-
1
-
-
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, Terwilliger J, Davis S, Weeks DE, Bui T, Jeunemaitre X, Velho G, Froguel P, Ratcliffe P, Corvol P, Soubrier F, Lathrop GM. Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. Hum Med Genet. 1997;6:2077-2086.
-
(1997)
Hum Med Genet
, vol.6
, pp. 2077-2086
-
-
Julier, C.1
Delepine, M.2
Keavney, B.3
Terwilliger, J.4
Davis, S.5
Weeks, D.E.6
Bui, T.7
Jeunemaitre, X.8
Velho, G.9
Froguel, P.10
Ratcliffe, P.11
Corvol, P.12
Soubrier, F.13
Lathrop, G.M.14
-
2
-
-
0032811792
-
Evidence for linkage between essential hypertension and a putative locus on human chromosome 17
-
Baima J, Nicolaou M, Schwartz F, DeStefano AL, Manolis A, Gavras I, Laffer C, Elijovich F, Farrer L, Baldwin CT, Gavras H. Evidence for linkage between essential hypertension and a putative locus on human chromosome 17. Hypertension. 1999:34:4-7.
-
(1999)
Hypertension
, vol.34
, pp. 4-7
-
-
Baima, J.1
Nicolaou, M.2
Schwartz, F.3
DeStefano, A.L.4
Manolis, A.5
Gavras, I.6
Laffer, C.7
Elijovich, F.8
Farrer, L.9
Baldwin, C.T.10
Gavras, H.11
-
3
-
-
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, O'Donnell CJ, Lifton RP, Gavras H, Cupples LA, Myers RH. 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;36:477-483.
-
(2000)
Hypertension
, vol.36
, pp. 477-483
-
-
Levy, D.1
DeStefano, A.L.2
Larson, M.G.3
O'Donnell, C.J.4
Lifton, R.P.5
Gavras, H.6
Cupples, L.A.7
Myers, R.H.8
-
4
-
-
0025946420
-
Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats
-
Hilbert P, Lindpainter K, Beckmann JS, Serikawa T, Soubrier F, Dubay C, Canwright P, De Gouyen B, Julier C, Takahashi S, Vincent M, D. Ganten D, Georges M, Lathrop GM. Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats. Nature. 1991;353:521-529.
-
(1991)
Nature
, vol.353
, pp. 521-529
-
-
Hilbert, P.1
Lindpainter, K.2
Beckmann, J.S.3
Serikawa, T.4
Soubrier, F.5
Dubay, C.6
Canwright, P.7
De Gouyen, B.8
Julier, C.9
Takahashi, S.10
Vincent, M.11
Ganten, D.D.12
Georges, M.13
Lathrop, G.M.14
-
5
-
-
0025936511
-
Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat
-
Jacob HJ, Lindpainter K, Lincoln SE, Kusumi K, Bunker RK, Mao Y-P, Ganten D, Dzau VJ, Lander ES. Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat. Cell. 1991;67: 213-224.
-
(1991)
Cell
, vol.67
, pp. 213-224
-
-
Jacob, H.J.1
Lindpainter, K.2
Lincoln, S.E.3
Kusumi, K.4
Bunker, R.K.5
Mao, Y.-P.6
Ganten, D.7
Dzau, V.J.8
Lander, E.S.9
-
6
-
-
17944373014
-
Human hypertension caused by mutations in WNK kinases
-
Wilson FH, Disse-Nicodeme S, Choate KA, Ishikawa K, Nelson-Williams C, Desitter I, Gunel M, Milford DV, Lipkin GW, Achard J-M, Feely MP, Dussol B, Berland Y, Unwin RJ, Mayan H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP. Human hypertension caused by mutations in WNK kinases. Science. 2001;293:1107-1112.
-
(2001)
Science
, vol.293
, pp. 1107-1112
-
-
Wilson, F.H.1
Disse-Nicodeme, S.2
Choate, K.A.3
Ishikawa, K.4
Nelson-Williams, C.5
Desitter, I.6
Gunel, M.7
Milford, D.V.8
Lipkin, G.W.9
Achard, J.-M.10
Feely, M.P.11
Dussol, B.12
Berland, Y.13
Unwin, R.J.14
Mayan, H.15
Simon, D.B.16
Farfel, Z.17
Jeunemaitre, X.18
Lifton, R.P.19
-
7
-
-
0037248330
-
Contrasting associations between aldosterone synthase gene polymorphisms and essential hypertension in blacks and in whites
-
Zhu H, Sagnella GA, Dong Y, Miller MA, Onipinla A, Markandu ND, MacGregor GA. Contrasting associations between aldosterone synthase gene polymorphisms and essential hypertension in blacks and in whites. J Hypertens. 2003;21:87-95.
-
(2003)
J Hypertens
, vol.21
, pp. 87-95
-
-
Zhu, H.1
Sagnella, G.A.2
Dong, Y.3
Miller, M.A.4
Onipinla, A.5
Markandu, N.D.6
MacGregor, G.A.7
-
8
-
-
0043095586
-
Haplotype analysis of aldosterone synthase gene (CYP11B2) polymorphisms shows association with essential hypertension
-
Kumar N, Benjafield AV, Lin RCY, Wang WYS, Stowasser M, Morris BJ. Haplotype analysis of aldosterone synthase gene (CYP11B2) polymorphisms shows association with essential hypertension. J Hypertens. 2003;21: 1331-1337.
-
(2003)
J Hypertens
, vol.21
, pp. 1331-1337
-
-
Kumar, N.1
Benjafield, A.V.2
Lin, R.C.Y.3
Wang, W.Y.S.4
Stowasser, M.5
Morris, B.J.6
-
9
-
-
0026580019
-
A chimeric 11β-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton RP, Dluhy RG, Powers M, Rich GM, Cook S, Ulick S, Lalouel J-M. A chimeric 11β-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature. 1992;355:262-265.
-
(1992)
Nature
, vol.355
, pp. 262-265
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, G.M.4
Cook, S.5
Ulick, S.6
Lalouel, J.-M.7
-
10
-
-
0032459346
-
Molecular genetics in childhood hypertension
-
Morris BJ. Molecular genetics in childhood hypertension (review). Prog Pediat Cardiol. 1999;9:203-212.
-
(1999)
Prog Pediat Cardiol
, vol.9
, pp. 203-212
-
-
Morris, B.J.1
-
11
-
-
0032499488
-
Association of hypertension with T594M mutation in β subunit of epithelial sodium channels in black people resident in London
-
Baker EH, Dong YB, Sagnella GA, Roghwell M, Onnipinla AK, Markandu ND, Cappuccio FP, Cook DG, Persu A, Corvol P. Association of hypertension with T594M mutation in β subunit of epithelial sodium channels in black people resident in London. Lancet. 1998;351:1388-1392.
-
(1998)
Lancet
, vol.351
, pp. 1388-1392
-
-
Baker, E.H.1
Dong, Y.B.2
Sagnella, G.A.3
Roghwell, M.4
Onnipinla, A.K.5
Markandu, N.D.6
Cappuccio, F.P.7
Cook, D.G.8
Persu, A.9
Corvol, P.10
-
13
-
-
0038652103
-
+ channel: Progressing from Liddle's syndrome to essential hypertension
-
+ channel: progressing from Liddle's syndrome to essential hypertension (Editorial comment). J Hypertens. 2003;21:855-857.
-
(2003)
J Hypertens
, vol.21
, pp. 855-857
-
-
Persu, A.1
-
14
-
-
0029092801
-
Hypertension caused by a truncated epithelial sodium channel γ subunit: Genetic heterogeneity of Liddle syndrome
-
Hansson JH, Nelson-Williams C, Suzuki H, Schild L, Shimkets R, Lu Y, Canessa C, Iwasaki T, Rossier B, Lifton RP. Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndrome. Nat Genet. 1995;11:76-82.
-
(1995)
Nat Genet
, vol.11
, pp. 76-82
-
-
Hansson, J.H.1
Nelson-Williams, C.2
Suzuki, H.3
Schild, L.4
Shimkets, R.5
Lu, Y.6
Canessa, C.7
Iwasaki, T.8
Rossier, B.9
Lifton, R.P.10
-
15
-
-
0037782086
-
Genetic variants of WNK4 in whiles and African Americans with hypertension
-
Erlich PM, Cui J, Chazaro I, Farrer, L. A., Baldwin CT, Gavras H, DeStefano AL. Genetic variants of WNK4 in whiles and African Americans with hypertension. Hypertension. 2003;41:1191-1195.
-
(2003)
Hypertension
, vol.41
, pp. 1191-1195
-
-
Erlich, P.M.1
Cui, J.2
Chazaro, I.3
Farrer, L.A.4
Baldwin, C.T.5
Gavras, H.6
DeStefano, A.L.7
-
16
-
-
0031044981
-
Association of angiotensin II type 1 receptor gene polymorphism with essential hypertension
-
Wang WYS, Zee RYL, Morris BJ. Association of angiotensin II type 1 receptor gene polymorphism with essential hypertension. Clin Genet. 1997; 51:31-34.
-
(1997)
Clin Genet
, vol.51
, pp. 31-34
-
-
Wang, W.Y.S.1
Zee, R.Y.L.2
Morris, B.J.3
-
17
-
-
16144367023
-
Glucagon receptor gene mutation in essential hypertension
-
Chambers SM, Morris BJ. Glucagon receptor gene mutation in essential hypertension. Nature Genet. 1996;12:122.
-
(1996)
Nature Genet
, vol.12
, pp. 122
-
-
Chambers, S.M.1
Morris, B.J.2
-
18
-
-
0032217177
-
G-protein β3 subunit gene (GNB3) variant in causation of essential hypertension
-
Benjafield AV, Jeyasingam CL, Nyholt DR, Griffiths LR, Morris BJ. G-protein β3 subunit gene (GNB3) variant in causation of essential hypertension. Hypertension. 1998;32:1094-1097.
-
(1998)
Hypertension
, vol.32
, pp. 1094-1097
-
-
Benjafield, A.V.1
Jeyasingam, C.L.2
Nyholt, D.R.3
Griffiths, L.R.4
Morris, B.J.5
-
19
-
-
0028123010
-
Different frequencies of angiotensin-converting enzyme genotypes in older hypertensive individuals
-
Morris BJ, Zee RYL, Schrader AP. Different frequencies of angiotensin-converting enzyme genotypes in older hypertensive individuals. J Clin Invest. 1994;94:1085-1089.
-
(1994)
J Clin Invest
, vol.94
, pp. 1085-1089
-
-
Morris, B.J.1
Zee, R.Y.L.2
Schrader, A.P.3
-
20
-
-
0016319012
-
Estimation of linkage disequilibrium in randomly mating populations
-
Hill WG. Estimation of linkage disequilibrium in randomly mating populations. Heredity. 1974;33:229-239.
-
(1974)
Heredity
, vol.33
, pp. 229-239
-
-
Hill, W.G.1
-
21
-
-
0028857007
-
Polygenic disease: Methods for mapping complex disease traits
-
Weeks DE, Lathrop M. Polygenic disease: methods for mapping complex disease traits. Trends Genet. 1995;11:513-519.
-
(1995)
Trends Genet
, vol.11
, pp. 513-519
-
-
Weeks, D.E.1
Lathrop, M.2
-
22
-
-
0042092604
-
Association of EDNRA, but not WNK4 or FKBPIB, polymorphisms with essential hypertension
-
Benjafield AV, Katyk K, Morris BJ. Association of EDNRA, but not WNK4 or FKBPIB, polymorphisms with essential hypertension. Clin Genet. 2003;63.
-
(2003)
Clin Genet
, pp. 63
-
-
Benjafield, A.V.1
Katyk, K.2
Morris, B.J.3
-
23
-
-
0037388270
-
The role of Wnk4 in polygenic hypertension: A candidate gene analysis on rat chromosome 10
-
Monti J, Zimdahl H, Schulz H, Plehm R, Ganten D, Hubner N. The role of Wnk4 in polygenic hypertension: a candidate gene analysis on rat chromosome 10. Hypertension. 2003;41:938-942.
-
(2003)
Hypertension
, vol.41
, pp. 938-942
-
-
Monti, J.1
Zimdahl, H.2
Schulz, H.3
Plehm, R.4
Ganten, D.5
Hubner, N.6
-
26
-
-
0038375052
-
Genome-wide mapping for human loci for essential hypertension
-
Caulfield M, Munroe P, Samani N, Pembroke J, Dominiczak A, Brown M, Benjamin N, Webster J, Ratcliffe P, O'Shea S, Papp J, Taylor E, Dobson R, Knight J, Newhouse S, Hooper J, Lee W, Brain N, Clayton D, Lathrop M, Farrall M, Connell J. Genome-wide mapping for human loci for essential hypertension. Lancet. 2003;361:2118-2123.
-
(2003)
Lancet
, vol.361
, pp. 2118-2123
-
-
Caulfield, M.1
Munroe, P.2
Samani, N.3
Pembroke, J.4
Dominiczak, A.5
Brown, M.6
Benjamin, N.7
Webster, J.8
Ratcliffe, P.9
O'Shea, S.10
Papp, J.11
Taylor, E.12
Dobson, R.13
Knight, J.14
Newhouse, S.15
Hooper, J.16
Lee, W.17
Brain, N.18
Clayton, D.19
Lathrop, M.20
Farrall, M.21
Connell, J.22
more..
|