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Obesity (nutrition)
Citations 1-10 of 39 total displayed.
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Most recent content
(1 Sep 2007):
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Letters to JMG
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension
- Ana Carolina Braga Marçano, Beverley Burke, Johannie Gungadoo, Chris Wallace, Pamela J Kaisaki, Peng Y Woon, Martin Farrall, David Clayton, Morris Brown, Anna Dominiczak, John M Connell, John Webster, Mark Lathrop, Mark Caulfield, Nilesh Samani, Dominique Gauguier, Patricia B Munroe
J. Med. Genet. 2007 44: 603 -605; published online before print as 10.1136/jmg.2007.049718
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Past content
(since Jun 1999):
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Original articles
Polymorphisms of the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with obesity phenotypes in a large family-based association study
- Yan-fang Guo, Dong-hai Xiong, Hui Shen, Lan-juan Zhao, Peng Xiao, Yan Guo, Wei Wang, Tie-lin Yang, Robert R Recker, Hong-wen Deng
J. Med. Genet. 2006 43: 798 -803; published online before print as 10.1136/jmg.2006.041715
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Letters to JMG
The oestrogen receptor gene is linked and/or associated with age of menarche in different ethnic groups
- J-R Long, H Xu, L-J Zhao, P-Y Liu, H Shen, Y-J Liu, D-H Xiong, P Xiao, Y-Z Liu, V Dvornyk, J-L Li, R R Recker, H-W Deng
J. Med. Genet. 2005; 42: 796-800.
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Original articles
A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families
- N Gaukrodger, B M Mayosi, H Imrie, P Avery, M Baker, J M C Connell, H Watkins, M Farrall, B Keavney
J. Med. Genet. 2005; 42: 474-478.
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Original articles
Evidence of an association between genetic variation of the coactivator PGC-1ß and obesity
- G Andersen, L Wegner, K Yanagisawa, C S Rose, J Lin, C Glümer, T Drivsholm, K Borch-Johnsen, T Jørgensen, T Hansen, B M Spiegelman, O Pedersen
J. Med. Genet. 2005; 42: 402-407.
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Electronic letters
Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys
- I M Heid, C Vollmert, A Hinney, A Döring, F Geller, H Löwel, H-E Wichmann, T Illig, J Hebebrand, F Kronenberg the KORA Group
J. Med. Genet. 2005; 42: e21.
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Electronic letters
The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy
- J Bond, K Flintoff, J Higgins, S Scott, C Bennet, J Parsons, J Mannon, H Jafri, Y Rashid, M Barrow, R Trembath, G Woodruff, E Rossa, S Lynch, J Sheilds, R Newbury-Ecob, A Falconer, P Holland, D Cockburn, G Karbani, S Malik, M Ahmed, E Roberts, G Taylor, C G Woods
J. Med. Genet. 2005; 42: e10.
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Original articles
A transgenic mouse bearing an antisense construct of regulatory subunit type 1A of protein kinase A develops endocrine and other tumours: comparison with Carney complex and other PRKAR1A induced lesions
- K J Griffin, L S Kirschner, L Matyakhina, S G Stergiopoulos, A Robinson-White, S M Lenherr, F D Weinberg, E S Claflin, D Batista, I Bourdeau, A Voutetakis, F Sandrini, E M Meoli, A J Bauer, Y S Cho-Chung, S R Bornstein, J A Carney, C A Stratakis
J. Med. Genet. 2004; 41: 923-931.
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Letters to JMG
A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome
- D Vallée, E Chevrier, G E Graham, M A Lazzaro, P A Lavigne, A G Hunter, D J Picketts
J. Med. Genet. 2004; 41: 778-783.
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Letters to JMG
Large quantitative effect of melanocortin-4 receptor gene mutations on body mass index
- A Dempfle, A Hinney, M Heinzel-Gutenbrunner, M Raab, F Geller, T Gudermann, H Schäfer, J Hebebrand
J. Med. Genet. 2004; 41: 795-800.
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