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Diabetes|March 22, 2008
The diabetic phenotype in HNF4A mutation carriers is moderated by the expression of HNF4A isoforms from the P1 promoter during fetal developmentLorna W Harries, Jonathan M Locke, Beverley Shields, et al.
BMC Medical Genetics|June 7, 2006
The functional "KL-VS" variant of KLOTHO is not associated with type 2 diabetes in 5028 UK CaucasiansRachel M Freathy, Michael N Weedon, David Melzer, et al.
The Pan African Medical Journal|July 1, 2024
Impact of haemoglobin variants on the diagnostic sensitivity of glycated haemoglobin (HbA1c) assay methodologies in sub-Saharan Africa: a laboratory-based method validation studyPriscilla Agatha Balungi, Anxious Jackson Niwaha, Rachel Nice, et al.
Diabetes|April 30, 2003
Genetic variation in the small heterodimer partner gene and young-onset type 2 diabetes, obesity, and birth weight in U.K. subjectsSimon M S Mitchell, Michael N Weedon, Katharine R Owen, et al.
Diabetes|October 27, 2004
Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. populationMichael N Weedon, Katharine R Owen, Beverley Shields, et al.
Plos Medicine|October 6, 2006
Combining information from common type 2 diabetes risk polymorphisms improves disease predictionMichael N Weedon, Mark I McCarthy, Graham Hitman, et al.
Diabetes|October 2, 2009
Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetesHana Lango Allen, Stefan Johansson, Sian Ellard, et al.
European Journal of Endocrinology|February 15, 2011
A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacementPeter N Taylor, Vijay Panicker, Adrian Sayers, et al.
Diabetes Care|June 9, 2016
Systematic Population Screening, Using Biomarkers and Genetic Testing, Identifies 2.5% of the U.K. Pediatric Diabetes Population With Monogenic DiabetesMaggie Shepherd, Beverley Shields, Suzanne Hammersley, et al.
Diabetes|December 29, 2007
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthoodEmma L Edghill, Sarah E Flanagan, Ann-Marie Patch, et al.
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