14 September 2018 | Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. | Pulit, SL; Stoneman, C; Morris, AP; et al. |
30 October 2018 | Cognitive, Neurological, and Behavioral Features in Adults With KCNJ11 Neonatal Diabetes | Bowman, P; Day, J; Torrens, L; et al. |
3 October 2018 | Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease | Wakeling, MN; Laver, TW; Wright, CF; 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. |
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. |
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 | Murray, A; Freathy, RM; Weedon, MN; 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. |
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. |