Minton JA - Search Results

1

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

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

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

4

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

5

Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities.

Rubio-Cabezas O, Minton JA, Kantor I, Williams D, Ellard S, Hattersley AT. Rubio-Cabezas O, et al. Among authors: minton ja. Diabetes. 2010 Sep;59(9):2326-31. doi: 10.2337/db10-0011. Epub 2010 Jun 23. Diabetes. 2010. PMID: 20573748 Free PMC article.

6

Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.

Rubio-Cabezas O, Minton JA, Caswell R, Shield JP, Deiss D, Sumnik Z, Cayssials A, Herr M, Loew A, Lewis V, Ellard S, Hattersley AT. Rubio-Cabezas O, et al. Among authors: minton ja. Diabetes Care. 2009 Jan;32(1):111-6. doi: 10.2337/dc08-1188. Epub 2008 Oct 17. Diabetes Care. 2009. PMID: 18931102 Free PMC article.

7

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

8

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.

9

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

10

Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology.

Edghill EL, Minton JA, Groves CJ, Flanagan SE, Patch AM, Rubio-Cabezas O, Shepherd M, Lenzen S, McCarthy MI, Ellard S, Hattersley AT. Edghill EL, et al. Among authors: minton ja. JOP. 2010 Jan 8;11(1):14-7. JOP. 2010. PMID: 20065546

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

26 results

Search Page