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Ischaemic heart disease

Citations 11-20 of 35 total displayed.

Past content (since Sep 2001):
Letters to JMG
Evidence for a gene influencing haematocrit on chromosome 6q23–24: genomewide scan in the Framingham Heart Study
J-P Lin, C J O’Donnell, D Levy, L A Cupples
J. Med. Genet. 2005; 42: 75-79. [Extract] [Full text] [PDF] [Request Permissions]  

Short reports
The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis
L Valenti, D Conte, A Piperno, P Dongiovanni, A L Fracanzani, M Fraquelli, A Vergani, C Gianni, L Carmagnola, S Fargion
J. Med. Genet. 2004; 41: 946-950. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Genetic polymorphism of CYP1A2 increases the risk of myocardial infarction
M C Cornelis, A El-Sohemy, H Campos
J. Med. Genet. 2004; 41: 758-762. [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Opposite effects of interleukin 10 common gene polymorphisms in cardiovascular diseases and in successful ageing: genetic background of male centenarians is protective against coronary heart disease
D Lio, G Candore, A Crivello, L Scola, G Colonna-Romano, L Cavallone, E Hoffmann, M Caruso, F Licastro, C M Caldarera, A Branzi, C Franceschi, C Caruso
J. Med. Genet. 2004; 41: 790-794. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Evidence of differing genotypic effects of PPAR{alpha} in women and men
Q H Khan, D E Pontefract, S Iyengar, S Ye
J. Med. Genet. 2004; 41: e79. [Extract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome
K Fukuchi, T Katsuya, K Sugimoto, M Kuremura, H D Kim, L Li, T Ogihara
J. Med. Genet. 2004; 41: e67. [Extract] [Full text] [PDF] [Request Permissions]  

Original articles
Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes
J J McCarthy, A Parker, R Salem, D J Moliterno, Q Wang, E F Plow, S Rao, G Shen, W J Rogers, L K Newby, R Cannata, K Glatt, E J Topol
J. Med. Genet. 2004; 41: 334-341. [Abstract] [Full text] [PDF] [Request Permissions] [ Web-only Table ]  

Letters to JMG
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes
A B Csoka, H Cao, P J Sammak, D Constantinescu, G P Schatten, R A Hegele
J. Med. Genet. 2004; 41: 304-308. [Extract] [Full text] [PDF] [Request Permissions]  

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
Common apolipoprotein E polymorphisms and risk of clinical malaria in the Gambia
C Aucan, A J Walley, A V S Hill
J. Med. Genet. 2004; 41: 21-24. [Extract] [Full text] [PDF] [Request Permissions]  

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