Hattersley AT - Search Results

1

A Mendelian Randomization Study Provides Evidence That Adiposity and Dyslipidemia Lead to Lower Urinary Albumin-to-Creatinine Ratio, a Marker of Microvascular Function.

Casanova F, Wood AR, Yaghootkar H, Beaumont RN, Jones SE, Gooding KM, Aizawa K, Strain WD, Hattersley AT, Khan F, Shore AC, Frayling TM, Tyrrell J. Casanova F, et al. Among authors: hattersley at. Diabetes. 2020 May;69(5):1072-1082. doi: 10.2337/db19-0862. Epub 2020 Jan 8. Diabetes. 2020. PMID: 31915152 Free PMC article.

2

Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K.

Frayling TM, Bulamn MP, Ellard S, Appleton M, Dronsfield MJ, Mackie AD, Baird JD, Kaisaki PJ, Yamagata K, Bell GI, Bain SC, Hattersley AT. Frayling TM, et al. Among authors: hattersley at. Diabetes. 1997 Apr;46(4):720-5. doi: 10.2337/diab.46.4.720. Diabetes. 1997. PMID: 9075818

3

A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young.

Bulman MP, Dronsfield MJ, Frayling T, Appleton M, Bain SC, Ellard S, Hattersley AT. Bulman MP, et al. Among authors: hattersley at. Diabetologia. 1997 Jul;40(7):859-62. doi: 10.1007/s001250050760. Diabetologia. 1997. PMID: 9243109

4

A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes.

Frayling TM, Bulman MP, Appleton M, Hattersley AT, Ellard S. Frayling TM, et al. Among authors: hattersley at. Hum Genet. 1997 Dec;101(3):351-4. doi: 10.1007/s004390050640. Hum Genet. 1997. PMID: 9439666

5

Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.

Beards F, Frayling T, Bulman M, Horikawa Y, Allen L, Appleton M, Bell GI, Ellard S, Hattersley AT. Beards F, et al. Among authors: hattersley at. Diabetes. 1998 Jul;47(7):1152-4. doi: 10.2337/diabetes.47.7.1152. Diabetes. 1998. PMID: 9648841 Review. No abstract available.

6

Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the young.

Ellard S, Bulman MP, Frayling TM, Allen LI, Dronsfield MJ, Tack CJ, Hattersley AT. Ellard S, et al. Among authors: hattersley at. Diabetes. 1999 Apr;48(4):921-3. doi: 10.2337/diabetes.48.4.921. Diabetes. 1999. PMID: 10102714 No abstract available.

7

A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3.

Turnpenny PD, Bulman MP, Frayling TM, Abu-Nasra TK, Garrett C, Hattersley AT, Ellard S. Turnpenny PD, et al. Among authors: hattersley at. Am J Hum Genet. 1999 Jul;65(1):175-82. doi: 10.1086/302464. Am J Hum Genet. 1999. PMID: 10364530 Free PMC article.

8

Impaired maximum microvascular hyperaemia in patients with MODY 3 (hepatocyte nuclear factor-1alpha gene mutations).

Lee BC, Appleton M, Shore AC, Tooke JE, Hattersley AT. Lee BC, et al. Among authors: hattersley at. Diabet Med. 1999 Sep;16(9):731-5. doi: 10.1046/j.1464-5491.1999.00129.x. Diabet Med. 1999. PMID: 10510948

9

Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.

Frayling TM, Walker M, McCarthy MI, Evans JC, Allen LI, Lynn S, Ayres S, Millauer B, Turner C, Turner RC, Sampson MJ, Hitman GA, Ellard S, Hattersley AT. Frayling TM, et al. Among authors: hattersley at. Diabetes. 1999 Dec;48(12):2475-9. doi: 10.2337/diabetes.48.12.2475. Diabetes. 1999. PMID: 10580439

10

Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles.

Huxtable SJ, Saker PJ, Haddad L, Walker M, Frayling TM, Levy JC, Hitman GA, O'Rahilly S, Hattersley AT, McCarthy MI. Huxtable SJ, et al. Among authors: hattersley at. Diabetes. 2000 Jan;49(1):126-30. doi: 10.2337/diabetes.49.1.126. Diabetes. 2000. PMID: 10615960

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