Farooqi IS - Search Results

1

A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome.

Bochukova EG, Lawler K, Croizier S, Keogh JM, Patel N, Strohbehn G, Lo KK, Humphrey J, Hokken-Koelega A, Damen L, Donze S, Bouret SG, Plagnol V, Farooqi IS. Bochukova EG, et al. Among authors: farooqi is. Cell Rep. 2018 Mar 27;22(13):3401-3408. doi: 10.1016/j.celrep.2018.03.018. Cell Rep. 2018. PMID: 29590610 Free PMC article.

2

Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency.

Farooqi IS, Yeo GS, Keogh JM, Aminian S, Jebb SA, Butler G, Cheetham T, O'Rahilly S. Farooqi IS, et al. J Clin Invest. 2000 Jul;106(2):271-9. doi: 10.1172/JCI9397. J Clin Invest. 2000. PMID: 10903343 Free PMC article.

3

The CART gene and human obesity: mutational analysis and population genetics.

Challis BG, Yeo GS, Farooqi IS, Luan J, Aminian S, Halsall DJ, Keogh JM, Wareham NJ, O'Rahilly S. Challis BG, et al. Among authors: farooqi is. Diabetes. 2000 May;49(5):872-5. doi: 10.2337/diabetes.49.5.872. Diabetes. 2000. PMID: 10905499

4

Partial leptin deficiency and human adiposity.

Farooqi IS, Keogh JM, Kamath S, Jones S, Gibson WT, Trussell R, Jebb SA, Lip GY, O'Rahilly S. Farooqi IS, et al. Nature. 2001 Nov 1;414(6859):34-5. doi: 10.1038/35102112. Nature. 2001. PMID: 11689931

5

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.

Challis BG, Pritchard LE, Creemers JW, Delplanque J, Keogh JM, Luan J, Wareham NJ, Yeo GS, Bhattacharyya S, Froguel P, White A, Farooqi IS, O'Rahilly S. Challis BG, et al. Among authors: farooqi is. Hum Mol Genet. 2002 Aug 15;11(17):1997-2004. doi: 10.1093/hmg/11.17.1997. Hum Mol Genet. 2002. PMID: 12165561

6

Beneficial effects of leptin on obesity, T cell hyporesponsiveness, and neuroendocrine/metabolic dysfunction of human congenital leptin deficiency.

Farooqi IS, Matarese G, Lord GM, Keogh JM, Lawrence E, Agwu C, Sanna V, Jebb SA, Perna F, Fontana S, Lechler RI, DePaoli AM, O'Rahilly S. Farooqi IS, et al. J Clin Invest. 2002 Oct;110(8):1093-103. doi: 10.1172/JCI15693. J Clin Invest. 2002. PMID: 12393845 Free PMC article.

7

Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms.

Yeo GS, Lank EJ, Farooqi IS, Keogh J, Challis BG, O'Rahilly S. Yeo GS, et al. Among authors: farooqi is. Hum Mol Genet. 2003 Mar 1;12(5):561-74. doi: 10.1093/hmg/ddg057. Hum Mol Genet. 2003. PMID: 12588803

8

Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene.

Farooqi IS, Keogh JM, Yeo GS, Lank EJ, Cheetham T, O'Rahilly S. Farooqi IS, et al. N Engl J Med. 2003 Mar 20;348(12):1085-95. doi: 10.1056/NEJMoa022050. N Engl J Med. 2003. PMID: 12646665 Free article.

9

Contribution of variants in the small heterodimer partner gene to birthweight, adiposity, and insulin levels: mutational analysis and association studies in multiple populations.

Hung CC, Farooqi IS, Ong K, Luan J, Keogh JM, Pembrey M, Yeo GS, Dunger D, Wareham NJ, O' Rahilly S. Hung CC, et al. Among authors: farooqi is. Diabetes. 2003 May;52(5):1288-91. doi: 10.2337/diabetes.52.5.1288. Diabetes. 2003. PMID: 12716767

10

Genetic variation in the corticotrophin-releasing factor receptors: identification of single-nucleotide polymorphisms and association studies with obesity in UK Caucasians.

Challis BG, Luan J, Keogh J, Wareham NJ, Farooqi IS, O'Rahilly S. Challis BG, et al. Among authors: farooqi is. Int J Obes Relat Metab Disord. 2004 Mar;28(3):442-6. doi: 10.1038/sj.ijo.0802564. Int J Obes Relat Metab Disord. 2004. PMID: 14724656

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