5 October 2014 | Defining the role of common variation in the genomic and biological architecture of adult human height. | Wood, AR; Esko, T; Yang, J; et al. |
17 December 2015 | Adherence to Oral Glucose-Lowering Therapies and Associations With 1-Year HbA1c: A Retrospective Cohort Analysis in a Large Primary Care Database. | Farmer, AJ; Rodgers, LR; Lonergan, M; et al. |
30 November 2017 | Frequency and phenotype of type 1 diabetes in the first six decades of life: a cross-sectional, genetically stratified survival analysis from UK Biobank. | Thomas, NJ; Jones, SE; Weedon, MN; et al. |
12 October 2017 | Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance | Patel, KA; Kettunen, J; Laakso, M; et al. |
17 July 2018 | PLIN1 haploinsufficiency is not associated with lipodystrophy | Laver, TW; Patel, KA; Colclough, K; et al. |
2 August 2016 | The common p.R114W HNF4A mutation causes a distinct clinical subtype of monogenic diabetes. | Laver, TW; Colclough, K; Shepherd, M; et al. |
1 August 2013 | An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy | Weedon, MN; Ellard, S; Prindle, MJ; et al. |
12 October 2017 | Cohort profile for the MASTERMIND study: Using the Clinical Practice Research Datalink (CPRD) to investigate stratification of response to treatment in patients with Type 2 diabetes | Rodgers, LR; Weedon, MN; Henley, WE; et al. |
5 April 2016 | Type 1 Diabetes Genetic Risk Score: a novel tool to discriminate monogenic and type 1 diabetes | Patel, KA; Oram, RA; Flanagan, SE; et al. |
1 May 2019 | Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors | Warrington, NM; Beaumont, RN; Horikoshi, M; et al. |