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. |
3 September 2016 | Beta cell function and ongoing autoimmunity in long-standing, childhood onset type 1 diabetes. | Williams, GM; Long, AE; Wilson, IV; et al. |
31 March 2016 | Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes | Babiker, T; Vedovato, N; Patel, K; et al. |
28 April 2016 | Practical Classification Guidelines for Diabetes in patients treated with insulin: a cross-sectional study of the accuracy of diabetes diagnosis. | Hope, SV; Wienand-Barnett, S; Shepherd, M; et al. |
1 September 2016 | Prematurity should not prevent genetic testing for neonatal diabetes | Besser, RE; Flanagan, SE; Mackay, DG; et al. |
1 October 2016 | Monogenic autoimmune diseases of the endocrine system | Johnson, MB; Hattersley, AT; Flanagan, SE |
28 September 2016 | Genome-wide associations for birth weight and correlations with adult disease | Horikoshi, M; Beaumont, RN; Day, FR; et al. |
8 April 2016 | Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors. | Fendler, W; Madzio, J; Kozinski, K; et al. |
27 April 2016 | Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk. | Vedovato, N; Cliff, E; Proks, P; et al. |
17 August 2016 | Hypogonadotropic hypogonadism and short stature in patients with diabetes due to neurogenin 3 deficiency | Rubio-Cabezas, O; Luis Gómez, J; Gleisner, A; et al. |