-
1
-
-
67649516363
-
Estudio del componente genético de la cardiopatía isquémica: De los estudios de ligamiento al genotipado integral del genoma
-
R. Elosua, C. Lluís, and G. Lucas Estudio del componente genético de la cardiopatía isquémica: de los estudios de ligamiento al genotipado integral del genoma Rev Esp Cardiol Supl. 9 Supl B 2009 B24 38
-
(2009)
Rev Esp Cardiol Supl.
, vol.9
, Issue.SUPPL. B
, pp. 24-38
-
-
Elosua, R.1
Lluís, C.2
Lucas, G.3
-
2
-
-
61349177857
-
New susceptibility locus for coronary artery disease on chromosome 3q22.3
-
J. Erdmann, A. Grosshennig, P.S. Braund, I.R. Konig, C. Hengstenberg, and A.S. Hall New susceptibility locus for coronary artery disease on chromosome 3q22.3 Nat Genet 41 2009 280 282
-
(2009)
Nat Genet
, vol.41
, pp. 280-282
-
-
Erdmann, J.1
Grosshennig, A.2
Braund, P.S.3
Konig, I.R.4
Hengstenberg, C.5
Hall, A.S.6
-
3
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
DOI 10.1126/science.1142842
-
A. Helgadottir, G. Thorleifsson, A. Manolescu, S. Gretarsdottir, T. Blondal, and A. Jonasdottir A common variant on chromosome 9p21 affects the risk of myocardial infarction Science 316 2007 1491 1493 (Pubitemid 46906618)
-
(2007)
Science
, vol.316
, Issue.5830
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
Jonasdottir, A.7
Sigurdsson, A.8
Baker, A.9
Palsson, A.10
Masson, G.11
Gudbjartsson, D.F.12
Magnusson, K.P.13
Andersen, K.14
Levey, A.I.15
Backman, V.M.16
Matthiasdottir, S.17
Jonsdottir, T.18
Palsson, S.19
Einarsdottir, H.20
Gunnarsdottir, S.21
Gylfason, A.22
Vaccarino, V.23
Hooper, W.C.24
Reilly, M.P.25
Granger, C.B.26
Austin, H.27
Rader, D.J.28
Shah, S.H.29
Quyyumi, A.A.30
Gulcher, J.R.31
Thorgeirsson, G.32
Thorsteinsdottir, U.33
Kong, A.34
Stefansson, K.35
more..
-
4
-
-
70749096913
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
S. Kathiresan, B.F. Voight, S. Purcell, K. Musunuru, D. Ardissino, and P.M. Mannucci Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Nat Genet 41 2009 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
-
5
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
R. McPherson, A. Pertsemlidis, N. Kavaslar, A. Stewart, R. Roberts, and D.R. Cox A common allele on chromosome 9 associated with coronary heart disease Science 316 2007 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
-
6
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
DOI 10.1056/NEJMoa072366
-
N.J. Samani, J. Erdmann, A.S. Hall, C. Hengstenberg, M. Mangino, and B. Mayer Genomewide association analysis of coronary artery disease N Engl J Med 357 2007 443 453 (Pubitemid 47204873)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.5
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
Dixon, R.J.7
Meitinger, T.8
Braund, P.9
Wichmann, H.-E.10
Barrett, J.H.11
Konig, I.R.12
Stevens, S.E.13
Szymczak, S.14
Tregouet, D.-A.15
Iles, M.M.16
Pahlke, F.17
Pollard, H.18
Lieb, W.19
Cambien, F.20
Fischer, M.21
Ouwehand, W.22
Blankenberg, S.23
Balmforth, A.J.24
Baessler, A.25
Ball, S.G.26
Strom, T.M.27
Braenne, I.28
Gieger, C.29
Deloukas, P.30
Tobin, M.D.31
Ziegler, A.32
Thompson, J.R.33
Schunkert, H.34
more..
-
7
-
-
61349137526
-
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease
-
D.A. Tregouet, I.R. Konig, J. Erdmann, A. Munteanu, P.S. Braund, and A.S. Hall Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease Nat Genet 41 2009 283 285
-
(2009)
Nat Genet
, vol.41
, pp. 283-285
-
-
Tregouet, D.A.1
Konig, I.R.2
Erdmann, J.3
Munteanu, A.4
Braund, P.S.5
Hall, A.S.6
-
8
-
-
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 447 2007 661 678
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
9
-
-
39749142228
-
The search for new cardiovascular biomarkers
-
R.E. Gerszten, and T.J. Wang The search for new cardiovascular biomarkers Nature 451 2008 949 952
-
(2008)
Nature
, vol.451
, pp. 949-952
-
-
Gerszten, R.E.1
Wang, T.J.2
-
10
-
-
0041766795
-
An adaptation of the Framingham coronary heart disease risk function to European Mediterranean areas
-
J. Marrugat, R. D'Agostino, L. Sullivan, R. Elosua, P. Wilson, and J. Ordovas An adaptation of the Framingham coronary heart disease risk function to European Mediterranean areas J Epidemiol Community Health 57 2003 634 638
-
(2003)
J Epidemiol Community Health
, vol.57
, pp. 634-638
-
-
Marrugat, J.1
D'Agostino, R.2
Sullivan, L.3
Elosua, R.4
Wilson, P.5
Ordovas, J.6
-
11
-
-
66349111734
-
Criteria for evaluation of novel markers of cardiovascular risk: A scientific statement from the American Heart Association
-
M.A. Hlatky, P. Greenland, D.K. Arnett, C.M. Ballantyne, M.H. Criqui, and M.S. Elkind Criteria for evaluation of novel markers of cardiovascular risk: a scientific statement from the American Heart Association Circulation 119 2009 2408 2416
-
(2009)
Circulation
, vol.119
, pp. 2408-2416
-
-
Hlatky, M.A.1
Greenland, P.2
Arnett, D.K.3
Ballantyne, C.M.4
Criqui, M.H.5
Elkind, M.S.6
-
12
-
-
32144461525
-
Cohort profile: 1958 British birth cohort (National Child Development Study)
-
C. Power, and J. Elliott Cohort profile: 1958 British birth cohort (National Child Development Study) Int J Epidemiol 35 2006 34 41
-
(2006)
Int J Epidemiol
, vol.35
, pp. 34-41
-
-
Power, C.1
Elliott, J.2
-
13
-
-
77957107429
-
-
EMBL-EBI. EMBL-EBI website [citado 2 Dic 2009]. Disponible en
-
EMBL-EBI. EMBL-EBI website [citado 2 Dic 2009]. Disponible en: http://www.ebi.ac.uk/ega/page.php?page=studies&name=WTCCCe
-
-
-
-
15
-
-
34047179603
-
SNPassoc: An R package to perform whole genome association studies
-
J.R. Gonzalez, L. Armengol, X. Sole, E. Guino, J.M. Mercader, and X. Estivill SNPassoc: an R package to perform whole genome association studies Bioinformatics 23 2007 644 645
-
(2007)
Bioinformatics
, vol.23
, pp. 644-645
-
-
Gonzalez, J.R.1
Armengol, L.2
Sole, X.3
Guino, E.4
Mercader, J.M.5
Estivill, X.6
-
16
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
C. Newton-Cheh, T. Johnson, V. Gateva, M.D. Tobin, M. Bochud, and L. Coin Genome-wide association study identifies eight loci associated with blood pressure Nat Genet 41 2009 666 676
-
(2009)
Nat Genet
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
Johnson, T.2
Gateva, V.3
Tobin, M.D.4
Bochud, M.5
Coin, L.6
-
17
-
-
75749086085
-
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
-
J. Dupuis, C. Langenberg, I. Prokopenko, R. Saxena, N. Soranzo, and A.U. Jackson New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Nat Genet 42 2010 105 116
-
(2010)
Nat Genet
, vol.42
, pp. 105-116
-
-
Dupuis, J.1
Langenberg, C.2
Prokopenko, I.3
Saxena, R.4
Soranzo, N.5
Jackson, A.U.6
-
18
-
-
65349192772
-
Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry
-
M.C. Cornelis, L. Qi, C. Zhang, P. Kraft, J. Manson, and T. Cai Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry Ann Intern Med 150 2009 541 550
-
(2009)
Ann Intern Med
, vol.150
, pp. 541-550
-
-
Cornelis, M.C.1
Qi, L.2
Zhang, C.3
Kraft, P.4
Manson, J.5
Cai, T.6
-
19
-
-
0037510020
-
Estimación del riesgo coronario en España mediante la ecuación de Framingham calibrada
-
DOI 10.1157/13043951
-
J. Marrugat, P. Solanas, R. D'Agostino, L. Sullivan, J. Ordovás, and F. Cordón Estimación del riesgo coronario en España mediante la ecuación de Framingham calibrada Rev Esp Cardiol 56 2003 253 261 (Pubitemid 36527246)
-
(2003)
Revista Espanola de Cardiologia
, vol.56
, Issue.3
, pp. 253-261
-
-
Marrugat, J.1
Solanas, P.2
D'Agostino, R.3
Sullivan, L.4
Ordovas, J.5
Cordon, F.6
Ramos, R.7
Sala, J.8
Masia, R.9
Rohlfs, I.10
Elosua, R.11
Kannel, W.B.12
-
20
-
-
70449513058
-
Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study
-
A. Brautbar, C.M. Ballantyne, K. Lawson, V. Nambi, L. Chambless, and A.R. Folsom Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study Circ Cardiovasc Genet 2 2009 279 285
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 279-285
-
-
Brautbar, A.1
Ballantyne, C.M.2
Lawson, K.3
Nambi, V.4
Chambless, L.5
Folsom, A.R.6
-
21
-
-
58749087343
-
Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3
-
N.P. Paynter, D.I. Chasman, J.E. Buring, D. Shiffman, N.R. Cook, and P.M. Ridker Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3 Ann Intern Med 150 2009 65 72
-
(2009)
Ann Intern Med
, vol.150
, pp. 65-72
-
-
Paynter, N.P.1
Chasman, D.I.2
Buring, J.E.3
Shiffman, D.4
Cook, N.R.5
Ridker, P.M.6
-
22
-
-
40449095630
-
Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men
-
P.J. Talmud, J.A. Cooper, J. Palmen, R. Lovering, F. Drenos, and A.D. Hingorani Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men Clin Chem 54 2008 467 474
-
(2008)
Clin Chem
, vol.54
, pp. 467-474
-
-
Talmud, P.J.1
Cooper, J.A.2
Palmen, J.3
Lovering, R.4
Drenos, F.5
Hingorani, A.D.6
-
23
-
-
34547555885
-
Prediction of coronary heart disease risk using a genetic risk score: The Atherosclerosis Risk in Communities Study
-
A.C. Morrison, L.A. Bare, L.E. Chambless, S.G. Ellis, M. Malloy, and J.P. Kane Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities Study Am J Epidemiol 166 2007 28 35
-
(2007)
Am J Epidemiol
, vol.166
, pp. 28-35
-
-
Morrison, A.C.1
Bare, L.A.2
Chambless, L.E.3
Ellis, S.G.4
Malloy, M.5
Kane, J.P.6
-
24
-
-
40949149395
-
Polymorphisms associated with cholesterol and risk of cardiovascular events
-
S. Kathiresan, O. Melander, D. Anevski, C. Guiducci, N.P. Burtt, and C. Roos Polymorphisms associated with cholesterol and risk of cardiovascular events N Engl J Med 358 2008 1240 1249
-
(2008)
N Engl J Med
, vol.358
, pp. 1240-1249
-
-
Kathiresan, S.1
Melander, O.2
Anevski, D.3
Guiducci, C.4
Burtt, N.P.5
Roos, C.6
-
25
-
-
58149161560
-
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
-
Y.S. Aulchenko, S. Ripatti, I. Lindqvist, D. Boomsma, I.M. Heid, and P.P. Pramstaller Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Nat Genet 41 2009 47 55
-
(2009)
Nat Genet
, vol.41
, pp. 47-55
-
-
Aulchenko, Y.S.1
Ripatti, S.2
Lindqvist, I.3
Boomsma, D.4
Heid, I.M.5
Pramstaller, P.P.6
-
26
-
-
77149120471
-
Association between a literature-based genetic risk score and cardiovascular events in women
-
N.P. Paynter, D.I. Chasman, G. Pare, J.E. Buring, N.R. Cook, and J.P. Miletich Association between a literature-based genetic risk score and cardiovascular events in women JAMA 303 2010 631 637
-
(2010)
JAMA
, vol.303
, pp. 631-637
-
-
Paynter, N.P.1
Chasman, D.I.2
Pare, G.3
Buring, J.E.4
Cook, N.R.5
Miletich, J.P.6
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