-
1
-
-
0002966223
-
Familial aggregation and genetic epidemiology of blood pressure
-
Laragh J, Brenner BM (editors). New York: Raven Press
-
Ward R. Familial aggregation and genetic epidemiology of blood pressure. In: Laragh J, Brenner BM (editors): Hypertension: pathophysiology, diagnosis and management. New York: Raven Press; 1990, pp. 81-100.
-
(1990)
Hypertension: Pathophysiology, Diagnosis and Management
, pp. 81-100
-
-
Ward, R.1
-
2
-
-
0037305164
-
Genome scans for hypertension and blood pressure regulation
-
Samani NJ. Genome scans for hypertension and blood pressure regulation. Am J Hypertens 2003; 16:167-171.
-
(2003)
Am J Hypertens
, vol.16
, pp. 167-171
-
-
Samani, N.J.1
-
3
-
-
12244274952
-
A meta-analysis of genome-wide linkage scans for hypertension: The National Heart, Lung and Blood Institute Family Blood Pressure Program
-
Province MA, Kardia SL, Ranade K, Rao DC, Thiel BA, Cooper RS, et al. A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program. Am J Hypertens 2003; 16:144-147.
-
(2003)
Am J Hypertens
, vol.16
, pp. 144-147
-
-
Province, M.A.1
Kardia, S.L.2
Ranade, K.3
Rao, D.C.4
Thiel, B.A.5
Cooper, R.S.6
-
4
-
-
0038375052
-
Genome-wide mapping of human loci for essential hypertension
-
Caulfield M, Munroe P, Pembroke J, Samani N, Dominiczak A, Brown M, et al. Genome-wide mapping of human loci for essential hypertension. Lancet 2003; 361:2118-2123.
-
(2003)
Lancet
, vol.361
, pp. 2118-2123
-
-
Caulfield, M.1
Munroe, P.2
Pembroke, J.3
Samani, N.4
Dominiczak, A.5
Brown, M.6
-
5
-
-
0036841585
-
Genome scan among Nigerians linking blood pressure to chromosomes 2, 3, and 19
-
Cooper RS, Luke A, Zhu X, Kan D, Adeyemo A, Rotimi C, et al. Genome scan among Nigerians linking blood pressure to chromosomes 2, 3, and 19. Hypertension 2002; 40:629-633.
-
(2002)
Hypertension
, vol.40
, pp. 629-633
-
-
Cooper, R.S.1
Luke, A.2
Zhu, X.3
Kan, D.4
Adeyemo, A.5
Rotimi, C.6
-
6
-
-
0030941604
-
Evaluation of an electronic blood pressure device for epidemiologlcal studies
-
Cooper R, Puras A, Tracy J, Kaufman J, Asuzu M, Ordunez P, et al. Evaluation of an electronic blood pressure device for epidemiologlcal studies. Blood Press Monit 1997; 2:35-40.
-
(1997)
Blood Press Monit
, vol.2
, pp. 35-40
-
-
Cooper, R.1
Puras, A.2
Tracy, J.3
Kaufman, J.4
Asuzu, M.5
Ordunez, P.6
-
7
-
-
0030997240
-
The prevalence of hypertension in seven populations of west African origin
-
Cooper R, Rotimi C, Ataman S, McGee D, Osotimehin B, Kadiri S, et al. The prevalence of hypertension in seven populations of west African origin. Am J Public Health 1997; 87:160-168.
-
(1997)
Am J Public Health
, vol.87
, pp. 160-168
-
-
Cooper, R.1
Rotimi, C.2
Ataman, S.3
McGee, D.4
Osotimehin, B.5
Kadiri, S.6
-
8
-
-
0033037577
-
Maximum-likelihood generalized heritability estimate for blood pressure in Nigerian families
-
Rotimi CN, Cooper RS, Cao G, Ogunbiyi O, Ladipo M, Owoaje E, et al. Maximum-likelihood generalized heritability estimate for blood pressure in Nigerian families. Hypertension 1999; 33:874-878.
-
(1999)
Hypertension
, vol.33
, pp. 874-878
-
-
Rotimi, C.N.1
Cooper, R.S.2
Cao, G.3
Ogunbiyi, O.4
Ladipo, M.5
Owoaje, E.6
-
9
-
-
0036338150
-
Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin - rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002; 30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
10
-
-
8844250042
-
Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis
-
Huang Q, Shete S, Amos CI. Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis. Am J Hum Genet 2004; 75:1106-1112.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1106-1112
-
-
Huang, Q.1
Shete, S.2
Amos, C.I.3
-
11
-
-
0029130796
-
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population
-
Excoffier L, Slatkin M. Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. Mol Biol Evol 1995; 12:921-927.
-
(1995)
Mol Biol Evol
, vol.12
, pp. 921-927
-
-
Excoffier, L.1
Slatkin, M.2
-
12
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis GR, Cardon LR, Cookson WO. A general test of association for quantitative traits in nuclear families. Am J Hum Genet 2000; 66:279-292.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
13
-
-
0031582196
-
A novel putative G-protein-coupled receptor expressed in lung, heart and lymphoid tissue
-
Kvingedal AM, Smeland EB. A novel putative G-protein-coupled receptor expressed in lung, heart and lymphoid tissue. FEBS Lett 1997; 407:59-62.
-
(1997)
FEBS Lett
, vol.407
, pp. 59-62
-
-
Kvingedal, A.M.1
Smeland, E.B.2
-
14
-
-
0037168586
-
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
-
Mammalian Gene Collection Program Team
-
Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, et al. Mammalian Gene Collection Program Team. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc Natl Acad Sci USA 2002; 99:16899-16903.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 16899-16903
-
-
Strausberg, R.L.1
Feingold, E.A.2
Grouse, L.H.3
Derge, J.G.4
Klausner, R.D.5
Collins, F.S.6
-
15
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science 1996; 273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
16
-
-
13944250687
-
Admixture mapping for hypertension loci with genome-scan markers
-
Zhu X, Luke A, Cooper RS, Quertermous T, Hanis C, Mosley T, et al. Admixture mapping for hypertension loci with genome-scan markers. Nat Genet 2005; 37:177-181.
-
(2005)
Nat Genet
, vol.37
, pp. 177-181
-
-
Zhu, X.1
Luke, A.2
Cooper, R.S.3
Quertermous, T.4
Hanis, C.5
Mosley, T.6
-
17
-
-
0036278171
-
Genomewide linkage scan of resting blood pressure: HERITAGE Family Study. Health, Risk Factors, Exercise Training, and Genetics
-
Rice T, Rankinen T, Chagnon YC, Province MA, Perusse L, Leon AS, et al. Genomewide linkage scan of resting blood pressure: HERITAGE Family Study. Health, Risk Factors, Exercise Training, and Genetics. Hypertension 2002; 39:1037-1043.
-
(2002)
Hypertension
, vol.39
, pp. 1037-1043
-
-
Rice, T.1
Rankinen, T.2
Chagnon, Y.C.3
Province, M.A.4
Perusse, L.5
Leon, A.S.6
-
18
-
-
0036318601
-
Genome scans for blood pressure and hypertension: The National Heart, Lung, and Blood Institute Family Heart Study
-
Hunt SC, Ellison RC, Atwood LD, Pankow JS, Province MA, Leppert MF. 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
Pankow, J.S.4
Province, M.A.5
Leppert, M.F.6
-
19
-
-
17944362243
-
The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome
-
Comuzzie AG, Funahashi T, Sonnenberg G, Martin LJ, Jacob HJ, Black AE, et al. The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome. J Clin Endocrinol Metab 2001; 86:4321-4325.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 4321-4325
-
-
Comuzzie, A.G.1
Funahashi, T.2
Sonnenberg, G.3
Martin, L.J.4
Jacob, H.J.5
Black, A.E.6
-
20
-
-
0037317663
-
Antihypertensive treatments obscure familial contributions to blood pressure variation
-
Cui JS, Hopper JL, Harrap SB. Antihypertensive treatments obscure familial contributions to blood pressure variation. Hypertension 2003; 41:207-210.
-
(2003)
Hypertension
, vol.41
, pp. 207-210
-
-
Cui, J.S.1
Hopper, J.L.2
Harrap, S.B.3
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