-
1
-
-
0028330005
-
Genetic susceptibility to death from coronary heart disease in a study of twins
-
Marenberg, M.E., Risch, N., Berkman, L.F., Floderus, B., de Faire, U., Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med 330 (1994), 1041–1046.
-
(1994)
N Engl J Med
, vol.330
, pp. 1041-1046
-
-
Marenberg, M.E.1
Risch, N.2
Berkman, L.F.3
Floderus, B.4
de Faire, U.5
-
2
-
-
0036378360
-
Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins
-
Zdravkovic, S., Wienke, A., Pedersen, N.L., Marenberg, M.E., Yashin, A.I., De Faire, U., Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins. J Intern Med 252 (2002), 247–254.
-
(2002)
J Intern Med
, vol.252
, pp. 247-254
-
-
Zdravkovic, S.1
Wienke, A.2
Pedersen, N.L.3
Marenberg, M.E.4
Yashin, A.I.5
De Faire, U.6
-
3
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
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
-
-
-
4
-
-
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
-
5
-
-
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
-
6
-
-
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
-
7
-
-
85038613029
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Myocardial Infarction Genetics Consortium. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet, 2009, 41334–41341.
-
(2009)
Nat Genet
, pp. 41334-41341
-
-
-
8
-
-
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
-
9
-
-
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
-
10
-
-
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. Arterioscler Thromb Vasc Biol 28 (2008), 360–365.
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 360-365
-
-
Shen, G.Q.1
Li, L.2
Rao, S.3
-
11
-
-
41649085340
-
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease
-
Schunkert, H., Gotz, A., Braund, P., et al. Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease. Circulation 117 (2008), 1675–1684.
-
(2008)
Circulation
, vol.117
, pp. 1675-1684
-
-
Schunkert, H.1
Gotz, A.2
Braund, P.3
-
12
-
-
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., PROCARDIS Consortium. 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
-
13
-
-
41649091577
-
Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations
-
Hinohara, K., Nakajima, T., Takahashi, M., et al. Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations. J Hum Genet 53 (2008), 357–359.
-
(2008)
J Hum Genet
, vol.53
, pp. 357-359
-
-
Hinohara, K.1
Nakajima, T.2
Takahashi, M.3
-
14
-
-
48049115182
-
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study
-
Assimes, T.L., Knowles, J.W., Basu, A., et al. Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Hum Mol Genet 17 (2008), 2320–2328.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 2320-2328
-
-
Assimes, T.L.1
Knowles, J.W.2
Basu, A.3
-
15
-
-
58749087343
-
Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3
-
Paynter, N.P., Chasman, D.I., Buring, J.E., Shiffman, D., Cook, N.R., Ridker, P.M., Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3. Ann Intern Med 150 (2009), 65–72.
-
(2009)
Ann Intern Med
, vol.150
, pp. 65-72
-
-
Paynter, N.P.1
Chasman, D.I.2
Buring, J.E.3
Shiffman, D.4
Cook, N.R.5
Ridker, P.M.6
-
16
-
-
77149160077
-
Association between 9p21 genomic markers and heart disease: a meta-analysis
-
Palomaki, G.E., Melillo, S., Bradley, L.A., Association between 9p21 genomic markers and heart disease: a meta-analysis. JAMA 303 (2010), 648–656.
-
(2010)
JAMA
, vol.303
, pp. 648-656
-
-
Palomaki, G.E.1
Melillo, S.2
Bradley, L.A.3
-
17
-
-
63149194355
-
Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease
-
Horne, B.D., Carllquist, J.F., Muhlestein, J.B., Bair, T.L., Anderson, J.L., Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease. Circ Cardiovasc Genet 1 (2008), 85–92.
-
(2008)
Circ Cardiovasc Genet
, vol.1
, pp. 85-92
-
-
Horne, B.D.1
Carllquist, J.F.2
Muhlestein, J.B.3
Bair, T.L.4
Anderson, J.L.5
-
18
-
-
56349096706
-
Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility
-
Anderson, J.L., Horne, B.D., Kolek, M.J., et al. Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility. Am Heart J 156 (2008), 1155–1162.
-
(2008)
Am Heart J
, vol.156
, pp. 1155-1162
-
-
Anderson, J.L.1
Horne, B.D.2
Kolek, M.J.3
-
19
-
-
47349129207
-
Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study
-
Ye, S., Willeit, J., Kronenberg, F., Xu, Q., Kiechl, S., Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study. J Am Coll Cardiol 52 (2008), 378–384.
-
(2008)
J Am Coll Cardiol
, vol.52
, pp. 378-384
-
-
Ye, S.1
Willeit, J.2
Kronenberg, F.3
Xu, Q.4
Kiechl, S.5
-
20
-
-
0028206843
-
Continuing evolution of therapy for coronary artery disease: Initial results from the era of coronary angioplasty
-
Mark, D.B., Nelson, C.L., Califf, R.M., et al. Continuing evolution of therapy for coronary artery disease: Initial results from the era of coronary angioplasty. Circulation 89 (1994), 2015–2025.
-
(1994)
Circulation
, vol.89
, pp. 2015-2025
-
-
Mark, D.B.1
Nelson, C.L.2
Califf, R.M.3
-
21
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel, S.B., Schaffner, S.F., Nguyen, H., et al. The structure of haplotype blocks in the human genome. Science 296 (2002), 2225–2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
-
22
-
-
67449103171
-
Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease
-
Muendlein, A., Saely, C.H., Rhomberg, S., et al. Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease. Atherosclerosis 205 (2009), 174–180.
-
(2009)
Atherosclerosis
, vol.205
, pp. 174-180
-
-
Muendlein, A.1
Saely, C.H.2
Rhomberg, S.3
|