-
1
-
-
33645830718
-
Hypertension: Trends in prevalence, incidence, and control
-
Hajjar I, Kotchen JM, Kotchen TA. Hypertension: trends in prevalence, incidence, and control. Annu Rev Public Health 2006; 27: 465-490.
-
(2006)
Annu Rev Public Health
, vol.27
, pp. 465-490
-
-
Hajjar, I.1
Kotchen, J.M.2
Kotchen, T.A.3
-
2
-
-
10044281466
-
Prevalence of hypertension, its awareness and control in adult population in Japan
-
Sekikawa A, Hayakawa T. Prevalence of hypertension, its awareness and control in adult population in Japan. J Hum Hypertens 2004; 18: 911-912.
-
(2004)
J Hum Hypertens
, vol.18
, pp. 911-912
-
-
Sekikawa, A.1
Hayakawa, T.2
-
3
-
-
67349188883
-
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
-
Cho YS, Go MJ, Kim YJ, Heo JY, Oh JH, Ban HJ et al. A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Nat Genet 2009; 41: 527-534.
-
(2009)
Nat Genet
, vol.41
, pp. 527-534
-
-
Cho, Y.S.1
Go, M.J.2
Kim, Y.J.3
Heo, J.Y.4
Oh, J.H.5
Ban, H.J.6
-
4
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
Newton-Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L et al. Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009; 41: 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
-
5
-
-
66149105886
-
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations
-
Org E, Eyheramendy S, Juhanson P, Gieger C, Lichtner P, Klopp N et al. Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. Hum Mol Genet 2009; 18: 2288-2296.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 2288-2296
-
-
Org, E.1
Eyheramendy, S.2
Juhanson, P.3
Gieger, C.4
Lichtner, P.5
Klopp, N.6
-
6
-
-
19044362161
-
A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide search
-
Angius A, Petretto E, Maestrale GB, Forabosco P, Casu G, Piras D et al. A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide search. Am J Hum Genet 2002; 71: 893-905.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 893-905
-
-
Angius, A.1
Petretto, E.2
Maestrale, G.B.3
Forabosco, P.4
Casu, G.5
Piras, D.6
-
7
-
-
0035139750
-
Linkage of hypertension to chromosome 2q14- q23 in Chinese families
-
Zhu DL, Wang HY, Xiong MM, He X, Chu SL, Jin L et al. Linkage of hypertension to chromosome 2q14- q23 in Chinese families. J Hypertens 2001; 19: 55-61.
-
(2001)
J Hypertens
, vol.19
, pp. 55-61
-
-
Zhu, D.L.1
Wang, H.Y.2
Xiong, M.M.3
He, X.4
Chu, S.L.5
Jin, L.6
-
8
-
-
21044442370
-
Hypertension susceptibility genes on chromosome 2p24-p25 in a general Japanese population
-
Kamide K, Kokubo Y, Yang J, Tanaka C, Hanada H, Takiuchi S et al. Hypertension susceptibility genes on chromosome 2p24-p25 in a general Japanese population. J Hypertens 2005; 23: 955-960.
-
(2005)
J Hypertens
, vol.23
, pp. 955-960
-
-
Kamide, K.1
Kokubo, Y.2
Yang, J.3
Tanaka, C.4
Hanada, H.5
Takiuchi, S.6
-
9
-
-
38949149650
-
Association of polymorphisms of ABCA1 and ROS1 with hypertension in Japanese individuals
-
Yamada Y, Kato K, Yoshida T, Yokoi K, Matsuo H, Watanabe S et al. Association of polymorphisms of ABCA1 and ROS1 with hypertension in Japanese individuals. Int J Mol Med 2008; 21: 83-89.
-
(2008)
Int J Mol Med
, vol.21
, pp. 83-89
-
-
Yamada, Y.1
Kato, K.2
Yoshida, T.3
Yokoi, K.4
Matsuo, H.5
Watanabe, S.6
-
10
-
-
33845370070
-
Association of genetic polymorphisms of ACADSB and COMT with human hypertension
-
Kamide K, Kokubo Y, Yang J, Matayoshi T, Inamoto N, Takiuchi S et al. Association of genetic polymorphisms of ACADSB and COMT with human hypertension. J Hypertens 2007; 25: 103-110.
-
(2007)
J Hypertens
, vol.25
, pp. 103-110
-
-
Kamide, K.1
Kokubo, Y.2
Yang, J.3
Matayoshi, T.4
Inamoto, N.5
Takiuchi, S.6
-
11
-
-
37349079875
-
Protein tyrosine kinase 2beta as a candidate gene for hypertension
-
Kamide K, Kokubo Y, Fukuhara S, Hanada H, Yang J, Kada A et al. Protein tyrosine kinase 2beta as a candidate gene for hypertension. Pharmacogenet Genomics 2007; 17: 931-939.
-
(2007)
Pharmacogenet Genomics
, vol.17
, pp. 931-939
-
-
Kamide, K.1
Kokubo, Y.2
Fukuhara, S.3
Hanada, H.4
Yang, J.5
Kada, A.6
-
12
-
-
50249110957
-
Influence of CYP11B2 gene polymorphism on the prevalence of hypertension and the blood pressure in Japanese men: Interaction with dietary salt intake
-
Song Y, Miyaki K, Araki J, Zhang L, Takahashi Y, Nakayama T et al. Influence of CYP11B2 gene polymorphism on the prevalence of hypertension and the blood pressure in Japanese men: interaction with dietary salt intake. J Nutrigenet Nutrigenomics 2008; 1: 252-258.
-
(2008)
J Nutrigenet Nutrigenomics
, vol.1
, pp. 252-258
-
-
Song, Y.1
Miyaki, K.2
Araki, J.3
Zhang, L.4
Takahashi, Y.5
Nakayama, T.6
-
13
-
-
0033060947
-
Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription
-
Xie T, Ho SL, Ramsden D. Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription. Mol Pharmacol 1999; 56: 31-38.
-
(1999)
Mol Pharmacol
, vol.56
, pp. 31-38
-
-
Xie, T.1
Ho, S.L.2
Ramsden, D.3
-
14
-
-
33845746879
-
High systolic blood pressure is associated with Val/Val genotype in the catechol-o-methyltransferase gene the Nord-Trøndelag Health Study (HUNT)
-
Hagen K, Pettersen E, Stovner LJ, Skorpen F, Holmen J, Zwart JA. High systolic blood pressure is associated with Val/Val genotype in the catechol-o-methyltransferase gene. The Nord-Trøndelag Health Study (HUNT). Am J Hypertens 2007; 20: 21-26.
-
(2007)
Am J Hypertens
, vol.20
, pp. 21-26
-
-
Hagen, K.1
Pettersen, E.2
Stovner, L.J.3
Skorpen, F.4
Holmen, J.5
Zwart, J.A.6
-
15
-
-
42949179424
-
Catechol-O-methyltransferase val158-met polymorphism is associated with abdominal obesity and blood pressure in men
-
Annerbrink K, Westberg L, Nilsson S, Rosmond R, Holm G, Eriksson E. Catechol-O-methyltransferase val158-met polymorphism is associated with abdominal obesity and blood pressure in men. Metabolism 2008; 57: 708-711.
-
(2008)
Metabolism
, vol.57
, pp. 708-711
-
-
Annerbrink, K.1
Westberg, L.2
Nilsson, S.3
Rosmond, R.4
Holm, G.5
Eriksson, E.6
-
16
-
-
0026609630
-
The Ca2+ pump of the plasma membrane
-
Carafoli E. The Ca2+ pump of the plasma membrane. J Biol Chem 1992; 267: 2115-2118.
-
(1992)
J Biol Chem
, vol.267
, pp. 2115-2118
-
-
Carafoli, E.1
-
17
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ et al. Finding the missing heritability of complex diseases. Nature 2009; 461: 747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
-
18
-
-
34948877698
-
Prediction of individual genetic risk to disease from genome-wide association studies
-
Wray NR, Goddard ME, Visscher PM. Prediction of individual genetic risk to disease from genome-wide association studies. Genome Res 2007; 17: 1520-1528.
-
(2007)
Genome Res
, vol.17
, pp. 1520-1528
-
-
Wray, N.R.1
Goddard, M.E.2
Visscher, P.M.3
-
19
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR et al. Common SNPs explain a large proportion of the heritability for human height. Nat Genet 2010; 42: 565-569.
-
(2010)
Nat Genet
, vol.42
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
Nyholt, D.R.6
-
20
-
-
56349096931
-
Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk
-
Lango H, , Palmer CN, Morris AD, Zeggini E, Hattersley ATet al. Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk. Diabetes 2008; 57: 3129-3135.
-
(2008)
Diabetes
, vol.57
, pp. 3129-3135
-
-
Lango, H.1
Palmer, C.N.2
Morris, A.D.3
Zeggini, E.4
Hattersley, A.T.5
-
21
-
-
84969213492
-
Genomewide 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. Genomewide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007; 447: 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
|