-
1
-
-
0033942498
-
Familial aggregation of blood pressure: A population-based family study in eastern Finland
-
Fuentes RM, Notkola IL, Shemeikka S, Tuomilehto J, Nissinen A., Familial aggregation of blood pressure: a population-based family study in eastern Finland. J Hum Hypertens 2000 14 441 445
-
(2000)
J Hum Hypertens
, vol.14
, pp. 441-445
-
-
Fuentes, R.M.1
Notkola, I.L.2
Shemeikka, S.3
Tuomilehto, J.4
Nissinen, A.5
-
2
-
-
0028114754
-
Genetic and environmental influences on blood pressure in elderly twins
-
Hong Y, de Faire U, Heller DA, McClearn GE, Pedersen N., 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.5
-
3
-
-
0024311243
-
Blood pressure as a risk factor for cardiovascular disease. The Framingham Study-30 years of follow-up
-
Stokes J 3rd, Kannel WB, Wolf PA, D'Agostino RB, Cupples LA., Blood pressure as a risk factor for cardiovascular disease. The Framingham Study-30 years of follow-up. Hypertension 1989 13 5 suppl I13 I18
-
(1989)
Hypertension
, vol.13
, Issue.5
, pp. I13-I18
-
-
Stokes, J.1
Kannel, W.B.2
Wolf, P.A.3
D'Agostino, R.B.4
Cupples, L.A.5
-
4
-
-
0037079309
-
Age-specific relevance of usual blood pressure to vascular mortality: A meta-analysis of individual data for one million adults in 61 prospective studies
-
Lewington S, Clarke R, Qizilbash N, Peto R, Collins R, Prospective Studies Collaboration Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet 2002 360 1903 1913
-
(2002)
Lancet
, vol.360
, pp. 1903-1913
-
-
Lewington, S.1
Clarke, R.2
Qizilbash, N.3
Peto, R.4
Collins, R.5
-
5
-
-
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, Wellcome Trust Case Control Consortium Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009 41 666 676. doi: 10.1038/ng.361.
-
(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
-
6
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, International Consortium for Blood Pressure Genome-Wide Association Studies Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011 478 103 109. doi: 10.1038/nature10405.
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
Munroe, P.B.2
Rice, K.M.3
Bochud, M.4
Johnson, A.D.5
Chasman, D.I.6
-
7
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Genome-wide association study of blood pressure and hypertension. Nat Genet 2009 41 677 687. doi: 10.1038/ng.384.
-
(2009)
Nat Genet
, vol.41
, pp. 677-687
-
-
Levy, D.1
Ehret, G.B.2
Rice, K.3
Verwoert, G.C.4
Launer, L.J.5
Dehghan, A.6
-
8
-
-
80053383403
-
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
-
Wain LV, Verwoert GC, O'Reilly PF, Shi G, Johnson T, Johnson AD, LifeLines Cohort Study; EchoGen consortium; AortaGen Consortium; CHARGE Consortium Heart Failure Working Group; KidneyGen consortium; CKDGen consortium; Cardiogenics consortium; CardioGram Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet 2011 43 1005 1011. doi: 10.1038/ng.922.
-
(2011)
Nat Genet
, vol.43
, pp. 1005-1011
-
-
Wain, L.V.1
Verwoert, G.C.2
O'Reilly, P.F.3
Shi, G.4
Johnson, T.5
Johnson, A.D.6
-
9
-
-
84883824600
-
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
-
Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Asian Genetic Epidemiology Network Consortium Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet 2013 93 545 554. doi: 10.1016/j.ajhg.2013.07.010.
-
(2013)
Am J Hum Genet
, vol.93
, pp. 545-554
-
-
Franceschini, N.1
Fox, E.2
Zhang, Z.3
Edwards, T.L.4
Nalls, M.A.5
Sung, Y.J.6
-
10
-
-
0035571328
-
Mutations in the Na-Cl cotransporter reduce blood pressure in humans
-
Cruz DN, Simon DB, Nelson-Williams C, Farhi A, Finberg K, Burleson L, Mutations in the Na-Cl cotransporter reduce blood pressure in humans. Hypertension 2001 37 1458 1464
-
(2001)
Hypertension
, vol.37
, pp. 1458-1464
-
-
Cruz, D.N.1
Simon, D.B.2
Nelson-Williams, C.3
Farhi, A.4
Finberg, K.5
Burleson, L.6
-
11
-
-
42649084334
-
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
-
Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet 2008 40 592 599. doi: 10.1038/ng.118.
-
(2008)
Nat Genet
, vol.40
, pp. 592-599
-
-
Ji, W.1
Foo, J.N.2
O'Roak, B.J.3
Zhao, H.4
Larson, M.G.5
Simon, D.B.6
-
12
-
-
84907494911
-
Sequence analysis of six blood pressure candidate regions in 4,178 individuals: The Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study
-
Morrison AC, Bis JC, Hwang SJ, Ehret GB, Lumley T, Rice K, Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study. PLoS One 2014 9 e109155. doi: 10.1371/journal.pone.0109155.
-
(2014)
PLoS One
, vol.9
, pp. e109155
-
-
Morrison, A.C.1
Bis, J.C.2
Hwang, S.J.3
Ehret, G.B.4
Lumley, T.5
Rice, K.6
-
13
-
-
84893720400
-
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
-
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang ZZ, NHLBI Grand Opportunity Exome Sequencing Project Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am J Hum Genet 2014 94 233 245. doi: 10.1016/j.ajhg.2014.01.010.
-
(2014)
Am J Hum Genet
, vol.94
, pp. 233-245
-
-
Lange, L.A.1
Hu, Y.2
Zhang, H.3
Xue, C.4
Schmidt, E.M.5
Tang, Z.Z.6
-
14
-
-
84922454111
-
Association of exome sequences with plasma C-reactive protein levels in >9000 participants
-
Schick UM, Auer PL, Bis JC, Lin H, Wei P, Pankratz N, Cohorts for Heart and Aging Research in Genomic Epidemiology; National Heart, Lung, and Blood Institute GO Exome Sequencing Project Association of exome sequences with plasma C-reactive protein levels in >9000 participants. Hum Mol Genet 2015 24 559 571. doi: 10.1093/hmg/ddu450.
-
(2015)
Hum Mol Genet
, vol.24
, pp. 559-571
-
-
Schick, U.M.1
Auer, P.L.2
Bis, J.C.3
Lin, H.4
Wei, P.5
Pankratz, N.6
-
15
-
-
63449100039
-
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts
-
Psaty BM, O'Donnell CJ, Gudnason V, Lunetta KL, Folsom AR, Rotter JI, CHARGE Consortium Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circ Cardiovasc Genet 2009 2 73 80. doi: 10.1161/CIRCGENETICS.108.829747.
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 73-80
-
-
Psaty, B.M.1
O'Donnell, C.J.2
Gudnason, V.3
Lunetta, K.L.4
Folsom, A.R.5
Rotter, J.I.6
-
16
-
-
0024591825
-
The Atherosclerosis Risk in Communities (ARIC) Study: Design and objectives. The ARIC Investigators
-
The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC Investigators. Am J Epidemiol 1989 129 687 702
-
(1989)
Am J Epidemiol
, vol.129
, pp. 687-702
-
-
-
17
-
-
0025913116
-
The Cardiovascular Health Study: Design and rationale
-
Fried LP, Borhani NO, Enright P, Furberg CD, Gardin JM, Kronmal RA, The Cardiovascular Health Study: design and rationale. Ann Epidemiol 1991 1 263 276
-
(1991)
Ann Epidemiol
, vol.1
, pp. 263-276
-
-
Fried, L.P.1
Borhani, N.O.2
Enright, P.3
Furberg, C.D.4
Gardin, J.M.5
Kronmal, R.A.6
-
19
-
-
84886623285
-
The Framingham Offspring Study. Design and preliminary data
-
Feinleib M, Kannel WB, Garrison RJ, McNamara PM, Castelli WP., The Framingham Offspring Study. Design and preliminary data. Prev Med 1975 4 518 525
-
(1975)
Prev Med
, vol.4
, pp. 518-525
-
-
Feinleib, M.1
Kannel, W.B.2
Garrison, R.J.3
McNamara, P.M.4
Castelli, W.P.5
-
20
-
-
29244477198
-
Toward resolution of cardiovascular health disparities in African Americans: Design and methods of the Jackson Heart Study
-
Taylor HA Jr, Wilson JG, Jones DW, Sarpong DF, Srinivasan A, Garrison RJ, Toward resolution of cardiovascular health disparities in African Americans: design and methods of the Jackson Heart Study. Ethn Dis 2005 15 4 suppl 6 S6 S4
-
(2005)
Ethn Dis
, vol.15
, Issue.4
, pp. S6-S14
-
-
Taylor, H.A.1
Wilson, J.G.2
Jones, D.W.3
Sarpong, D.F.4
Srinivasan, A.5
Garrison, R.J.6
-
21
-
-
6844255857
-
Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group
-
Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group. Control Clin Trials 1998 19 61 109
-
(1998)
Control Clin Trials
, vol.19
, pp. 61-109
-
-
-
22
-
-
0036840537
-
Multi-Ethnic Study of Atherosclerosis: Objectives and design
-
Bild DE, Bluemke DA, Burke GL, Detrano R, Diez Roux AV, Folsom AR, Multi-Ethnic Study of Atherosclerosis: objectives and design. Am J Epidemiol 2002 156 871 881
-
(2002)
Am J Epidemiol
, vol.156
, pp. 871-881
-
-
Bild, D.E.1
Bluemke, D.A.2
Burke, G.L.3
Detrano, R.4
Diez Roux, A.V.5
Folsom, A.R.6
-
23
-
-
36148941777
-
The Rotterdam Study: Objectives and design update
-
Hofman A, Breteler MM, van Duijn CM, Krestin GP, Pols HA, Stricker BH, The Rotterdam Study: objectives and design update. Eur J Epidemiol 2007 22 819 829. doi: 10.1007/s10654-007-9199-x.
-
(2007)
Eur J Epidemiol
, vol.22
, pp. 819-829
-
-
Hofman, A.1
Breteler, M.M.2
Van Duijn, C.M.3
Krestin, G.P.4
Pols, H.A.5
Stricker, B.H.6
-
24
-
-
18144362129
-
The effect of genetic drift in a young genetically isolated population
-
Pardo LM, MacKay I, Oostra B, van Duijn CM, Aulchenko YS., The effect of genetic drift in a young genetically isolated population. Ann Hum Genet 2005 69 pt 3 288 295. doi: 10.1046/j.1529-8817.2005.00162.x.
-
(2005)
Ann Hum Genet
, vol.69
, pp. 288-295
-
-
Pardo, L.M.1
MacKay, I.2
Oostra, B.3
Van Duijn, C.M.4
Aulchenko, Y.S.5
-
25
-
-
26444496137
-
Adjusting for treatment effects in studies of quantitative traits: Antihypertensive therapy and systolic blood pressure
-
Tobin MD, Sheehan NA, Scurrah KJ, Burton PR., Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure. Stat Med 2005 24 2911 2935. doi: 10.1002/sim.2165.
-
(2005)
Stat Med
, vol.24
, pp. 2911-2935
-
-
Tobin, M.D.1
Sheehan, N.A.2
Scurrah, K.J.3
Burton, P.R.4
-
26
-
-
22844447499
-
A summary of the effects of antihypertensive medications on measured blood pressure
-
Wu J, Kraja AT, Oberman A, Lewis CE, Ellison RC, Arnett DK, A summary of the effects of antihypertensive medications on measured blood pressure. Am J Hypertens 2005 18 935 942. doi: 10.1016/j.amjhyper.2005.01.011.
-
(2005)
Am J Hypertens
, vol.18
, pp. 935-942
-
-
Wu, J.1
Kraja, A.T.2
Oberman, A.3
Lewis, C.E.4
Ellison, R.C.5
Arnett, D.K.6
-
27
-
-
79960572198
-
Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities
-
Bainbridge MN, Wang M, Wu Y, Newsham I, Muzny DM, Jefferies JL, Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities. Genome Biol 2011 12 R68. doi: 10.1186/gb-2011-12-7-r68.
-
(2011)
Genome Biol
, vol.12
, pp. R68
-
-
Bainbridge, M.N.1
Wang, M.2
Wu, Y.3
Newsham, I.4
Muzny, D.M.5
Jefferies, J.L.6
-
28
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang K, Li M, Hakonarson H., ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 2010 38 e164. doi: 10.1093/nar/gkq603.
-
(2010)
Nucleic Acids Res
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
29
-
-
84881613239
-
DbNSFP v2.0: A database of human non-synonymous SNVs and their functional predictions and annotations
-
Liu X, Jian X, Boerwinkle E., dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations. Hum Mutat 2013 34 E2393 E2402. doi: 10.1002/humu.22376.
-
(2013)
Hum Mutat
, vol.34
, pp. E2393-E2402
-
-
Liu, X.1
Jian, X.2
Boerwinkle, E.3
-
30
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D., Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006 38 904 909. doi: 10.1038/ng1847.
-
(2006)
Nat Genet
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
31
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
-
Li B, Leal SM., Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am J Hum Genet 2008 83 311 321. doi: 10.1016/j.ajhg.2008.06.024.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
32
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu MC, Lee S, Cai T, Li Y, Boehnke M, Lin X., Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet 2011 89 82 93. doi: 10.1016/j.ajhg.2011.05.029.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
Lin, X.6
-
33
-
-
84888132259
-
Identifying multiple causative genes at a single GWAS locus
-
Flister MJ, Tsaih SW, O'Meara CC, Endres B, Hoffman MJ, Geurts AM, Identifying multiple causative genes at a single GWAS locus. Genome Res 2013 23 1996 2002. doi: 10.1101/gr.160283.113.
-
(2013)
Genome Res
, vol.23
, pp. 1996-2002
-
-
Flister, M.J.1
Tsaih, S.W.2
O'Meara, C.C.3
Endres, B.4
Hoffman, M.J.5
Geurts, A.M.6
-
34
-
-
84875168008
-
Genes for blood pressure: An opportunity to understand hypertension
-
Ehret GB, Caulfield MJ., Genes for blood pressure: an opportunity to understand hypertension. Eur Heart J 2013 34 951 961. doi: 10.1093/eurheartj/ehs455.
-
(2013)
Eur Heart J
, vol.34
, pp. 951-961
-
-
Ehret, G.B.1
Caulfield, M.J.2
-
35
-
-
0036083537
-
Molecular structure and physiological function of chloride channels
-
Jentsch TJ, Stein V, Weinreich F, Zdebik AA., Molecular structure and physiological function of chloride channels. Physiol Rev 2002 82 503 568. doi: 10.1152/physrev.00029.2001.
-
(2002)
Physiol Rev
, vol.82
, pp. 503-568
-
-
Jentsch, T.J.1
Stein, V.2
Weinreich, F.3
Zdebik, A.A.4
-
36
-
-
85047691317
-
CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations
-
Scott JW, Hawley SA, Green KA, Anis M, Stewart G, Scullion GA, CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations. J Clin Invest 2004 113 274 284. doi: 10.1172/JCI19874.
-
(2004)
J Clin Invest
, vol.113
, pp. 274-284
-
-
Scott, J.W.1
Hawley, S.A.2
Green, K.A.3
Anis, M.4
Stewart, G.5
Scullion, G.A.6
-
37
-
-
0035969520
-
Barttin is a Cl-channel beta-subunit crucial for renal Cl-reabsorption and inner ear K+ secretion
-
Estévez R, Boettger T, Stein V, Birkenhäger R, Otto E, Hildebrandt F, Barttin is a Cl-channel beta-subunit crucial for renal Cl-reabsorption and inner ear K+ secretion. Nature 2001 414 558 561. doi: 10.1038/35107099.
-
(2001)
Nature
, vol.414
, pp. 558-561
-
-
Estévez, R.1
Boettger, T.2
Stein, V.3
Birkenhäger, R.4
Otto, E.5
Hildebrandt, F.6
-
38
-
-
16944366243
-
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
-
Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet 1997 17 171 178. doi: 10.1038/ng1097-171.
-
(1997)
Nat Genet
, vol.17
, pp. 171-178
-
-
Simon, D.B.1
Bindra, R.S.2
Mansfield, T.A.3
Nelson-Williams, C.4
Mendonca, E.5
Stone, R.6
-
39
-
-
79957585975
-
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
-
Kato N, Takeuchi F, Tabara Y, Kelly TN, Go MJ, Sim X, Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat Genet 2011 43 531 538. doi: 10.1038/ng.834.
-
(2011)
Nat Genet
, vol.43
, pp. 531-538
-
-
Kato, N.1
Takeuchi, F.2
Tabara, Y.3
Kelly, T.N.4
Go, M.J.5
Sim, X.6
-
40
-
-
84886434475
-
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci
-
Kelly TN, Takeuchi F, Tabara Y, Edwards TL, Kim YJ, Chen P, Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci. Hypertension 2013 62 853 859. doi: 10.1161/HYPERTENSIONAHA.113.01148.
-
(2013)
Hypertension
, vol.62
, pp. 853-859
-
-
Kelly, T.N.1
Takeuchi, F.2
Tabara, Y.3
Edwards, T.L.4
Kim, Y.J.5
Chen, P.6
-
41
-
-
84868592524
-
Genome-wide linkage and association scans for pulse pressure in Chinese twins
-
Zhang D, Pang Z, Li S, Jiang W, Wang S, Thomassen M, Genome-wide linkage and association scans for pulse pressure in Chinese twins. Hypertens Res 2012 35 1051 1057. doi: 10.1038/hr.2012.90.
-
(2012)
Hypertens Res
, vol.35
, pp. 1051-1057
-
-
Zhang, D.1
Pang, Z.2
Li, S.3
Jiang, W.4
Wang, S.5
Thomassen, M.6
-
42
-
-
42349112088
-
Genome-wide association studies for complex traits: Consensus, uncertainty and challenges
-
McCarthy MI, Abecasis GR, Cardon LR, Goldstein DB, Little J, Ioannidis JP, Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet 2008 9 356 369. doi: 10.1038/nrg2344.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
Goldstein, D.B.4
Little, J.5
Ioannidis, J.P.6
-
43
-
-
84904048618
-
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations
-
Ganesh SK, Chasman DI, Larson MG, Guo X, Verwoert G, Bis JC, Global Blood Pressure Genetics Consortium Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Am J Hum Genet 2014 95 49 65. doi: 10.1016/j.ajhg.2014.06.002.
-
(2014)
Am J Hum Genet
, vol.95
, pp. 49-65
-
-
Ganesh, S.K.1
Chasman, D.I.2
Larson, M.G.3
Guo, X.4
Verwoert, G.5
Bis, J.C.6
|