-
1
-
-
33644840046
-
Genetic susceptibility to coronary artery disease: from promise to progress
-
Watkins H., Farrall M. Genetic susceptibility to coronary artery disease: from promise to progress. Nat Rev Genet 2006, 7:163-173.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 163-173
-
-
Watkins, H.1
Farrall, M.2
-
2
-
-
0023263185
-
Coronary risk prediction in adults (the Framingham Heart Study)
-
Wilson P.W., Castelli W.P., Kannel W.B. Coronary risk prediction in adults (the Framingham Heart Study). Am J Cardiol 1987, 59:91G-94G.
-
(1987)
Am J Cardiol
, vol.59
-
-
Wilson, P.W.1
Castelli, W.P.2
Kannel, W.B.3
-
3
-
-
0029091696
-
Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation
-
Ferrieres J., Lambert J., Lussier-Cacan S., Davignon J. Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation. Circulation 1995, 92:290-295.
-
(1995)
Circulation
, vol.92
, pp. 290-295
-
-
Ferrieres, J.1
Lambert, J.2
Lussier-Cacan, S.3
Davignon, J.4
-
4
-
-
18544372620
-
A comprehensive linkage analysis for myocardial infarction and its related risk factors
-
Broeckel U., Hengstenberg C., Mayer B., et al. A comprehensive linkage analysis for myocardial infarction and its related risk factors. Nat Genet 2002, 30:210-214.
-
(2002)
Nat Genet
, vol.30
, pp. 210-214
-
-
Broeckel, U.1
Hengstenberg, C.2
Mayer, B.3
-
5
-
-
70749096913
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Kathiresan S., Voight B.F., Purcell S., 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
-
6
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
Willer C.J., Sanna S., Jackson A.U., et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet 2008, 40:161-169.
-
(2008)
Nat Genet
, vol.40
, pp. 161-169
-
-
Willer, C.J.1
Sanna, S.2
Jackson, A.U.3
-
7
-
-
58249135635
-
Cytochrome P450 2C19 polymorphism in young patients treated with clopidogrel after myocardial infarction: a cohort study
-
Collet J.P., Hulot J.S., Pena A., et al. Cytochrome P450 2C19 polymorphism in young patients treated with clopidogrel after myocardial infarction: a cohort study. Lancet 2009, 373:309-317.
-
(2009)
Lancet
, vol.373
, pp. 309-317
-
-
Collet, J.P.1
Hulot, J.S.2
Pena, A.3
-
8
-
-
10744233196
-
Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis
-
Wang Q., Rao S., Shen G.Q., et al. Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis. Am J Hum Genet 2004, 74:262-271.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 262-271
-
-
Wang, Q.1
Rao, S.2
Shen, G.Q.3
-
9
-
-
0141919767
-
Meta-analysis of 4 coronary heart disease genome-wide linkage studies confirms a susceptibility locus on chromosome 3q
-
Chiodini B.D., Lewis C.M. Meta-analysis of 4 coronary heart disease genome-wide linkage studies confirms a susceptibility locus on chromosome 3q. Arterioscler Thromb Vasc Biol 2003, 23:1863-1868.
-
(2003)
Arterioscler Thromb Vasc Biol
, vol.23
, pp. 1863-1868
-
-
Chiodini, B.D.1
Lewis, C.M.2
-
10
-
-
0036094165
-
Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2
-
Harrap S.B., Zammit K.S., Wong Z.Y., et al. Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2. Arterioscler Thromb Vasc Biol 2002, 22:874-878.
-
(2002)
Arterioscler Thromb Vasc Biol
, vol.22
, pp. 874-878
-
-
Harrap, S.B.1
Zammit, K.S.2
Wong, Z.Y.3
-
11
-
-
0035717515
-
Genome-wide linkage analysis reveals evidence of multiple regions that influence variation in plasma lipid and apolipoprotein levels associated with risk of coronary heart disease
-
Klos K.L., Kardia S.L., Ferrell R.E., et al. Genome-wide linkage analysis reveals evidence of multiple regions that influence variation in plasma lipid and apolipoprotein levels associated with risk of coronary heart disease. Arterioscler Thromb Vasc Biol 2001, 21:971-978.
-
(2001)
Arterioscler Thromb Vasc Biol
, vol.21
, pp. 971-978
-
-
Klos, K.L.1
Kardia, S.L.2
Ferrell, R.E.3
-
12
-
-
77953072265
-
A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease
-
Mathias R.A., Kim Y., Sung H., et al. A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease. BMC Med Genomics 2010, 3:22.
-
(2010)
BMC Med Genomics
, vol.3
, pp. 22
-
-
Mathias, R.A.1
Kim, Y.2
Sung, H.3
-
13
-
-
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
-
14
-
-
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
-
15
-
-
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 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
-
16
-
-
58149161560
-
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
-
Aulchenko Y.S., Ripatti S., Lindqvist I., et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet 2009, 41:47-55.
-
(2009)
Nat Genet
, vol.41
, pp. 47-55
-
-
Aulchenko, Y.S.1
Ripatti, S.2
Lindqvist, I.3
-
17
-
-
61349177857
-
New susceptibility locus for coronary artery disease on chromosome 3q22.3
-
Erdmann J., Grosshennig A., Braund P.S., et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 2009, 41:280-282.
-
(2009)
Nat Genet
, vol.41
, pp. 280-282
-
-
Erdmann, J.1
Grosshennig, A.2
Braund, P.S.3
-
18
-
-
61349137526
-
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease
-
Tregouet D.A., Konig I.R., Erdmann J., et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet 2009, 41:283-285.
-
(2009)
Nat Genet
, vol.41
, pp. 283-285
-
-
Tregouet, D.A.1
Konig, I.R.2
Erdmann, J.3
-
19
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
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. The Wellcome Trust Case Control Consortium.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
20
-
-
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 2008, 117:1675-1684.
-
(2008)
Circulation
, vol.117
, pp. 1675-1684
-
-
Schunkert, H.1
Gotz, A.2
Braund, P.3
-
21
-
-
73649141739
-
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease
-
Linsel-Nitschke P., Heeren J., Aherrahrou Z., et al. Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. Atherosclerosis 2009, 208:183-189.
-
(2009)
Atherosclerosis
, vol.208
, pp. 183-189
-
-
Linsel-Nitschke, P.1
Heeren, J.2
Aherrahrou, Z.3
-
22
-
-
70349569056
-
Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus
-
Jarinova O., Stewart A.F., 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.2
Roberts, R.3
-
23
-
-
33847144011
-
Generation of transgenic mice for cardiovascular research
-
Tian X.L., Wang Q.K. Generation of transgenic mice for cardiovascular research. Methods Mol Med 2006, 129:69-81.
-
(2006)
Methods Mol Med
, vol.129
, pp. 69-81
-
-
Tian, X.L.1
Wang, Q.K.2
-
24
-
-
70350359126
-
Genetic association of FOXO1A and FOXO3A with longevity trait in Han Chinese populations
-
Li Y., Wang W.J., Cao H., et al. Genetic association of FOXO1A and FOXO3A with longevity trait in Han Chinese populations. Hum Mol Genet 2009, 18:4897-4904.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4897-4904
-
-
Li, Y.1
Wang, W.J.2
Cao, H.3
-
25
-
-
0002294347
-
A simple sequentially rejective Bonferroni test procedure
-
Holm S. A simple sequentially rejective Bonferroni test procedure. Scand J Stat 1979, 65-70.
-
(1979)
Scand J Stat
, pp. 65-70
-
-
Holm, S.1
-
26
-
-
40749097651
-
Methods for handling multiple testing
-
Rice T.K., Schork N.J., Rao D.C. Methods for handling multiple testing. Adv Genet 2008, 60:293-308.
-
(2008)
Adv Genet
, vol.60
, pp. 293-308
-
-
Rice, T.K.1
Schork, N.J.2
Rao, D.C.3
-
27
-
-
56049111301
-
Structural characterization of soluble E-Syt2
-
Groer G.J., Haslbeck M., Roessle M., Gessner A. Structural characterization of soluble E-Syt2. FEBS Lett 2008, 582:3941-3947.
-
(2008)
FEBS Lett
, vol.582
, pp. 3941-3947
-
-
Groer, G.J.1
Haslbeck, M.2
Roessle, M.3
Gessner, A.4
-
29
-
-
0030729777
-
Novel small GTPase M-Ras participates in reorganization of actin cytoskeleton
-
Matsumoto K., Asano T., Endo T. Novel small GTPase M-Ras participates in reorganization of actin cytoskeleton. Oncogene 1997, 15:2409-2417.
-
(1997)
Oncogene
, vol.15
, pp. 2409-2417
-
-
Matsumoto, K.1
Asano, T.2
Endo, T.3
-
30
-
-
33745728166
-
Silencing of Peroxiredoxin 2 and aberrant methylation of 33 CpG islands in putative promoter regions in human malignant melanomas
-
Furuta J., Nobeyama Y., Umebayashi Y., et al. Silencing of Peroxiredoxin 2 and aberrant methylation of 33 CpG islands in putative promoter regions in human malignant melanomas. Cancer Res 2006, 66:6080-6086.
-
(2006)
Cancer Res
, vol.66
, pp. 6080-6086
-
-
Furuta, J.1
Nobeyama, Y.2
Umebayashi, Y.3
|