1 October 2014 | RA autoantibodies as predictors of rheumatoid arthritis in non-cystic fibrosis bronchiectasis patients.
| Perry, E; Stenton, C; Kelly, C; et al. |
23 January 2017 | Rab32 connects ER stress to mitochondrial defects in multiple sclerosis
| Haile, Y; Deng, X; Ortiz-Sandoval, C; et al. |
1 January 2012 | Radon and skin cancer in southwest England: an ecologic study
| Wheeler, BW; Allen, James; Depledge, MH; et al. |
5 October 2017 | Random non-fasting C-peptide testing can identify patients with insulin-treated type 2 diabetes at high risk of hypoglycaemia.
| Hope, SV; Knight, BA; Shields, BM; 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. |
19 September 2016 | Rapid hepatic clearance of full length CCN-2/CTGF: a putative role for LRP1-mediated endocytosis
| Gerritsen, KGF; Bovenschen, N; Nguyen, TQ; et al. |
23 October 2019 | Rapid treatment of moderate to severe hypertension using a novel protocol in a single-centre, before and after interventional study.
| Jordan, AN; Anning, C; Wilkes, L; et al. |
1 February 2017 | Rare and low-frequency coding variants alter human adult height
| Marouli, E; Graff, M; Medina-Gomez, C; et al. |
4 August 2015 | Rare coding variants and X-linked loci associated with age at menarche
| Lunetta, KL; Day, FR; Sulem, P; et al. |
1 October 2015 | Rates of lateral gene transfer in prokaryotes: high but why?
| Vos, Michiel; Hesselman, MC; te Beek, TA; et al. |
1 May 2019 | Rationale for enteroviral vaccination and antiviral therapies in human type 1 diabetes
| Dunne, JL; Richardson, SJ; Atkinson, MA; et al. |
1 June 2016 | Reactivity to low-flow as a potential determinant for brachial artery flow-mediated vasodilatation
| Aizawa, K; Elyas, S; Adingupu, DD; et al. |
26 June 2021 | Reappearance of C-Peptide During the Third Trimester of Pregnancy in Type 1 Diabetes: Pancreatic Regeneration or Fetal Hyperinsulinism?
| Meek, CL; Oram, RA; McDonald, TJ; et al. |
12 June 2015 | Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73
| Jinks, RN; Puffenberger, EG; Baple, Emma Louise; et al. |
4 May 2017 | Recessively inherited LRBA mutations cause autoimmunity presenting as neonatal diabetes
| Johnson, MB; De Franco, E; Lango Allen, H; et al. |
1 July 2015 | Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation
| Chakera, AJ; Steele, AM; Gloyn, Anna L.; et al. |
30 January 2020 | Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism
| Gunning, AC; Strucinska, K; Muñoz Oreja, M; et al. |
28 September 2017 | Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers
| Pilling, LC; Atkins, JL; Duff, MO; et al. |
13 September 2018 | Red cell distribution width and common disease onsets in 240,477 healthy volunteers followed for up to 9 years
| Pilling, LC; Atkins, JL; Kuchel, GA; et al. |
5 June 2009 | Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births.
| Slingerland, AS; Shields, BM; Flanagan, SE; et al. |