new Graves disease susceptibility locus at chromosome 18q21.

Vaidya B, Imrie H, Perros P, Young ET, Kelly WF, Carr D, Large DM, Toft AD, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. Am J Hum Genet. 2000 May;66(5):1710-4. doi: 10.1086/302908. Epub 2000 Apr 3. Am J Hum Genet. 2000. PMID: 10762555 Free PMC article.

9

CTLA4 gene and Graves' disease: association of Graves' disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphism.

Vaidya B, Oakes EJ, Imrie H, Dickinson AJ, Perros P, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. Clin Endocrinol (Oxf). 2003 Jun;58(6):732-5. doi: 10.1046/j.1365-2265.2003.01778.x. Clin Endocrinol (Oxf). 2003. PMID: 12780750

10

Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease.

Vaidya B, Imrie H, Geatch DR, Perros P, Ball SG, Baylis PH, Carr D, Hurel SJ, James RA, Kelly WF, Kemp EH, Young ET, Weetman AP, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: imrie h. J Clin Endocrinol Metab. 2000 Feb;85(2):688-91. doi: 10.1210/jcem.85.2.6369. J Clin Endocrinol Metab. 2000. PMID: 10690877

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