Timothy Barrett
Timothy Barrett
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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
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
Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome
TG Barrett, SE Bundey, AF Macleod
The Lancet 346 (8988), 1458-1463, 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
Type 2 diabetes mellitus in UK children–an emerging problem
S Ehtisham, TG Barrett, NJ Shaw
Diabetic medicine 17 (12), 867-871, 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
Wolfram (DIDMOAD) syndrome.
TG Barrett, SE Bundey
Journal of medical genetics 34 (10), 838-841, 1997
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
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
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
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
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
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
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
WFS1/wolframin mutations, Wolfram syndrome, and associated diseases
F Khanim, J Kirk, F Latif, TG Barrett
Human mutation 17 (5), 357-367, 2001
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
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
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
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
Metformin in obese children and adolescents: the MOCA trial
D Kendall, A Vail, R Amin, T Barrett, P Dimitri, F Ivison, M Kibirige, ...
The Journal of Clinical Endocrinology & Metabolism 98 (1), 322-329, 2013
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