-
1
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
The Wellcome Trust Case Control Consortium
-
The 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
-
-
-
2
-
-
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 2007, 316:1488-1491.
-
(2007)
Science
, vol.316
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
-
3
-
-
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 2007, 316:1491-1493.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
-
4
-
-
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. New Engl J Med 2007, 357:443-453.
-
(2007)
New Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
-
6
-
-
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 2008, 17:806-814.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 806-814
-
-
Broadbent, H.M.1
Peden, J.F.2
Lorkowski, S.3
-
7
-
-
57049150338
-
Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes
-
Doria A., Wojcik J., Xu R., et al. Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes. JAMA 2008, 300:2389-2397.
-
(2008)
JAMA
, vol.300
, pp. 2389-2397
-
-
Doria, A.1
Wojcik, J.2
Xu, R.3
-
8
-
-
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 2008, 53:357-359.
-
(2008)
J Hum Genet
, vol.53
, pp. 357-359
-
-
Hinohara, K.1
Nakajima, T.2
Takahashi, M.3
-
9
-
-
48749121090
-
Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population
-
Hiura Y., Fukushima Y., Yuno M., et al. Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population. Circ J 2008, 72:1213-1217.
-
(2008)
Circ J
, vol.72
, pp. 1213-1217
-
-
Hiura, Y.1
Fukushima, Y.2
Yuno, M.3
-
10
-
-
41649085340
-
For the 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., et al. for the 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
-
11
-
-
40449095630
-
Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men
-
Talmud P.J., Cooper J.A., Palmen J., et al. Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men. Clin Chem 2008, 54:467-474.
-
(2008)
Clin Chem
, vol.54
, pp. 467-474
-
-
Talmud, P.J.1
Cooper, J.A.2
Palmen, J.3
-
12
-
-
70349622023
-
Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke
-
Lemmens R., Abboud S., Robberecht W., et al. Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke. Eur J Hum Genet 2009, 17:1287-1293.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1287-1293
-
-
Lemmens, R.1
Abboud, S.2
Robberecht, W.3
-
13
-
-
79551623339
-
Haplotypes on 9p21 modify the risk for coronary artery disease among Indians
-
[Epub ahead of print]
-
AshokKumar M., Emmanuel C., Dhandapany P.S., et al. Haplotypes on 9p21 modify the risk for coronary artery disease among Indians. DNA Cell Biol 2011, 30:105-110. [Epub ahead of print].
-
(2011)
DNA Cell Biol
, vol.30
, pp. 105-110
-
-
AshokKumar, M.1
Emmanuel, C.2
Dhandapany, P.S.3
-
14
-
-
77950955511
-
Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population
-
Gori F., Specchia C., Pietri S., et al. Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population. BMC Med Genet 2010, 11:60.
-
(2010)
BMC Med Genet
, vol.11
, pp. 60
-
-
Gori, F.1
Specchia, C.2
Pietri, S.3
-
15
-
-
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 2010, 303:648-656.
-
(2010)
JAMA
, vol.303
, pp. 648-656
-
-
Palomaki, G.E.1
Melillo, S.2
Bradley, L.A.3
-
16
-
-
34249888775
-
-
Diabetes Genetics Initiative of Broad Institute of Harvard and MIT, Lund University, and Novartis Institutes of BioMedical Research. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science
-
Diabetes Genetics Initiative of Broad Institute of Harvard and MIT, Lund University, and Novartis Institutes of BioMedical Research. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 2007;316:1331-6.
-
(2007)
, vol.316
, pp. 1331-6
-
-
-
17
-
-
34249895023
-
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
-
Zeggini E., Weedon M.N., Lindgren C.M., et al. Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 2007, 316:1336-1341.
-
(2007)
Science
, vol.316
, pp. 1336-1341
-
-
Zeggini, E.1
Weedon, M.N.2
Lindgren, C.M.3
-
18
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
Scott L.J., Mohlke K.L., Bonnycastle L.L., et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 2007, 316:1341-1345.
-
(2007)
Science
, vol.316
, pp. 1341-1345
-
-
Scott, L.J.1
Mohlke, K.L.2
Bonnycastle, L.L.3
-
19
-
-
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 2008, 40:217-224.
-
(2008)
Nat Genet
, vol.40
, pp. 217-224
-
-
Helgadottir, A.1
Thorleifsson, G.2
Magnusson, K.P.3
-
20
-
-
44449176689
-
For the ISGS investigators. Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21
-
Matarin M., Brown W.M., Singleton A., Hardy J.A., Meschia J.F. for the ISGS investigators. Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21. Stroke 2008, 39:1586-1589.
-
(2008)
Stroke
, vol.39
, pp. 1586-1589
-
-
Matarin, M.1
Brown, W.M.2
Singleton, A.3
Hardy, J.A.4
Meschia, J.F.5
-
21
-
-
71849099015
-
The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people
-
Cluett C., McDermott M.M., Guralnik J., et al. The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people. Circ Cardiovasc Genet 2009, 2:347-353.
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 347-353
-
-
Cluett, C.1
McDermott, M.M.2
Guralnik, J.3
-
22
-
-
73449091829
-
A common variant at 9p21 is associated with sudden and arrhythmic cardiac death
-
Newton-Cheh C., Cook N.R., VanDenburgh H., et al. A common variant at 9p21 is associated with sudden and arrhythmic cardiac death. Circulation 2009, 120:2062-2068.
-
(2009)
Circulation
, vol.120
, pp. 2062-2068
-
-
Newton-Cheh, C.1
Cook, N.R.2
VanDenburgh, H.3
-
23
-
-
33747587608
-
Regulation of the INK4b-ARF-INK4a tumour suppressor locus: all for one or one for all
-
Gil J., Peters G. Regulation of the INK4b-ARF-INK4a tumour suppressor locus: all for one or one for all. Nat Rev Mol Cell Biol 2006, 7:667-677.
-
(2006)
Nat Rev Mol Cell Biol
, vol.7
, pp. 667-677
-
-
Gil, J.1
Peters, G.2
-
24
-
-
77952363272
-
Chromosome 9p21 SNPs associated with multiple disease phenotypes correlate with ANRIL expression
-
Cunnington M.S., Santibanez Koref M., Mayosi B.M., Burn J., Keavney B. Chromosome 9p21 SNPs associated with multiple disease phenotypes correlate with ANRIL expression. PLoS Genet 2010, 6:e1000899.
-
(2010)
PLoS Genet
, vol.6
-
-
Cunnington, M.S.1
Santibanez Koref, M.2
Mayosi, B.M.3
Burn, J.4
Keavney, B.5
-
25
-
-
79151486394
-
Expression of Chr9p21 genes CDKN2B (p15INK4b), CDKN2A (p16INK4a, p14ARF) and MTAP in human atherosclerotic plaque
-
Holdt L.M., Sass K., Gäbel G., et al. Expression of Chr9p21 genes CDKN2B (p15INK4b), CDKN2A (p16INK4a, p14ARF) and MTAP in human atherosclerotic plaque. Atherosclerosis 2011, 214:264-270.
-
(2011)
Atherosclerosis
, vol.214
, pp. 264-270
-
-
Holdt, L.M.1
Sass, K.2
Gäbel, G.3
-
26
-
-
70349569056
-
Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus
-
Jarinova O., Stewart A.F.R., Roberts R., 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.R.2
Roberts, R.3
-
27
-
-
64549083268
-
INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis
-
Liu Y., Sanoff H.K., Cho H., et al. INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis. PLoS ONE. 2009, 4:e5027.
-
(2009)
PLoS ONE.
, vol.4
-
-
Liu, Y.1
Sanoff, H.K.2
Cho, H.3
-
28
-
-
35348983887
-
-
The International HapMap Consortium. A second generation human haplotype map of over 3.1 million SNPs. Nature
-
The International HapMap Consortium. A second generation human haplotype map of over 3.1 million SNPs. Nature 2007;449:851-61.
-
(2007)
, vol.449
, pp. 851-61
-
-
-
29
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
Barrett J.C., Fry B., Maller J., Daly M.J. 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
-
30
-
-
38849091997
-
Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond
-
Pencina M.J., D'Agostino R.B., D'Agostino R.B., Vasan R.S. Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond. Stat Med 2008, 27:157-172.
-
(2008)
Stat Med
, vol.27
, pp. 157-172
-
-
Pencina, M.J.1
D'Agostino, R.B.2
D'Agostino, R.B.3
Vasan, R.S.4
-
31
-
-
34848886609
-
Two common gene variants on chromosome 9 and risk of atherothrombosis
-
Zee R.Y.L., Ridker P.M. Two common gene variants on chromosome 9 and risk of atherothrombosis. Stroke 2007, 38:e111.
-
(2007)
Stroke
, vol.38
-
-
Zee, R.Y.L.1
Ridker, P.M.2
-
32
-
-
55849100737
-
Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study
-
Dehghan A., van Hoek M., Sijbrands E.J.G., et al. Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study. BMC Med 2008, 6:30.
-
(2008)
BMC Med
, vol.6
, pp. 30
-
-
Dehghan, A.1
van Hoek, M.2
Sijbrands, E.J.G.3
-
33
-
-
77949915560
-
Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population
-
Ghazouani L., Khalifa S.B.H., Abboud N., et al. Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population. J Thromb Thrombolysis 2010, 29:114-118.
-
(2010)
J Thromb Thrombolysis
, vol.29
, pp. 114-118
-
-
Ghazouani, L.1
Khalifa, S.B.H.2
Abboud, N.3
-
34
-
-
77951676608
-
Control of cell proliferation in atherosclerosis: insights from animal models and human studies
-
Fuster J.J., Fernández P., González-Navarro H., et al. Control of cell proliferation in atherosclerosis: insights from animal models and human studies. Cardiovasc Res 2010, 86:254-264.
-
(2010)
Cardiovasc Res
, vol.86
, pp. 254-264
-
-
Fuster, J.J.1
Fernández, P.2
González-Navarro, H.3
|