-
1
-
-
84990161111
-
Atherosclerosis precursors in finnish children and adolescents. I. General description of the cross-sectional study of 1980, and an account of the children's and families' state of health
-
Akerblom HK, Viikari J, Uhari M, Räsänen L, Byckling T, Louhivuori K, et al. Atherosclerosis precursors in Finnish children and adolescents. I. General description of the cross-sectional study of 1980, and an account of the children's and families' state of health. Acta Paediatr Scand Suppl. 1985;318:49-63.
-
(1985)
Acta Paediatr Scand Suppl
, vol.318
, pp. 49-63
-
-
Akerblom, H.K.1
Viikari, J.2
Uhari, M.3
Räsänen, L.4
Byckling, T.5
Louhivuori, K.6
-
2
-
-
4243138387
-
Coronary disease among united states soldiers killed in action in korea; preliminary report
-
Enos WF, Holmes RH, Beyer J. Coronary disease among United States soldiers killed in action in Korea; preliminary report. J Am Med Assoc. 1953;152:1090-1093.
-
(1953)
J Am Med Assoc
, vol.152
, pp. 1090-1093
-
-
Enos, W.F.1
Holmes, R.H.2
Beyer, J.3
-
3
-
-
77149160077
-
Association between 9p21 genomic markers and heart disease: A meta-Analysis
-
Palomaki GE, Melillo S, Bradley LA. Association between 9p21 genomic markers and heart disease: a meta-Analysis. JAMA. 2010;303:648-656.
-
(2010)
JAMA
, vol.303
, pp. 648-656
-
-
Palomaki, G.E.1
Melillo, S.2
Bradley, L.A.3
-
4
-
-
0036378360
-
Heritability of death from coronary heart disease: A 36-year follow-up of 20 966 swedish twins
-
Zdravkovic S, Wienke A, Pedersen NL, Marenberg ME, Yashin AI, De Faire U. Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins. J Intern Med. 2002;252:247-254.
-
(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
-
5
-
-
79951473520
-
9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response
-
Harismendy O, Notani D, Song X, Rahim NG, Tanasa B, Heintzman N, et al. 9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response. Nature. 2011;470:264-268.
-
(2011)
Nature
, vol.470
, pp. 264-268
-
-
Harismendy, O.1
Notani, D.2
Song, X.3
Rahim, N.G.4
Tanasa, B.5
Heintzman, N.6
-
6
-
-
84856136800
-
Recent studies of the human chromosome 9p21 locus, which is associated with atherosclerosis in human populations
-
Holdt LM, Teupser D. Recent studies of the human chromosome 9p21 locus, which is associated with atherosclerosis in human populations. Arterioscler Thromb Vasc Biol. 2012;32:196-206.
-
(2012)
Arterioscler Thromb Vasc Biol
, vol.32
, pp. 196-206
-
-
Holdt, L.M.1
Teupser, D.2
-
7
-
-
70349569056
-
Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus
-
Jarinova O, Stewart AF, Roberts R, Wells G, Lau P, Naing T, et al. Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus. Arterioscler Thromb Vasc Biol. 2009;29:1671-1677.
-
(2009)
Arterioscler Thromb Vasc Biol
, vol.29
, pp. 1671-1677
-
-
Jarinova, O.1
Stewart, A.F.2
Roberts, R.3
Wells, G.4
Lau, P.5
Naing, T.6
-
8
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007;316:1491-1493.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
-
9
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, Roberts R, Cox DR, et al. A common allele on chromosome 9 associated with coronary heart disease. Science. 2007;316:1488-1491.
-
(2007)
Science
, vol.316
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
Stewart, A.4
Roberts, R.5
Cox, D.R.6
-
10
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
WTCCC and the Cardiogenics Consortium
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, et al WTCCC and the Cardiogenics Consortium. Genomewide association analysis of coronary artery disease. N Engl J Med. 2007;357:443-453.
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
-
11
-
-
77149122355
-
9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population
-
Ding H, Xu Y, Wang X, Wang Q, Zhang L, Tu Y, et al. 9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population. Circ Cardiovasc Genet. 2009;2:338-346.
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 338-346
-
-
Ding, H.1
Xu, Y.2
Wang, X.3
Wang, Q.4
Zhang, L.5
Tu, Y.6
-
12
-
-
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, Hohda S, Sasaoka T, Nakahara K, et al. Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations. J Hum Genet. 2008;53:357-359.
-
(2008)
J Hum Genet
, vol.53
, pp. 357-359
-
-
Hinohara, K.1
Nakajima, T.2
Takahashi, M.3
Hohda, S.4
Sasaoka, T.5
Nakahara, K.6
-
13
-
-
41649085340
-
Cardiogenics consortium. Repeated replication and a prospective meta-Analysis of the association between chromosome 9p21.3 and coronary artery disease
-
Schunkert H, Götz A, Braund P, McGinnis R, Tregouet DA, Mangino M, et al Cardiogenics Consortium. Repeated replication and a prospective meta-Analysis of the association between chromosome 9p21.3 and coronary artery disease. Circulation. 2008;117:1675-1684.
-
(2008)
Circulation
, vol.117
, pp. 1675-1684
-
-
Schunkert, H.1
Götz, A.2
Braund, P.3
McGinnis, R.4
Tregouet, D.A.5
Mangino, M.6
-
14
-
-
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 GQ, Li L, Rao S, Abdullah KG, Ban JM, Lee BS, 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. 2008;28:360-365.
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 360-365
-
-
Shen, G.Q.1
Li, L.2
Rao, S.3
Abdullah, K.G.4
Ban, J.M.5
Lee, B.S.6
-
15
-
-
77955438579
-
Gene dosage of the common variant 9p21 predicts severity of coronary artery disease
-
Dandona S, Stewart AF, Chen L, Williams K, So D, O'Brien E, et al. Gene dosage of the common variant 9p21 predicts severity of coronary artery disease. J Am Coll Cardiol. 2010;56:479-486.
-
(2010)
J Am Coll Cardiol
, vol.56
, pp. 479-486
-
-
Dandona, S.1
Stewart, A.F.2
Chen, L.3
Williams, K.4
So, D.5
O'Brien, E.6
-
16
-
-
63149194355
-
Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease
-
Horne BD, Carlquist JF, Muhlestein JB, Bair TL, Anderson JL. Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease. Circ Cardiovasc Genet. 2008;1:85-92.
-
(2008)
Circ Cardiovasc Genet
, vol.1
, pp. 85-92
-
-
Horne, B.D.1
Carlquist, J.F.2
Muhlestein, J.B.3
Bair, T.L.4
Anderson, J.L.5
-
17
-
-
79251619566
-
Identification of adamts7 as a novel locus for coronary atherosclerosis and association of abo with myocardial infarction in the presence of coronary atherosclerosis: Two genome-wide association studies
-
Myocardial Infarction Genetics Consortium. Wellcome Trust Case Control Consortium
-
Reilly MP, Li M, He J, Ferguson JF, Stylianou IM, Mehta NN, et al Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Lancet. 2011;377:383-392.
-
(2011)
Lancet
, vol.377
, pp. 383-392
-
-
Reilly, M.P.1
Li, M.2
He, J.3
Ferguson, J.F.4
Stylianou, I.M.5
Mehta, N.N.6
-
18
-
-
56849128391
-
Gene-environment interactions in the etiology of obesity: Defining the fundamentals
-
Bouchard C. Gene-environment interactions in the etiology of obesity: defining the fundamentals. Obesity (Silver Spring). 2008;16(Suppl 3):S5-S10.
-
(2008)
Obesity (Silver Spring
, vol.16
, Issue.SUPPL. 3
-
-
Bouchard, C.1
-
19
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, Chen H, et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007;316:1331-1336.
-
(2007)
Science
, vol.316
, pp. 1331-1336
-
-
Saxena, R.1
Voight, B.F.2
Lyssenko, V.3
Burtt, N.P.4
De Bakker, P.I.5
Chen, H.6
-
20
-
-
78649379906
-
Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies
-
Davies RW, Dandona S, Stewart AF, Chen L, Ellis SG, Tang WH, et al. Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies. Circ Cardiovasc Genet. 2010;3:468-474.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 468-474
-
-
Davies, R.W.1
Dandona, S.2
Stewart, A.F.3
Chen, L.4
Ellis, S.G.5
Tang, W.H.6
-
21
-
-
13444269543
-
Haploview: Analysis and visualization of ld and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005;21:263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
22
-
-
34548292504
-
Plink: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007;81:559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
-
23
-
-
80053316001
-
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction
-
Italian Atherosclerosis, Thrombosis and Vascular Biology Investigators
-
Ardissino D, Berzuini C, Merlini PA, Mannuccio Mannucci P, Surti A, Burtt N, et al; Italian Atherosclerosis, Thrombosis and Vascular Biology Investigators. Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction. J Am Coll Cardiol. 2011;58:426-434.
-
(2011)
J Am Coll Cardiol
, vol.58
, pp. 426-434
-
-
Ardissino, D.1
Berzuini, C.2
Merlini, P.A.3
Mannuccio, M.P.4
Surti, A.5
Burtt, N.6
-
24
-
-
78650316598
-
The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease
-
Patel RS, Su S, Neeland IJ, Ahuja A, Veledar E, Zhao J, et al. The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease. Eur Heart J. 2010;31:3017-3023.
-
(2010)
Eur Heart J
, vol.31
, pp. 3017-3023
-
-
Patel, R.S.1
Su, S.2
Neeland, I.J.3
Ahuja, A.4
Veledar, E.5
Zhao, J.6
-
25
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007;447:661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
26
-
-
70749096913
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet. 2009;41:334-341.
-
(2009)
Nat Genet
, vol.41
, pp. 334-341
-
-
Kathiresan, S.1
Voight, B.F.2
Purcell, S.3
Musunuru, K.4
Ardissino, D.5
Mannucci, P.M.6
-
27
-
-
79959710790
-
Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease
-
Gong Y, Beitelshees AL, Cooper-DeHoff RM, Lobmeyer MT, Langaee TY, Wu J, et al. Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease. Circ Cardiovasc Genet. 2011;4:169-178.
-
(2011)
Circ Cardiovasc Genet
, vol.4
, pp. 169-178
-
-
Gong, Y.1
Beitelshees, A.L.2
Cooper-DeHoff, R.M.3
Lobmeyer, M.T.4
Langaee, T.Y.5
Wu, J.6
-
28
-
-
0028063408
-
Increased expression of matrix metalloproteinases and matrix degrading activity in vulnerable regions of human atherosclerotic plaques
-
Galis ZS, Sukhova GK, Lark MW, Libby P. Increased expression of matrix metalloproteinases and matrix degrading activity in vulnerable regions of human atherosclerotic plaques. J Clin Invest. 1994;94:2493-2503.
-
(1994)
J Clin Invest
, vol.94
, pp. 2493-2503
-
-
Galis, Z.S.1
Sukhova, G.K.2
Lark, M.W.3
Libby, P.4
-
29
-
-
0034687333
-
Coronary artery injury and the biology of atherosclerosis: Inflammation, thrombosis, and stabilization
-
discussion 8J
-
Libby P. Coronary artery injury and the biology of atherosclerosis: inflammation, thrombosis, and stabilization. Am J Cardiol. 2000;86(8B):3J-8J; discussion 8J.
-
(2000)
Am J Cardiol
, vol.86
, Issue.8 B
-
-
Libby, P.1
-
30
-
-
0028085059
-
Site of intimal rupture or erosion of thrombosed coronary atherosclerotic plaques is characterized by an inflammatory process irrespective of the dominant plaque morphology
-
van der Wal AC, Becker AE, van der Loos CM, Das PK. Site of intimal rupture or erosion of thrombosed coronary atherosclerotic plaques is characterized by an inflammatory process irrespective of the dominant plaque morphology. Circulation. 1994;89:36-44.
-
(1994)
Circulation
, vol.89
, pp. 36-44
-
-
Van Der Wal, A.C.1
Becker, A.E.2
Van Der Loos, C.M.3
Das, P.K.4
-
31
-
-
78649354925
-
Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: A potential mechanism for increased vascular disease
-
Musunuru K, Post WS, Herzog W, Shen H, O'Connell JR, McArdle PF, et al. Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease. Circ Cardiovasc Genet. 2010;3:445-453.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 445-453
-
-
Musunuru, K.1
Post, W.S.2
Herzog, W.3
Shen, H.4
O'Connell, J.R.5
McArdle, P.F.6
-
32
-
-
84867164045
-
Platelets in atherosclerosis and thrombosis
-
Schulz C, Massberg S. Platelets in atherosclerosis and thrombosis. Handb Exp Pharmacol. 2012:111-133.
-
(2012)
Handb Exp Pharmacol
, pp. 111-133
-
-
Schulz, C.1
Massberg, S.2
|