Simmonds MJ - Search Results

1

Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease.

Chand S, Chue CD, Edwards NC, Hodson J, Simmonds MJ, Hamilton A, Gough SC, Harper L, Steeds RP, Townend JN, Ferro CJ, Borrows R. Chand S, et al. Among authors: simmonds mj. PLoS One. 2015 Jan 22;10(1):e0116160. doi: 10.1371/journal.pone.0116160. eCollection 2015. PLoS One. 2015. PMID: 25612295 Free PMC article. Clinical Trial.

2

Caveolin-1 single-nucleotide polymorphism and arterial stiffness in non-dialysis chronic kidney disease.

Chand S, Edwards NC, Chue CD, Jesky M, Stringer S, Simmonds MJ, Duff CE, Cockwell P, Harper L, Steeds RP, Townend JN, Ferro CJ, Borrows R. Chand S, et al. Among authors: simmonds mj. Nephrol Dial Transplant. 2016 Jul;31(7):1140-4. doi: 10.1093/ndt/gfv350. Epub 2015 Oct 3. Nephrol Dial Transplant. 2016. PMID: 26433014

3

Genetic developments in autoimmune thyroid disease: an evolutionary process.

Zeitlin AA, Simmonds MJ, Gough SC. Zeitlin AA, et al. Among authors: simmonds mj. Clin Endocrinol (Oxf). 2008 May;68(5):671-82. doi: 10.1111/j.1365-2265.2007.03075.x. Epub 2007 Dec 13. Clin Endocrinol (Oxf). 2008. PMID: 18081880 Review.

4

Association of caveolin-1 gene polymorphism with kidney transplant fibrosis and allograft failure.

Moore J, McKnight AJ, Simmonds MJ, Courtney AE, Hanvesakul R, Brand OJ, Briggs D, Ball S, Cockwell P, Patterson CC, Maxwell AP, Gough SC, Borrows R. Moore J, et al. Among authors: simmonds mj. JAMA. 2010 Apr 7;303(13):1282-7. doi: 10.1001/jama.2010.356. JAMA. 2010. PMID: 20371787

5

Caveolin-1 single nucleotide polymorphism in antineutrophil cytoplasmic antibody associated vasculitis.

Chand S, Holle JU, Hilhorst M, Simmonds MJ, Smith S, Kamesh L, Hewins P, McKnight AJ, Maxwell AP, Cohen Tervaert JW, Wieczorek S, Harper L, Borrows R. Chand S, et al. Among authors: simmonds mj. PLoS One. 2013 Jul 19;8(7):e69022. doi: 10.1371/journal.pone.0069022. Print 2013. PLoS One. 2013. PMID: 23894397 Free PMC article.

6

A single nucleotide polymorphism in the CD40 gene on chromosome 20q (GD-2) provides no evidence for susceptibility to Graves' disease in UK Caucasians.

Heward JM, Simmonds MJ, Carr-Smith J, Foxall H, Franklyn JA, Gough SC. Heward JM, et al. Among authors: simmonds mj. Clin Endocrinol (Oxf). 2004 Aug;61(2):269-72. doi: 10.1111/j.1365-2265.2004.02099.x. Clin Endocrinol (Oxf). 2004. PMID: 15272925

7

The search for the genetic contribution to autoimmune thyroid disease: the never ending story?

Simmonds MJ, Gough SC. Simmonds MJ, et al. Brief Funct Genomics. 2011 Mar;10(2):77-90. doi: 10.1093/bfgp/elq036. Brief Funct Genomics. 2011. PMID: 21436304 Review.

8

Donor ABCB1 variant associates with increased risk for kidney allograft failure.

Moore J, McKnight AJ, Döhler B, Simmonds MJ, Courtney AE, Brand OJ, Briggs D, Ball S, Cockwell P, Patterson CC, Maxwell AP, Gough SC, Opelz G, Borrows R. Moore J, et al. Among authors: simmonds mj. J Am Soc Nephrol. 2012 Nov;23(11):1891-9. doi: 10.1681/ASN.2012030260. Epub 2012 Oct 11. J Am Soc Nephrol. 2012. PMID: 23064017 Free PMC article.

9

Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression.

Yesmin K, Hargreaves C, Newby PR, Brand OJ, Heward JM, Franklyn JA, Gough SC, Simmonds MJ. Yesmin K, et al. Among authors: simmonds mj. Clin Endocrinol (Oxf). 2010 Jul;73(1):119-25. doi: 10.1111/j.1365-2265.2010.03780.x. Epub 2010 Feb 10. Clin Endocrinol (Oxf). 2010. PMID: 20148910

10

The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency.

Wood AM, Simmonds MJ, Bayley DL, Newby PR, Gough SC, Stockley RA. Wood AM, et al. Among authors: simmonds mj. Respir Res. 2008 Jul 11;9(1):52. doi: 10.1186/1465-9921-9-52. Respir Res. 2008. PMID: 18620570 Free PMC article.

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