Hattersley AT - Search Results

1

Primate-specific ZNF808 is essential for pancreatic development in humans.

De Franco E, Owens NDL, Montaser H, Wakeling MN, Saarimäki-Vire J, Triantou A, Ibrahim H, Balboa D, Caswell RC, Jennings RE, Kvist JA, Johnson MB, Muralidharan S, Ellard S, Wright CF, Maddirevula S, Alkuraya FS; Pancreatic Agenesis Gene Discovery Consortium; Hanley NA, Flanagan SE, Otonkoski T, Hattersley AT, Imbeault M. De Franco E, et al. Among authors: hattersley at. Nat Genet. 2023 Dec;55(12):2075-2081. doi: 10.1038/s41588-023-01565-x. Epub 2023 Nov 16. Nat Genet. 2023. PMID: 37973953 Free PMC article.

2

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

3

Mutations in the glucokinase gene of the fetus result in reduced birth weight.

Hattersley AT, Beards F, Ballantyne E, Appleton M, Harvey R, Ellard S. Hattersley AT, et al. Nat Genet. 1998 Jul;19(3):268-70. doi: 10.1038/953. Nat Genet. 1998. PMID: 9662401

4

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.

5

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis.

Bulman MP, Kusumi K, Frayling TM, McKeown C, Garrett C, Lander ES, Krumlauf R, Hattersley AT, Ellard S, Turnpenny PD. Bulman MP, et al. Among authors: hattersley at. Nat Genet. 2000 Apr;24(4):438-41. doi: 10.1038/74307. Nat Genet. 2000. PMID: 10742114

6

Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY).

Ellard S, Bulman MP, Frayling TM, Shepherd M, Hattersley AT. Ellard S, et al. Among authors: hattersley at. Hum Mutat. 2000 Sep;16(3):273. doi: 10.1002/1098-1004(200009)16:3<273::AID-HUMU18>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 10980542

7

Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics.

Owen KR, Shepherd M, Stride A, Ellard S, Hattersley AT. Owen KR, et al. Among authors: hattersley at. Diabet Med. 2002 Sep;19(9):758-61. doi: 10.1046/j.1464-5491.2002.00766.x. Diabet Med. 2002. PMID: 12207813

8

Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers.

Stride A, Shepherd M, Frayling TM, Bulman MP, Ellard S, Hattersley AT. Stride A, et al. Among authors: hattersley at. Diabetes Care. 2002 Dec;25(12):2287-91. doi: 10.2337/diacare.25.12.2287. Diabetes Care. 2002. PMID: 12453975

9

Identifying hepatic nuclear factor 1alpha mutations in children and young adults with a clinical diagnosis of type 1 diabetes.

Lambert AP, Ellard S, Allen LI, Gallen IW, Gillespie KM, Bingley PJ, Hattersley AT. Lambert AP, et al. Among authors: hattersley at. Diabetes Care. 2003 Feb;26(2):333-7. doi: 10.2337/diacare.26.2.333. Diabetes Care. 2003. PMID: 12547858

10

Etiological investigation of diabetes in young adults presenting with apparent type 2 diabetes.

Owen KR, Stride A, Ellard S, Hattersley AT. Owen KR, et al. Among authors: hattersley at. Diabetes Care. 2003 Jul;26(7):2088-93. doi: 10.2337/diacare.26.7.2088. Diabetes Care. 2003. PMID: 12832318

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