Keavney B - Search Results

1

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.

Griffin HR, Hall DH, Topf A, Eden J, Stuart AG, Parsons J, Peart I, Deanfield JE, O'Sullivan J, Babu-Narayan SV, Gatzoulis MA, Bu'lock FA, Bhattacharya S, Bentham J, Farrall M, Granados Riveron J, Brook JD, Burn J, Cordell HJ, Goodship JA, Keavney B. Griffin HR, et al. Among authors: keavney b. PLoS One. 2009;4(3):e4978. doi: 10.1371/journal.pone.0004978. Epub 2009 Mar 24. PLoS One. 2009. PMID: 19308252 Free PMC article.

2

Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci.

McKenzie CA, Julier C, Forrester T, McFarlane-Anderson N, Keavney B, Lathrop GM, Ratcliffe PJ, Farrall M. McKenzie CA, et al. Among authors: keavney b. Am J Hum Genet. 1995 Dec;57(6):1426-35. Am J Hum Genet. 1995. PMID: 8533773 Free PMC article.

3

Measured haplotype analysis of the angiotensin-I converting enzyme gene.

Keavney B, McKenzie CA, Connell JM, Julier C, Ratcliffe PJ, Sobel E, Lathrop M, Farrall M. Keavney B, et al. Hum Mol Genet. 1998 Oct;7(11):1745-51. doi: 10.1093/hmg/7.11.1745. Hum Mol Genet. 1998. PMID: 9736776

4

Measured haplotype analysis of the aldosterone synthase gene and heart size.

Mayosi BM, Keavney B, Watkins H, Farrall M. Mayosi BM, et al. Among authors: keavney b. Eur J Hum Genet. 2003 May;11(5):395-401. doi: 10.1038/sj.ejhg.5200967. Eur J Hum Genet. 2003. PMID: 12734545

5

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. 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

6

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: keavney b. J Med Genet. 2005 Jun;42(6):474-8. doi: 10.1136/jmg.2004.027631. J Med Genet. 2005. PMID: 15937081 Free PMC article.

7

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: keavney b. Diabetes. 2005 Aug;54(8):2492-6. doi: 10.2337/diabetes.54.8.2492. Diabetes. 2005. PMID: 16046320

8

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: keavney b. Stroke. 2005 Oct;36(10):2215-9. doi: 10.1161/01.STR.0000182254.47941.96. Epub 2005 Sep 22. Stroke. 2005. PMID: 16179573

9

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. Among authors: keavney b. 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

10

INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 families.

Hall DH, Rahman T, Avery PJ, Keavney B. Hall DH, et al. Among authors: keavney b. BMC Med Genet. 2006 Nov 30;7:83. doi: 10.1186/1471-2350-7-83. BMC Med Genet. 2006. PMID: 17137505 Free PMC article.

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