-
1
-
-
60349120503
-
Association of genetic variation on chromosome 9p21.3 and arterial stiffness
-
Bjorck HM, Lanne T, Alehagen U, Persson K, et al. (2009). Association of genetic variation on chromosome 9p21.3 and arterial stiffness. J. Intern. Med. 265: 373-381.
-
(2009)
J. Intern. Med
, vol.265
, pp. 373-381
-
-
Bjorck, H.M.1
Lanne, T.2
Alehagen, U.3
Persson, K.4
-
2
-
-
33748053016
-
GATA2 is associated with familial early-onset coronary artery disease
-
Connelly JJ, Wang T, Cox JE, Haynes C, et al. (2006). GATA2 is associated with familial early-onset coronary artery disease. PLoS Genet. 2: e139.
-
(2006)
PLoS Genet
, vol.2
-
-
Connelly, J.J.1
Wang, T.2
Cox, J.E.3
Haynes, C.4
-
3
-
-
77449156564
-
The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies
-
Dandona S, Chen L, Fan M, Alam MA, et al. (2010). The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies. Hum. Genet. 127: 101-105.
-
(2010)
Hum. Genet
, vol.127
, pp. 101-105
-
-
Dandona, S.1
Chen, L.2
Fan, M.3
Alam, M.A.4
-
4
-
-
77149122355
-
9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population. Circ. Cardiovasc
-
Ding H, Xu Y, Wang X, Wang Q, et al. (2009). 9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population. Circ. Cardiovasc. Genet. 2: 338-346.
-
(2009)
Genet
, vol.2
, pp. 338-346
-
-
Ding, H.1
Xu, Y.2
Wang, X.3
Wang, Q.4
-
5
-
-
77953845368
-
Association of the polymorphism of synaptobrevins/vesicle-associated membrane proteins 8 gene with coronary heart disease in Chinese Han population
-
Duan CC, Xu LX and Chen Q (2010). Association of the polymorphism of synaptobrevins/vesicle-associated membrane proteins 8 gene with coronary heart disease in Chinese Han population. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 27: 329-332.
-
(2010)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.27
, pp. 329-332
-
-
Duan, C.C.1
Xu, L.X.2
Chen, Q.3
-
6
-
-
0031661313
-
E1B 55-kilodalton-associated protein: A cellular protein with RNA-binding activity implicated in nucleocytoplasmic transport of adenovirus and cellular mRNAs
-
Gabler S, Schutt H, Groitl P, Wolf H, et al. (1998). E1B 55-kilodalton-associated protein: a cellular protein with RNA-binding activity implicated in nucleocytoplasmic transport of adenovirus and cellular mRNAs. J. Virol. 72: 7960-7971.
-
(1998)
J. Virol
, vol.72
, pp. 7960-7971
-
-
Gabler, S.1
Schutt, H.2
Groitl, P.3
Wolf, H.4
-
7
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, et al. (2007). A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 316: 1491-1493.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
-
8
-
-
0141739796
-
Haplotypes and the systematic analysis of genetic variation in genes and genomes
-
Hoehe MR (2003). Haplotypes and the systematic analysis of genetic variation in genes and genomes. Pharmacogenomics 4: 547-570.
-
(2003)
Pharmacogenomics
, vol.4
, pp. 547-570
-
-
Hoehe, M.R.1
-
9
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, et al. (2007). A common allele on chromosome 9 associated with coronary heart disease. Science 316: 1488-1491.
-
(2007)
Science
, vol.316
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
Stewart, A.4
-
10
-
-
0036792816
-
On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles
-
Morris RW and Kaplan NL (2002). On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles. Genet. Epidemiol. 23: 221-233.
-
(2002)
Genet. Epidemiol
, vol.23
, pp. 221-233
-
-
Morris, R.W.1
Kaplan, N.L.2
-
11
-
-
0036683001
-
Vesicle-associated membrane protein 3 (VAMP-3) and VAMP-8 are present in human platelets and are required for granule secretion
-
Polgar J, Chung SH and Reed GL (2002). Vesicle-associated membrane protein 3 (VAMP-3) and VAMP-8 are present in human platelets and are required for granule secretion. Blood 100: 1081-1083.
-
(2002)
Blood
, vol.100
, pp. 1081-1083
-
-
Polgar, J.1
Chung, S.H.2
Reed, G.L.3
-
12
-
-
33846857559
-
Heart disease and stroke statistics - 2007 update: A report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee
-
Rosamond W, Flegal K, Friday G, Furie K, et al. (2007). Heart disease and stroke statistics - 2007 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation 115: e69-171.
-
(2007)
Circulation
, vol.115
-
-
Rosamond, W.1
Flegal, K.2
Friday, G.3
Furie, K.4
-
13
-
-
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, 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
-
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. Arterioscler Thromb
-
Shen GQ, Li L, Rao S, Abdullah KG, et al. (2008a). 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: 360-365.
-
(2008)
Vasc. Biol
, vol.28
, pp. 360-365
-
-
Shen, G.Q.1
Li, L.2
Rao, S.3
Abdullah, K.G.4
-
15
-
-
38949209549
-
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population
-
Shen GQ, Rao S, Martinelli N, Li L, et al. (2008b). Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population. J. Hum. Genet. 53: 144-150.
-
(2008)
J. Hum. Genet
, vol.53
, pp. 144-150
-
-
Shen, G.Q.1
Rao, S.2
Martinelli, N.3
Li, L.4
-
16
-
-
33745948419
-
Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction. Arterioscler Thromb
-
Shiffman D, Rowland CM, Louie JZ, Luke MM, et al. (2006). Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction. Arterioscler Thromb. Vasc. Biol. 26: 1613-1618.
-
(2006)
Vasc. Biol
, vol.26
, pp. 1613-1618
-
-
Shiffman, D.1
Rowland, C.M.2
Louie, J.Z.3
Luke, M.M.4
-
17
-
-
33846921101
-
Gene-environment interaction and its impact on coronary heart disease risk
-
Talmud PJ (2007). Gene-environment interaction and its impact on coronary heart disease risk. Nutr. Metab. Cardiovasc. Dis. 17: 148-152.
-
(2007)
Nutr. Metab. Cardiovasc. Dis
, vol.17
, pp. 148-152
-
-
Talmud, P.J.1
-
18
-
-
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, Howard VJ, et al. (2006). Heart disease and stroke statistics - 2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation 113: e85-151.
-
(2006)
Circulation
, vol.113
-
-
Thom, T.1
Haase, N.2
Rosamond, W.3
Howard, V.J.4
-
19
-
-
33749018788
-
Genetic susceptibility to myocardial infarction and coronary artery disease
-
Spec. No. 2
-
Topol EJ, Smith J, Plow EF and Wang QK (2006). Genetic susceptibility to myocardial infarction and coronary artery disease. Hum. Mol. Genet. 15 (Spec. No. 2): R117-R123.
-
(2006)
Hum. Mol. Genet
, vol.15
-
-
Topol, E.J.1
Smith, J.2
Plow, E.F.3
Wang, Q.K.4
-
20
-
-
84858981200
-
Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease
-
Virani SS, Brautbar A, Lee VV, MacArthur E, et al. (2012). Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease. Circ. J. 76:950-956.
-
(2012)
Circ. J
, vol.76
, pp. 950-956
-
-
Virani, S.S.1
Brautbar, A.2
Lee, V.V.3
Macarthur, E.4
-
21
-
-
34147144860
-
Peakwide mapping on chromosome 3q13 identifes the kalirin gene as a novel candidate gene for coronary artery disease
-
Wang L, Hauser ER, Shah SH, Pericak-Vance MA, et al. (2007). Peakwide mapping on chromosome 3q13 identifes the kalirin gene as a novel candidate gene for coronary artery disease. Am. J. Hum. Genet. 80: 650-663.
-
(2007)
Am. J. Hum. Genet
, vol.80
, pp. 650-663
-
-
Wang, L.1
Hauser, E.R.2
Shah, S.H.3
Pericak-Vance, M.A.4
-
22
-
-
0035960630
-
Global burden of cardiovascular diseases: Part I: General considerations, the epidemiologic transition, risk factors, and impact of urbanization
-
Yusuf S, Reddy S, Ôunpuu S and Anand S (2001). Global burden of cardiovascular diseases: Part I: general considerations, the epidemiologic transition, risk factors, and impact of urbanization. Circulation 104: 2746-2753.
-
(2001)
Circulation
, vol.104
, pp. 2746-2753
-
-
Yusuf, S.1
Reddy, S.2
Ôunpuu, S.3
Anand, S.4
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