A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism von Koulouri, O, Nicholas, A. K, Schoenmakers, E, Mokrosinski, J, Lane, F, Cole, T, Kirk, J, Farooqi, I. S, Chatterjee, V. K, Gurnell, M, Schoenmakers, N

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Two Novel Missense Mutations in G Protein-Coupled Receptor 54 in a Patient with Hypogonadotropic Hypogonadism von Semple, R. K., Achermann, J. C., Ellery, J., Farooqi, I. S., Karet, F. E., Stanhope, R. G., O’Rahilly, S., Aparicio, S. A.

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Prolonged successful therapy for hyperinsulinaemic hypoglycaemia after gastric bypass: the pathophysiological role of GLP1 and its response to a somatostatin analogue von Myint, K S, Greenfield, J R, Farooqi, I S, Henning, E, Holst, J J, Finer, N

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Early childhood infection and atopic disorder von Farooqi, I Sadaf, Hopkin, Julian M

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Functional characterization of human NTRK2 mutations identified in patients with severe early-onset obesity von Gray, J, Yeo, G, Hung, C, Keogh, J, Clayton, P, Banerjee, K, McAulay, A, O'Rahilly, S, Farooqi, I S

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WNT10B mutations in human obesity von Christodoulides, C, Scarda, A, Granzotto, M, Milan, G, Dalla Nora, E, Keogh, J, De Pergola, G, Stirling, H, Pannacciulli, N, Sethi, J. K, Federspil, G, Vidal-Puig, A, Farooqi, I. S, O'Rahilly, S, Vettor, R

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Effects of Recombinant Leptin Therapy in a Child with Congenital Leptin Deficiency von Farooqi, I. Sadaf, Jebb, Susan A, Langmack, Gill, Lawrence, Elizabeth, Cheetham, Christopher H, Prentice, Andrew M, Hughes, Ieuan A, McCamish, Mark A, O'Rahilly, Stephen

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Food images engage subliminal motivation to seek food von Ziauddeen, H, Subramaniam, N, Gaillard, R, Burke, L K, Farooqi, I S, Fletcher, P C

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A frameshift mutation in MC4R associated with dominantly inherited human obesity von Yeo, Giles S.H., Farooqi, I. Sadaf, Aminian, Shiva, Halsall, David J., Stanhope, Richard G., O'Rahilly, Stephen

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New advances in the genetics of early onset obesity von Farooqi, I S, O'Rahilly, S

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Increased body mass index is associated with specific regional alterations in brain structure von Medic, N, Ziauddeen, H, Ersche, K D, Farooqi, I S, Bullmore, E T, Nathan, P J, Ronan, L, Fletcher, P C

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Congenital leptin deficiency is associated with severe early-onset obesity in humans von MONTAGUE, C. T, FAROOQI, I. S, CHEETHAM, C. H, EARLEY, A. R, BARNETT, A. H, PRINS, J. B, O'RAHILLY, S, WHITEHEAD, J. P, SOOS, M. A, RAU, H, WAREHAM, N. J, SEWTER, C. P, DIGBY, J. E, MOHAMMED, S. N, HURST, J. A

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Human obesity as a heritable disorder of the central control of energy balance von O'Rahilly, S, Farooqi, I.S

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Genetic factors in human obesity von Farooqi, I. S., O'Rahilly, S.

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Studies of the SIM1 gene in relation to human obesity and obesity-related traits von Hung, C.C.C, Luan, J, Sims, M, Keogh, J.M, Hall, C, Wareham, N.J, O'Rahilly, S, Farooqi, I.S

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TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency von Metherell, LA, Savage, MO, Dattani, M, Walker, J, Clayton, PE, Farooqi, IS, Clark, AJ

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Uncoupling protein 3 genetic variants in human obesity : the c-55t promoter polymorphism is negatively correlated with body mass index in a UK Caucasian population von HALSALL, D. J, LUAN, J, SAKER, P, HUXTABLE, S, FAROOQI, I. S, KEOGH, J, WAREHAM, N. J, O'RAHILLY, S

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Sequential alterations in haemorheology, endothelial dysfunction, platelet activation and thrombogenesis in relation to prognosis following acute stroke: The West Birmingham Stroke... von Lip, G Y. H, Blann, A D, Farooqi, I S, Zarifis, J, Sagar, G, Beevers, D G

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Genetic variation in the corticotrophin-releasing factor receptors: identification of single-nucleotide polymorphisms and association studies with obesity in UK Caucasians von Challis, B G, Luan, J, Keogh, J, Wareham, N J, Farooqi, I S, O'Rahilly, S

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Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity von Mazen, I., El-Gammal, M., Abdel-Hamid, M., Farooqi, I.S., Amr, K.

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