-
1
-
-
33947609211
-
Risk factors for acute myocardial infarction in Latin America: The INTERHEART Latin American study
-
INTERHEART Investigators in Latin America
-
Lanas F, Avezum A, Bautista LE, Díaz R, Luna M, Islam S, Yusuf S, INTERHEART Investigators in Latin America: Risk factors for acute myocardial infarction in Latin America: the INTERHEART Latin American study. Circulation 2007;115: 1067-1074.
-
(2007)
Circulation
, vol.115
, pp. 1067-1074
-
-
Lanas, F.1
Avezum, A.2
Bautista, L.E.3
Díaz, R.4
Luna, M.5
Islam, S.6
Yusuf, S.7
-
2
-
-
33846603166
-
Genetics and heritability of coronary artery disease and myocardial infarction
-
Mayer B, Erdmann J, Schunkert H: Genetics and heritability of coronary artery disease and myocardial infarction. Clin Res Cardiol 2007;96:1-7.
-
(2007)
Clin Res Cardiol
, vol.96
, pp. 1-7
-
-
Mayer, B.1
Erdmann, J.2
Schunkert, H.3
-
3
-
-
33746839281
-
Endothelial nitric oxide synthase G894T gene polymorphism in Chilean subjects with coronary artery disease and controls
-
Jaramillo PC, Muñoz A, Lanas C, Lanas F, Salazar LA: Endothelial nitric oxide synthase G894T gene polymorphism in Chilean subjects with coronary artery disease and controls. Clin Chim Acta 2006;371:102-106.
-
(2006)
Clin Chim Acta
, vol.371
, pp. 102-106
-
-
Jaramillo, P.C.1
Muñoz, A.2
Lanas, C.3
Lanas, F.4
Salazar, L.A.5
-
4
-
-
35948940878
-
786T>C polymorphism of the endothelial nitric oxide synthase gene in Chilean subjects with coronary artery disease and controls
-
Jaramillo PC, Lanas C, Lanas F, Salazar LA: -786T>C polymorphism of the endothelial nitric oxide synthase gene in Chilean subjects with coronary artery disease and controls. Clin Chim Acta 2008;387:105-108.
-
(2008)
Clin Chim Acta
, vol.387
, pp. 105-108
-
-
Jaramillo, P.C.1
Lanas, C.2
Lanas, F.3
Salazar, L.A.4
-
5
-
-
34147109232
-
Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol
-
Pare G, Serre D, Brisson D, Anand SS, Montpetit A, Tremblay G, Engert JC, Hudson TJ, Gaudet D: Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol. Am J Hum Genet 2007;80:673-682.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 673-682
-
-
Pare, G.1
Serre, D.2
Brisson, D.3
Anand, S.S.4
Montpetit, A.5
Tremblay, G.6
Engert, J.C.7
Hudson, T.J.8
Gaudet, D.9
-
6
-
-
0033843695
-
Seven DNA polymorphisms at the candidate genes of atherosclerosis in Brazilian women with angiographically documented coronary artery disease
-
Salazar LA, Hirata MH, Giannini SD, Forti N, Diament J, Lima TM, Hirata RD: Seven DNA polymorphisms at the candidate genes of atherosclerosis in Brazilian women with angiographically documented coronary artery disease. Clin Chim Acta 2000;300:139-149.
-
(2000)
Clin Chim Acta
, vol.300
, pp. 139-149
-
-
Salazar, L.A.1
Hirata, M.H.2
Giannini, S.D.3
Forti, N.4
Diament, J.5
Lima, T.M.6
Hirata, R.D.7
-
7
-
-
0035877010
-
Correlation of polymorphism to coagulation and biochemical risk factors for cardiovascular diseases
-
Wu A, Tsongalis G: Correlation of polymorphism to coagulation and biochemical risk factors for cardiovascular diseases. Am J Cardiol 2001;87:1361-1366.
-
(2001)
Am J Cardiol
, vol.87
, pp. 1361-1366
-
-
Wu, A.1
Tsongalis, G.2
-
8
-
-
33750807530
-
Sequence variations within the genes related to hemostatic imbalance and their impact on coronary artery disease in Turkish population
-
Taymaz H, Erarslan S, Oner ET, Alkan T, Aǧirbaşli M, Kirdar B: Sequence variations within the genes related to hemostatic imbalance and their impact on coronary artery disease in Turkish population. Thromb Res 2007;119:55-62.
-
(2007)
Thromb Res
, vol.119
, pp. 55-62
-
-
Taymaz, H.1
Erarslan, S.2
Oner, E.T.3
Alkan, T.4
Aǧirbaşli, M.5
Kirdar, B.6
-
9
-
-
45249086825
-
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis
-
Martinelli N, Trabetti E, Pinotti M, Olivieri O, Sandri M, Friso S, Pizzolo F, Bozzini C, Caruso PP, Cavallari U, Cheng S, Pignatti PF, Bernardi F, Corrocher R, Girelli D: Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. PLoS ONE 2008;3:e1523.
-
(2008)
PLoS ONE
, vol.3
-
-
Martinelli, N.1
Trabetti, E.2
Pinotti, M.3
Olivieri, O.4
Sandri, M.5
Friso, S.6
Pizzolo, F.7
Bozzini, C.8
Caruso, P.P.9
Cavallari, U.10
Cheng, S.11
Pignatti, P.F.12
Bernardi, F.13
Corrocher, R.14
Girelli, D.15
-
10
-
-
0036840704
-
Association of the factor XII 46C>T polymorphism with risk of coronary heart disease (CHD) in the WOSCOPS study
-
Zito F, Lowe G, Rumley A, McMahon A, Humphries S: Association of the factor XII 46C>T polymorphism with risk of coronary heart disease (CHD) in the WOSCOPS study. Atherosclerosis 2002;165:153-158.
-
(2002)
Atherosclerosis
, vol.165
, pp. 153-158
-
-
Zito, F.1
Lowe, G.2
Rumley, A.3
McMahon, A.4
Humphries, S.5
-
11
-
-
3242748377
-
Homozygosity of the T allele of the 46 C>T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population
-
Santamaría A, Mateo J, Tirado I, Oliver A, Belvís R, Martí-Fábregas J, Felices R, Soria JM, Souto JC, Fontcuberta J: Homozygosity of the T allele of the 46 C>T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population. Stroke 2004;35:1795-1799.
-
(2004)
Stroke
, vol.35
, pp. 1795-1799
-
-
Santamaría, A.1
Mateo, J.2
Tirado, I.3
Oliver, A.4
Belvís, R.5
Martí-Fábregas, J.6
Felices, R.7
Soria, J.M.8
Souto, J.C.9
Fontcuberta, J.10
-
12
-
-
3242749842
-
Homozygosity of the T allele of the 46 C>T polymorphism in the F12 gene is a risk factor for acute coronary artery disease in the Spanish population
-
Santamaría A, Martinez-Rubio A, Mateo J, Tirado I, Soria J, Fontcuberta J: Homozygosity of the T allele of the 46 C>T polymorphism in the F12 gene is a risk factor for acute coronary artery disease in the Spanish population. Haematologica 2004;89: 878-879.
-
(2004)
Haematologica
, vol.89
, pp. 878-879
-
-
Santamaría, A.1
Martinez-Rubio, A.2
Mateo, J.3
Tirado, I.4
Soria, J.5
Fontcuberta, J.6
-
13
-
-
2442465593
-
Association after linkage analysis indicates that homozygosity for the 46C>T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis
-
Tirado I, Soria JM, Mateo J, Oliver A, Souto JC, Santamaria A, Felices R, Borrell M, Fontcuberta J: Association after linkage analysis indicates that homozygosity for the 46C>T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis. Thromb Haemost 2004;91:899-904.
-
(2004)
Thromb Haemost
, vol.91
, pp. 899-904
-
-
Tirado, I.1
Soria, J.M.2
Mateo, J.3
Oliver, A.4
Souto, J.C.5
Santamaria, A.6
Felices, R.7
Borrell, M.8
Fontcuberta, J.9
-
14
-
-
0035543840
-
Homozygosity for the C>T polymorphism at nucleotide 46 in the 5′untraslated region of the factor XII gene protects from development of acute coronary syndrome
-
Endler G, Mannhalter C, Sunder-Plassmann H, Lalouschek W, Kapiotis S, Exner M, Jordanova N, Meier S, Kunze F, Wagner O, Huber K: Homozygosity for the C>T polymorphism at nucleotide 46 in the 5′untraslated region of the factor XII gene protects from development of acute coronary syndrome. Br J Haematol 2001;115:1007-1009.
-
(2001)
Br J Haematol
, vol.115
, pp. 1007-1009
-
-
Endler, G.1
Mannhalter, C.2
Sunder-Plassmann, H.3
Lalouschek, W.4
Kapiotis, S.5
Exner, M.6
Jordanova, N.7
Meier, S.8
Kunze, F.9
Wagner, O.10
Huber, K.11
-
15
-
-
0035864343
-
A common C->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activity
-
Endler G, Exner M, Mannhalter C, Meier S, Ruzicka K, Handler S, Panzer S, Wagner O, Quehenberger P: A common C->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activity. Thromb Res 2001;101:255-260.
-
(2001)
Thromb Res
, vol.101
, pp. 255-260
-
-
Endler, G.1
Exner, M.2
Mannhalter, C.3
Meier, S.4
Ruzicka, K.5
Handler, S.6
Panzer, S.7
Wagner, O.8
Quehenberger, P.9
-
16
-
-
0031873791
-
Optimized procedure DNA isolation from fresh and cryopreserved clotted human blood useful in clinical molecular testing
-
Salazar LA, Hirata MH, Cavalli SA, Machado MO, Hirata RD: Optimized procedure DNA isolation from fresh and cryopreserved clotted human blood useful in clinical molecular testing. Clin Chem 1998;44:1748-1750.
-
(1998)
Clin Chem
, vol.44
, pp. 1748-1750
-
-
Salazar, L.A.1
Hirata, M.H.2
Cavalli, S.A.3
Machado, M.O.4
Hirata, R.D.5
-
17
-
-
0034711163
-
Epidemiological and genetic association of activated factor XII concentration with factor VII activity, fibrinopeptide A concentration, and risk of coronary heart disease in men
-
Zito F, Drummond F, Bujac SR, Esnouf MP, Morrissey JH, Humphries SE, Miller GJ: Epidemiological and genetic association of activated factor XII concentration with factor VII activity, fibrinopeptide A concentration, and risk of coronary heart disease in men. Circulation 2000;102:2058-2062.
-
(2000)
Circulation
, vol.102
, pp. 2058-2062
-
-
Zito, F.1
Drummond, F.2
Bujac, S.R.3
Esnouf, M.P.4
Morrissey, J.H.5
Humphries, S.E.6
Miller, G.J.7
-
18
-
-
0035019737
-
Rapid factor XII (46 C>T) genotyping by fluorescence resonance energy transfer in patients with coronary artery disease or thrombophilia
-
Orth M, Westphal S, Dierkes J, Luley C, Schlatterer K: Rapid factor XII (46 C>T) genotyping by fluorescence resonance energy transfer in patients with coronary artery disease or thrombophilia. Clin Chem 2001;47:1117-1119.
-
(2001)
Clin Chem
, vol.47
, pp. 1117-1119
-
-
Orth, M.1
Westphal, S.2
Dierkes, J.3
Luley, C.4
Schlatterer, K.5
-
19
-
-
0036269750
-
Activated factor XII levels and factor XII 46C>T genotype in relation to coronary artery calcification in patients with type I diabetes and healthy subjects
-
Colhoun H, Zito F, Chan N, Rubens M, Fuler J, Humphries S: Activated factor XII levels and factor XII 46C>T genotype in relation to coronary artery calcification in patients with type I diabetes and healthy subjects. Atherosclerosis 2002;163:363-369.
-
(2002)
Atherosclerosis
, vol.163
, pp. 363-369
-
-
Colhoun, H.1
Zito, F.2
Chan, N.3
Rubens, M.4
Fuler, J.5
Humphries, S.6
-
20
-
-
0033125184
-
FXII (46C>T) polymorphism and in vivo generation of FXII activity-gene frequencies and relationship in patients with coronary artery disease
-
Kohler H, Futers T, Grant P: FXII (46C>T) polymorphism and in vivo generation of FXII activity-gene frequencies and relationship in patients with coronary artery disease. Thromb Haemost 1999;81:745-747.
-
(1999)
Thromb Haemost
, vol.81
, pp. 745-747
-
-
Kohler, H.1
Futers, T.2
Grant, P.3
-
21
-
-
38349171226
-
Coagulation factor XII (FXII) activity, activated FXII, distribution of FXII C46T gene polymorphism and coronary risk
-
Bach J, Endler G, Winkelmann BR, Boehm BO, Maerz W, Mannhalter C, Hellstern P: Coagulation factor XII (FXII) activity, activated FXII, distribution of FXII C46T gene polymorphism and coronary risk. J Thromb Haemost 2008;6: 291-296.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 291-296
-
-
Bach, J.1
Endler, G.2
Winkelmann, B.R.3
Boehm, B.O.4
Maerz, W.5
Mannhalter, C.6
Hellstern, P.7
-
22
-
-
29244452575
-
Synergistic association between hypercholesterolemia and the C46T factor XII polymorphism for developing premature myocardial infarction
-
Roldán V, Corral J, Marín F, Pineda J, Vicente V, González-Conejero R: Synergistic association between hypercholesterolemia and the C46T factor XII polymorphism for developing premature myocardial infarction. Thromb Haemost 2005;94:1294-1299.
-
(2005)
Thromb Haemost
, vol.94
, pp. 1294-1299
-
-
Roldán, V.1
Corral, J.2
Marín, F.3
Pineda, J.4
Vicente, V.5
González-Conejero, R.6
-
23
-
-
18244384262
-
A quantitative-trait locus in the human factor XII gene influences both plasma factor levels and susceptibility to thrombotic disease
-
Soria JM, Almasy L, Souto JC, Bacq D, Buil A, Faure A, Martínez-Marchán E, Mateo J, Borrell M, Stone W, Lathrop M, Fontcuberta J, Blangero J: A quantitative-trait locus in the human factor XII gene influences both plasma factor levels and susceptibility to thrombotic disease. Am J Hum Genet 2002;70:567-574.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 567-574
-
-
Soria, J.M.1
Almasy, L.2
Souto, J.C.3
Bacq, D.4
Buil, A.5
Faure, A.6
Martínez-Marchán, E.7
Mateo, J.8
Borrell, M.9
Stone, W.10
Lathrop, M.11
Fontcuberta, J.12
Blangero, J.13
-
24
-
-
34147150283
-
Homozygosity for the C46T polymorphism of the F12 gene is a risk factor for venous thrombosis during the first pregnancy
-
Cochery-Nouvellon E, Mercier E, Lissalde-Lavigne G, Daurès JP, Quéré I, Dauzat M, Marès P, Gris JC: Homozygosity for the C46T polymorphism of the F12 gene is a risk factor for venous thrombosis during the first pregnancy. J Thromb Haemost 2007;5:700-707.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 700-707
-
-
Cochery-Nouvellon, E.1
Mercier, E.2
Lissalde-Lavigne, G.3
Daurès, J.P.4
Quéré, I.5
Dauzat, M.6
Marès, P.7
Gris, J.C.8
-
25
-
-
37849040691
-
Factor XII C46T gene polymorphism and the risk of cerebral venous thrombosis
-
Reuner KH, Jenetzky E, Aleu A, Litfin F, Mellado P, Kloss M, Jüttler E, Grau AJ, Rickmann H, Patscheke H, Lichy C: Factor XII C46T gene polymorphism and the risk of cerebral venous thrombosis. Neurology 2008;70:129-132.
-
(2008)
Neurology
, vol.70
, pp. 129-132
-
-
Reuner, K.H.1
Jenetzky, E.2
Aleu, A.3
Litfin, F.4
Mellado, P.5
Kloss, M.6
Jüttler, E.7
Grau, A.J.8
Rickmann, H.9
Patscheke, H.10
Lichy, C.11
-
26
-
-
43749117957
-
Coagulation factor XII (FXII) activity, activated factor XII, distribution of factor XII C46T gene polymorphism and coronary risk: Reply to a rebuttal
-
Bach J, Endler G, Mannhalter C, Hellstern P: Coagulation factor XII (FXII) activity, activated factor XII, distribution of factor XII C46T gene polymorphism and coronary risk: reply to a rebuttal. J Thromb Haemost 2008;6:1055-1056.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 1055-1056
-
-
Bach, J.1
Endler, G.2
Mannhalter, C.3
Hellstern, P.4
-
27
-
-
34548065409
-
Phenotypic and genotypic differences in factor XII between African Americans and Caucasians
-
Miller CH, Hooper C: Phenotypic and genotypic differences in factor XII between African Americans and Caucasians. J Thromb Haemost 2007;5:1981-1982.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1981-1982
-
-
Miller, C.H.1
Hooper, C.2
-
28
-
-
16544382991
-
Evaluation of the interactions of common genetic mutations in stroke
-
Szolnoki Z: Evaluation of the interactions of common genetic mutations in stroke. Methods Mol Med 2005;104:241-250.
-
(2005)
Methods Mol Med
, vol.104
, pp. 241-250
-
-
Szolnoki, Z.1
-
29
-
-
0031964489
-
Levels of activated FXII in survivors of myocardial infarction - Association with circulating risk factors and extent of coronary artery disease
-
Kohler HP, Carter AM, Stickland MH, Grant PJ: Levels of activated FXII in survivors of myocardial infarction - Association with circulating risk factors and extent of coronary artery disease. Thromb Haemost 1998;79:14-18.
-
(1998)
Thromb Haemost
, vol.79
, pp. 14-18
-
-
Kohler, H.P.1
Carter, A.M.2
Stickland, M.H.3
Grant, P.J.4
-
30
-
-
11144232409
-
Activated factor XII in patients with hyperglycaemia and dyslipidaemia
-
Prusa R, Zadina J, Bronský J: Activated factor XII in patients with hyperglycaemia and dyslipidaemia. Vnitr Lek 2004;50:917-922.
-
(2004)
Vnitr Lek
, vol.50
, pp. 917-922
-
-
Prusa, R.1
Zadina, J.2
Bronský, J.3
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