-
1
-
-
2642554707
-
Atherosclerotic Vascular Disease Conference: Writing Group I: Epidemiology
-
Pasternak, R. C., Criqui, M. H., Benjamin, E. J., Fowkes, F. G., Isselbacher, E. M., McCullough, P. A. et al. Atherosclerotic Vascular Disease Conference: Writing Group I: epidemiology. Circulation 109, 2605-2612 (2004).
-
(2004)
Circulation
, vol.109
, pp. 2605-2612
-
-
Pasternak, R.C.1
Criqui, M.H.2
Benjamin, E.J.3
Fowkes, F.G.4
Isselbacher, E.M.5
McCullough, P.A.6
-
2
-
-
84969213492
-
Genome-wide association study of 14 000 cases of seven common diseases and 3000 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 3000 shared controls. Nature 447, 661-678 (2007).
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
3
-
-
44449176689
-
Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21
-
Matarin, M., Brown, W. M., Singleton, A., Hardy, J. A., Meschia, J. F. & ISGS investigators Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21. Stroke 39, 1586-1589 (2008).
-
(2008)
Stroke
, vol.39
, pp. 1586-1589
-
-
Matarin, M.1
Brown, W.M.2
Singleton, A.3
Hardy, J.A.4
Meschia, J.F.5
-
4
-
-
67249112107
-
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke
-
Gschwendtner, A., Bevan, S., Cole, J. W., Plourde, A., Matarin, M., Ross-Adams, H. et al. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Ann. Neurol. 65, 531-539 (2009).
-
(2009)
Ann. Neurol.
, vol.65
, pp. 531-539
-
-
Gschwendtner, A.1
Bevan, S.2
Cole, J.W.3
Plourde, A.4
Matarin, M.5
Ross-Adams, H.6
-
5
-
-
34247116957
-
Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction
-
Hata, J., Matsuda, K., Ninomiya, T., Yonemoto, K., Matsushita, T., Ohnishi, Y. et al. Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction. Hum. Mol. Genet. 16, 630-639 (2007).
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 630-639
-
-
Hata, J.1
Matsuda, K.2
Ninomiya, T.3
Yonemoto, K.4
Matsushita, T.5
Ohnishi, Y.6
-
6
-
-
41649091577
-
Replication of association between a chromosome 9p21 polymorphism with coronary artery disease in Japanese and Korean populations
-
Hinohara, K., Nakajima, T., Takahashi, M., Hohda, S., Sasaoka, T., Nakahara, K. et al. Replication of association between a chromosome 9p21 polymorphism with coronary artery disease in Japanese and Korean populations. J. Hum. Genet. 53, 357-359 (2008).
-
(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
-
7
-
-
66249119374
-
Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations
-
Hinohara, K., Nakajima, T., Sasaoka, T., Sawabe, M., Lee, B. S., Ban, J. et al. Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations. J. Hum. Genet. 54, 248-251 (2009).
-
(2009)
J. Hum. Genet.
, vol.54
, pp. 248-251
-
-
Hinohara, K.1
Nakajima, T.2
Sasaoka, T.3
Sawabe, M.4
Lee, B.S.5
Ban, J.6
-
8
-
-
70350139601
-
Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease
-
doi: 10.1007/s00439-009-0698-6.
-
Hinohara, K., Nakajima, T., Yasunami, M., Houda, S., Sasaoka, T., Yamamoto, K. et al. Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease. Hum. Genet. (2009)doi: 10.1007/s00439-009-0698-6.
-
(2009)
Hum. Genet.
-
-
Hinohara, K.1
Nakajima, T.2
Yasunami, M.3
Houda, S.4
Sasaoka, T.5
Yamamoto, K.6
-
9
-
-
4344610941
-
Association study of CD14 polymorphism with myocardial infarction in a Japanese population
-
Hohda, S., Kimura, A., Sasaoka, T., Hayashi, T., Ueda, K., Yasunami, M. et al. Association study of CD14 polymorphism with myocardial infarction in a Japanese population. Jpn. Heart. J. 44, 613-622 (2003).
-
(2003)
Jpn. Heart. J.
, vol.44
, pp. 613-622
-
-
Hohda, S.1
Kimura, A.2
Sasaoka, T.3
Hayashi, T.4
Ueda, K.5
Yasunami, M.6
-
10
-
-
34247850787
-
Lack of association between LTA and LGALS2 polymorphisms and myocardial infarction in Japanese and Korean populations
-
Kimura, A., Takahashi, M., Choi, B. Y., Bae, S. W., Hohta, S., Sasaoka, T. et al. Lack of association between LTA and LGALS2 polymorphisms and myocardial infarction in Japanese and Korean populations. Tissue Antigens 69, 265-269 (2007).
-
(2007)
Tissue Antigens
, vol.69
, pp. 265-269
-
-
Kimura, A.1
Takahashi, M.2
Choi, B.Y.3
Bae, S.W.4
Hohta, S.5
Sasaoka, T.6
-
11
-
-
44149127481
-
PGA: Power calculator for case-control genetic association analyses
-
Menashe, I., Rosenberg, P. S. & Chen, B. E. PGA: Power calculator for case-control genetic association analyses. BMC Genetics. 9, 36 (2008).
-
(2008)
BMC Genetics.
, vol.9
, pp. 36
-
-
Menashe, I.1
Rosenberg, P.S.2
Chen, B.E.3
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