Ischaemic heart disease

Citations 1-10 of 35 total displayed.

Original articles
Premature death in adults with 22q11.2 deletion syndrome

A S Bassett, E W C Chow, J Husted, K A Hodgkinson, E Oechslin, L Harris, C Silversides
J. Med. Genet. 2009 46: 324 -330; published online before print as 10.1136/jmg.2008.063800 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
A PCSK9 variant and familial combined hyperlipidaemia

M Abifadel, L Bernier, G Dubuc, G Nuel, J-P Rabès, J Bonneau, A Marques, M Marduel, M Devillers, A Munnich, D Erlich, M Varret, M Roy, J Davignon, C Boileau
J. Med. Genet. 2008 45: 780 -786; published online before print as 10.1136/jmg.2008.059980 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population

Y Yamada, K Kato, M Oguri, T Fujimaki, K Yokoi, H Matsuo, S Watanabe, N Metoki, H Yoshida, K Satoh, S Ichihara, Y Aoyagi, A Yasunaga, H Park, M Tanaka, Y Nozawa
J. Med. Genet. 2008 45: 216 -221; published online before print as 10.1136/jmg.2007.054387 [Abstract] [Full text] [PDF] [Request Permissions] [ web only table ]  

Letters to JMG
Association of arginase 1 gene polymorphisms with the risk of myocardial infarction and common carotid intima–media thickness

Julie Dumont, Mahmoud Zureik, Dominique Cottel, Michèle Montaye, Pierre Ducimetière, Philippe Amouyel, Thierry Brousseau
J. Med. Genet. 2007 44: 526 -531; published online before print as 10.1136/jmg.2006.047449 [Abstract] [Full text] [PDF] [Request Permissions] [ web only figure ]  

Original articles
Three single-nucleotide polymorphisms in LPA account for most of the increase in lipoprotein(a) level elevation in African Americans compared with European Americans

J-P Chretien, J Coresh, Y Berthier-Schaad, W H L Kao, N E Fink, M J Klag, S M Marcovina, F Giaculli, M W Smith
J. Med. Genet. 2006 43: 917 -923; published online before print as 10.1136/jmg.2006.042119 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk

S E Humphries, R A Whittall, C S Hubbart, S Maplebeck, J A Cooper, A K Soutar, R Naoumova, G R Thompson, M Seed, P N Durrington, J P Miller, D J B Betteridge, H A W Neil for the Simon Broome Familial Hyperlipidaemia Register Group and Scientific Steering Committee
J. Med. Genet. 2006; 43: 943-949. [Abstract] [Full text] [PDF] [Request Permissions] [ web only appendix ]  

Letters to JMG
The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction

P González, M García-Castro, J R Reguero, A Batalla, A G Ordóñez, R L Palop, I Lozano, M Montes, V Álvarez, E Coto
J. Med. Genet. 2006 43: 167 -169; published online before print as 10.1136/jmg.2005.035071 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
VEGF polymorphisms and severity of atherosclerosis

W M Howell, S Ali, M J Rose-Zerilli, S Ye
J. Med. Genet. 2005; 42: 485-490. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traits

M R Abdollahi, T R Gaunt, H E Syddall, C Cooper, D I W Phillips, S Ye, I N M Day
J. Med. Genet. 2005; 42: 396-401. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam Study

F A Sayed-Tabatabaei, A F C Schut, A Arias Vásquez, A M Bertoli-Avella, A Hofman, J C M Witteman, C M van Duijn
J. Med. Genet. 2005; 42: 26-30. [Abstract] [Full text] [PDF] [Request Permissions]