Now showing items 1-20 of 23

    Issue DateTitleAuthor(s)
    17 September 2020UK psychiatrists’ experience of withdrawal of antipsychotics prescribed for challenging behaviours in adults with intellectual disabilities and/or autism  Deb, S; Nancarrow, T; Limbu, B; et al.
    2017Understanding the barriers and improving care in type 2 diabetes: Brazilian perspective in time to do more in diabetes  Vencio, S; Paldánius, PM; Blüher, M; et al.
    3 August 2018Unexpected subcellular distribution of a specific isoform of the Coxsackie and adenovirus receptor, CAR-SIV, in human pancreatic beta cells  Ifie, E; Russell, M; Leete, P; et al.
    22 September 2015Unfolding the complexities of ER chaperones in health and disease: Report on the 11th International Calreticulin Workshop  Gold, L; Williams, D; Groenendyk, J; et al.
    2 October 2019Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinism  Houghton, JAL; Banerjee, I; Shaikh, G; et al.
    6 February 2020Update of variants identified in the pancreatic beta‐cell K ATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes  De Franco, E; Saint‐Martin, C; Brusgaard, K; et al.
    15 August 2012Urinary bisphenol a concentration and angiography-defined coronary artery stenosis.  Melzer, D; Gates, P; Osborne, NJ; et al.
    27 March 2012Urinary bisphenol A concentration and risk of future coronary artery disease in apparently healthy men and women  Melzer, D; Osborne, NJ; Henley, William E.; et al.
    1 November 2013Urinary C-peptide creatinine ratio detects absolute insulin deficiency in Type 2 diabetes  Hope, SV; Jones, AG; Goodchild, E; et al.
    18 December 2013Urine C-peptide creatinine ratio can be used to assess insulin resistance and insulin production in people without diabetes: an observational study  Oram, RA; Rawlingson, A; Shields, BM; et al.
    16 February 2021Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation  Weedon, MN; Jackson, L; Harrison, JW; et al.
    20 September 2018Use of vascular assessments and novel biomarkers to predict cardiovascular events in type 2 diabetes: The Summit VIP study  Shore, AC; Colhoun, HM; Natali, A; et al.
    23 July 2019Using a two-sample Mendelian randomization design to investigate a possible causal effect of maternal lipid concentrations on offspring birth weight  Hwang, L-D; Lawlor, DA; Freathy, RM; et al.
    1 July 2015Using Genetic Variants to Assess the Relationship Between Circulating Lipids and Type 2 Diabetes  Fall, T; Xie, W; Poon, W; et al.
    10 February 2020Using human genetics to understand the disease impacts of testosterone in men and women  Ruth, KS; Day, FR; Tyrrell, J; et al.
    3 October 2017Using induced pluripotent stem cells to explore genetic and epigenetic variation associated with Alzheimer's disease  Imm, J; Kerrigan, TL; Jeffries, A; et al.
    8 June 2021Using Mendelian Randomisation methods to understand whether diurnal preference is causally related to mental health  O’Loughlin, J; Casanova, F; Jones, SE; et al.
    6 February 2020Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389  Yau, D; Laver, TW; Dastamani, A; et al.
    27 August 2019Using structural analysis in silico to assess the impact of missense variants in MEN1  Caswell, RC; Owens, MM; Gunning, AC; et al.
    13 February 2018Using Structural Equation Modelling to Jointly Estimate Maternal and Fetal Effects on Birthweight in the UK Biobank  Warrington, NM; Freathy, RM; Neale, MC; et al.