Yeo GS - Search Results

1

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.

de Smith AJ, Purmann C, Walters RG, Ellis RJ, Holder SE, Van Haelst MM, Brady AF, Fairbrother UL, Dattani M, Keogh JM, Henning E, Yeo GS, O'Rahilly S, Froguel P, Farooqi IS, Blakemore AI. de Smith AJ, et al. Among authors: yeo gs. Hum Mol Genet. 2009 Sep 1;18(17):3257-65. doi: 10.1093/hmg/ddp263. Epub 2009 Jun 4. Hum Mol Genet. 2009. PMID: 19498035 Free PMC article.

2

A frameshift mutation in MC4R associated with dominantly inherited human obesity.

Yeo GS, Farooqi IS, Aminian S, Halsall DJ, Stanhope RG, O'Rahilly S. Yeo GS, et al. Nat Genet. 1998 Oct;20(2):111-2. doi: 10.1038/2404. Nat Genet. 1998. PMID: 9771698 No abstract available.

3

The role of melanocortin signalling in the control of body weight: evidence from human and murine genetic models.

Yeo GS, Farooqi IS, Challis BG, Jackson RS, O'Rahilly S. Yeo GS, et al. QJM. 2000 Jan;93(1):7-14. doi: 10.1093/qjmed/93.1.7. QJM. 2000. PMID: 10623776 Review.

4

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. Among authors: yeo gs. J Clin Invest. 2000 Jul;106(2):271-9. doi: 10.1172/JCI9397. J Clin Invest. 2000. PMID: 10903343 Free PMC article.

5

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: yeo gs. Diabetes. 2000 May;49(5):872-5. doi: 10.2337/diabetes.49.5.872. Diabetes. 2000. PMID: 10905499

6

Obesity therapy: altering the energy intake-and-expenditure balance sheet.

Crowley VE, Yeo GS, O'Rahilly S. Crowley VE, et al. Among authors: yeo gs. Nat Rev Drug Discov. 2002 Apr;1(4):276-86. doi: 10.1038/nrd770. Nat Rev Drug Discov. 2002. PMID: 12120279 Review.

7

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: yeo gs. Hum Mol Genet. 2002 Aug 15;11(17):1997-2004. doi: 10.1093/hmg/11.17.1997. Hum Mol Genet. 2002. PMID: 12165561

8

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. Hum Mol Genet. 2003 Mar 1;12(5):561-74. doi: 10.1093/hmg/ddg057. Hum Mol Genet. 2003. PMID: 12588803

9

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. Among authors: yeo gs. N Engl J Med. 2003 Mar 20;348(12):1085-95. doi: 10.1056/NEJMoa022050. N Engl J Med. 2003. PMID: 12646665 Free article.

10

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: yeo gs. Diabetes. 2003 May;52(5):1288-91. doi: 10.2337/diabetes.52.5.1288. Diabetes. 2003. PMID: 12716767

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