-
1
-
-
24944498879
-
Genetic contributors toward increased risk for ischemic heart disease
-
Nordlie MA, Wold LE, Kloner RA. Genetic contributors toward increased risk for ischemic heart disease. J Mol Cell Cardiol 2005; 39:667-679.
-
(2005)
J Mol Cell Cardiol
, vol.39
, pp. 667-679
-
-
Nordlie, M.A.1
Wold, L.E.2
Kloner, R.A.3
-
2
-
-
4344698768
-
Pathobiology of atherosclerosis: Are there racial and ethnic differences?
-
Watson KE, Topol EJ. Pathobiology of atherosclerosis: are there racial and ethnic differences? Rev Cardiovasc Med 2004; 5 (suppl 3):S14-S21.
-
(2004)
Rev Cardiovasc Med
, vol.5
, Issue.3 SUPPL.
-
-
Watson, K.E.1
Topol, E.J.2
-
3
-
-
5444239280
-
Novel features of nitric oxide, endothelial nitric oxide synthase, and atherosclerosis
-
Ignarro LJ, Napoli C. Novel features of nitric oxide, endothelial nitric oxide synthase, and atherosclerosis. Curr Atheroscler Rep 2004; 6:281-287.
-
(2004)
Curr Atheroscler Rep
, vol.6
, pp. 281-287
-
-
Ignarro, L.J.1
Napoli, C.2
-
4
-
-
0344395113
-
The association of homocysteine and coronary artery disease
-
Gauthier GM, Keevil JG, McBride PE. The association of homocysteine and coronary artery disease. Clin Cardiol 2003; 26:563-568.
-
(2003)
Clin Cardiol
, vol.26
, pp. 563-568
-
-
Gauthier, G.M.1
Keevil, J.G.2
McBride, P.E.3
-
5
-
-
13844306360
-
Pivotal role of plasminogen-activator inhibitor 1 in vascular disease
-
Agirbasli M. Pivotal role of plasminogen-activator inhibitor 1 in vascular disease. Int J Clin Pract 2005; 59:102-106.
-
(2005)
Int J Clin Pract
, vol.59
, pp. 102-106
-
-
Agirbasli, M.1
-
6
-
-
0031979233
-
PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: Relation to environmental and genetic determinants
-
Margaglione M, Capucci G, d'Addedda M, Colaizzo D, Giuliani N, Vecchione G, et al. PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: relation to environmental and genetic determinants. Arterioscl Thromb Vasc Biol 1998; 18:562-567.
-
(1998)
Arterioscl Thromb Vasc Biol
, vol.18
, pp. 562-567
-
-
Margaglione, M.1
Capucci, G.2
D'Addedda, M.3
Colaizzo, D.4
Giuliani, N.5
Vecchione, G.6
-
7
-
-
0032564442
-
High plasminogen activator inhibitor and tissue plasminogen activator levels in plasma precede a first acute myocardial infarction in both men and women: Evidence for the fibrinolytic system as an independent primary risk factor
-
Thogersen AM, Jansson JH, Boman K, Nilsson TK, Weinehall L, Huhtasaari F, et al. High plasminogen activator inhibitor and tissue plasminogen activator levels in plasma precede a first acute myocardial infarction in both men and women: evidence for the fibrinolytic system as an independent primary risk factor. Circulation 1998; 98:2241-2247.
-
(1998)
Circulation
, vol.98
, pp. 2241-2247
-
-
Thogersen, A.M.1
Jansson, J.H.2
Boman, K.3
Nilsson, T.K.4
Weinehall, L.5
Huhtasaari, F.6
-
8
-
-
0033933395
-
Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle aged Finnish men who died suddenly
-
Mikkelsson J, Perola M, Wartiovaara U, Peltonen L, Palotie A, Penttila A, et al. Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle aged Finnish men who died suddenly. Thromb Haemost 2000; 84:78-82.
-
(2000)
Thromb Haemost
, vol.84
, pp. 78-82
-
-
Mikkelsson, J.1
Perola, M.2
Wartiovaara, U.3
Peltonen, L.4
Palotie, A.5
Penttila, A.6
-
9
-
-
0030762720
-
Plasminogen activation inhibitor-1 (PAI-1) content in platelets from healthy individuals genotyped for the 4G/5G polymorphism in the PAI-1 gene
-
Nordenhem A, Wiman B. Plasminogen activation inhibitor-1 (PAI-1) content in platelets from healthy individuals genotyped for the 4G/5G polymorphism in the PAI-1 gene. Scand J Clin Lab Invest 1997; 57:453-461.
-
(1997)
Scand J Clin Lab Invest
, vol.57
, pp. 453-461
-
-
Nordenhem, A.1
Wiman, B.2
-
10
-
-
0028901713
-
Allele-specific increase in basal transcription of the plasminogen activator inhibitor-1 gene is associated with myocardial infarction
-
Eriksson P, Kallin B, van't Hooft FM, Bavenholm P, Hamsten A. Allele-specific increase in basal transcription of the plasminogen activator inhibitor-1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA 1995; 92:1851-1855.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 1851-1855
-
-
Eriksson, P.1
Kallin, B.2
Van't Hooft, F.M.3
Bavenholm, P.4
Hamsten, A.5
-
11
-
-
0026016865
-
Genetic variations at the plasminogen activator inhibitor-1 locus is associated with altered levels of plasminogen activator inhibitor-1 activity
-
Dawson S, Hamsten A, Wiman B, Henney A, Humphries S. Genetic variations at the plasminogen activator inhibitor-1 locus is associated with altered levels of plasminogen activator inhibitor-1 activity. Arterioscl Thromb 1991; 11:183-190.
-
(1991)
Arterioscl Thromb
, vol.11
, pp. 183-190
-
-
Dawson, S.1
Hamsten, A.2
Wiman, B.3
Henney, A.4
Humphries, S.5
-
12
-
-
0034435074
-
Genetic determinants of hyperhomocysteinaemia: The roles of cystathionine beta-synthase and 5,10-methylenetetrahydrofolate reductase
-
Blom HJ. Genetic determinants of hyperhomocysteinaemia: the roles of cystathionine beta-synthase and 5,10-methylenetetrahydrofolate reductase. Eur J Pediatr 2000; 159 (suppl 3):S208-S212.
-
(2000)
Eur J Pediatr
, vol.159
, Issue.3 SUPPL.
-
-
Blom, H.J.1
-
13
-
-
0034190659
-
5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A HUGE review
-
Botto LD, Yang Q. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HUGE review. Am J Epidemiol 2000; 151:862-877.
-
(2000)
Am J Epidemiol
, vol.151
, pp. 862-877
-
-
Botto, L.D.1
Yang, Q.2
-
14
-
-
4944266004
-
Genetic basis of atherosclerosis: Part II clinical implications
-
Lusis AJ, Fogelman AM, Fonarow GC. Genetic basis of atherosclerosis: Part II clinical implications. Circulation 2004; 110:2066-2071.
-
(2004)
Circulation
, vol.110
, pp. 2066-2071
-
-
Lusis, A.J.1
Fogelman, A.M.2
Fonarow, G.C.3
-
15
-
-
0037163849
-
MTHFR 677C→T polymorphism and risk of coronary artery disease: A meta analysis
-
Klerk M, Verhoef P, Clarke R, Blom HJ, Kok FJ, Schouten EG; MTHFR Studies Collaboration Group. MTHFR 677C→T polymorphism and risk of coronary artery disease: a meta analysis. JAMA 2002; 288:2023-2031.
-
(2002)
JAMA
, vol.288
, pp. 2023-2031
-
-
Klerk, M.1
Verhoef, P.2
Clarke, R.3
Blom, H.J.4
Kok, F.J.5
Schouten, E.G.6
-
16
-
-
4444233897
-
Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease
-
Almawi WY, Ameen G, Tamim H, Finan RR, Irani-Hakime N. Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease. J Thromb Thrombolysis 2004; 17:199-205.
-
(2004)
J Thromb Thrombolysis
, vol.17
, pp. 199-205
-
-
Almawi, W.Y.1
Ameen, G.2
Tamim, H.3
Finan, R.R.4
Irani-Hakime, N.5
-
17
-
-
0033140292
-
Genetic polymorphisms of homocysteine metabolism related enzymes in patients with coronary heart disease
-
Xu H, Chen Z, Tang J. Genetic polymorphisms of homocysteine metabolism related enzymes in patients with coronary heart disease. Zhonghua Yi Xue Za Zhi 1999; 79:414-416.
-
(1999)
Zhonghua Yi Xue Za Zhi
, vol.79
, pp. 414-416
-
-
Xu, H.1
Chen, Z.2
Tang, J.3
-
18
-
-
0030006275
-
Molecular variant of 5,10-methylenetetrahydrofolate reductase is a risk factor of ischemic heart disease in the Japanese population
-
Izumi M, Iwai N, Ohmichi N, Nakamura Y, Shimoike H, Kinoshita M. Molecular variant of 5,10-methylenetetrahydrofolate reductase is a risk factor of ischemic heart disease in the Japanese population. Atherosclerosis 1996; 121:293-294.
-
(1996)
Atherosclerosis
, vol.121
, pp. 293-294
-
-
Izumi, M.1
Iwai, N.2
Ohmichi, N.3
Nakamura, Y.4
Shimoike, H.5
Kinoshita, M.6
-
19
-
-
0035319508
-
Methylene tetrahydrofolate reductase gene polymorphism and the risk of premature myocardial infarction
-
Gulec S, Aras O, Akar E, Tutar E, Omurlu K, Avci F, et al. Methylene tetrahydrofolate reductase gene polymorphism and the risk of premature myocardial infarction. Clin Cardiol 2001; 24:281-284.
-
(2001)
Clin Cardiol
, vol.24
, pp. 281-284
-
-
Gulec, S.1
Aras, O.2
Akar, E.3
Tutar, E.4
Omurlu, K.5
Avci, F.6
-
20
-
-
0032763113
-
Methylenetetrahydrofolate reductase genotypes and early-onset coronary artery disease
-
Mager A, Lalezari S, Shohat T, Birnbaum Y, Adler Y, Magal N, Shohat M. Methylenetetrahydrofolate reductase genotypes and early-onset coronary artery disease. Circulation 1999; 100:2406-2410.
-
(1999)
Circulation
, vol.100
, pp. 2406-2410
-
-
Mager, A.1
Lalezari, S.2
Shohat, T.3
Birnbaum, Y.4
Adler, Y.5
Magal, N.6
Shohat, M.7
-
21
-
-
0037233375
-
Nitric oxide, atherosclerosis and the clinical relevance of endothelial dysfunction
-
Anderson TJ. Nitric oxide, atherosclerosis and the clinical relevance of endothelial dysfunction. Heart Fail Rev 2003; 8:71-86.
-
(2003)
Heart Fail Rev
, vol.8
, pp. 71-86
-
-
Anderson, T.J.1
-
22
-
-
0034616273
-
Genotype dependent and cigarette specific effects on endothelial nitric oxide synthase gene expression and enzyme activity
-
Wang XL, Sim AS, Wang MX, Murrell GA, Trudinger B, Wang J. Genotype dependent and cigarette specific effects on endothelial nitric oxide synthase gene expression and enzyme activity. FEBS Lett 2000; 471:45-50.
-
(2000)
FEBS Lett
, vol.471
, pp. 45-50
-
-
Wang, X.L.1
Sim, A.S.2
Wang, M.X.3
Murrell, G.A.4
Trudinger, B.5
Wang, J.6
-
23
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylene tetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylene tetrahydrofolate reductase. Nat Genet 1995; 10:111-113.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
24
-
-
0034087967
-
Association of the 4G/5G polymorphism in the promoter region of the plasminogen activator inhibitor-1 with abdominal aortic aneurysms
-
Rossaak JI, Van Rij AM, Jones GT, Harris EL. Association of the 4G/5G polymorphism in the promoter region of the plasminogen activator inhibitor-1 with abdominal aortic aneurysms. J Vasc Surg 2000; 31:1026-1032.
-
(2000)
J Vasc Surg
, vol.31
, pp. 1026-1032
-
-
Rossaak, J.I.1
Van Rij, A.M.2
Jones, G.T.3
Harris, E.L.4
-
25
-
-
0030048029
-
A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene
-
Wang LX, Sim AS, Badenhop RF, McCredie RM, Wilcken DE. A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene. Nat Med 1996; 2:41-45.
-
(1996)
Nat Med
, vol.2
, pp. 41-45
-
-
Wang, L.X.1
Sim, A.S.2
Badenhop, R.F.3
McCredie, R.M.4
Wilcken, D.E.5
-
26
-
-
0034973569
-
Multifactor dimensionality reduction reveals high-order interactions among estrogen metabolism genes in sporadic breast cancer
-
Ritchie MD, Hahn LW, Roodi N, Bailey LR, Dupont WD, Parl FF, et al. Multifactor dimensionality reduction reveals high-order interactions among estrogen metabolism genes in sporadic breast cancer. Am J Hum Genet 2001; 69:138-147.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 138-147
-
-
Ritchie, M.D.1
Hahn, L.W.2
Roodi, N.3
Bailey, L.R.4
Dupont, W.D.5
Parl, F.F.6
-
27
-
-
0037433052
-
Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions
-
Hahn LW, Ritchie MD, Moore JH. Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions. Bioinformatics 2003; 19:376-382.
-
(2003)
Bioinformatics
, vol.19
, pp. 376-382
-
-
Hahn, L.W.1
Ritchie, M.D.2
Moore, J.H.3
-
29
-
-
0040326195
-
-
Free computer program for the analysis of allelic data distributed by the authors over the Internet from the GDA home page
-
Lewis PO, Zaykin D. Genetic data analysis Version 1.0 (d12). Free computer program for the analysis of allelic data distributed by the authors over the Internet from the GDA home page at http://alleyn.eeb.uconn.edu/gda/ ;1999.
-
(1999)
Genetic Data Analysis Version 1.0 (D12)
-
-
Lewis, P.O.1
Zaykin, D.2
-
30
-
-
0033990339
-
Model free analysis and permutation test for allelic associations
-
Zhao JH, Curtis D, Sham PC. Model free analysis and permutation test for allelic associations. Hum Hered 2000; 50:133-139.
-
(2000)
Hum Hered
, vol.50
, pp. 133-139
-
-
Zhao, J.H.1
Curtis, D.2
Sham, P.C.3
-
31
-
-
0027514896
-
Molecular and statistical approaches to the detection and correction of errors in genotype databases
-
Brzustowics LM, Merette J, Xie X, Townsend L, Gilla TC, Ott J. Molecular and statistical approaches to the detection and correction of errors in genotype databases. Am J Hum Genet 1993; 53:1137-1145.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1137-1145
-
-
Brzustowics, L.M.1
Merette, J.2
Xie, X.3
Townsend, L.4
Gilla, T.C.5
Ott, J.6
-
32
-
-
0033854953
-
Combinations of variations in multiple genes are associated with hypertension
-
Williams SM, Addy JH, Phillips JA 3rd, Dai M, Kpodonu J, Afful J, et al. Combinations of variations in multiple genes are associated with hypertension. Hypertension 2000; 36:2-6.
-
(2000)
Hypertension
, vol.36
, pp. 2-6
-
-
Williams, S.M.1
Addy, J.H.2
Phillips III, J.A.3
Dai, M.4
Kpodonu, J.5
Afful, J.6
-
33
-
-
2342475667
-
Multilocus analysis of hypertension: A hierarchical approach
-
Williams SM, Ritchie MD, Phillips JA 3rd, Dawson E, Prince M, Dzhura E, et al. Multilocus analysis of hypertension: a hierarchical approach. Hum Hered 2004; 57:28-38.
-
(2004)
Hum Hered
, vol.57
, pp. 28-38
-
-
Williams, S.M.1
Ritchie, M.D.2
Phillips III, J.A.3
Dawson, E.4
Prince, M.5
Dzhura, E.6
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