Imrie H - Search Results

1

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

2

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

3

A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.

Gaukrodger N, Mayosi BM, Imrie H, Avery P, Baker M, Connell JM, Watkins H, Farrall M, Keavney B. Gaukrodger N, et al. Among authors: imrie h. J Med Genet. 2005 Jun;42(6):474-8. doi: 10.1136/jmg.2004.027631. J Med Genet. 2005. PMID: 15937081 Free PMC article.

4

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.

Baker M, Gaukrodger N, Mayosi BM, Imrie H, Farrall M, Watkins H, Connell JM, Avery PJ, Keavney B. Baker M, et al. Among authors: imrie h. Diabetes. 2005 Aug;54(8):2492-6. doi: 10.2337/diabetes.54.8.2492. Diabetes. 2005. PMID: 16046320

5

Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysis.

Mayosi BM, Avery PJ, Baker M, Gaukrodger N, Imrie H, Green FR, Farrall M, Watkins H, Keavney B. Mayosi BM, et al. Among authors: imrie h. Stroke. 2005 Oct;36(10):2215-9. doi: 10.1161/01.STR.0000182254.47941.96. Epub 2005 Sep 22. Stroke. 2005. PMID: 16179573

6

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

7

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

8

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

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

Vascular insulin-like growth factor-I resistance and diet-induced obesity.

Imrie H, Abbas A, Viswambharan H, Rajwani A, Cubbon RM, Gage M, Kahn M, Ezzat VA, Duncan ER, Grant PJ, Ajjan R, Wheatcroft SB, Kearney MT. Imrie H, et al. Endocrinology. 2009 Oct;150(10):4575-82. doi: 10.1210/en.2008-1641. Epub 2009 Jul 16. Endocrinology. 2009. PMID: 19608653

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