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Issue Date Title Author(s)
18 September 2018 A UK nationwide prospective study of treatment change in MODY: genetic subtype and clinical characteristics predict optimal glycaemic control after discontinuing insulin and metformin
Shepherd, MH; Shields, BM; Hudson, M; et al.
23 October 2018 Genome-wide and abdominal MRI data provide evidence that a genetically determined favorable adiposity phenotype is characterized by lower ectopic liver fat and lower risk of type 2 diabetes, heart disease, and hypertension
; ; ; et al.
8 April 2019 Trisomy 21 is a Cause of Permanent Neonatal Diabetes that is Autoimmune but not HLA Associated
; ; ; et al.
20 February 2018 Genetic risk scores in adult-onset type 1 diabetes - Authors' reply
Thomas, NJ; Jones, SE; Weedon, MN; et al.
13 June 2018 Permanent neonatal diabetes: combining sulfonylureas with insulin may be an effective treatment.
Misra, S; Vedovato, N; Cliff, E; et al.
30 January 2018 Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic
Clissold, RL; Fulford, J; Hudson, M; et al.
23 November 2016 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
Ried, JS; Jeff M, J; Chu, AY; et al.
1 November 2016 Low IgE is a useful tool to identify STAT3 gain-of-functionmMutations.
Johnson, MB; Flanagan, SE; Martins, TB; et al.
24 May 2016 Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder.
Clissold, RL; Shaw-Smith, C; Turnpenny, P; et al.
28 December 2012 Identifying clinical criteria to predict Type 1 diabetes, as defined by absolute insulin deficiency: a systematic review protocol.
Shields, BM; Peters, JL; Cooper, C; et al.