-
1
-
-
0037264105
-
Incidence of diagnosed deep vein thrombosis in the general population: systematic review
-
Fowkes F.J., Price J.F., and Fowkes G. Incidence of diagnosed deep vein thrombosis in the general population: systematic review. Eur J Vasc Endovasc Surg 25 (2004) 1-5
-
(2004)
Eur J Vasc Endovasc Surg
, vol.25
, pp. 1-5
-
-
Fowkes, F.J.1
Price, J.F.2
Fowkes, G.3
-
2
-
-
0038042011
-
Risk factors for venous thromboembolism
-
Anderson F., and Spencer F. Risk factors for venous thromboembolism. Circulation 107 (2003) I9-I16
-
(2003)
Circulation
, vol.107
-
-
Anderson, F.1
Spencer, F.2
-
3
-
-
0033832644
-
Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population
-
Angchaisuksiri P., Pingsuthiwong S., Aryuchai K., et al. Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population. Am J Hematol 65 (2000) 119-122
-
(2000)
Am J Hematol
, vol.65
, pp. 119-122
-
-
Angchaisuksiri, P.1
Pingsuthiwong, S.2
Aryuchai, K.3
-
4
-
-
26244460048
-
Factor V Leiden, prothrombin 20210A, methylenetetrahydrofolate reductase 677 T, and population genetics
-
Bauduer F., and Lacombe D. Factor V Leiden, prothrombin 20210A, methylenetetrahydrofolate reductase 677 T, and population genetics. Mol Genet Metabol 86 (2005) 91-99
-
(2005)
Mol Genet Metabol
, vol.86
, pp. 91-99
-
-
Bauduer, F.1
Lacombe, D.2
-
5
-
-
0036544888
-
Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population
-
Lu Y., Zhao Y., Liu G., et al. Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population. Thromb Res 106 (2002) 7-12
-
(2002)
Thromb Res
, vol.106
, pp. 7-12
-
-
Lu, Y.1
Zhao, Y.2
Liu, G.3
-
6
-
-
34250855052
-
Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls
-
Chinnery P., Mowbray C., Pate S., et al. Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls. J Med Genet 44 (2007) e80
-
(2007)
J Med Genet
, vol.44
-
-
Chinnery, P.1
Mowbray, C.2
Pate, S.3
-
7
-
-
48649083598
-
Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients
-
Rosa A., Fonseca B., Krug T., et al. Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients. BMC Med Genet 9 (2008) 57-67
-
(2008)
BMC Med Genet
, vol.9
, pp. 57-67
-
-
Rosa, A.1
Fonseca, B.2
Krug, T.3
-
8
-
-
43449087360
-
Mitochondrial haplogroups: ischemic cardiovascular disease, other diseases, mortality, and longevity in the general population
-
Benn M., Schwartz M., Nordestgaard B., and Tybjærg-Hansen A. Mitochondrial haplogroups: ischemic cardiovascular disease, other diseases, mortality, and longevity in the general population. Circulation 117 (2008) 2492-2501
-
(2008)
Circulation
, vol.117
, pp. 2492-2501
-
-
Benn, M.1
Schwartz, M.2
Nordestgaard, B.3
Tybjærg-Hansen, A.4
-
9
-
-
0026046333
-
African populations and the evolution of human mitochondrial DNA
-
Vigilant I., Stoneking M., Harpending H., Hawkes K., and Wilson A. African populations and the evolution of human mitochondrial DNA. Science 253 (1991) 1503-1507
-
(1991)
Science
, vol.253
, pp. 1503-1507
-
-
Vigilant, I.1
Stoneking, M.2
Harpending, H.3
Hawkes, K.4
Wilson, A.5
-
10
-
-
0026063965
-
Branching pattern in the evolutionary tree for human mitochondrial DNA
-
Di Renzo A., and Wilson A. Branching pattern in the evolutionary tree for human mitochondrial DNA. PNAS 88 (1991) 1597-1601
-
(1991)
PNAS
, vol.88
, pp. 1597-1601
-
-
Di Renzo, A.1
Wilson, A.2
-
11
-
-
75049085501
-
Founder mitochondrial haplogroups in Amerindian populations
-
Bailliet G., Rothhamer F., Carnese F., Bravi C., and Bianchi N. Founder mitochondrial haplogroups in Amerindian populations. Am J Hum Genet 50 (1994) 592-601
-
(1994)
Am J Hum Genet
, vol.50
, pp. 592-601
-
-
Bailliet, G.1
Rothhamer, F.2
Carnese, F.3
Bravi, C.4
Bianchi, N.5
-
12
-
-
0029790032
-
Multipler founder haplotypes of mitochondrial DNA Amerindians revealed by RFLP and sequency
-
Santos S., Ribeiro-Dos Santos A., Meyer D., and Zago M. Multipler founder haplotypes of mitochondrial DNA Amerindians revealed by RFLP and sequency. Ann Hum Genet 60 (1996) 305-319
-
(1996)
Ann Hum Genet
, vol.60
, pp. 305-319
-
-
Santos, S.1
Ribeiro-Dos Santos, A.2
Meyer, D.3
Zago, M.4
-
13
-
-
3343017432
-
Mitochondrial DNA diversity in South America and the genetic history of Andean Highlanders
-
Fuselli S., Tarazona-Santos E., Dupanloup I., Soto A., Luiselli D., and Pettener D. Mitochondrial DNA diversity in South America and the genetic history of Andean Highlanders. Mol Biol Evol 20 (2003) 1682-1691
-
(2003)
Mol Biol Evol
, vol.20
, pp. 1682-1691
-
-
Fuselli, S.1
Tarazona-Santos, E.2
Dupanloup, I.3
Soto, A.4
Luiselli, D.5
Pettener, D.6
-
14
-
-
0033838985
-
Mitochondrial DNA polymorphisms in Chilean aboriginal populations: implications for the peopling of the southern cone of the continent
-
Moraga M., Rocco P., Miquel J., et al. Mitochondrial DNA polymorphisms in Chilean aboriginal populations: implications for the peopling of the southern cone of the continent. Am J Phys Anthropol 113 (2000) 19-29
-
(2000)
Am J Phys Anthropol
, vol.113
, pp. 19-29
-
-
Moraga, M.1
Rocco, P.2
Miquel, J.3
-
15
-
-
0036484684
-
Composición genética de la población chilena: Distribución de polimorfismos de DNA mitocondrial en grupos originarios y en la población mixta de Santiago
-
Rocco P., Morales C., Moraga M., et al. Composición genética de la población chilena: Distribución de polimorfismos de DNA mitocondrial en grupos originarios y en la población mixta de Santiago. Rev Med Chile 130 (2002) 125-131
-
(2002)
Rev Med Chile
, vol.130
, pp. 125-131
-
-
Rocco, P.1
Morales, C.2
Moraga, M.3
-
16
-
-
33144458775
-
mtDNA microevolution in Southern Chile's archipelagos
-
García F., Moraga M., Vera S., et al. mtDNA microevolution in Southern Chile's archipelagos. Am J Phys Anthropol 129 (2006) 473-481
-
(2006)
Am J Phys Anthropol
, vol.129
, pp. 473-481
-
-
García, F.1
Moraga, M.2
Vera, S.3
-
17
-
-
0031873791
-
Optimized procedure DNA isolation from fresh and cryopreserved clotted human blood useful in clinical molecular testing
-
Salazar L.A., Hirata M., Cavalli S., et al. Optimized procedure DNA isolation from fresh and cryopreserved clotted human blood useful in clinical molecular testing. Clin Chem 44 8 (1998) 1748-1750
-
(1998)
Clin Chem
, vol.44
, Issue.8
, pp. 1748-1750
-
-
Salazar, L.A.1
Hirata, M.2
Cavalli, S.3
-
18
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina R.M., Koeleman B.P.C., Koster T., et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 369 (1994) 64-67
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
-
19
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort S.R., Rosendaal F.R., Reitsma P.H., and Bertina R.M. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 88 10 (1996) 3698-3703
-
(1996)
Blood
, vol.88
, Issue.10
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
20
-
-
0029049553
-
A candidate genetic risk factor for vascular diseases: a common mutation in methylenetetrahydrofolate reductase
-
Frosst P., Blom H., Milos R., et al. A candidate genetic risk factor for vascular diseases: a common mutation in methylenetetrahydrofolate reductase. Nature Genet 10 (1995) 111-113
-
(1995)
Nature Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.2
Milos, R.3
-
21
-
-
0035658140
-
Mutation in the promotor region of the β-fibrinogen gene and the risk of future myocardial infarction, stroke and venous thrombosis
-
Blake G., Schmitz C., Lindpaintner K., and Ridker P. Mutation in the promotor region of the β-fibrinogen gene and the risk of future myocardial infarction, stroke and venous thrombosis. Eur Heart J 22 (2001) 2262-2266
-
(2001)
Eur Heart J
, vol.22
, pp. 2262-2266
-
-
Blake, G.1
Schmitz, C.2
Lindpaintner, K.3
Ridker, P.4
-
22
-
-
0031055330
-
A single early migration for the peopling of the Americas supported by mitochondrial DNA sequence data
-
Bonatto S., and Salzano F. A single early migration for the peopling of the Americas supported by mitochondrial DNA sequence data. PNAS 94 (1997) 1866-1871
-
(1997)
PNAS
, vol.94
, pp. 1866-1871
-
-
Bonatto, S.1
Salzano, F.2
-
23
-
-
33748509495
-
Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy
-
Castro M.G., Huerta C., Reguero J.R., et al. Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy. Int J Cardiol 112 (2006) 202-206
-
(2006)
Int J Cardiol
, vol.112
, pp. 202-206
-
-
Castro, M.G.1
Huerta, C.2
Reguero, J.R.3
-
24
-
-
33846352842
-
Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males
-
Nishigaki Y., Yamada Y., Fuku N., et al. Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males. Hum Genet 120 (2007) 827-836
-
(2007)
Hum Genet
, vol.120
, pp. 827-836
-
-
Nishigaki, Y.1
Yamada, Y.2
Fuku, N.3
-
25
-
-
0031023757
-
A single genetic origin for a common Caucasian risk factor for venous thrombosis
-
Zivelin A., Griffin J., Xu X., et al. A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood 89 (1997) 397-402
-
(1997)
Blood
, vol.89
, pp. 397-402
-
-
Zivelin, A.1
Griffin, J.2
Xu, X.3
-
26
-
-
33745105401
-
Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24 000 years ago
-
Zivelin A., Mor-Cohen R., Kovalsky V., et al. Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24 000 years ago. Blood 107 (2006) 4666-4668
-
(2006)
Blood
, vol.107
, pp. 4666-4668
-
-
Zivelin, A.1
Mor-Cohen, R.2
Kovalsky, V.3
-
27
-
-
11444268843
-
Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients
-
Rodrigues C., Rocha L., Morelli V., Franco R., and Lourenco D. Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients. J Thromb Haemost 2 (2004) 1211-1212
-
(2004)
J Thromb Haemost
, vol.2
, pp. 1211-1212
-
-
Rodrigues, C.1
Rocha, L.2
Morelli, V.3
Franco, R.4
Lourenco, D.5
-
28
-
-
0034324872
-
Prevalence of three prothrombotic polymorphisms: factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T in Argentina
-
Genoud V., Castañon M., Annichino-Bizzacchi J., Korin J., and Kordich L. Prevalence of three prothrombotic polymorphisms: factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T in Argentina. Thromb Res 100 (2000) 127-131
-
(2000)
Thromb Res
, vol.100
, pp. 127-131
-
-
Genoud, V.1
Castañon, M.2
Annichino-Bizzacchi, J.3
Korin, J.4
Kordich, L.5
-
29
-
-
33645904206
-
Relevant genetic contribution of Amerindian to the extant population of Argentina
-
Corach D., Marino M., and Sala A. Relevant genetic contribution of Amerindian to the extant population of Argentina. Int Congress Series 1288 (2006) 397-399
-
(2006)
Int Congress Series
, vol.1288
, pp. 397-399
-
-
Corach, D.1
Marino, M.2
Sala, A.3
-
30
-
-
0030155494
-
Resistencia a la Proteína C Activada: Estudio de laboratorio y prevalencia del defecto in población chilena
-
Pereira J., Quiroga T., Goycoolea M., et al. Resistencia a la Proteína C Activada: Estudio de laboratorio y prevalencia del defecto in población chilena. Rev Med Chile 124 (1996) 663-668
-
(1996)
Rev Med Chile
, vol.124
, pp. 663-668
-
-
Pereira, J.1
Quiroga, T.2
Goycoolea, M.3
-
31
-
-
32244447480
-
Factor V Leiden y mutación de la protrombina G20210A en pacientes con trombosis venosa y arterial
-
Palomo I., Pereira J., Alarcón M., et al. Factor V Leiden y mutación de la protrombina G20210A en pacientes con trombosis venosa y arterial. Rev Med Chile 133 (2005) 1425-1433
-
(2005)
Rev Med Chile
, vol.133
, pp. 1425-1433
-
-
Palomo, I.1
Pereira, J.2
Alarcón, M.3
-
32
-
-
0036484684
-
Composición genética de la población chilena. Distribución de polimorfismos de DNA mitocondrial en grupos originarios y en la población mixta de Santiago.
-
Rocco P., Morales C., Moraga M., et al. Composición genética de la población chilena. Distribución de polimorfismos de DNA mitocondrial en grupos originarios y en la población mixta de Santiago. Rev Med Chile 130 (2002) 125-131
-
(2002)
Rev Med Chile
, vol.130
, pp. 125-131
-
-
Rocco, P.1
Morales, C.2
Moraga, M.3
-
33
-
-
0031902128
-
Prevalence of the mutation C677 > T in the Methylenetetrahydrofolate reductase gene among distinct ethnic groups in Brazil
-
Arruda V., Siqueira L., Gonçalves M., et al. Prevalence of the mutation C677 > T in the Methylenetetrahydrofolate reductase gene among distinct ethnic groups in Brazil. Am J Med Genet 78 (1998) 332-335
-
(1998)
Am J Med Genet
, vol.78
, pp. 332-335
-
-
Arruda, V.1
Siqueira, L.2
Gonçalves, M.3
-
34
-
-
0032042477
-
Frequency of factor V (FV) Leiden and C677T Methylenetetrahydrofolate reductase (MTHFR) mutation in Colombians
-
Camacho O., Giusti B., Restrepo Fernandez C.M., Abbate R., and Pepe G. Frequency of factor V (FV) Leiden and C677T Methylenetetrahydrofolate reductase (MTHFR) mutation in Colombians. Thromb Haemost 79 (1998) 883-884
-
(1998)
Thromb Haemost
, vol.79
, pp. 883-884
-
-
Camacho, O.1
Giusti, B.2
Restrepo Fernandez, C.M.3
Abbate, R.4
Pepe, G.5
-
35
-
-
0032231408
-
Heterogeneity in world distribution of the thermolabile C677T mutation in 5, 10-methylenetetrahydrofolate reductase
-
Pepe G., Camacho V., Giusti T., et al. Heterogeneity in world distribution of the thermolabile C677T mutation in 5, 10-methylenetetrahydrofolate reductase. Am J Hum Genet 63 (1998) 917-920
-
(1998)
Am J Hum Genet
, vol.63
, pp. 917-920
-
-
Pepe, G.1
Camacho, V.2
Giusti, T.3
-
36
-
-
0036488108
-
A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians
-
Mukherjee M., Joshi S., Bagadi S., Dalvi M., Rao A., and Shetty K.R. A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians. Clin Genet 61 (2002) 155-159
-
(2002)
Clin Genet
, vol.61
, pp. 155-159
-
-
Mukherjee, M.1
Joshi, S.2
Bagadi, S.3
Dalvi, M.4
Rao, A.5
Shetty, K.R.6
-
37
-
-
0030747763
-
Prevalence of factor V Leiden mutation in various populations
-
Herrmann F.H., Koesling M., Schroder W., et al. Prevalence of factor V Leiden mutation in various populations. Genet Epidemiol 14 (1997) 403-411
-
(1997)
Genet Epidemiol
, vol.14
, pp. 403-411
-
-
Herrmann, F.H.1
Koesling, M.2
Schroder, W.3
-
38
-
-
20444445722
-
Homocysteine, MTHFR and risk of venous thrombosis: a meta-analysis of published epidemiological studies
-
Den Heijer M., Lewington S., and Clarke R. Homocysteine, MTHFR and risk of venous thrombosis: a meta-analysis of published epidemiological studies. J Thromb Haemost 3 (2005) 292-299
-
(2005)
J Thromb Haemost
, vol.3
, pp. 292-299
-
-
Den Heijer, M.1
Lewington, S.2
Clarke, R.3
-
39
-
-
0141484369
-
The epidemiology of venous thromboembolism in Caucasians and African-Americans: the GATE study
-
Dowling N., Austin H., Dilley A., Wiitsett C., Evatt B.L., and Hooper W.C. The epidemiology of venous thromboembolism in Caucasians and African-Americans: the GATE study. J Thromb Haemost 1 (2003) 80-87
-
(2003)
J Thromb Haemost
, vol.1
, pp. 80-87
-
-
Dowling, N.1
Austin, H.2
Dilley, A.3
Wiitsett, C.4
Evatt, B.L.5
Hooper, W.C.6
-
40
-
-
0037373178
-
Serum homocysteine, thermolabile variant of metylenetetrahydrofolate reductase (MTHFR), and venous thromboembolism: longitudinal investigation of thromboembolism (LITE)
-
Tsai A.W., Cushman M., Tsai M.Y., et al. Serum homocysteine, thermolabile variant of metylenetetrahydrofolate reductase (MTHFR), and venous thromboembolism: longitudinal investigation of thromboembolism (LITE). Am J Hematol 72 (2003) 192-200
-
(2003)
Am J Hematol
, vol.72
, pp. 192-200
-
-
Tsai, A.W.1
Cushman, M.2
Tsai, M.Y.3
|