Ratcliffe PJ - Search Results

1

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: ratcliffe pj. Am J Hum Genet. 1995 Dec;57(6):1426-35. Am J Hum Genet. 1995. PMID: 8533773 Free PMC article.

2

UK prospective diabetes study (UKPDS) 14: association of angiotensin-converting enzyme insertion/deletion polymorphism with myocardial infarction in NIDDM.

Keavney BD, Dudley CR, Stratton IM, Holman RR, Matthews DR, Ratcliffe PJ, Turner RC. Keavney BD, et al. Among authors: ratcliffe pj. Diabetologia. 1995 Aug;38(8):948-52. doi: 10.1007/BF00400584. Diabetologia. 1995. PMID: 7589881

3

U.K. Prospective Diabetes Study. XV: Relationship of renin-angiotensin system gene polymorphisms with microalbuminuria in NIDDM.

Dudley CR, Keavney B, Stratton IM, Turner RC, Ratcliffe PJ. Dudley CR, et al. Among authors: ratcliffe pj. Kidney Int. 1995 Dec;48(6):1907-11. doi: 10.1038/ki.1995.490. Kidney Int. 1995. PMID: 8587251 Free article. Clinical Trial.

4

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. Among authors: ratcliffe pj. Hum Mol Genet. 1998 Oct;7(11):1745-51. doi: 10.1093/hmg/7.11.1745. Hum Mol Genet. 1998. PMID: 9736776

5

Screening for the GRA mutation in Jamaica.

McKenzie CA, Keavney B, Forrester T, Julier C, Ratcliffe PJ. McKenzie CA, et al. Among authors: ratcliffe pj. J Hum Hypertens. 2000 Feb;14(2):157-8. doi: 10.1038/sj.jhh.1000840. J Hum Hypertens. 2000. PMID: 10723126 No abstract available.

6

Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE).

McKenzie CA, Abecasis GR, Keavney B, Forrester T, Ratcliffe PJ, Julier C, Connell JM, Bennett F, McFarlane-Anderson N, Lathrop GM, Cardon LR. McKenzie CA, et al. Among authors: ratcliffe pj. Hum Mol Genet. 2001 May 1;10(10):1077-84. doi: 10.1093/hmg/10.10.1077. Hum Mol Genet. 2001. PMID: 11331618

7

Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass.

Mayosi BM, Keavney B, Kardos A, Davies CH, Ratcliffe PJ, Farrall M, Watkins H. Mayosi BM, et al. Among authors: ratcliffe pj. Eur Heart J. 2002 Dec;23(24):1963-71. doi: 10.1053/euhj.2002.3288. Eur Heart J. 2002. PMID: 12473259

8

HLA has strongest association with IgA nephropathy in genome-wide analysis.

Feehally J, Farrall M, Boland A, Gale DP, Gut I, Heath S, Kumar A, Peden JF, Maxwell PH, Morris DL, Padmanabhan S, Vyse TJ, Zawadzka A, Rees AJ, Lathrop M, Ratcliffe PJ. Feehally J, et al. Among authors: ratcliffe pj. J Am Soc Nephrol. 2010 Oct;21(10):1791-7. doi: 10.1681/ASN.2010010076. Epub 2010 Jul 1. J Am Soc Nephrol. 2010. PMID: 20595679 Free PMC article.

9

PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nepsilon-dimethyl lysine demethylase.

Loenarz C, Ge W, Coleman ML, Rose NR, Cooper CD, Klose RJ, Ratcliffe PJ, Schofield CJ. Loenarz C, et al. Among authors: ratcliffe pj. Hum Mol Genet. 2010 Jan 15;19(2):217-22. doi: 10.1093/hmg/ddp480. Epub 2009 Oct 19. Hum Mol Genet. 2010. PMID: 19843542 Free PMC article.

10

A Ribosomopathy Reveals Decoding Defective Ribosomes Driving Human Dysmorphism.

Paolini NA, Attwood M, Sondalle SB, Vieira CMDS, van Adrichem AM, di Summa FM, O'Donohue MF, Gleizes PE, Rachuri S, Briggs JW, Fischer R, Ratcliffe PJ, Wlodarski MW, Houtkooper RH, von Lindern M, Kuijpers TW, Dinman JD, Baserga SJ, Cockman ME, MacInnes AW. Paolini NA, et al. Among authors: ratcliffe pj. Am J Hum Genet. 2017 Mar 2;100(3):506-522. doi: 10.1016/j.ajhg.2017.01.034. Am J Hum Genet. 2017. PMID: 28257692 Free PMC article.

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