相似文献
1
The genetics of heart attack.
Heart. 2006 Jun;92(6):855-61. doi: 10.1136/hrt.2005.060202.
2
[Genome-wide SNP association study to identify genes related to myocardial infarction and their functional analyses].
Tanpakushitsu Kakusan Koso. 2004 Nov;49(14):2215-21.
3
Genome-wide linkage approach yields novel early onset myocardial infarction locus in East Asians.
Circ Cardiovasc Genet. 2013 Dec;6(6):531-2. doi: 10.1161/CIRCGENETICS.113.000378.
4
Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis.
Circ Cardiovasc Genet. 2013 Dec;6(6):569-78. doi: 10.1161/CIRCGENETICS.111.000027. Epub 2013 Oct 11.
5
Genome-wide association study to identify single-nucleotide polymorphisms conferring risk of myocardial infarction.
Methods Mol Med. 2006;128:173-80. doi: 10.1007/978-1-59745-159-8_12.
6
Mapping complex disease loci in whole-genome association studies.
Nature. 2004 May 27;429(6990):446-52. doi: 10.1038/nature02623.
7
Simon Dack Lecture. The genomic basis of myocardial infarction.
J Am Coll Cardiol. 2005 Oct 18;46(8):1456-65. doi: 10.1016/j.jacc.2005.06.064. Epub 2005 Sep 28.
8
Cardiovascular genomics.
Circulation. 2006 Mar 21;113(11):e450-5. doi: 10.1161/CIRCULATIONAHA.105.560151.
9
On the significance of linkage studies of complex traits.
Am J Hum Genet. 2004 Jul;75(1):151-2; author reply 152-4. doi: 10.1086/422220.
10
Progress in unraveling the genetics of coronary artery disease and myocardial infarction.
Curr Atheroscler Rep. 2007 Sep;9(3):179-86. doi: 10.1007/s11883-007-0017-4.
引用本文的文献
1
Stroke genetics: a review and update.
J Stroke. 2014 Sep;16(3):114-23. doi: 10.5853/jos.2014.16.3.114. Epub 2014 Sep 30.
本文引用的文献
1
A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction.
Nat Genet. 2006 Jan;38(1):68-74. doi: 10.1038/ng1692. Epub 2005 Nov 10.
2
Identification of four gene variants associated with myocardial infarction.
Am J Hum Genet. 2005 Oct;77(4):596-605. doi: 10.1086/491674. Epub 2005 Aug 26.
3
The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction.
J Med Genet. 2006 Feb;43(2):167-9. doi: 10.1136/jmg.2005.035071. Epub 2005 Jun 15.
4
Miscues on the "lack of MEF2A mutations" in coronary artery disease.
J Clin Invest. 2005 Jun;115(6):1399-400; author reply 1400-1. doi: 10.1172/JCI25475.
5
Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial.
JAMA. 2005 May 11;293(18):2245-56. doi: 10.1001/jama.293.18.2245.
6
Lack of MEF2A mutations in coronary artery disease.
J Clin Invest. 2005 Apr;115(4):1016-20. doi: 10.1172/JCI24186.
7
Whole-genome patterns of common DNA variation in three human populations.
Science. 2005 Feb 18;307(5712):1072-9. doi: 10.1126/science.1105436.
8
Genome-wide association studies for common diseases and complex traits.
Nat Rev Genet. 2005 Feb;6(2):95-108. doi: 10.1038/nrg1521.
9
Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction.
Circulation. 2005 Feb 22;111(7):855-62. doi: 10.1161/01.CIR.0000155611.41961.BB. Epub 2005 Feb 14.
10
Transcription factor MEF2A mutations in patients with coronary artery disease.
Hum Mol Genet. 2004 Dec 15;13(24):3181-8. doi: 10.1093/hmg/ddh329. Epub 2004 Oct 20.
Zotero 插件