| 18 April 2019 | A specific CNOT1 mutation results in a novel syndrome of pancreatic agenesis and holoprosencephaly through impaired pancreatic and neurological development | De Franco, E; Watson, RA; Weninger, WJ; et al. |
| 18 December 2019 | Patterns of postmeal insulin secretion in individuals with sulfonylurea-treated KCNJ11 neonatal diabetes show predominance of non-K ATP -channel pathways | Bowman, P; McDonald, TJ; Knight, BA; et al. |
| 8 November 2019 | Absence of islet autoantibodies and modestly raised glucose values at diabetes diagnosis should lead to testing for MODY: Lessons from a 5-year pediatric Swedish national cohort study | Carlsson, A; Shepherd, M; Ellard, S; et al. |
| 18 November 2010 | Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus | Bell, CG; Finer, S; Lindgren, CM; et al. |
| 4 June 2018 | Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study | Bowman, P; Sulen, Å; Barbetti, F; et al. |
| 12 June 2018 | The Common HNF1A Variant I27L is a Modifier of Age at Diabetes Diagnosis in HNF1A-MODY Individuals. | Locke, JM; Saint-Martin, C; Laver, TW; et al. |
| 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. |
| 20 October 2019 | A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio. | Casanova, F; Tyrrell, J; Beaumont, RN; 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. |
| 7 May 2018 | Time trends and geographical variation in prescribing of drugs for diabetes in England 1998-2017 | Curtis, HJ; Dennis, JM; Shields, BM; et al. |
