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Diabetes Care|June 25, 2015
Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase MutationAli J Chakera, Anna M Steele, Anna L Gloyn, et al.
Journal of Negative Results in Biomedicine|November 28, 2006
A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian populationRachel M Freathy, Simon M S Mitchell, Beatrice Knight, et al.
Diabetes Care|November 19, 2015
A Type 1 Diabetes Genetic Risk Score Can Aid Discrimination Between Type 1 and Type 2 Diabetes in Young AdultsRichard A Oram, Kashyap Patel, Anita Hill, et al.
Diabetes|July 28, 2005
A large-scale association analysis of common variation of the HNF1alpha gene with type 2 diabetes in the U.K. Caucasian populationMichael N Weedon, Katharine R Owen, Beverley Shields, et al.
BMJ Open|March 21, 2020
Strategies to identify individuals with monogenic diabetes: results of an economic evaluationJaime L Peters, Rob Anderson, Beverley Shields, et al.
BMJ Open|September 28, 2019
Development and validation of multivariable clinical diagnostic models to identify type 1 diabetes requiring rapid insulin therapy in adults aged 18-50 yearsAnita Lynam, Timothy McDonald, Anita Hill, et al.
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.
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.
Diabetes Care|December 19, 2015
Adherence to Oral Glucose-Lowering Therapies and Associations With 1-Year HbA1c: A Retrospective Cohort Analysis in a Large Primary Care DatabaseAndrew J Farmer, Lauren R Rodgers, Mike Lonergan, et al.
Human Molecular Genetics|May 12, 2009
A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancyRachel M Freathy, Susan M Ring, Beverley Shields, et al.
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