EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome M Delépine, M Nicolino, T Barrett, M Golamaully, G Mark Lathrop, C Julier Nature genetics 25 (4), 406-409, 2000 | 1021 | 2000 |
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation ECH Friesema, A Grueters, H Biebermann, H Krude, A Von Moers, ... The Lancet 364 (9443), 1435-1437, 2004 | 759 | 2004 |
Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome TG Barrett, SE Bundey, AF Macleod The Lancet 346 (8988), 1458-1463, 1995 | 734 | 1995 |
Macrosomia and Hyperinsulinaemic Hypoglycaemia in Patients with Heterozygous Mutations in the HNF4A Gene ER Pearson, SF Boj, AM Steele, T Barrett, K Stals, JP Shield, S Ellard, ... PLoS medicine 4 (4), e118, 2007 | 526 | 2007 |
Type 2 diabetes mellitus in UK children–an emerging problem S Ehtisham, TG Barrett, NJ Shaw Diabetic medicine 17 (12), 867-871, 2000 | 356 | 2000 |
Rising incidence of type 2 diabetes in children in the UK L Haines, KC Wan, R Lynn, TG Barrett, JPH Shield Diabetes care 30 (5), 1097-1101, 2007 | 314 | 2007 |
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness V Labay, T Raz, D Baron, H Mandel, H Williams, T Barrett, R Szargel, ... nature genetics 22 (3), 300-304, 1999 | 310 | 1999 |
Wolfram (DIDMOAD) syndrome. TG Barrett, SE Bundey Journal of medical genetics 34 (10), 838-841, 1997 | 306 | 1997 |
Liraglutide in children and adolescents with type 2 diabetes WV Tamborlane, M Barrientos-Pérez, U Fainberg, H Frimer-Larsen, ... New England Journal of Medicine 381 (7), 637-646, 2019 | 295 | 2019 |
First UK survey of paediatric type 2 diabetes and MODY S Ehtisham, AT Hattersley, DB Dunger, TG Barrett Archives of disease in childhood 89 (6), 526-529, 2004 | 274 | 2004 |
Once-weekly semaglutide in adolescents with obesity D Weghuber, T Barrett, M Barrientos-Pérez, I Gies, D Hesse, ... New England Journal of Medicine 387 (24), 2245-2257, 2022 | 252 | 2022 |
Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1 C Hardy, F Khanim, R Torres, M Scott-Brown, A Seller, J Poulton, ... The American Journal of Human Genetics 65 (5), 1279-1290, 1999 | 240 | 1999 |
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity V Senée, KM Vattem, M Delépine, LA Rainbow, C Haton, A Lecoq, ... Diabetes 53 (7), 1876-1883, 2004 | 238 | 2004 |
Multi-scale investigation of the performance of limestone in concrete DP Bentz, A Ardani, T Barrett, SZ Jones, D Lootens, MA Peltz, T Sato, ... Construction and Building Materials 75, 1-10, 2015 | 229 | 2015 |
Type 2 diabetes in the child and adolescent. P Zeitler, J Fu, N Tandon, K Nadeau, T Urakami, T Barrett, D Maahs Pediatric diabetes 15, 2014 | 209 | 2014 |
Ethnic differences in insulin resistance and body composition in United Kingdom adolescents S Ehtisham, N Crabtree, P Clark, N Shaw, T Barrett The Journal of Clinical Endocrinology & Metabolism 90 (7), 3963-3969, 2005 | 209 | 2005 |
WFS1/wolframin mutations, Wolfram syndrome, and associated diseases F Khanim, J Kirk, F Latif, TG Barrett Human mutation 17 (5), 357-367, 2001 | 208 | 2001 |
Effectiveness of a childhood obesity prevention programme delivered through schools, targeting 6 and 7 year olds: cluster randomised controlled trial (WAVES study) P Adab, MJ Pallan, ER Lancashire, K Hemming, E Frew, T Barrett, ... bmj 360, 2018 | 185 | 2018 |
Dysregulation of autophagy as a common mechanism in lysosomal storage diseases E Seranova, KJ Connolly, M Zatyka, TR Rosenstock, T Barrett, ... Essays in biochemistry 61 (6), 733-749, 2017 | 175 | 2017 |
Premature adrenarche: novel lessons from early onset androgen excess J Idkowiak, GG Lavery, V Dhir, TG Barrett, PM Stewart, N Krone, W Arlt European Journal of Endocrinology 165 (2), 189-207, 2011 | 167 | 2011 |