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JOP : Journal of the Pancreas|May 11, 2006
Functional variation in VEGF is not associated with type 2 diabetes in a United Kingdom Caucasian populationRachel M Freathy, Michael N Weedon, Beverley Shields, et al.
Diabetes Care|February 1, 2020
Homozygous Hypomorphic HNF1A Alleles Are a Novel Cause of Young-Onset Diabetes and Result in Sulfonylurea-Sensitive DiabetesShivani Misra, Neelam Hassanali, Amanda J Bennett, et al.
The Journal of Biological Chemistry|April 2, 2011
Discovery of a novel site regulating glucokinase activity following characterization of a new mutation causing hyperinsulinemic hypoglycemia in humansNicola L Beer, Martijn van de Bunt, Kevin Colclough, et al.
Ebiomedicine|April 19, 2026
Genotype-first approach reveals monogenic lipodystrophy is underdiagnosed, with health and mortality risksLuke N Sharp, Kevin Colclough, Jacques Murray Leech, et al.
Diabetologia|March 18, 2026
Polygenic background contributes to GCK-MODY clinical presentation and glycaemic variabilityJacques Murray Leech, Ankit M Arni, V Kartik Chundru, et al.
Diabetes|February 2, 2022
Evaluation of Evidence for Pathogenicity Demonstrates That BLK, KLF11, and PAX4 Should Not Be Included in Diagnostic Testing for MODYThomas W Laver, Matthew N Wakeling, Olivia Knox, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 2025
Population prevalence, penetrance, and mortality for genetically confirmed MODYLuke N Sharp, Kevin Colclough, Jacques Murray Leech, et al.
BMJ Open|December 29, 2020
TriMaster: randomised double-blind crossover study of a DPP4 inhibitor, SGLT2 inhibitor and thiazolidinedione as second-line or third-line therapy in patients with type 2 diabetes who have suboptimal glycaemic control on metformin treatment with or without a sulfonylurea-a MASTERMIND study protocolCatherine Angwin, Caroline Jenkinson, Angus Jones, et al.
Human Molecular Genetics|April 15, 2006
A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetesPeter Proks, Amanda L Arnold, Jan Bruining, et al.
Kidney International Reports|September 14, 2019
HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During ChildhoodShazia Adalat, Wesley N Hayes, William A Bryant, et al.
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