-
1
-
-
0028114754
-
Genetic and environmental influences on blood pressure in elderly twins
-
Hong Y, de Faire U, Heller DA, McClearn GE, Pedersen NK. Genetic and environmental influences on blood pressure in elderly twins. Hypertension. 1994;24:663-670.
-
(1994)
Hypertension
, vol.24
, pp. 663-670
-
-
Hong, Y.1
De Faire, U.2
Heller, D.A.3
McClearn, G.E.4
Pedersen, N.K.5
-
2
-
-
0028240980
-
Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping
-
Reed PW, Davies JL, Copeman JB, Bennett ST, Palmer SM, Pritchard LE, Cough SCL, Kawaguchi Y, Cordell HJ, Balfour KM, Jenkins SC, Powell EE, Vignal A, Todd JA. Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping Nat Genet 1994;7:390-395.
-
(1994)
Nat Genet
, vol.7
, pp. 390-395
-
-
Reed, P.W.1
Davies, J.L.2
Copeman, J.B.3
Bennett, S.T.4
Palmer, S.M.5
Pritchard, L.E.6
Cough, S.C.L.7
Kawaguchi, Y.8
Cordell, H.J.9
Balfour, K.M.10
Jenkins, S.C.11
Powell, E.E.12
Vignal, A.13
Todd, J.A.14
-
3
-
-
0029908532
-
The causes of essential hypertension
-
Brown MJ. The causes of essential hypertension. Br J Clin Pharmacol. 1996;42:21-27.
-
(1996)
Br J Clin Pharmacol
, vol.42
, pp. 21-27
-
-
Brown, M.J.1
-
4
-
-
0028832203
-
Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers
-
Holmans P, Clayton D. Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers. Am J Hum Genet. 1995;57:1221-1232.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1221-1232
-
-
Holmans, P.1
Clayton, D.2
-
5
-
-
16044374799
-
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families
-
Mahtani MM, Widen E, Lehto M, Thomas J, McCarthy M, Brayer J, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyak L, Munnelly K, Parkkonen M, Reeve-Daly MP, Weaver A, Brettin T, Duyk G, Lander ES, Groop LC. Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. Nat Genet. 1996;14:90-94.
-
(1996)
Nat Genet
, vol.14
, pp. 90-94
-
-
Mahtani, M.M.1
Widen, E.2
Lehto, M.3
Thomas, J.4
McCarthy, M.5
Brayer, J.6
Bryant, B.7
Chan, G.8
Daly, M.9
Forsblom, C.10
Kanninen, T.11
Kirby, A.12
Kruglyak, L.13
Munnelly, K.14
Parkkonen, M.15
Reeve-Daly, M.P.16
Weaver, A.17
Brettin, T.18
Duyk, G.19
Lander, E.S.20
Groop, L.C.21
more..
-
6
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies JL, Kawaguchi Y, Bennett ST, Copeman JB, Cordell HJ. Pritchard LE., Reed PW, Gough SC, Jenkins SC, Palmer SM, Balfour KM, Rowe BR, Farrall M, Barnett AH, Bain SC, Todd JA. A genome-wide search for human type 1 diabetes susceptibility genes. Nature. 1994;371:130-136.
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawaguchi, Y.2
Bennett, S.T.3
Copeman, J.B.4
Cordell, H.J.5
Pritchard, L.E.6
Reed, P.W.7
Gough, S.C.8
Jenkins, S.C.9
Palmer, S.M.10
Balfour, K.M.11
Rowe, B.R.12
Farrall, M.13
Barnett, A.H.14
Bain, S.C.15
Todd, J.A.16
-
7
-
-
0030023292
-
Complex traits on a map
-
Ott J. Complex traits on a map. Nature. 1996;379:772-773.
-
(1996)
Nature
, vol.379
, pp. 772-773
-
-
Ott, J.1
-
8
-
-
0028877463
-
Genertc dissection of complex trails: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L. Genertc dissection of complex trails: guidelines for interpreting and reporting linkage results. Nat Genet. 1995;11: 241-247.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
10
-
-
0030118739
-
Genetic dissection of complex traits
-
Curtis D. Genetic dissection of complex traits. Nat Genet. 1996;12: 356-357.
-
(1996)
Nat Genet
, vol.12
, pp. 356-357
-
-
Curtis, D.1
-
11
-
-
0026669336
-
Molecular basis of human hypertension: Role of angiotensinogen
-
Jeunemaitre X, Soubrier F, Kotelevtsev YV, Lifton RP, Williams GS, Charru A, Hunt SC, Hopkins PN, Williams RR, Lalouel J, Corvol P. Molecular basis of human hypertension: role of angiotensinogen. Cell. 1992;71:169-180.
-
(1992)
Cell
, vol.71
, pp. 169-180
-
-
Jeunemaitre, X.1
Soubrier, F.2
Kotelevtsev, Y.V.3
Lifton, R.P.4
Williams, G.S.5
Charru, A.6
Hunt, S.C.7
Hopkins, P.N.8
Williams, R.R.9
Lalouel, J.10
Corvol, P.11
-
12
-
-
0031884504
-
Evaluation of the angiotensinogen locus in human essential hypertension: A European study
-
Brand E, Chatelain N, Keavney B, Caulfield M, Citterio L, Connell JMC, Grobbee DE, Schmidt S, Schunkert H, Schuster H, Sharma AM, Soubrier F. Evaluation of the angiotensinogen locus in human essential hypertension: a European study. Hypertension. 1998;31:725-729.
-
(1998)
Hypertension
, vol.31
, pp. 725-729
-
-
Brand, E.1
Chatelain, N.2
Keavney, B.3
Caulfield, M.4
Citterio, L.5
Connell, J.M.C.6
Grobbee, D.E.7
Schmidt, S.8
Schunkert, H.9
Schuster, H.10
Sharma, A.M.11
Soubrier, F.12
-
14
-
-
17344372511
-
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus
-
Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, Mitra M, Farmer J, Williams SR, Cox NJ, Bell GI, Risch N, Spielman RS. A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat Genet. 1998;19: 292-296.
-
(1998)
Nat Genet
, vol.19
, pp. 292-296
-
-
Concannon, P.1
Gogolin-Ewens, K.J.2
Hinds, D.A.3
Wapelhorst, B.4
Morrison, V.A.5
Stirling, B.6
Mitra, M.7
Farmer, J.8
Williams, S.R.9
Cox, N.J.10
Bell, G.I.11
Risch, N.12
Spielman, R.S.13
-
15
-
-
0033361891
-
An extreme-sib-pair genome scan for genes regulating blood pressure
-
Xu X, Rogus JJ, Terwedow HA, Yang J, Wang Z, Chen C, Niu T, Wang B, Xu H, Weiss S, Schork NJ, Fang Z. An extreme-sib-pair genome scan for genes regulating blood pressure. Am J Hum Genet. 1999;64:1694-1701.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1694-1701
-
-
Xu, X.1
Rogus, J.J.2
Terwedow, H.A.3
Yang, J.4
Wang, Z.5
Chen, C.6
Niu, T.7
Wang, B.8
Xu, H.9
Weiss, S.10
Schork, N.J.11
Fang, Z.12
-
16
-
-
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;99:1407-1410.
-
(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
-
17
-
-
0029001682
-
Extreme discordant sib pairs for mapping quantitative trait loci in humans
-
Risch N, Zhang H. Extreme discordant sib pairs for mapping quantitative trait loci in humans. Science. 1995;268:1584-1589.
-
(1995)
Science
, vol.268
, pp. 1584-1589
-
-
Risch, N.1
Zhang, H.2
-
18
-
-
0029794875
-
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK
-
Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad SA, Lifton RP. Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK. Nat Genet. 1996;14:152-156.
-
(1996)
Nat Genet
, vol.14
, pp. 152-156
-
-
Simon, D.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
Hamdan, J.H.4
Dipietro, A.5
Trachtman, H.6
Sanjad, S.A.7
Lifton, R.P.8
-
19
-
-
0027946089
-
Liddle's syndrome: Heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel
-
Shimkets RA, Warnock DG, Bositis CM, Nelson-Williams C, Hansson JH, Schambelan M, Gill JR, Ulick S, Milora RV, Findling JW, Canessa CM, Rossier BC, Lifton RP. Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel. Cell. 1994;79:407-414.
-
(1994)
Cell
, vol.79
, pp. 407-414
-
-
Shimkets, R.A.1
Warnock, D.G.2
Bositis, C.M.3
Nelson-Williams, C.4
Hansson, J.H.5
Schambelan, M.6
Gill, J.R.7
Ulick, S.8
Milora, R.V.9
Findling, J.W.10
Canessa, C.M.11
Rossier, B.C.12
Lifton, R.P.13
-
20
-
-
0026580019
-
A chimaeric 11b-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. A chimaeric 11b-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.7
-
21
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
-
Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitelman HJ, Lifton RP. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat Genet. 1996;12:24-30.
-
(1996)
Nat Genet
, vol.12
, pp. 24-30
-
-
Simon, D.B.1
Nelson-Williams, C.2
Bia, M.J.3
Ellison, D.4
Karet, F.E.5
Molina, A.M.6
Vaara, I.7
Iwata, F.8
Cushner, H.M.9
Koolen, M.10
Gainza, F.J.11
Gitelman, H.J.12
Lifton, R.P.13
-
22
-
-
0030032699
-
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
-
Simon DB, Karet FE, Hamdan JM, Di Pietro A, Sanjad SA, Lifton RP. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat Genet. 1996;13:183-188.
-
(1996)
Nat Genet
, vol.13
, pp. 183-188
-
-
Simon, D.B.1
Karet, F.E.2
Hamdan, J.M.3
Di Pietro, A.4
Sanjad, S.A.5
Lifton, R.P.6
-
23
-
-
0030140024
-
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12
-
Schuster H, Wienker TE, Bahring S, Bilginturan N, Toka HR, Neitzel H, Jeschke E, Toka O, Gilbert D, Lowe A, Ott J, Haller H, Luft FC. Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12. Nat Genet. 1996;13:98-100.
-
(1996)
Nat Genet
, vol.13
, pp. 98-100
-
-
Schuster, H.1
Wienker, T.E.2
Bahring, S.3
Bilginturan, N.4
Toka, H.R.5
Neitzel, H.6
Jeschke, E.7
Toka, O.8
Gilbert, D.9
Lowe, A.10
Ott, J.11
Haller, H.12
Luft, F.C.13
-
24
-
-
0029160972
-
Human hypertension caused by mutations in the kidney isozyme of 11b-hydroxysteroid dehydrogenase
-
Mune T, Rogerson FM, Nikkila H, Agarwal AK, White PC. Human hypertension caused by mutations in the kidney isozyme of 11b-hydroxysteroid dehydrogenase. Nat Genet. 1995;10:394-399.
-
(1995)
Nat Genet
, vol.10
, pp. 394-399
-
-
Mune, T.1
Rogerson, F.M.2
Nikkila, H.3
Agarwal, A.K.4
White, P.C.5
-
25
-
-
19244386918
-
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21
-
Mansfield TA, Simon DB, Farfel Z, Bia M, Tucci JR, Lebel M, Gutkin M, Vialettes B, Christofilis MA, Kauppinen-Makelin R, Mayan H, Risch N, Lifton RP. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21. Nat Genet. 1997;16:202-205.
-
(1997)
Nat Genet
, vol.16
, pp. 202-205
-
-
Mansfield, T.A.1
Simon, D.B.2
Farfel, Z.3
Bia, M.4
Tucci, J.R.5
Lebel, M.6
Gutkin, M.7
Vialettes, B.8
Christofilis, M.A.9
Kauppinen-Makelin, R.10
Mayan, H.11
Risch, N.12
Lifton, R.P.13
-
26
-
-
13344295074
-
Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1
-
Chang SS, Grunder S, Hanukoglu A, Rosler A, Mathew PM, Hanukoglu I, Schild L, Lu Y, Shimkets RA, Nelson-Williams C, Rossier BC, Lifton RP. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nature Genet. 1996;12:248-253.
-
(1996)
Nature Genet
, vol.12
, pp. 248-253
-
-
Chang, S.S.1
Grunder, S.2
Hanukoglu, A.3
Rosler, A.4
Mathew, P.M.5
Hanukoglu, I.6
Schild, L.7
Lu, Y.8
Shimkets, R.A.9
Nelson-Williams, C.10
Rossier, B.C.11
Lifton, R.P.12
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