-
1
-
-
33646799069
-
Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data
-
Lopez A.D., Mathers C.D., Ezzati M., Jamison D.T., and Murray C.J. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet 367 (2006) 1747-1757
-
(2006)
Lancet
, vol.367
, pp. 1747-1757
-
-
Lopez, A.D.1
Mathers, C.D.2
Ezzati, M.3
Jamison, D.T.4
Murray, C.J.5
-
2
-
-
72949132104
-
Factors of risk in the development of coronary heart disease-six year follow-up experience. The Framingham Study
-
Kannel W.B., Dawber T.R., Kagan A., Revotskie N., and Stokes III J. Factors of risk in the development of coronary heart disease-six year follow-up experience. The Framingham Study. Ann Intern Med 55 (1961) 33-50
-
(1961)
Ann Intern Med
, vol.55
, pp. 33-50
-
-
Kannel, W.B.1
Dawber, T.R.2
Kagan, A.3
Revotskie, N.4
Stokes III, J.5
-
3
-
-
0034945516
-
Validation of the Framingham coronary heart disease prediction scores: results of a multiple ethnic groups investigation
-
D'Agostino Sr. R.B., Grundy S., Sullivan L.M., and Wilson P. Validation of the Framingham coronary heart disease prediction scores: results of a multiple ethnic groups investigation. JAMA 286 (2001) 180-187
-
(2001)
JAMA
, vol.286
, pp. 180-187
-
-
D'Agostino Sr., R.B.1
Grundy, S.2
Sullivan, L.M.3
Wilson, P.4
-
4
-
-
2542437775
-
Predictive value for the Chinese population of the Framingham CHD risk assessment tool compared with the Chinese Multi-Provincial Cohort Study
-
Liu J., Hong Y., D'Agostino Sr. R.B., Wu Z., Wang W., Sun J., et al. Predictive value for the Chinese population of the Framingham CHD risk assessment tool compared with the Chinese Multi-Provincial Cohort Study. JAMA 291 (2004) 2591-2599
-
(2004)
JAMA
, vol.291
, pp. 2591-2599
-
-
Liu, J.1
Hong, Y.2
D'Agostino Sr., R.B.3
Wu, Z.4
Wang, W.5
Sun, J.6
-
5
-
-
0038579421
-
Estimation of ten-year risk of fatal cardiovascular disease in Europe: the SCORE project
-
Conroy R.M., Pyörälä K., Fitzgerald A.P., Sans S., Menotti A., De Backer G., et al. Estimation of ten-year risk of fatal cardiovascular disease in Europe: the SCORE project. Eur Heart J 24 (2003) 987-1003
-
(2003)
Eur Heart J
, vol.24
, pp. 987-1003
-
-
Conroy, R.M.1
Pyörälä, K.2
Fitzgerald, A.P.3
Sans, S.4
Menotti, A.5
De Backer, G.6
-
6
-
-
0032510639
-
Prediction of coronary heart disease using risk factor categories
-
Wilson P.W., D'Agostino R.B., Levy D., Belanger A.M., Silbershatz H., and Kannel W.B. Prediction of coronary heart disease using risk factor categories. Circulation 97 (1998) 1837-1847
-
(1998)
Circulation
, vol.97
, pp. 1837-1847
-
-
Wilson, P.W.1
D'Agostino, R.B.2
Levy, D.3
Belanger, A.M.4
Silbershatz, H.5
Kannel, W.B.6
-
7
-
-
4444382796
-
Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study
-
Yusuf S., Hawken S., Ounpuu S., Dans T., Avezum A., Lanas F., et al. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet 364 (2004) 937-952
-
(2004)
Lancet
, vol.364
, pp. 937-952
-
-
Yusuf, S.1
Hawken, S.2
Ounpuu, S.3
Dans, T.4
Avezum, A.5
Lanas, F.6
-
8
-
-
0035943071
-
Maternal and paternal history of myocardial infarction and risk of cardiovascular disease in men and women
-
Sesso H.D., Lee I.M., Gaziano J.M., Rexrode K.M., Glynn R.J., and Buring J.E. Maternal and paternal history of myocardial infarction and risk of cardiovascular disease in men and women. Circulation 104 (2001) 393-398
-
(2001)
Circulation
, vol.104
, pp. 393-398
-
-
Sesso, H.D.1
Lee, I.M.2
Gaziano, J.M.3
Rexrode, K.M.4
Glynn, R.J.5
Buring, J.E.6
-
9
-
-
0035015076
-
Family history as a risk factor for early onset myocardial infarction in young women
-
Friedlander Y., Arbogast P., Schwartz S.M., Marcovina S.M., Austin M.A., Rosendaal F.R., et al. Family history as a risk factor for early onset myocardial infarction in young women. Atherosclerosis 156 (2001) 201-207
-
(2001)
Atherosclerosis
, vol.156
, pp. 201-207
-
-
Friedlander, Y.1
Arbogast, P.2
Schwartz, S.M.3
Marcovina, S.M.4
Austin, M.A.5
Rosendaal, F.R.6
-
10
-
-
0018749850
-
Familial occurrence of coronary heart disease: effect of age at diagnosis
-
Rissanen A.M. Familial occurrence of coronary heart disease: effect of age at diagnosis. Am J Cardiol 44 (1979) 60-66
-
(1979)
Am J Cardiol
, vol.44
, pp. 60-66
-
-
Rissanen, A.M.1
-
11
-
-
29544440820
-
Sibling cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults
-
Murabito J.M., Pencina M.J., Nam B.H., D'Agostino Sr. R.B., Wang T.J., Lloyd-Jones D., et al. Sibling cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults. JAMA 294 (2005) 3117-3123
-
(2005)
JAMA
, vol.294
, pp. 3117-3123
-
-
Murabito, J.M.1
Pencina, M.J.2
Nam, B.H.3
D'Agostino Sr., R.B.4
Wang, T.J.5
Lloyd-Jones, D.6
-
12
-
-
0028330005
-
Genetic susceptibility to death from coronary heart disease in a study of twins
-
Marenberg M.E., Risch N., Berkman L.F., Floderus B., and de Faire U. Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med 330 (1994) 1041-1046
-
(1994)
N Engl J Med
, vol.330
, pp. 1041-1046
-
-
Marenberg, M.E.1
Risch, N.2
Berkman, L.F.3
Floderus, B.4
de Faire, U.5
-
13
-
-
16444371114
-
The heritability of CHD mortality in Danish twins after controlling for smoking and BMI
-
Wienke A., Herskind A.M., Christensen K., Skytthe A., and Yashin A.I. The heritability of CHD mortality in Danish twins after controlling for smoking and BMI. Twin Res Hum Genet 8 (2005) 53-59
-
(2005)
Twin Res Hum Genet
, vol.8
, pp. 53-59
-
-
Wienke, A.1
Herskind, A.M.2
Christensen, K.3
Skytthe, A.4
Yashin, A.I.5
-
14
-
-
0037418247
-
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
-
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group
-
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group. No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age. Circulation 107 (2003) 1117-1122
-
(2003)
Circulation
, vol.107
, pp. 1117-1122
-
-
-
15
-
-
33846185489
-
Genetics of ischaemic stroke
-
Dichgans M. Genetics of ischaemic stroke. Lancet Neurol 6 (2007) 149-161
-
(2007)
Lancet Neurol
, vol.6
, pp. 149-161
-
-
Dichgans, M.1
-
16
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Sequencing Consortium
-
International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome. Nature 409 (2001) 860-921
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
-
17
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R., Ishikawa S., Fitch K.R., Feuk L., Perry G.H., Andrews T.D., et al. Global variation in copy number in the human genome. Nature 444 (2006) 444-454
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
-
18
-
-
79959524146
-
A haplotype map of the human genome
-
International HapMap Consortium
-
International HapMap Consortium. A haplotype map of the human genome. Nature 437 (2005) 1299-1320
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
19
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
International HapMap Consortium
-
International HapMap Consortium. A second generation human haplotype map of over 3.1 million SNPs. Nature 449 (2007) 851-861
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
-
20
-
-
65949104586
-
Genomewide association studies and human disease
-
Hardy J., and Singleton A. Genomewide association studies and human disease. N Engl J Med 360 (2009) 1759-1768
-
(2009)
N Engl J Med
, vol.360
, pp. 1759-1768
-
-
Hardy, J.1
Singleton, A.2
-
21
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn J.N., and Daly M.J. Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 6 (2005) 95-108
-
(2005)
Nat Rev Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
22
-
-
34247144499
-
Non validation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study
-
Morgan T.M., Krumholz H.M., Lifton R.P., and Spertus J.A. Non validation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study. JAMA 297 (2007) 1551-1561
-
(2007)
JAMA
, vol.297
, pp. 1551-1561
-
-
Morgan, T.M.1
Krumholz, H.M.2
Lifton, R.P.3
Spertus, J.A.4
-
23
-
-
0027407565
-
Apolipoprotein E: high-avidity binding to β-amyloid and increased frequency of type 4 allele in late-onset Alzheimer disease
-
Strittmatter W.J., Saunders A.M., Schmechel D., Pericak-Vance M., Enghild J., Salvesen G.S., et al. Apolipoprotein E: high-avidity binding to β-amyloid and increased frequency of type 4 allele in late-onset Alzheimer disease. Proc Natl Acad Sci USA 90 (1993) 1977-1981
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 1977-1981
-
-
Strittmatter, W.J.1
Saunders, A.M.2
Schmechel, D.3
Pericak-Vance, M.4
Enghild, J.5
Salvesen, G.S.6
-
24
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder E.H., Saunders A.M., Strittmatter W.J., Schmechel D.E., Gaskell P.C., Small G.W., et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science 261 (1993) 921-923
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
Small, G.W.6
-
25
-
-
77649182817
-
Factor V Leiden, but not prothrombin G20120A, is associated with premature myocardial infarction
-
Spreafico M., Peyvandi F., Foco L., Bernardinelli L., Duga S., Asselta S., et al. Factor V Leiden, but not prothrombin G20120A, is associated with premature myocardial infarction. Circulation 118 (2008) S_956
-
(2008)
Circulation
, vol.118
-
-
Spreafico, M.1
Peyvandi, F.2
Foco, L.3
Bernardinelli, L.4
Duga, S.5
Asselta, S.6
-
27
-
-
42349112088
-
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
-
McCarthy M.I., Abecasis G.R., Cardon L.R., Goldstein D.B., Little J., Ioannidis J.P., et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet 9 (2008) 356-369
-
(2008)
Nat Rev Genet
, vol.9
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
Goldstein, D.B.4
Little, J.5
Ioannidis, J.P.6
-
28
-
-
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 447 (2007) 661-678
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
29
-
-
58049217860
-
-
Available at:, accessed
-
Hindorff, L.A., Junkins, H.A., Mehta, J.P., Manolio, T.A. A Catalog of Published Genome-Wide Association Studies. Available at: www.genome.gov/gwastudies. [accessed 11/14/2009].
-
(2009)
A Catalog of Published Genome-Wide Association Studies
, pp. 11-14
-
-
Hindorff, L.A.1
Junkins, H.A.2
Mehta, J.P.3
Manolio, T.A.4
-
30
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
McPherson R., Pertsemlidis A., Kavaslar N., Stewart A., Roberts R., Cox D.R., et al. 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
-
31
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A., Thorleifsson G., Manolescu A., Gretarsdottir S., Blondal T., Jonasdottir A., et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 316 (2007) 1491-1493
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
-
32
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani N.J., Erdmann J., Hall A.S., Hengstenberg C., Mangino M., Mayer B., et al. Genomewide association analysis of coronary artery disease. N Engl J Med 357 (2007) 443-453
-
(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
Mayer, B.6
-
33
-
-
61349137526
-
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease
-
Trégouët D.A., König I.R., Erdmann J., Munteanu A., Braund P.S., Hall A.S., et al. 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
-
-
Trégouët, D.A.1
König, I.R.2
Erdmann, J.3
Munteanu, A.4
Braund, P.S.5
Hall, A.S.6
-
34
-
-
70749096913
-
Genome-wide association of early onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Myocardial Infarction Genetics Consortium
-
Myocardial Infarction Genetics Consortium. 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
-
-
-
35
-
-
61349177857
-
New susceptibility locus for coronary artery disease on chromosome 3q22.3
-
Erdmann J., Grosshennig A., Braund P.S., König I.R., Hengstenberg C., Hall A.S., et al. 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
König, I.R.4
Hengstenberg, C.5
Hall, A.S.6
-
36
-
-
48049115182
-
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study
-
Assimes T.L., Knowles J.W., Basu A., Iribarren C., Southwick A., Tang H., et al. Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Hum Mol Genet 17 (2008) 2320-2328
-
(2008)
Hum Mol Genet
, vol.17
, pp. 2320-2328
-
-
Assimes, T.L.1
Knowles, J.W.2
Basu, A.3
Iribarren, C.4
Southwick, A.5
Tang, H.6
-
37
-
-
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
-
Shen G.Q., Li L., Rao S., Abdullah K.G., Ban J.M., Lee B.S., et al. 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 (2008) 360-365
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 360-365
-
-
Shen, G.Q.1
Li, L.2
Rao, S.3
Abdullah, K.G.4
Ban, J.M.5
Lee, B.S.6
-
38
-
-
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., Hohda S., Sasaoka T., Nakahara K., et al. Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations. J Hum Genet 53 (2008) 357-359
-
(2008)
J Hum Genet
, vol.53
, pp. 357-359
-
-
Hinohara, K.1
Nakajima, T.2
Takahashi, M.3
Hohda, S.4
Sasaoka, T.5
Nakahara, K.6
-
39
-
-
55449112465
-
Associations between single nucleotide polymorphisms on chromosome 9p21 and risk of coronary heart disease in Chinese Han population
-
Zhou L., Zhang X., He M., Cheng L., Chen Y., Hu F.B., et al. Associations between single nucleotide polymorphisms on chromosome 9p21 and risk of coronary heart disease in Chinese Han population. Arterioscler Thromb Vasc Biol 28 (2008) 2085-2089
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 2085-2089
-
-
Zhou, L.1
Zhang, X.2
He, M.3
Cheng, L.4
Chen, Y.5
Hu, F.B.6
-
40
-
-
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., Sawamura H., Kokubo Y., Okamura T., et al. Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population. Circ J 72 (2008) 1213-1217
-
(2008)
Circ J
, vol.72
, pp. 1213-1217
-
-
Hiura, Y.1
Fukushima, Y.2
Yuno, M.3
Sawamura, H.4
Kokubo, Y.5
Okamura, T.6
-
41
-
-
69449102288
-
A common variant in chromosome 9p21 associated with coronary artery disease in Asian Indians
-
Maitra A., Dash D., John S., Sannappa P.R., Das A.P., Shanker J., et al. A common variant in chromosome 9p21 associated with coronary artery disease in Asian Indians. J Genet 88 (2009) 113-118
-
(2009)
J Genet
, vol.88
, pp. 113-118
-
-
Maitra, A.1
Dash, D.2
John, S.3
Sannappa, P.R.4
Das, A.P.5
Shanker, J.6
-
42
-
-
38649091662
-
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
-
Helgadottir A., Thorleifsson G., Magnusson K.P., Grétarsdottir S., Steinthorsdottir V., Manolescu A., et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet 40 (2008) 217-224
-
(2008)
Nat Genet
, vol.40
, pp. 217-224
-
-
Helgadottir, A.1
Thorleifsson, G.2
Magnusson, K.P.3
Grétarsdottir, S.4
Steinthorsdottir, V.5
Manolescu, A.6
-
43
-
-
63149194355
-
Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease
-
Horne B.D., Carlquist J.F., Muhlestein J.B., Bair T.L., and Anderson J.L. Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease. Circ Cardiovasc Genet 1 (2008) 85-92
-
(2008)
Circ Cardiovasc Genet
, vol.1
, pp. 85-92
-
-
Horne, B.D.1
Carlquist, J.F.2
Muhlestein, J.B.3
Bair, T.L.4
Anderson, J.L.5
-
44
-
-
47349129207
-
Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study
-
Ye S., Willeit J., Kronenberg F., Xu Q., and Kiechl S. Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study. J Am Coll Cardiol 52 (2008) 378-384
-
(2008)
J Am Coll Cardiol
, vol.52
, pp. 378-384
-
-
Ye, S.1
Willeit, J.2
Kronenberg, F.3
Xu, Q.4
Kiechl, S.5
-
45
-
-
66249105018
-
A genetic variant on chromosome 9p21 and incident heart failure in the ARIC study
-
ARIC investigators
-
Yamagishi K., Folsom A.R., Rosamond W.D., Boerwinkle E., and ARIC investigators. A genetic variant on chromosome 9p21 and incident heart failure in the ARIC study. Eur Heart J 30 (2009) 1222-1228
-
(2009)
Eur Heart J
, vol.30
, pp. 1222-1228
-
-
Yamagishi, K.1
Folsom, A.R.2
Rosamond, W.D.3
Boerwinkle, E.4
-
46
-
-
34047274599
-
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release
-
Matarín M., Brown W.M., Scholz S., et al. A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. Lancet Neurol 6 (2007) 414-420
-
(2007)
Lancet Neurol
, vol.6
, pp. 414-420
-
-
Matarín, M.1
Brown, W.M.2
Scholz, S.3
-
47
-
-
70350574629
-
Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
-
Yamada Y., Fuku N., Tanaka M., Aoyagi Y., Sawabe M., Metoki N., et al. Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. Atherosclerosis 207 (2009) 144-149
-
(2009)
Atherosclerosis
, vol.207
, pp. 144-149
-
-
Yamada, Y.1
Fuku, N.2
Tanaka, M.3
Aoyagi, Y.4
Sawabe, M.5
Metoki, N.6
-
48
-
-
55849100349
-
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
-
Gretarsdottir S., Thorleifsson G., Manolescu A., Styrkarsdottir U., Helgadottir A., Gschwendtner A., et al. Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. Ann Neurol 64 (2008) 402-409
-
(2008)
Ann Neurol
, vol.64
, pp. 402-409
-
-
Gretarsdottir, S.1
Thorleifsson, G.2
Manolescu, A.3
Styrkarsdottir, U.4
Helgadottir, A.5
Gschwendtner, A.6
-
49
-
-
34447515621
-
Variants conferring risk of atrial fibrillation on chromosome 4q25
-
Gudbjartsson D.F., Arnar D.O., Helgadottir A., Gretarsdottir S., Holm H., Sigurdsson A., et al. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature 448 (2007) 353-357
-
(2007)
Nature
, vol.448
, pp. 353-357
-
-
Gudbjartsson, D.F.1
Arnar, D.O.2
Helgadottir, A.3
Gretarsdottir, S.4
Holm, H.5
Sigurdsson, A.6
-
50
-
-
68149137739
-
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
-
Gudbjartsson D.F., Holm H., Gretarsdottir S., Thorleifsson G., Walters G.B., Thorgeirsson G., et al. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat Genet 41 (2009) 876-878
-
(2009)
Nat Genet
, vol.41
, pp. 876-878
-
-
Gudbjartsson, D.F.1
Holm, H.2
Gretarsdottir, S.3
Thorleifsson, G.4
Walters, G.B.5
Thorgeirsson, G.6
-
51
-
-
65949090748
-
Genomewide association studies of stroke
-
Ikram M.A., Seshadri S., Bis J.C., Fornage M., DeStefano A.L., Aulchenko Y.S., et al. Genomewide association studies of stroke. N Engl J Med 360 (2009) 1718-1728
-
(2009)
N Engl J Med
, vol.360
, pp. 1718-1728
-
-
Ikram, M.A.1
Seshadri, S.2
Bis, J.C.3
Fornage, M.4
DeStefano, A.L.5
Aulchenko, Y.S.6
-
52
-
-
65949099120
-
Genetic risk prediction - are we there yet?
-
Kraft P., and Hunter D.J. Genetic risk prediction - are we there yet?. N Engl J Med 360 17 (2009) 1701-1703
-
(2009)
N Engl J Med
, vol.360
, Issue.17
, pp. 1701-1703
-
-
Kraft, P.1
Hunter, D.J.2
-
53
-
-
65949124249
-
Genomewide association studies - illuminating biologic pathways
-
Hirschhorn J.N. Genomewide association studies - illuminating biologic pathways. N Engl J Med 360 17 (2009) 1699-1701
-
(2009)
N Engl J Med
, vol.360
, Issue.17
, pp. 1699-1701
-
-
Hirschhorn, J.N.1
-
54
-
-
55549097849
-
The diploid genome sequence of an Asian individual
-
Wang J., Wang W., Li R., Li Y., Tian G., Goodman L., et al. The diploid genome sequence of an Asian individual. Nature 456 (2008) 60-65
-
(2008)
Nature
, vol.456
, pp. 60-65
-
-
Wang, J.1
Wang, W.2
Li, R.3
Li, Y.4
Tian, G.5
Goodman, L.6
-
55
-
-
42249087308
-
The complete genome of an individual by massively parallel DNA sequencing
-
Wheeler D.A., Srinivasan M., Egholm M., Shen Y., Chen L., McGuire A., et al. The complete genome of an individual by massively parallel DNA sequencing. Nature 452 (2008) 872-876
-
(2008)
Nature
, vol.452
, pp. 872-876
-
-
Wheeler, D.A.1
Srinivasan, M.2
Egholm, M.3
Shen, Y.4
Chen, L.5
McGuire, A.6
|