-
1
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, et al. (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447: 661-78.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
Burton, P.R.1
Clayton, D.G.2
Cardon, L.R.3
Craddock, N.4
Deloukas, P.5
-
2
-
-
34547623750
-
Genome-wide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, et al. (2007) Genome-wide association analysis of coronary artery disease. N Engl J Med 357: 443-53.
-
(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
-
3
-
-
79960221315
-
The chromosome 9p21 region and myocardial infarction in a European population
-
Koch W, Türk S, Erl A, Hoppmann P, Pfeufer A, et al. (2011) The chromosome 9p21 region and myocardial infarction in a European population. Atherosclerosis 217: 220-6.
-
(2011)
Atherosclerosis
, vol.217
, pp. 220-226
-
-
Koch, W.1
Türk, S.2
Erl, A.3
Hoppmann, P.4
Pfeufer, A.5
-
4
-
-
34250010480
-
A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction
-
Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, et al. (2007) A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction. Science 316: 1491-93.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
-
5
-
-
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, et al. (2009) Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy-number variants. Nat Genet 41: 334-41.
-
(2009)
Nat Genet
, vol.41
, pp. 334-341
-
-
Kathiresan, S.1
Voight, B.F.2
Purcell, S.3
Musunuru, K.4
Ardissino, D.5
-
6
-
-
84155163079
-
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction
-
O'Donnell CJ, Kavousi M, Smith AV, Kardia SL, Feitosa MF, et al. (2011) Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation 124: 2855-64.
-
(2011)
Circulation
, vol.124
, pp. 2855-2864
-
-
O'Donnell, C.J.1
Kavousi, M.2
Smith, A.V.3
Kardia, S.L.4
Feitosa, M.F.5
-
7
-
-
84857192818
-
Genome-wide association study of coronary artery disease in the Japanese
-
Takeuchi F, Yokota M, Yamamoto K, Nakashima E, Katsuya T, et al. (2012) Genome-wide association study of coronary artery disease in the Japanese. Eur J Hum Genet 20: 333-40.
-
(2012)
Eur J Hum Genet
, vol.20
, pp. 333-340
-
-
Takeuchi, F.1
Yokota, M.2
Yamamoto, K.3
Nakashima, E.4
Katsuya, T.5
-
8
-
-
84875467239
-
A genome-wide association study of a coronary artery disease risk variant
-
Lee JY, Lee BS, Shin DJ, Woo Park K, Shin YA, et al. (2013) A genome-wide association study of a coronary artery disease risk variant. J Hum Genet 58: 120-6.
-
(2013)
J Hum Genet
, vol.58
, pp. 120-126
-
-
Lee, J.Y.1
Lee, B.S.2
Shin, D.J.3
Woo Park, K.4
Shin, Y.A.5
-
9
-
-
80053452394
-
Large-scale gene-centric analysis identifies novel variants for coronary artery disease
-
Butterworth AS, Braund PS, Farrall M, Hardwick RJ, Saleheen D, et al. (2011) Large-scale gene-centric analysis identifies novel variants for coronary artery disease. PLoS Genet 7: e1002260.
-
(2011)
PLoS Genet
, vol.7
-
-
Butterworth, A.S.1
Braund, P.S.2
Farrall, M.3
Hardwick, R.J.4
Saleheen, D.5
-
10
-
-
79952351224
-
Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry
-
Scheffold T, Kullmann S, Huge A, Binner P, Ochs HR, et al. (2011) Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry. BMC Cardiovasc Disord 11: 9.
-
(2011)
BMC Cardiovasc Disord
, vol.11
, pp. 9
-
-
Scheffold, T.1
Kullmann, S.2
Huge, A.3
Binner, P.4
Ochs, H.R.5
-
11
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
Lyssenko V, Burtt NP, de Bakker PI, Chen H, Roix JJ, et al. (2007) Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 316: 1331-6.
-
(2007)
Science
, vol.316
, pp. 1331-1336
-
-
Lyssenko, V.1
Burtt, N.P.2
de Bakker, P.I.3
Chen, H.4
Roix, J.J.5
-
12
-
-
34249895023
-
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
-
Zeggini E, Weedon MN, Lindgren CM, Frayling TM, Elliott KS, et al. (2007) Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 316: 1336-41.
-
(2007)
Science
, vol.316
, pp. 1336-1341
-
-
Zeggini, E.1
Weedon, M.N.2
Lindgren, C.M.3
Frayling, T.M.4
Elliott, K.S.5
-
13
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
Scott LJ, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, et al. (2007) A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 316: 1341-5.
-
(2007)
Science
, vol.316
, pp. 1341-1345
-
-
Scott, L.J.1
Mohlke, K.L.2
Bonnycastle, L.L.3
Willer, C.J.4
Li, Y.5
-
14
-
-
84864074200
-
Type 2 diabetes and polymorphisms on chromosome 9p21: A meta-analysis
-
Cugino D, Gianfagna F, Santimone I, de Gaetano G, Donati MB, et al. (2012) Type 2 diabetes and polymorphisms on chromosome 9p21: A meta-analysis. Nutr Metab Cardiovasc Dis 22: 619-25.
-
(2012)
Nutr Metab Cardiovasc Dis
, vol.22
, pp. 619-625
-
-
Cugino, D.1
Gianfagna, F.2
Santimone, I.3
de Gaetano, G.4
Donati, M.B.5
-
15
-
-
84859814666
-
The 9p21 genetic variant is additive to carotid intima media thickness and plaque in improving coronary heart disease risk prediction in white participants of the Atherosclerosis Risk in Communities (ARIC) Study
-
Nambi V, Boerwinkle E, Lawson K, Brautbar A, Chambless L, et al. (2012) The 9p21 genetic variant is additive to carotid intima media thickness and plaque in improving coronary heart disease risk prediction in white participants of the Atherosclerosis Risk in Communities (ARIC) Study. Atherosclerosis 222: 135-7.
-
(2012)
Atherosclerosis
, vol.222
, pp. 135-137
-
-
Nambi, V.1
Boerwinkle, E.2
Lawson, K.3
Brautbar, A.4
Chambless, L.5
-
16
-
-
0028059330
-
Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma
-
Caldas C, Hahn SA, da Costa LT, Redston MS, Schutte M, et al. (1994) Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma. Nat Genet 8: 27-32.
-
(1994)
Nat Genet
, vol.8
, pp. 27-32
-
-
Caldas, C.1
Hahn, S.A.2
da Costa, L.T.3
Redston, M.S.4
Schutte, M.5
-
17
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22
-
Cannon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, et al. (1992) Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science 258: 1148-52.
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
Lewis, C.M.4
Anderson, D.E.5
-
18
-
-
3943049366
-
Smad expression in human atherosclerotic lesions: evidence for impaired TGF-b/Smad signaling in smooth muscle cells of fibrofatty lesions. Arterioscler
-
Kalinina N, Agrotis A, Antropova Y, Ilyinskaya O, Smirnov V, et al. (2004) Smad expression in human atherosclerotic lesions: evidence for impaired TGF-b/Smad signaling in smooth muscle cells of fibrofatty lesions. Arterioscler. Thromb Vasc Biol 24: 1391n6.
-
(2004)
Thromb Vasc Biol
, vol.24
-
-
Kalinina, N.1
Agrotis, A.2
Antropova, Y.3
Ilyinskaya, O.4
Smirnov, V.5
-
19
-
-
0034706909
-
A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer
-
Schmid M, Sen M, Rosenbach MD, Carrera CJ, Friedman H, et al. (2000) A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer. Oncogene 19: 5747-54.
-
(2000)
Oncogene
, vol.19
, pp. 5747-5754
-
-
Schmid, M.1
Sen, M.2
Rosenbach, M.D.3
Carrera, C.J.4
Friedman, H.5
-
20
-
-
77956637896
-
Genetics and beyond-the transcriptome of human monocytes and disease susceptibility
-
Zeller T, Wild P, Szymczak S, Rotival M, Schillert A, et al. (2010) Genetics and beyond-the transcriptome of human monocytes and disease susceptibility. PLoS One 5: e10693.
-
(2010)
PLoS One
, vol.5
-
-
Zeller, T.1
Wild, P.2
Szymczak, S.3
Rotival, M.4
Schillert, A.5
-
21
-
-
77952055198
-
A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: The GRACE Genetics Study
-
Buysschaert I, Carruthers KF, Dunbar DR, Peuteman G, Rietzschel E, et al. (2010) A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: The GRACE Genetics Study. Eur Heart J 31: 1132-41.
-
(2010)
Eur Heart J
, vol.31
, pp. 1132-1141
-
-
Buysschaert, I.1
Carruthers, K.F.2
Dunbar, D.R.3
Peuteman, G.4
Rietzschel, E.5
-
22
-
-
77955899532
-
A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality
-
Ellis KL, Pilbrow AP, Frampton CM, Doughty RN, Whalley GA, et al. (2010) A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality. Circ Cardiovasc Genet 3: 286-93.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 286-293
-
-
Ellis, K.L.1
Pilbrow, A.P.2
Frampton, C.M.3
Doughty, R.N.4
Whalley, G.A.5
-
23
-
-
70349512029
-
Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese
-
Peng WH, Lu L, Zhang Q, Zhang RY, Wang LJ, et al. (2009) Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese. Clin Chem Lab Med 47: 917-22.
-
(2009)
Clin Chem Lab Med
, vol.47
, pp. 917-922
-
-
Peng, W.H.1
Lu, L.2
Zhang, Q.3
Zhang, R.Y.4
Wang, L.J.5
-
24
-
-
0041353672
-
Global Registry of Acute Coronary Events Investigators. Predictors of hospital mortality in the Global Registry of Acute Coronary Events
-
Granger CB, Goldberg RJ, Dabbous O, Pieper KS, Eagle KA, et al. (2003) Global Registry of Acute Coronary Events Investigators. Predictors of hospital mortality in the Global Registry of Acute Coronary Events. Arch Intern Med 163: 2345-2353.
-
(2003)
Arch Intern Med
, vol.163
, pp. 2345-2353
-
-
Granger, C.B.1
Goldberg, R.J.2
Dabbous, O.3
Pieper, K.S.4
Eagle, K.A.5
-
25
-
-
84884192185
-
-
Available:. Accessed: 25 Jul 2013
-
Global Registry of Acute Coronary Events website. Available: http://www.outcomes-umassmed.org/GRACE/grace_risk_table.aspx. Accessed: 25 Jul 2013.
-
Global Registry of Acute Coronary Events website
-
-
-
26
-
-
84864459998
-
Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21
-
Gioli-Pereira L, Santos PC, Ferreira NE, Hueb WA, Krieger JE, et al. (2012) Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21. BMC Cardiovasc Disord 12: 61.
-
(2012)
BMC Cardiovasc Disord
, vol.12
, pp. 61
-
-
Gioli-Pereira, L.1
Santos, P.C.2
Ferreira, N.E.3
Hueb, W.A.4
Krieger, J.E.5
-
27
-
-
73449091829
-
A common variant at 9p21 is associated with sudden and arrhythmic cardiac death
-
Newton-Cheh C, Cook NR, VanDenburgh M, Rimm EB, Ridker PM, et al. (2009) A common variant at 9p21 is associated with sudden and arrhythmic cardiac death. Circulation 120: 2062-8.
-
(2009)
Circulation
, vol.120
, pp. 2062-2068
-
-
Newton-Cheh, C.1
Cook, N.R.2
VanDenburgh, M.3
Rimm, E.B.4
Ridker, P.M.5
-
28
-
-
80053316001
-
Investigators. Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction
-
Ardissino D, Berzuini C, Merlini PA, Mannuccio Mannucci P, Surti A, et al. (2011) Investigators. Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction. J Am Coll Cardiol 58: 426-34.
-
(2011)
J Am Coll Cardiol
, vol.58
, pp. 426-434
-
-
Ardissino, D.1
Berzuini, C.2
Merlini, P.A.3
Mannuccio Mannucci, P.4
Surti, A.5
-
29
-
-
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, et al. (2010) The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease. Eur Heart J 31: 3017-24.
-
(2010)
Eur Heart J
, vol.31
, pp. 3017-3024
-
-
Patel, R.S.1
Su, S.2
Neeland, I.J.3
Ahuja, A.4
Veledar, E.5
-
30
-
-
78651231695
-
Polymorphism on chromosome 9p21.3 contributes to early-onset and severity of coronary artery disease in non-diabetic and type 2 diabetic patients
-
Wang W, Peng WH, Lu L, Zhang RY, Zhang Q, et al. (2011) Polymorphism on chromosome 9p21.3 contributes to early-onset and severity of coronary artery disease in non-diabetic and type 2 diabetic patients. Chin Med J 124: 66-71.
-
(2011)
Chin Med J
, vol.124
, pp. 66-71
-
-
Wang, W.1
Peng, W.H.2
Lu, L.3
Zhang, R.Y.4
Zhang, Q.5
|