-
1
-
-
24944542337
-
Major causes of death among men and women in China
-
DOI 10.1056/NEJMsa050467
-
J He D Gu X Wu, et al. 2005 Major causes of death among men and women in China N Engl J Med 353 1124 1134 10.1056/NEJMsa050467 1:CAS:528: DC%2BD2MXhtVWhsbnK 16162883 (Pubitemid 41317435)
-
(2005)
New England Journal of Medicine
, vol.353
, Issue.11
, pp. 1124-1134
-
-
He, J.1
Gu, D.2
Wu, X.3
Reynolds, K.4
Duan, X.5
Yao, C.6
Wang, J.7
Chen, C.-S.8
Chen, J.9
Wildman, R.P.10
Klag, M.J.11
Whelton, P.K.12
-
2
-
-
0028330005
-
Genetic susceptibility to death from coronary heart disease in a study of twins
-
DOI 10.1056/NEJM199404143301503
-
ME Marenberg N Risch LF Berkman, et al. 1994 Genetic susceptibility to death from coronary heart disease in a study of twins N Engl J Med 330 1041 1046 10.1056/NEJM199404143301503 1:STN:280:DyaK2c7ntlaqtg%3D%3D 8127331 (Pubitemid 24106561)
-
(1994)
New England Journal of Medicine
, vol.330
, Issue.15
, pp. 1041-1046
-
-
Marenberg, M.E.1
Risch, N.2
Berkman, L.F.3
Floderus, B.4
De Faire, U.5
-
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, et al. 2007 A common variant on chromosome 9p21 affects the risk of myocardial infarction Science 316 1491 1493 10.1126/science.1142842 1:CAS:528:DC%2BD2sXmtFSjtro%3D 17478679 (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
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
DOI 10.1126/science.1142447
-
R McPherson A Pertsemlidis N Kavaslar, et al. 2007 A common allele on chromosome 9 associated with coronary heart disease Science 316 1488 1491 10.1126/science.1142447 1:CAS:528:DC%2BD2sXmtFSjtr0%3D 17478681 (Pubitemid 46906617)
-
(2007)
Science
, vol.316
, Issue.5830
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
Stewart, A.4
Roberts, R.5
Cox, D.R.6
Hinds, D.A.7
Pennacchio, L.A.8
Tybjaerg-Hansen, A.9
Folsom, A.R.10
Boerwinkle, E.11
Hobbs, H.H.12
Cohen, J.C.13
-
5
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
DOI 10.1056/NEJMoa072366
-
NJ Samani J Erdmann AS Hall, et al. 2007 WTCCC and the cardiogenics consortium. Genomewide association analysis of coronary artery disease N Engl J Med 357 443 453 10.1056/NEJMoa072366 1:CAS:528:DC%2BD2sXos1emsrk%3D 17634449 (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..
-
6
-
-
63949087448
-
A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease
-
10.1007/s11033-008-9259-7 1:CAS:528:DC%2BD1MXjvFaqur4%3D 18459066
-
Z Chen Q Qian G Ma, et al. 2009 A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease Mol Biol Rep 36 889 893 10.1007/s11033-008-9259-7 1:CAS:528:DC%2BD1MXjvFaqur4%3D 18459066
-
(2009)
Mol Biol Rep
, vol.36
, pp. 889-893
-
-
Chen, Z.1
Qian, Q.2
Ma, G.3
-
7
-
-
0034112689
-
Mild hypercholesterolemia and premature heart disease: Do the national criteria underestimate disease risk?
-
DOI 10.1016/S0735-1097(00)00556-8, PII S0735109700005568
-
KO Akosah E Gower L Groon, et al. 2000 Mild hypercholesterolemia and premature heart disease: do the national criteria underestimate disease risk? J Am Coll Cardiol 35 1178 1184 10.1016/S0735-1097(00)00556-8 1:STN:280: DC%2BD3c3itVOjug%3D%3D 10758958 (Pubitemid 30206892)
-
(2000)
Journal of the American College of Cardiology
, vol.35
, Issue.5
, pp. 1178-1184
-
-
Akosah, K.O.1
Gower, E.2
Groon, L.3
Rooney, B.L.4
Schaper, A.5
-
8
-
-
0034176697
-
Clinical profile and long-term prognosis of women ≤50 years of age referred for coronary angiography for evaluation of chest pain
-
DOI 10.1016/S0002-9149(99)00871-1, PII S0002914999008711
-
O Gurevitz M Jonas V Boyko, et al. 2000 Clinical profile and long-term prognosis of women < or = 50 years of age referred for coronary angiography for evaluation of chest pain Am J Cardiol 85 806 809 10.1016/S0002-9149(99) 00871-1 1:STN:280:DC%2BD3c3itVKiug%3D%3D 10758917 (Pubitemid 30157843)
-
(2000)
American Journal of Cardiology
, vol.85
, Issue.7
, pp. 806-809
-
-
Gurevitz, O.1
Jonas, M.2
Boyko, V.3
Rabinowitz, B.4
Reicher-Reiss, H.5
-
9
-
-
0036230486
-
Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p
-
10.2337/diabetes.51.4.1247 1:CAS:528:DC%2BD38Xis1Ois7k%3D 11916952
-
Y Mori S Otabe C Dina, et al. 2002 Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p Diabetes 51 1247 1255 10.2337/diabetes.51.4.1247 1:CAS:528:DC%2BD38Xis1Ois7k%3D 11916952
-
(2002)
Diabetes
, vol.51
, pp. 1247-1255
-
-
Mori, Y.1
Otabe, S.2
Dina, C.3
-
10
-
-
20144369480
-
Genome-wide linkage analysis of type 2 diabetes mellitus reconfirms the susceptibility locus on 11p13-p12 in Japanese
-
DOI 10.1007/s10038-004-0199-3
-
H Nawata S Shirasawa N Nakashima, et al. 2004 Genome-wide linkage analysis of type 2 diabetes mellitus reconfirms the susceptibility locus on 11p13-p12 in Japanese J Hum Genet 49 629 634 10.1007/s10038-004-0199-3 1:CAS:528:DC%2BD2cXhtVShsLjP 15490285 (Pubitemid 40385252)
-
(2004)
Journal of Human Genetics
, vol.49
, Issue.11
, pp. 629-634
-
-
Nawata, H.1
Shirasawa, S.2
Nakashima, N.3
Araki, E.4
Hashiguchi, J.5
Miyake, S.6
Yamauchi, T.7
Hamaguchi, K.8
Yoshimatsu, H.9
Takeda, H.10
Fukushima, H.11
Sasahara, T.12
Yamaguchi, K.13
Sonoda, N.14
Sonoda, T.15
Matsumoto, M.16
Tanaka, Y.17
Sugimoto, H.18
Tsubouchi, H.19
Inoguchi, T.20
Yanase, T.21
Wake, N.22
Narazaki, K.23
Eto, T.24
Umeda, F.25
Nakazaki, M.26
Ono, J.27
Asano, T.28
Ito, Y.29
Akazawa, S.30
Hazegawa, I.31
Takasu, N.32
Shinohara, M.33
Nishikawa, T.34
Nagafuchi, S.35
Okeda, T.36
Eguchi, K.37
Iwase, M.38
Ishikawa, M.39
Aoki, M.40
Keicho, N.41
Kato, N.42
Yasuda, K.43
Yamamoto, K.44
Sasazuki, T.45
more..
-
11
-
-
50449085212
-
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
-
10.1038/ng.208 1:CAS:528:DC%2BD1cXhtVGgt77E 18711366
-
H Unoki A Takahashi T Kawaguchi, et al. 2008 SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations Nat Genet 40 1098 1102 10.1038/ng.208 1:CAS:528:DC%2BD1cXhtVGgt77E 18711366
-
(2008)
Nat Genet
, vol.40
, pp. 1098-1102
-
-
Unoki, H.1
Takahashi, A.2
Kawaguchi, T.3
-
12
-
-
50449085998
-
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus
-
10.1038/ng.207 1:CAS:528:DC%2BD1cXhtVGgt77M 18711367
-
K Yasuda K Miyake Y Horikawa, et al. 2008 Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus Nat Genet 40 1092 1097 10.1038/ng.207 1:CAS:528:DC%2BD1cXhtVGgt77M 18711367
-
(2008)
Nat Genet
, vol.40
, pp. 1092-1097
-
-
Yasuda, K.1
Miyake, K.2
Horikawa, Y.3
-
13
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
DOI 10.1126/science.1142358
-
Diabetes Genetics Initiative of Broad Institute of Harvard and MIT Lund University Novartis Institutes of BioMedical Research R Saxena BF Voight V Lyssenko, et al. 2007 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Science 316 1331 1336 10.1126/science.1142358 1:CAS:528:DC%2BD2sXmtVyitrk%3D 17463246 (Pubitemid 46871653)
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1331-1336
-
-
Saxena, R.1
Voight, B.F.2
Lyssenko, V.3
Burtt, N.P.4
De Bakker, P.I.W.5
Chen, H.6
Roix, J.J.7
Kathiresan, S.8
Hirschhorn, J.N.9
Daly, M.J.10
Hughes, T.E.11
Groop, L.12
Altshuler, D.13
-
14
-
-
34249895023
-
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
-
DOI 10.1126/science.1142364
-
E Zeggini MN Weedon CM Lindgren, et al. 2007 Wellcome trust case control consortium (WTCCC), McCarthy MI, Hattersley AT. Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Science 316 1336 1340 10.1126/science.1142364 1:CAS:528:DC%2BD2sXmtVymtb0%3D 17463249 (Pubitemid 46871654)
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1336-1341
-
-
Zeggini, E.1
Weedon, M.N.2
Lindgren, C.M.3
Frayling, T.M.4
Elliott, K.S.5
Lango, H.6
Timpson, N.J.7
Perry, J.R.B.8
Rayner, N.W.9
Freathy, R.M.10
Barrett, J.C.11
Shields, B.12
Morris, A.P.13
Ellard, S.14
Groves, C.J.15
Harries, L.W.16
Marchini, J.L.17
Owen, K.R.18
Knight, B.19
Cardon, L.R.20
Walker, M.21
Hitman, G.A.22
Morris, A.D.23
Doney, A.S.F.24
McCarthy, M.I.25
Hattersley, A.T.26
Bruce, I.N.27
Donovan, H.28
Eyre, S.29
Gilbert, P.D.30
Hider, S.L.31
Hinks, A.M.32
John, S.L.33
Potter, C.34
Silman, A.J.35
Symmons, D.P.M.36
Thomson, W.37
Worthington, J.38
more..
-
15
-
-
66649101376
-
Genetic variation in KCNQ1 associates with fasting glucose and beta-cell function: A study of 3, 734 subjects comprising three ethnicities living in Singapore
-
10.2337/db08-1138 1:CAS:528:DC%2BD1MXntFanu7k%3D 19252135
-
JT Tan S Nurbaya D Gardner, et al. 2009 Genetic variation in KCNQ1 associates with fasting glucose and beta-cell function: a study of 3, 734 subjects comprising three ethnicities living in Singapore Diabetes 58 1445 1449 10.2337/db08-1138 1:CAS:528:DC%2BD1MXntFanu7k%3D 19252135
-
(2009)
Diabetes
, vol.58
, pp. 1445-1449
-
-
Tan, J.T.1
Nurbaya, S.2
Gardner, D.3
-
16
-
-
67349205597
-
Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population
-
Mar 24. [Epub ahead of print]
-
Hu C, Wang C, Zhang R et al. (2009) Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population. Diabetologia Mar 24. [Epub ahead of print]
-
(2009)
Diabetologia
-
-
Hu, C.1
Wang, C.2
Zhang, R.3
-
17
-
-
0035574654
-
Cardiovascular risk factors associated with insulin resistance cluster in families with early-onset coronary artery disease
-
10.1161/hq0801.093655 1:CAS:528:DC%2BD3MXmtVartrg%3D 11498464
-
A Kareinen L Viitanen P Halonen, et al. 2001 Cardiovascular risk factors associated with insulin resistance cluster in families with early-onset coronary artery disease Arterioscler Thromb Vasc Biol 21 1346 1352 10.1161/hq0801.093655 1:CAS:528:DC%2BD3MXmtVartrg%3D 11498464
-
(2001)
Arterioscler Thromb Vasc Biol
, vol.21
, pp. 1346-1352
-
-
Kareinen, A.1
Viitanen, L.2
Halonen, P.3
-
18
-
-
0004061789
-
-
World Health Organization. World Health Organization Geneva. Switzerland
-
World Health Organization (1990) MONICA manual; CVD/MNC. World Health Organization, Geneva. Switzerland
-
(1990)
MONICA Manual; CVD/MNC
-
-
-
19
-
-
0034121447
-
Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2
-
DOI 10.1038/75452
-
R Favis JP Day NP Gerry, et al. 2000 Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2 Nat Biotechnol 18 561 564 10.1038/75452 1:CAS:528:DC%2BD3cXjsVOmsbs%3D 10802632 (Pubitemid 30313972)
-
(2000)
Nature Biotechnology
, vol.18
, Issue.5
, pp. 561-564
-
-
Favis, R.1
Day, J.P.2
Gerry, N.P.3
Phelan, C.4
Narod, S.5
Barany, F.6
-
20
-
-
33644621288
-
A novel method based on ligase detection reaction for low abundant YIDD mutants detection in hepatitis B virus
-
DOI 10.1016/j.hepres.2005.12.007, PII S1386634605004705
-
Z Xiao J Xiao Y Jiang, et al. 2006 A novel method based on ligase detection reaction for low abundant YIDD mutants detection in hepatitis B virus Hepatol Res 34 150 155 10.1016/j.hepres.2005.12.007 1:CAS:528: DC%2BD28XitVKnsLs%3D 16500145 (Pubitemid 43316510)
-
(2006)
Hepatology Research
, vol.34
, Issue.3
, pp. 150-155
-
-
Xiao, Z.1
Xiao, J.2
Jiang, Y.3
Zhang, S.4
Yu, M.5
Zhao, J.6
Wei, D.7
Cao, H.8
-
21
-
-
28344448471
-
Ks channel inhibitors in insulin-secreting INS-1 cells
-
DOI 10.1007/s00424-005-1479-2
-
S Ullrich J Su F Ranta, et al. 2005 Effects of I(Ks) channel inhibitors in insulin-secreting INS-1 cells Pflugers Arch 451 428 436 10.1007/s00424-005- 1479-2 1:CAS:528:DC%2BD2MXht1GlsLfP 16133261 (Pubitemid 41719574)
-
(2005)
Pflugers Archiv European Journal of Physiology
, vol.451
, Issue.3
, pp. 428-436
-
-
Ullrich, S.1
Su, J.2
Ranta, F.3
Wittekindt, O.H.4
Ris, F.5
Rosler, M.6
Gerlach, U.7
Heitzmann, D.8
Warth, R.9
Lang, F.10
-
22
-
-
9644265449
-
Insulin secretion capacity in the development from normal glucose tolerance to type 2 diabetes
-
DOI 10.1016/j.diabres.2003.11.024, PII S0168822704001603
-
M Fukushima H Suzuki Y Seino 2004 Insulin secretion capacity in the development from normal glucose tolerance to type 2 diabetes Diabetes Res Clin Pract 66 S37 S43 10.1016/j.diabres.2003.11.024 1:CAS:528:DC%2BD2cXhtVantrfE 15563978 (Pubitemid 39572582)
-
(2004)
Diabetes Research and Clinical Practice
, vol.66
, Issue.SUPPL.
-
-
Fukushima, M.1
Suzuki, H.2
Seino, Y.3
-
23
-
-
41649085340
-
Cardiogenics consortium. Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease
-
10.1161/CIRCULATIONAHA.107.730614 18362232
-
H Schunkert A Götz P Braund, et al. 2008 Cardiogenics consortium. Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease Circulation 117 1675 1684 10.1161/CIRCULATIONAHA.107.730614 18362232
-
(2008)
Circulation
, vol.117
, pp. 1675-1684
-
-
Schunkert, H.1
Götz, A.2
Braund, P.3
-
24
-
-
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
-
DOI 10.1161/ATVBAHA.107.157248, PII 0004360520080200000025
-
GQ Shen L Li S Rao, et al. 2008 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 10.1161/ATVBAHA.107.157248 1:CAS:528:DC%2BD1cXosVygsQ%3D%3D 18048766 (Pubitemid 351161212)
-
(2008)
Arteriosclerosis, Thrombosis, and Vascular Biology
, vol.28
, Issue.2
, 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
Park, J.E.7
Wang, Q.K.8
-
25
-
-
49549087336
-
Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest)
-
10.1111/j.1469-1809.2008.00454.x 1:CAS:528:DC%2BD1cXhtFajt7%2FF 18505420
-
KG Abdullah L Li GQ Shen, et al. 2008 Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest) Ann Hum Genet 72 Pt 5 654 657 10.1111/j.1469-1809.2008.00454.x 1:CAS:528:DC%2BD1cXhtFajt7%2FF 18505420
-
(2008)
Ann Hum Genet
, vol.72
, Issue.PART 5
, pp. 654-657
-
-
Abdullah, K.G.1
Li, L.2
Shen, G.Q.3
|