| 1 October 2014 | RA autoantibodies as predictors of rheumatoid arthritis in non-cystic fibrosis bronchiectasis patients.
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| 23 January 2017 | Rab32 connects ER stress to mitochondrial defects in multiple sclerosis
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| 1 January 2012 | Radon and skin cancer in southwest England: an ecologic study
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| 5 October 2017 | Random non-fasting C-peptide testing can identify patients with insulin-treated type 2 diabetes at high risk of hypoglycaemia.
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| 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
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| 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
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| 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. |
| 21 July 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
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| 28 September 2017 | Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers
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| 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. |
| 4 August 2020 | Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome
| Banerjee, I; Senniappan, S; Laver, TW; et al. |
