Minton JA - Search Results

1

Common variations in the ALMS1 gene do not contribute to susceptibility to type 2 diabetes in a large white UK population.

Patel S, Minton JA, Weedon MN, Frayling TM, Ricketts C, Hitman GA, McCarthy MI, Hattersley AT, Walker M, Barrett TG. Patel S, et al. Among authors: minton ja. Diabetologia. 2006 Jun;49(6):1209-13. doi: 10.1007/s00125-006-0227-2. Epub 2006 Apr 7. Diabetologia. 2006. PMID: 16601972

2

Association analysis of 6,736 U.K. subjects provides replication and confirms TCF7L2 as a type 2 diabetes susceptibility gene with a substantial effect on individual risk.

Groves CJ, Zeggini E, Minton J, Frayling TM, Weedon MN, Rayner NW, Hitman GA, Walker M, Wiltshire S, Hattersley AT, McCarthy MI. Groves CJ, et al. Diabetes. 2006 Sep;55(9):2640-4. doi: 10.2337/db06-0355. Diabetes. 2006. PMID: 16936215

3

Syndromic obesity and diabetes: changes in body composition with age and mutation analysis of ALMS1 in 12 United Kingdom kindreds with Alstrom syndrome.

Minton JA, Owen KR, Ricketts CJ, Crabtree N, Shaikh G, Ehtisham S, Porter JR, Carey C, Hodge D, Paisey R, Walker M, Barrett TG. Minton JA, et al. J Clin Endocrinol Metab. 2006 Aug;91(8):3110-6. doi: 10.1210/jc.2005-2633. Epub 2006 May 23. J Clin Endocrinol Metab. 2006. PMID: 16720663

4

Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction.

Minton JAL, van de Bunt M, Boustred C, Hussain K, Hattersley AT, Ellard S, Gloyn AL. Minton JAL, et al. Diabetologia. 2007 Sep;50(9):2019-2022. doi: 10.1007/s00125-007-0748-3. Epub 2007 Jul 6. Diabetologia. 2007. PMID: 17618412 No abstract available.

5

Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations.

Minton JA, Hattersley AT, Owen K, McCarthy MI, Walker M, Latif F, Barrett T, Frayling TM. Minton JA, et al. Diabetes. 2002 Apr;51(4):1287-90. doi: 10.2337/diabetes.51.4.1287. Diabetes. 2002. PMID: 11916957

6

Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.

Ricketts CJ, Minton JA, Samuel J, Ariyawansa I, Wales JK, Lo IF, Barrett TG. Ricketts CJ, et al. Among authors: minton ja. Acta Paediatr. 2006 Jan;95(1):99-104. doi: 10.1080/08035250500323715. Acta Paediatr. 2006. PMID: 16373304

7

Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic development.

Edghill EL, Bingham C, Slingerland AS, Minton JA, Noordam C, Ellard S, Hattersley AT. Edghill EL, et al. Among authors: minton ja. Diabet Med. 2006 Dec;23(12):1301-6. doi: 10.1111/j.1464-5491.2006.01999.x. Diabet Med. 2006. PMID: 17116179

8

Novel GLIS3 mutations demonstrate an extended multisystem phenotype.

Dimitri P, Warner JT, Minton JA, Patch AM, Ellard S, Hattersley AT, Barr S, Hawkes D, Wales JK, Gregory JW. Dimitri P, et al. Among authors: minton ja. Eur J Endocrinol. 2011 Mar;164(3):437-43. doi: 10.1530/EJE-10-0893. Epub 2010 Dec 7. Eur J Endocrinol. 2011. PMID: 21139041

9

Wolfram syndrome.

Minton JA, Rainbow LA, Ricketts C, Barrett TG. Minton JA, et al. Rev Endocr Metab Disord. 2003 Mar;4(1):53-9. doi: 10.1023/a:1021875403463. Rev Endocr Metab Disord. 2003. PMID: 12618560 Review. No abstract available.

10

The impact of the angiotensin-converting enzyme insertion/deletion polymorphism on severe hypoglycemia in Type 2 diabetes.

Freathy RM, Lonnen KF, Steele AM, Minton JA, Frayling TM, Hattersley AT, Macleod KM. Freathy RM, et al. Among authors: minton ja. Rev Diabet Stud. 2006 Summer;3(2):76-81. doi: 10.1900/RDS.2006.3.76. Epub 2006 Aug 10. Rev Diabet Stud. 2006. PMID: 17487330 Free PMC article.

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