Obesity (nutrition)

Citations 11-20 of 39 total displayed.

Electronic letters
Hepatic lipase C-480T polymorphism modifies the effect of HDL cholesterol on the risk of acute myocardial infarction in men: a prospective population based study

Y M Fan, J T Salonen, T A Koivu, T-P Tuomainen, K Nyyssönen, T A Lakka, R Salonen, K Seppänen, S T Nikkari, E Tahvanainen, T Lehtimäki
J. Med. Genet. 2004; 41: e28. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
APOE and TGF-ß1 genes are associated with obesity phenotypes

J-R Long, P-Y Liu, Y-J Liu, Y Lu, D-H Xiong, L Elze, R R Recker, H-W Deng
J. Med. Genet. 2003; 40: 918-924. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Effect of the peroxisome proliferator activated receptor- gene Pro12Ala variant on body mass index: a meta-analysis

S Masud, S Ye
J. Med. Genet. 2003; 40: 773-780. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Receptor mediated effect of serotonergic transmission in patients with bipolar affective disorder

Y M J Lin, H C Yang, T J Lai, C S J Fann, H S Sun
J. Med. Genet. 2003; 40: 781-786. [Extract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Further support for digenic inheritance in Bardet-Biedl syndrome

S Fauser, M Munz, D Besch
J. Med. Genet. 2003; 40: e104. [Extract] [Full text] [PDF] [Request Permissions]  

Original articles
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

D C Bittel, N Kibiryeva, Z Talebizadeh, M G Butler
J. Med. Genet. 2003; 40: 568-574. [Abstract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Death in adults with Prader-Willi syndrome may be correlated with maternal uniparental disomy

A Smith, G Loughnan, K Steinbeck
J. Med. Genet. 2003; 40: e63. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay

L G Dietz, A A Wylie, K A Rauen, S K Murphy, R L Jirtle, P D Cotter
J. Med. Genet. 2003; 40: e46. [Extract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Novel PHF6 mutation p.D333del causes Börjeson-Forssman-Lehmann syndrome

A Baumstark, K M Lower, A Sinkus, I Andriuskeviciute, L Jurkeniene, J Gécz, W Just
J. Med. Genet. 2003; 40: e50. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

V Cormier-Daire, F Molinari, M Rio, O Raoul, M-C de Blois, S Romana, M Vekemans, A Munnich, L Colleaux
J. Med. Genet. 2003; 40: 300-303. [Extract] [Full text] [PDF] [Request Permissions]