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Journal of Medical Genetics|June 3, 2005
Mutations in hepatocyte nuclear factor-1beta and their related phenotypesE L Edghill, C Bingham, S Ellard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|November 23, 2006
Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic developmentE L Edghill, C Bingham, A S Slingerland, et al.
Diabetologia|April 13, 2006
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotypeS E Flanagan, E L Edghill, A L Gloyn, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 17, 2012
HNF1B deletions in patients with young-onset diabetes but no known renal diseaseE L Edghill, K Stals, R A Oram, et al.
Diabetologia|April 16, 2004
Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndromeL W Harries, S Ellard, R W A Jones, et al.
Diabetologia|October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODYP Bowman, S E Flanagan, E L Edghill, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|November 11, 2009
Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetesO Rubio-Cabezas, E L Edghill, J Argente, et al.
Diabetologia|February 26, 2008
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the youngS Ellard, C Bellanné-Chantelot, A T Hattersley, et al.
Clinical Medicine (London, England)|April 10, 2014
Ten years of the national genetic diabetes nurse network: a model for the translation of genetic information into clinical careM Shepherd, K Colclough, S Ellard, et al.
Diabetes Care|November 28, 2001
ACE gene polymorphism as a prognostic indicator in patients with type 2 diabetes and established renal diseaseS Fava, J Azzopardi, S Ellard, et al.
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