-
1
-
-
0002966223
-
Familial aggregation and genetic epidemiology of blood pressure
-
Laragh JH, Brenner BM (eds). New York: Raven Press
-
Ward R. Familial aggregation and genetic epidemiology of blood pressure. In: Laragh JH, Brenner BM (eds). Hypertension: pathophysiology, diagnosis and management, second edition. New York: Raven Press, 1995: 67-88.
-
(1995)
Hypertension: Pathophysiology, Diagnosis and Management, Second Edition
, pp. 67-88
-
-
Ward, R.1
-
2
-
-
0037318295
-
Haplotype analysis of the human renin gene and essential hypertension
-
Hasimu B, Nakayama T, Mizutani Y et al. Haplotype analysis of the human renin gene and essential hypertension. Hypertension 2003; 41: 308-12.
-
(2003)
Hypertension
, vol.41
, pp. 308-312
-
-
Hasimu, B.1
Nakayama, T.2
Mizutani, Y.3
-
3
-
-
0036915585
-
Functionality of two new polymorphisms in the human renin gene enhancer region
-
Fuchs S, Philippe J, Germain S et al. Functionality of two new polymorphisms in the human renin gene enhancer region. J Hypertens 2002; 20: 2391-8.
-
(2002)
J Hypertens
, vol.20
, pp. 2391-2398
-
-
Fuchs, S.1
Philippe, J.2
Germain, S.3
-
4
-
-
0026651907
-
Evidence from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels
-
Tiret L, Rigat B, Visvikis S et al. Evidence from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels. Am J Hum Genet 1992; 51: 197-210.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 197-210
-
-
Tiret, L.1
Rigat, B.2
Visvikis, S.3
-
5
-
-
0003150944
-
The Angiotensin-Converting Enzyme: Molecular Biology and Implication of the Gene Polymorphism in Cardiovascular Diseases
-
Laragh JH (ed.) New York: Raven Press
-
nd ed. New York: Raven Press, 1995; 1667-82.
-
(1995)
nd Ed.
, pp. 1667-1682
-
-
Cambien, F.1
Soubrier, F.2
-
6
-
-
0010676445
-
Angiotensinogen and hypertension
-
Dominiczak AF, Connell JMC, Soubrier, F. (eds). Oxford: BIOS Scientific Publishers Ltd
-
Jeunemaitre X, Gimenez-Roqueplo A-P, Célérier J, Soubrier F, Corvol P. Angiotensinogen and hypertension. In: Dominiczak AF, Connell JMC, Soubrier, F. (eds). Molecular Genetics of Hypertension. Oxford: BIOS Scientific Publishers Ltd, 1999; 201-30.
-
(1999)
Molecular Genetics of Hypertension
, pp. 201-230
-
-
Jeunemaitre, X.1
Gimenez-Roqueplo, A.-P.2
Célérier, J.3
Soubrier, F.4
Corvol, P.5
-
7
-
-
0032975096
-
M235T angiotensinogen polymorphism and cardiovascular renal risk
-
Staessen JA, Kuznetsova T, Wang JG, Emelianov D, Vlietinck R, Fagard R. M235T angiotensinogen polymorphism and cardiovascular renal risk. J Hypertens 1999; 17: 9-17.
-
(1999)
J Hypertens
, vol.17
, pp. 9-17
-
-
Staessen, J.A.1
Kuznetsova, T.2
Wang, J.G.3
Emelianov, D.4
Vlietinck, R.5
Fagard, R.6
-
8
-
-
0028290165
-
Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension
-
Bonnardeaux A, Davies E, Jeunemaitre X et al. Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension. Hypertension 1994; 24: 63-9.
-
(1994)
Hypertension
, vol.24
, pp. 63-69
-
-
Bonnardeaux, A.1
Davies, E.2
Jeunemaitre, X.3
-
9
-
-
0033755905
-
Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings
-
Perola M, Kainulainen K, Pajukanta P et al. Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings. J Hypertens. 2000; 18: 1579-85.
-
(2000)
J Hypertens
, vol.18
, pp. 1579-1585
-
-
Perola, M.1
Kainulainen, K.2
Pajukanta, P.3
-
10
-
-
0033034853
-
Aldosterone secretion rate and blood pressure in essential hypertension are related to polymorphic differences in the aldosterone synthase gene CYP11B2
-
Davies E, Holloway CD, Ingram MC et al. Aldosterone secretion rate and blood pressure in essential hypertension are related to polymorphic differences in the aldosterone synthase gene CYP11B2. Hypertension 1999; 33: 703-7.
-
(1999)
Hypertension
, vol.33
, pp. 703-707
-
-
Davies, E.1
Holloway, C.D.2
Ingram, M.C.3
-
11
-
-
8944243072
-
Hypertension-associated point mutation in the adducin a et b subunits affet actin cytoskeleton and ion transport
-
Tripodi G, Valtorta F, Torielli L et al. Hypertension-associated point mutation in the adducin a et b subunits affet actin cytoskeleton and ion transport. J Clin Invest 1996; 97: 2815-22.
-
(1996)
J Clin Invest
, vol.97
, pp. 2815-2822
-
-
Tripodi, G.1
Valtorta, F.2
Torielli, L.3
-
12
-
-
0030898258
-
Polymorphism of a-adducin and salt-sensitivity in patients with essential hypertension
-
Cusi D, Barlassina C, Azzani T et al. Polymorphism of a-adducin and salt-sensitivity in patients with essential hypertension. Lancet 1997; 349: 1353-7.
-
(1997)
Lancet
, vol.349
, pp. 1353-1357
-
-
Cusi, D.1
Barlassina, C.2
Azzani, T.3
-
13
-
-
17344366286
-
Association of a human G-protein beta3 subunit variant with hypertension
-
Siffert W, Rosskopf D, Siffert G et al. Association of a human G-protein beta3 subunit variant with hypertension. Nat Genet 1998; 18: 45-8.
-
(1998)
Nat Genet
, vol.18
, pp. 45-48
-
-
Siffert, W.1
Rosskopf, D.2
Siffert, G.3
-
14
-
-
0033541569
-
Genetic linkage of beta and gamma subunits of epithelial sodium channel to systolic blood pressure
-
Wong ZY, Stebbing M, Ellis JA, Lamantia A, Harrap SB. Genetic linkage of beta and gamma subunits of epithelial sodium channel to systolic blood pressure. Lancet 1999; 353: 1222-5.
-
(1999)
Lancet
, vol.353
, pp. 1222-1225
-
-
Wong, Z.Y.1
Stebbing, M.2
Ellis, J.A.3
Lamantia, A.4
Harrap, S.B.5
-
15
-
-
0031927840
-
Genetic analysis of the subunit of the epithelial Na+ Channel in essential Hypertension
-
Persu A, Barbry P, Bassilina F et al. Genetic analysis of the subunit of the epithelial Na+ Channel in essential Hypertension. Hypertension 1998; 32: 129-37.
-
(1998)
Hypertension
, vol.32
, pp. 129-137
-
-
Persu, A.1
Barbry, P.2
Bassilina, F.3
-
16
-
-
0032499488
-
Association of hypertension associated with T594M mutation in b subunit of the epithelial sodium channel in black people resident in London
-
Dong YB, Baker EH, Sagnella GA et al. Association of hypertension associated with T594M mutation in b subunit of the epithelial sodium channel in black people resident in London. Lancet 1998; 351: 1388-92.
-
(1998)
Lancet
, vol.351
, pp. 1388-1392
-
-
Dong, Y.B.1
Baker, E.H.2
Sagnella, G.A.3
-
18
-
-
0032702619
-
Genetic variants in the epithelial sodium channel in relation to aldosterone and potassium excretion and risk for hypertension
-
Ambrosius WT, Bloem U, Zhou L et al. Genetic variants in the epithelial sodium channel in relation to aldosterone and potassium excretion and risk for hypertension. Hypertension 1999; 34: 631-7.
-
(1999)
Hypertension
, vol.34
, pp. 631-637
-
-
Ambrosius, W.T.1
Bloem, U.2
Zhou, L.3
-
19
-
-
0033596973
-
Genome-wide linkage analyses of systolic blood pressure using highly discordant siblings
-
Krushkal J, Ferrell R, Mockrin SC, Turner ST, Sing CF, Boerwinkle E. Genome-wide linkage analyses of systolic blood pressure using highly discordant siblings. Circulation 1999; 99: 1407-10.
-
(1999)
Circulation
, vol.99
, pp. 1407-1410
-
-
Krushkal, J.1
Ferrell, R.2
Mockrin, S.C.3
Turner, S.T.4
Sing, C.F.5
Boerwinkle, E.6
-
20
-
-
0034720848
-
Positional genomic analysis identifies the beta (2)-adrenergic receptor gene as a susceptibility locus for human hypertension
-
Bray MS, Krushkal J, Ferrell R et al. Positional genomic analysis identifies the beta (2)-adrenergic receptor gene as a susceptibility locus for human hypertension. Circulation 2000; 101: 2877-82.
-
(2000)
Circulation
, vol.101
, pp. 2877-2882
-
-
Bray, M.S.1
Krushkal, J.2
Ferrell, R.3
-
21
-
-
0034680349
-
Genome-wide linkage analysis of systolic and diastolic blood pressure: The Quebec Family Study
-
Rice T, Rankinen T, Province MA et al. Genome-wide linkage analysis of systolic and diastolic blood pressure: The Quebec Family Study. Circulation 2000; 102: 1956-63.
-
(2000)
Circulation
, vol.102
, pp. 1956-1963
-
-
Rice, T.1
Rankinen, T.2
Province, M.A.3
-
22
-
-
0033770421
-
Evidence for a gene influencing blood pressure on chromosome 17: Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham heart study
-
Levy D, DeStefano AL, Larson MG et al. Evidence for a gene influencing blood pressure on chromosome 17: genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham heart study. Hypertension 2000; 36: 477-83.
-
(2000)
Hypertension
, vol.36
, pp. 477-483
-
-
Levy, D.1
DeStefano, A.L.2
Larson, M.G.3
-
23
-
-
9844221411
-
Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10
-
Julier C, Delepine M, Keavney B et al. Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. Hum Mol Genet 1997; 6: 2077-85.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2077-2085
-
-
Julier, C.1
Delepine, M.2
Keavney, B.3
-
24
-
-
17944373014
-
Human hypertension caused by mutations in WNK kinases
-
Wilson F, Disse-Nicodème S, Choate K et al. Human hypertension caused by mutations in WNK kinases. Science 2001; 293: 1107-12.
-
(2001)
Science
, vol.293
, pp. 1107-1112
-
-
Wilson, F.1
Disse-Nicodème, S.2
Choate, K.3
-
25
-
-
0036278171
-
Genomewide linkage scan of resting blood pressure: HERITAGE Family Study
-
Health, Risk Factors, Exercise Training, and Genetics
-
Rice T, Rankinen T, Chagnon YC et al. Genomewide linkage scan of resting blood pressure: HERITAGE Family Study. Health, Risk Factors, Exercise Training, and Genetics. Hypertension 2002; 39: 1037-43.
-
(2002)
Hypertension
, vol.39
, pp. 1037-1043
-
-
Rice, T.1
Rankinen, T.2
Chagnon, Y.C.3
-
26
-
-
0036318601
-
Genome scans for blood pressure and hypertension: The National Heart, Lung, and Blood Institute Family Heart Study
-
Hunt SC, Ellison RC, Atwood LD et al. Genome scans for blood pressure and hypertension: the National Heart, Lung, and Blood Institute Family Heart Study. Hypertension 2002; 40: 1-6.
-
(2002)
Hypertension
, vol.40
, pp. 1-6
-
-
Hunt, S.C.1
Ellison, R.C.2
Atwood, L.D.3
-
27
-
-
0038375052
-
Genome-wide mapping human loci for essential hypertension
-
Caulfield M, Munroe P, Pembroke J. Genome-wide mapping human loci for essential hypertension. Lancet 2003; 361: 2118-23.
-
(2003)
Lancet
, vol.361
, pp. 2118-2123
-
-
Caulfield, M.1
Munroe, P.2
Pembroke, J.3
-
28
-
-
10744219593
-
A genome wide scan for early onset primary hypertension in Scandinavians
-
Von Wowern F, Bengtsson K, Lindgren CM et al. A genome wide scan for early onset primary hypertension in Scandinavians. Hum Mol Genet 2005; 12: 2077-81.
-
(2005)
Hum Mol Genet
, vol.12
, pp. 2077-2081
-
-
Von Wowern, F.1
Bengtsson, K.2
Lindgren, C.M.3
-
29
-
-
0034691278
-
QTL influencing blood pressure maps to the region of PPH1 on chromosome 2931-34 in Old Order Amish
-
Hsueh WC, Mitchell BD, Schneider JL et al. QTL influencing blood pressure maps to the region of PPH1 on chromosome 2931-34 in Old Order Amish. Circulation 2000; 101: 2810-6.
-
(2000)
Circulation
, vol.101
, pp. 2810-2816
-
-
Hsueh, W.C.1
Mitchell, B.D.2
Schneider, J.L.3
-
30
-
-
19044362161
-
A new essential hypertension susceptibility locus on chromosome 2p24-25, detected by genomewide search
-
Angius A, Petretto E, Maestrale GB et al. A new essential hypertension susceptibility locus on chromosome 2p24-25, 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
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