18 June 2019 | Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis | Thompson, WD; Tyrrell, J; Borges, MC; et al. |
8 April 2019 | Trisomy 21 is a Cause of Permanent Neonatal Diabetes that is Autoimmune but not HLA Associated | Johnson, MBJ; De Franco, E; Atma W Greeley, S; et al. |
5 July 2019 | Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of < 5 years in the Iranian population | Yaghootkar, H; Abbasi, F; Ghaemi, N; et al. |
3 May 2017 | Dominant ER Stress-Inducing WFS1 Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts | De Franco, E; Flanagan, SE; Yagi, T; et al. |
3 January 2018 | Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics | Beaumont, RN; Warrington, NM; Cavadino, A; et al. |
6 April 2016 | Should Studies of Diabetes Treatment Stratification Correct for Baseline HbA1c? | Jones, AG; Lonergan, M; Henley, WE; et al. |
21 April 2016 | Random non-fasting C-peptide: bringing robust assessment of endogenous insulin secretion to the clinic | Hope, SV; Knight, BA; Shields, BM; et al. |
7 February 2017 | Hyperglycaemia-related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetes | Day, JO; Flanagan, SE; Shepherd, MH; 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. |
27 December 2019 | De novo mutations in EIF2B1 affecting eIF2 signaling cause neonatal/early onset diabetes and transient hepatic dysfunction | De Franco, E; Caswell, R; Johnson, M; et al. |