-
1
-
-
34249906772
-
American Heart Association Council on Epidemiology and Prevention; American Heart Association Stroke Council; Functional Genomics and Translational Biology Interdisciplinary Working Group. Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council
-
Arnett D.K., Baird A.E., Barkley R.A., et al. American Heart Association Council on Epidemiology and Prevention; American Heart Association Stroke Council; Functional Genomics and Translational Biology Interdisciplinary Working Group. Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Translational Biology Interdisciplinary Working Group. Circulation 115 (2007) 2878-2901
-
(2007)
Circulation
, vol.115
, pp. 2878-2901
-
-
Arnett, D.K.1
Baird, A.E.2
Barkley, R.A.3
-
2
-
-
0037418247
-
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
-
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group
-
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group. No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age. Circulation 107 (2003) 1117-1122
-
(2003)
Circulation
, vol.107
, pp. 1117-1122
-
-
-
3
-
-
0030905250
-
Cardiovascular disease burden increases, NIH funding decreases
-
Breslow J.L. Cardiovascular disease burden increases, NIH funding decreases. Nat Med 3 (1997) 600-601
-
(1997)
Nat Med
, vol.3
, pp. 600-601
-
-
Breslow, J.L.1
-
4
-
-
40549109924
-
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
-
Broadbent H.M., Peden J.F., Lorkowski S., et al. Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Hum Mol Genet 17 (2008) 806-814
-
(2008)
Hum Mol Genet
, vol.17
, pp. 806-814
-
-
Broadbent, H.M.1
Peden, J.F.2
Lorkowski, S.3
-
5
-
-
18544372620
-
A comprehensive linkage analysis for myocardial infarction and its related risk factors
-
Broeckel U., Hengstenberg C., Mayer B., et al. A comprehensive linkage analysis for myocardial infarction and its related risk factors. Nat Genet 30 (2002) 210-214
-
(2002)
Nat Genet
, vol.30
, pp. 210-214
-
-
Broeckel, U.1
Hengstenberg, C.2
Mayer, B.3
-
6
-
-
35148835708
-
Genetics of cardiovascular diseases: from single mutations to the whole genome
-
Cambien F., and Tiret L. Genetics of cardiovascular diseases: from single mutations to the whole genome. Circulation 116 (2007) 1714-1724
-
(2007)
Circulation
, vol.116
, pp. 1714-1724
-
-
Cambien, F.1
Tiret, L.2
-
7
-
-
33750445938
-
Genetic approaches to coronary heart disease
-
Cohen J.C. Genetic approaches to coronary heart disease. J Am Coll Cardiol 48 (2006) 10-14
-
(2006)
J Am Coll Cardiol
, vol.48
, pp. 10-14
-
-
Cohen, J.C.1
-
8
-
-
35748959936
-
Future use of genomics in coronary artery disease
-
Damani S.B., and Topol E.J. Future use of genomics in coronary artery disease. J Am Coll Cardiol 50 (2007) 1933-1940
-
(2007)
J Am Coll Cardiol
, vol.50
, pp. 1933-1940
-
-
Damani, S.B.1
Topol, E.J.2
-
9
-
-
33744900610
-
Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17
-
Farrall M., Green F.R., Peden J.F., et al. Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17. PloS Genetics 2 (2006) e72
-
(2006)
PloS Genetics
, vol.2
-
-
Farrall, M.1
Green, F.R.2
Peden, J.F.3
-
10
-
-
18244398717
-
A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27
-
Francke S., Manraj M., Lacquemant C., et al. A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27. Hum Mol Genet 10 (2001) 2751-2765
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2751-2765
-
-
Francke, S.1
Manraj, M.2
Lacquemant, C.3
-
11
-
-
0036094165
-
Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2
-
Harrap S.B., Zammit K.S., Wong Z.Y., et al. Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2. Arterioscler Thromb Vasc Biol 22 (2002) 874-878
-
(2002)
Arterioscler Thromb Vasc Biol
, vol.22
, pp. 874-878
-
-
Harrap, S.B.1
Zammit, K.S.2
Wong, Z.Y.3
-
12
-
-
4143098058
-
A genome wide scan for early-onset coronary artery disease in 438 families: the GENECARD Study
-
Hauser E.R., Crossman D.C., Granger C.B., et al. A genome wide scan for early-onset coronary artery disease in 438 families: the GENECARD Study. Am J Hum Genet 75 (2004) 436-447
-
(2004)
Am J Hum Genet
, vol.75
, pp. 436-447
-
-
Hauser, E.R.1
Crossman, D.C.2
Granger, C.B.3
-
13
-
-
10744220794
-
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke
-
Helgadottir A., Manolescu A., Thorleifsson G., et al. The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke. Nat Genet 36 (2004) 233-239
-
(2004)
Nat Genet
, vol.36
, pp. 233-239
-
-
Helgadottir, A.1
Manolescu, A.2
Thorleifsson, G.3
-
14
-
-
13844289142
-
Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population
-
Helgadottir A., Gretarsdottir S., St Clair D., et al. Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population. Am J Hum Genet 76 (2005) 505-509
-
(2005)
Am J Hum Genet
, vol.76
, pp. 505-509
-
-
Helgadottir, A.1
Gretarsdottir, S.2
St Clair, D.3
-
15
-
-
29444444748
-
A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction
-
Helgadottir A., Manolescu A., Helgason A., et al. A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction. Nat Genet 38 (2006) 68-74
-
(2006)
Nat Genet
, vol.38
, pp. 68-74
-
-
Helgadottir, A.1
Manolescu, A.2
Helgason, A.3
-
16
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A., Thorleifsson G., Manolescu A., et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 316 (2007) 1491-1493
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
-
17
-
-
38649091662
-
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
-
Helgadottir A., Thorleifsson G., Magnusson K.P., et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet. 40 (2008) 217-224
-
(2008)
Nat Genet.
, vol.40
, pp. 217-224
-
-
Helgadottir, A.1
Thorleifsson, G.2
Magnusson, K.P.3
-
18
-
-
33751162818
-
Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS
-
Iakoubova O.A., Tong C.H., Chokkalingam A.P., et al. Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS. Arterioscler Thromb Vasc Biol 26 (2006) 2763-2768
-
(2006)
Arterioscler Thromb Vasc Biol
, vol.26
, pp. 2763-2768
-
-
Iakoubova, O.A.1
Tong, C.H.2
Chokkalingam, A.P.3
-
19
-
-
38349118892
-
Association of the Trp719Arg polymorphism in kinesin-like protein 6 with myocardial infarction and coronary heart disease in 2 prospective trials: the CARE and WOSCOPS trials
-
Iakoubova O.A., Tong C.H., Rowland C.M., et al. Association of the Trp719Arg polymorphism in kinesin-like protein 6 with myocardial infarction and coronary heart disease in 2 prospective trials: the CARE and WOSCOPS trials. J Am Coll Cardiol 51 (2008) 435-443
-
(2008)
J Am Coll Cardiol
, vol.51
, pp. 435-443
-
-
Iakoubova, O.A.1
Tong, C.H.2
Rowland, C.M.3
-
20
-
-
35748960247
-
Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes
-
Larson M.G., Atwood L.D., Benjamin E.J., et al. Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. BMC Med Genet 8 Suppl 1 (2007) S5
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Larson, M.G.1
Atwood, L.D.2
Benjamin, E.J.3
-
21
-
-
34548171994
-
A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease
-
Luke M.M., Kane J.P., Liu D.M., et al. A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease. Arterioscler Thromb Vasc Biol 27 (2007) 2030-2036
-
(2007)
Arterioscler Thromb Vasc Biol
, vol.27
, pp. 2030-2036
-
-
Luke, M.M.1
Kane, J.P.2
Liu, D.M.3
-
22
-
-
2342591299
-
Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes
-
McCarthy J.J., Parker A., Salem R., et al. Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes. J Med Genet 41 (2004) 334-341
-
(2004)
J Med Genet
, vol.41
, pp. 334-341
-
-
McCarthy, J.J.1
Parker, A.2
Salem, R.3
-
23
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
McPherson R., Pertsemlidis A., Kavaslar N., et al. A common allele on chromosome 9 associated with coronary heart disease. Science 316 (2007) 1488-1491
-
(2007)
Science
, vol.316
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
-
24
-
-
34247144499
-
Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study
-
Morgan T.M., Krumholz H.M., Lifton R.P., and Spertus J.A. Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study. JAMA 297 (2007) 1551-1561
-
(2007)
JAMA
, vol.297
, pp. 1551-1561
-
-
Morgan, T.M.1
Krumholz, H.M.2
Lifton, R.P.3
Spertus, J.A.4
-
26
-
-
18744407845
-
Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction
-
Ozaki K., Ohnishi Y., Iida A., et al. Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction. Nat Genet 32 (2002) 650-654
-
(2002)
Nat Genet
, vol.32
, pp. 650-654
-
-
Ozaki, K.1
Ohnishi, Y.2
Iida, A.3
-
27
-
-
2342480580
-
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro
-
Ozaki K., Inoue K., Sato H., et al. Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro. Nature 429 (2004) 72-75
-
(2004)
Nature
, vol.429
, pp. 72-75
-
-
Ozaki, K.1
Inoue, K.2
Sato, H.3
-
28
-
-
0033658950
-
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland
-
Pajukanta P., Cargill M., Viitanen L., et al. Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland. Am J Hum Genet 67 (2000) 1481-1493
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1481-1493
-
-
Pajukanta, P.1
Cargill, M.2
Viitanen, L.3
-
29
-
-
34250727671
-
Past and future of genetic research in thrombosis
-
Reitsma P.H., and Rosendaal F.R. Past and future of genetic research in thrombosis. J Thromb Haemost 5 Suppl. 1 (2007) 264-269
-
(2007)
J Thromb Haemost
, vol.5
, Issue.SUPPL. 1
, pp. 264-269
-
-
Reitsma, P.H.1
Rosendaal, F.R.2
-
30
-
-
34547629039
-
Scanning the genome for coronary risk
-
Rosenzweig A. Scanning the genome for coronary risk. N Engl J Med 357 (2007) 497-499
-
(2007)
N Engl J Med
, vol.357
, pp. 497-499
-
-
Rosenzweig, A.1
-
31
-
-
28144451633
-
A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study
-
Samani N.J., Burton P., Manigno M., et al. A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study. Am J Hum Genet 77 (2005) 1011-1020
-
(2005)
Am J Hum Genet
, vol.77
, pp. 1011-1020
-
-
Samani, N.J.1
Burton, P.2
Manigno, M.3
-
32
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani N.J., Erdmann J., Hall A.S., et al. Genomewide association analysis of coronary artery disease. N Engl J Med 357 (2007) 443-453
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
-
33
-
-
0037023783
-
Loss of lymphotoxin-alpha but not tumor necrosis factor-alpha reduces atherosclerosis in mice
-
Schreyer S.A., Vick C.M., and LeBoeuf R.C. Loss of lymphotoxin-alpha but not tumor necrosis factor-alpha reduces atherosclerosis in mice. J Biol Chem 277 (2002) 12364-12368
-
(2002)
J Biol Chem
, vol.277
, pp. 12364-12368
-
-
Schreyer, S.A.1
Vick, C.M.2
LeBoeuf, R.C.3
-
34
-
-
38949209549
-
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population
-
Shen G.Q., Rao S., Martinelli N., et al. Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population. J Hum Genet 53 (2008) 144-150
-
(2008)
J Hum Genet
, vol.53
, pp. 144-150
-
-
Shen, G.Q.1
Rao, S.2
Martinelli, N.3
-
35
-
-
38549092257
-
Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease
-
Shen G.Q., Li L., Rao S., et al. Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease. Artherioscler Thromb Vasc Biol 28 (2008) 360-365
-
(2008)
Artherioscler Thromb Vasc Biol
, vol.28
, pp. 360-365
-
-
Shen, G.Q.1
Li, L.2
Rao, S.3
-
36
-
-
25444523242
-
Identification of four gene variants associated with myocardial infarction
-
Shiffman D., Ellis S.G., Rowland C.M., et al. Identification of four gene variants associated with myocardial infarction. Am J Hum Genet 77 (2005) 596-605
-
(2005)
Am J Hum Genet
, vol.77
, pp. 596-605
-
-
Shiffman, D.1
Ellis, S.G.2
Rowland, C.M.3
-
37
-
-
33745948419
-
Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction
-
Shiffman D., Rowland C.M., Louie J.Z., et al. Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction. Arterioscler Thromb Vasc Biol 26 (2006) 1613-1618
-
(2006)
Arterioscler Thromb Vasc Biol
, vol.26
, pp. 1613-1618
-
-
Shiffman, D.1
Rowland, C.M.2
Louie, J.Z.3
-
38
-
-
37549058754
-
Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study
-
Shiffman D., O'Meara E.S., Bare L.A., et al. Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. Arterioscler Thomb Vasc Biol 28 (2008) 173-179
-
(2008)
Arterioscler Thomb Vasc Biol
, vol.28
, pp. 173-179
-
-
Shiffman, D.1
O'Meara, E.S.2
Bare, L.A.3
-
40
-
-
3142706539
-
Meta-analysis: apolipoprotein E genotypes and risk for coronary heart disease
-
Song Y., Stampfer M.J., and Liu S. Meta-analysis: apolipoprotein E genotypes and risk for coronary heart disease. Ann Intern Med 141 (2004) 137-147
-
(2004)
Ann Intern Med
, vol.141
, pp. 137-147
-
-
Song, Y.1
Stampfer, M.J.2
Liu, S.3
-
41
-
-
79959503826
-
The International HapMap Project
-
The International HapMap Consortium. The International HapMap Project. Nature 426 (2003) 789-796
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
The International HapMap Consortium1
-
42
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
The Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447 (2007) 661-678
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
The Wellcome Trust Case Control Consortium1
-
43
-
-
33644849222
-
Heart disease and stroke statistics-2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee
-
Thom T., Haase N., Rosamond W., et al. Heart disease and stroke statistics-2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation 113 (2006) 85-151
-
(2006)
Circulation
, vol.113
, pp. 85-151
-
-
Thom, T.1
Haase, N.2
Rosamond, W.3
-
44
-
-
0035960593
-
Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction
-
Topol E.J., McCarthy J., Gabriel S., et al. Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction. Circulation 104 (2001) 2641-2644
-
(2001)
Circulation
, vol.104
, pp. 2641-2644
-
-
Topol, E.J.1
McCarthy, J.2
Gabriel, S.3
-
46
-
-
0344827206
-
Mutation of MEF2A in an inherited disorder with features of coronary artery disease
-
Wang L., Fan C., Topol E., et al. Mutation of MEF2A in an inherited disorder with features of coronary artery disease. Science 302 (2003) 1578-1581
-
(2003)
Science
, vol.302
, pp. 1578-1581
-
-
Wang, L.1
Fan, C.2
Topol, E.3
-
47
-
-
10744233196
-
Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genome wide linkage analysis
-
Wang Q., Rao S., Shen G.Q., et al. Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genome wide linkage analysis. Am J Hum Genet 74 (2004) 262-271
-
(2004)
Am J Hum Genet
, vol.74
, pp. 262-271
-
-
Wang, Q.1
Rao, S.2
Shen, G.Q.3
-
48
-
-
0037069779
-
Prediction of the risk of myocardial infarction from polymorphisms in candidate genes
-
Yamada Y., Izawa H., Ichihara S., et al. Prediction of the risk of myocardial infarction from polymorphisms in candidate genes. N Engl J Med 347 (2002) 1916-1923
-
(2002)
N Engl J Med
, vol.347
, pp. 1916-1923
-
-
Yamada, Y.1
Izawa, H.2
Ichihara, S.3
-
49
-
-
3843138430
-
Lack of association of polymorphisms of the lymphotoxin alpha gene with myocardial infarction in Japanese
-
Yamada A., Ichihara S., Murase Y., et al. Lack of association of polymorphisms of the lymphotoxin alpha gene with myocardial infarction in Japanese. J Mol Med 82 (2004) 477-483
-
(2004)
J Mol Med
, vol.82
, pp. 477-483
-
-
Yamada, A.1
Ichihara, S.2
Murase, Y.3
-
50
-
-
33344478392
-
Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66,155 cases and 91,307 controls
-
Ye Z., Liu E.H., Higgins J.P., et al. Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66,155 cases and 91,307 controls. Lancet 367 (2006) 651-658
-
(2006)
Lancet
, vol.367
, pp. 651-658
-
-
Ye, Z.1
Liu, E.H.2
Higgins, J.P.3
-
51
-
-
33747179855
-
The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size
-
Zwicker J.I., Peyvandi F., Palla R., et al. The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size. Blood 108 (2006) 1280-1283
-
(2006)
Blood
, vol.108
, pp. 1280-1283
-
-
Zwicker, J.I.1
Peyvandi, F.2
Palla, R.3
|