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WNT10B mutations in human obesity.
Published in:
Diabetologia, 2006, v. 49, n. 4, p. 678, doi. 10.1007/s00125-006-0144-4
By:
- Christodoulides, C.;
- Scarda, A.;
- Granzotto, M.;
- Milan, G.;
- Nora, E. Dalla;
- 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.
Publication type:
Article
Genetic factors in human obesity.
Published in:
Obesity Reviews, 2007, v. 8, p. 37, doi. 10.1111/j.1467-789X.2007.00315.x
By:
- Farooqi, I. S.;
- O'Rahilly, S.
Publication type:
Article
ANDRE-MAYER AWARD AW0002 The leptin-melanocortin pathway in human physiology: insights from genetics.
Published in:
Obesity Reviews, 2006, v. 7, p. 35, doi. 10.1111/j.1467-7881.2006.00280_2.x
By:
- Farooqi, I. S.
Publication type:
Article
A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism.
Published in:
2016
By:
- 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
Publication type:
journal article
Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.
Published in:
2005
By:
- Semple, R K;
- Achermann, J C;
- Ellery, J;
- Farooqi, I S;
- Karet, F E;
- Stanhope, R G;
- O'rahilly, S;
- Aparicio, S A
Publication type:
journal article
Scientific Business Abstracts of the 113th Annual Meeting of the Association of Physicians of Great Britain and Ireland.
Published in:
QJM: An International Journal of Medicine, 2019, v. 112, n. 9, p. 724, doi. 10.1093/qjmed/hcz175
By:
- Cacciottolo, T M;
- Perikari, A;
- Klaauw, A van der;
- Henning, E;
- Stadler, L K J;
- Keogh, J;
- Farooqi, I S;
- Tenin, G;
- Keavney, B;
- Ryan, E;
- Budd, R;
- Bewley, M;
- Coelho, P;
- Rumsey, W;
- Sanchez, Y;
- McCafferty, J;
- Dockrell, D;
- Walmsley, S;
- Whyte, M;
- Liu, Y
Publication type:
Article
Prolonged successful therapy for hyperinsulinaemic hypoglycaemia after gastric bypass: the pathophysiological role of GLP1 and its response to a somatostatin analogue.
Published in:
European Journal of Endocrinology, 2012, v. 166, n. 5, p. 951, doi. 10.1530/EJE-11-1065
By:
- Myint, K. S.;
- Greenfield, J. R.;
- Farooqi, I. S.;
- Henning, E;
- Holst, J. J.;
- Finer, N.
Publication type:
Article
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency.
Published in:
European Journal of Endocrinology, 2004, v. 151, n. 4, p. 0463
By:
- L A Metherell;
- M O Savage;
- M Dattani;
- J Walker;
- P E Clayton;
- I S Farooqi;
- A J L Clark
Publication type:
Article
Food images engage subliminal motivation to seek food.
Published in:
International Journal of Obesity, 2012, v. 36, n. 9, p. 1245, doi. 10.1038/ijo.2011.239
By:
- Ziauddeen, H;
- Subramaniam, N;
- Gaillard, R;
- Burke, L K;
- Farooqi, I S;
- Fletcher, P C
Publication type:
Article
The CART gene and human obesity: mutational analysis and population genetics.
Published in:
2000
By:
- Challis, B G;
- Yeo, G S;
- Farooqi, I S;
- Luan, J;
- Aminian, S;
- Halsall, D J;
- Keogh, J M;
- Wareham, N J;
- O'Rahilly, S
Publication type:
journal article
Genetic variation in the corticotrophin-releasing factor receptors: identification of single-nucleotide polymorphisms and association studies with obesity in UK Caucasians.
Published in:
International Journal of Obesity & Related Metabolic Disorders, 2004, v. 28, n. 3, p. 442, doi. 10.1038/sj.ijo.0802564
By:
- Challis, B G;
- Luan, J;
- Keogh, J;
- Wareham, N J;
- Farooqi, I S
Publication type:
Article
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.
Published in:
International Journal of Obesity & Related Metabolic Disorders, 2001, v. 25, n. 4, p. 472, doi. 10.1038/sj.ijo.0801584
By:
- Halsall, D J;
- Luan, J;
- Saker, P;
- Huxtable, S;
- Farooqi, I S;
- Keogh, J;
- Wareham, N J;
- O'Rahilly, S
Publication type:
Article
Human obesity as a heritable disorder of the central control of energy balance.
Published in:
International Journal of Obesity, 2008, v. 32, p. S55, doi. 10.1038/ijo.2008.239
By:
- O'Rahilly, S.;
- Farooqi, I. S.
Publication type:
Article
Human obesity as a heritable disorder of the central control of energy balance.
Published in:
2008
By:
- O'Rahilly S;
- Farooqi IS;
- O'Rahilly, S;
- Farooqi, I S
Publication type:
journal article
Studies of the SIM1 gene in relation to human obesity and obesity-related traits.
Published in:
2007
By:
- Hung, C.-C. C.;
- Luan, J.;
- Sims, M.;
- Keogh, J. M.;
- Hall, C.;
- Wareham, N. J.;
- O'Rahilly, S.;
- Farooqi, I. S.
Publication type:
journal article
Functional characterization of human NTRK2 mutations identified in patients with severe early-onset obesity.
Published in:
2007
By:
- Gray, J.;
- Yeo, G.;
- Hung, C.;
- Keogh, J.;
- Clayton, P.;
- Banerjee, K.;
- McAulay, A.;
- O'Rahilly, S.;
- Farooqi, I. S.
Publication type:
journal article
New advances in the genetics of early onset obesity.
Published in:
2005
By:
- Farooqi, I. S.;
- O'Rahilly, S.
Publication type:
Editorial

Found: 17