-
1
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA. A map of human genome variation from population-scale sequencing. Nature 467: 1061-1073, 2010.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Abecasis, G.R.1
Altshuler, D.2
Auton, A.3
Brooks, L.D.4
Durbin, R.M.5
Gibbs, R.A.6
Hurles, M.E.7
McVean, G.A.8
-
2
-
-
36849037025
-
Relationship between GSTs gene polymorphism and susceptibility to end stage renal disease among North Indians
-
Agrawal S, Tripathi G, Khan F, Sharma R, Baburaj VP. Relationship between GSTs gene polymorphism and susceptibility to end stage renal disease among North Indians. Ren Fail 29: 947-953, 2007.
-
(2007)
Ren Fail
, vol.29
, pp. 947-953
-
-
Agrawal, S.1
Tripathi, G.2
Khan, F.3
Sharma, R.4
Baburaj, V.P.5
-
3
-
-
0030900338
-
Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats
-
Aitman TJ, Gotoda T, Evans AL, Imrie H, Heath KE, Trembling PM, Truman H, Wallace CA, Rahman A, Dore C, Flint J, Kren V, Zidek V, Kurtz TW, Pravenec M, Scott J. Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats. Nat Genet 16: 197-201, 1997.
-
(1997)
Nat Genet
, vol.16
, pp. 197-201
-
-
Aitman, T.J.1
Gotoda, T.2
Evans, A.L.3
Imrie, H.4
Heath, K.E.5
Trembling, P.M.6
Truman, H.7
Wallace, C.A.8
Rahman, A.9
Dore, C.10
Flint, J.11
Kren, V.12
Zidek, V.13
Kurtz, T.W.14
Pravenec, M.15
Scott, J.16
-
4
-
-
80054746492
-
Exome sequencing as a tool for Mendelian disease gene discovery
-
Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J. Exome sequencing as a tool for Mendelian disease gene discovery. Nat Rev Genet 12: 745-755, 2011.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 745-755
-
-
Bamshad, M.J.1
Ng, S.B.2
Bigham, A.W.3
Tabor, H.K.4
Emond, M.J.5
Nickerson, D.A.6
Shendure, J.7
-
5
-
-
46249126356
-
Estimating coverage and power for genetic association studies using near-complete variation data
-
Bhangale TR, Rieder MJ, Nickerson DA. Estimating coverage and power for genetic association studies using near-complete variation data. Nat Genet 40: 841-843, 2008.
-
(2008)
Nat Genet
, vol.40
, pp. 841-843
-
-
Bhangale, T.R.1
Rieder, M.J.2
Nickerson, D.A.3
-
6
-
-
0015654620
-
The hypertensive role of the kidney in spontaneously hypertensive rats
-
Bianchi G, Fox U, Di Francesco GF, Bardi U, Radice M. The hypertensive role of the kidney in spontaneously hypertensive rats. Clin Sci Mol Med Suppl 45, Suppl 1: 135s-139s, 1973.
-
(1973)
Clin Sci Mol Med Suppl
, vol.45
, Issue.SUPPL. 1
-
-
Bianchi, G.1
Fox, U.2
Di Francesco, G.F.3
Bardi, U.4
Radice, M.5
-
7
-
-
0028270493
-
Two point mutations within the adducin genes are involved in blood pressure variation
-
Bianchi G, Tripodi G, Casari G, Salardi S, Barber BR, Garcia R, Leoni P, Torielli L, Cusi D, Ferrandi M, Pinna LA, Barelles FE, Ferrari P. Two point mutations within the adducin genes are involved in blood pressure variation. Proc Natl Acad Sci USA 91: 3999-4003, 1994.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3999-4003
-
-
Bianchi, G.1
Tripodi, G.2
Casari, G.3
Salardi, S.4
Barber, B.R.5
Garcia, R.6
Leoni, P.7
Torielli, L.8
Cusi, D.9
Ferrandi, M.10
Pinna, L.A.11
Barelles, F.E.12
Ferrari, P.13
-
8
-
-
34147216956
-
A review of the genetics of essential hypertension
-
Binder A. A review of the genetics of essential hypertension. Curr Opin Cardiol 22: 176-184, 2007.
-
(2007)
Curr Opin Cardiol
, vol.22
, pp. 176-184
-
-
Binder, A.1
-
9
-
-
84857654651
-
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes
-
Bonnefond A, Clement N, Fawcett K, Yengo L, Vaillant E, Guillaume JL, Dechaume A, Payne F, Roussel R, Czernichow S, Hercberg S, Hadjadj S, Balkau B, Marre M, Lantieri O, Langenberg C, Bouatia-Naji N, Charpentier G, Vaxillaire M, Rocheleau G, Wareham NJ, Sladek R, McCarthy MI, Dina C, Barroso I, Jockers R, Froguel P. Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Nat Genet 44: 297-301, 2012.
-
(2012)
Nat Genet
, vol.44
, pp. 297-301
-
-
Bonnefond, A.1
Clement, N.2
Fawcett, K.3
Yengo, L.4
Vaillant, E.5
Guillaume, J.L.6
Dechaume, A.7
Payne, F.8
Roussel, R.9
Czernichow, S.10
Hercberg, S.11
Hadjadj, S.12
Balkau, B.13
Marre, M.14
Lantieri, O.15
Langenberg, C.16
Bouatia-Naji, N.17
Charpentier, G.18
Vaxillaire, M.19
Rocheleau, G.20
Wareham, N.J.21
Sladek, R.22
McCarthy, M.I.23
Dina, C.24
Barroso, I.25
Jockers, R.26
Froguel, P.27
more..
-
10
-
-
0028942436
-
Prevalence of hypertension in the US adult population. Results from the Third National Health and Nutrition Examination Survey, 1988-1991
-
Burt VL, Whelton P, Roccella EJ, Brown C, Cutler JA, Higgins M, Horan MJ, Labarthe D. Prevalence of hypertension in the US adult population. Results from the Third National Health and Nutrition Examination Survey, 1988-1991. Hypertension 25: 305-313, 1995.
-
(1995)
Hypertension
, vol.25
, pp. 305-313
-
-
Burt, V.L.1
Whelton, P.2
Roccella, E.J.3
Brown, C.4
Cutler, J.A.5
Higgins, M.6
Horan, M.J.7
Labarthe, D.8
-
12
-
-
0028966390
-
Association of the alpha-adducin locus with essential hypertension
-
Casari G, Barlassina C, Cusi D, Zagato L, Muirhead R, Righetti M, Nembri P, Amar K, Gatti M, Macciardi F, Binelli G, Bianchi G. Association of the alpha-adducin locus with essential hypertension. Hypertension 25: 320-326, 1995.
-
(1995)
Hypertension
, vol.25
, pp. 320-326
-
-
Casari, G.1
Barlassina, C.2
Cusi, D.3
Zagato, L.4
Muirhead, R.5
Righetti, M.6
Nembri, P.7
Amar, K.8
Gatti, M.9
McCiardi, F.10
Binelli, G.11
Bianchi, G.12
-
13
-
-
77951768942
-
Genetic loci influencing kidney function and chronic kidney disease
-
Chambers JC, Zhang W, Lord GM, van der Harst P, Lawlor DA, Sehmi JS, Gale DP, Wass MN, Ahmadi KR, Bakker SJ, Beckmann J, Bilo HJ, Bochud M, Brown MJ, Caulfield MJ, Connell JM, Cook HT, Cotlarciuc I, Davey Smith G, de Silva R, Deng G, Devuyst O, Dikkeschei LD, Dimkovic N, Dockrell M, Dominiczak A, Ebrahim S, Eggermann T, Farrall M, Ferrucci L, Floege J, Forouhi NG, Gansevoort RT, Han X, Hedblad B, Homan van der Heide JJ, Hepkema BG, Hernandez-Fuentes M, Hypponen E, Johnson T, de Jong PE, Kleefstra N, Lagou V, Lapsley M, Li Y, Loos RJ, Luan J, Luttropp K, Marechal C, Melander O, Munroe PB, Nordfors L, Parsa A, Peltonen L, Penninx BW, Perucha E, Pouta A, Prokopenko I, Roderick PJ, Ruokonen A, Samani NJ, Sanna S, Schalling M, Schlessinger D, Schlieper G, Seelen MA, Shuldiner AR, Sjogren M, Smit JH, Snieder H, Soranzo N, Spector TD, Stenvinkel P, Sternberg MJ, Swaminathan R, Tanaka T, Ubink-Veltmaat LJ, Uda M, Vollenweider P, Wallace C, Waterworth D, Zerres K, Waeber G, Wareham NJ, Maxwell PH, McCarthy MI, Jarvelin MR, Mooser V, Abecasis GR, Lightstone L, Scott J, Navis G, Elliott P, Kooner JS. Genetic loci influencing kidney function and chronic kidney disease. Nat Genet 42: 373-375, 2010.
-
(2010)
Nat Genet
, vol.42
, pp. 373-375
-
-
Chambers, J.C.1
Zhang, W.2
Lord, G.M.3
van der Harst, P.4
Lawlor, D.A.5
Sehmi, J.S.6
Gale, D.P.7
Wass, M.N.8
Ahmadi, K.R.9
Bakker, S.J.10
Beckmann, J.11
Bilo, H.J.12
Bochud, M.13
Brown, M.J.14
Caulfield, M.J.15
Connell, J.M.16
Cook, H.T.17
Cotlarciuc, I.18
Davey Smith, G.19
de Silva, R.20
Deng, G.21
Devuyst, O.22
Dikkeschei, L.D.23
Dimkovic, N.24
Dockrell, M.25
Dominiczak, A.26
Ebrahim, S.27
Eggermann, T.28
Farrall, M.29
Ferrucci, L.30
Floege, J.31
Forouhi, N.G.32
Gansevoort, R.T.33
Han, X.34
Hedblad, B.35
van der Heide Homan, J.J.36
Hepkema, B.G.37
Hernandez-Fuentes, M.38
Hypponen, E.39
Johnson, T.40
de Jong, P.E.41
Kleefstra, N.42
Lagou, V.43
Lapsley, M.44
Li, Y.45
Loos, R.J.46
Luan, J.47
Luttropp, K.48
Marechal, C.49
Melander, O.50
Munroe, P.B.51
Nordfors, L.52
Parsa, A.53
Peltonen, L.54
Penninx, B.W.55
Perucha, E.56
Pouta, A.57
Prokopenko, I.58
Roderick, P.J.59
Ruokonen, A.60
Samani, N.J.61
Sanna, S.62
Schalling, M.63
Schlessinger, D.64
Schlieper, G.65
Seelen, M.A.66
Shuldiner, A.R.67
Sjogren, M.68
Smit, J.H.69
Snieder, H.70
Soranzo, N.71
Spector, T.D.72
Stenvinkel, P.73
Sternberg, M.J.74
Swaminathan, R.75
Tanaka, T.76
Ubink-Veltmaat, L.J.77
Uda, M.78
Vollenweider, P.79
Wallace, C.80
Waterworth, D.81
Zerres, K.82
Waeber, G.83
Wareham, N.J.84
Maxwell, P.H.85
McCarthy, M.I.86
Jarvelin, M.R.87
Mooser, V.88
Abecasis, G.R.89
Lightstone, L.90
Scott, J.91
Navis, G.92
Elliott, P.93
Kooner, J.S.94
more..
-
14
-
-
84874085595
-
Loss of GSTM1, a NRF2 target, is associated with accelerated progression of hypertensive kidney disease in the African American Study of Kidney Disease (AASK)
-
Chang J, Ma JZ, Zeng Q, Cechova S, Gantz A, Nievergelt C, O'Connor D, Lipkowitz M, Le TH. Loss of GSTM1, a NRF2 target, is associated with accelerated progression of hypertensive kidney disease in the African American Study of Kidney Disease (AASK). Am J Physiol Renal Physiol 304: F348-F355, 2013.
-
(2013)
Am J Physiol Renal Physiol
, vol.304
-
-
Chang, J.1
Ma, J.Z.2
Zeng, Q.3
Cechova, S.4
Gantz, A.5
Nievergelt, C.6
O'Connor, D.7
Lipkowitz, M.8
Le, T.H.9
-
15
-
-
34249997024
-
Replicating genotype-phenotype associations
-
Chanock SJ, Manolio T, Boehnke M, Boerwinkle E, Hunter DJ, Thomas G, Hirschhorn JN, Abecasis G, Altshuler D, Bailey-Wilson JE, Brooks LD, Cardon LR, Daly M, Donnelly P, Fraumeni JF Jr, Freimer NB, Gerhard DS, Gunter C, Guttmacher AE, Guyer MS, Harris EL, Hoh J, Hoover R, Kong CA, Merikangas KR, Morton CC, Palmer LJ, Phimister EG, Rice JP, Roberts J, Rotimi C, Tucker MA, Vogan KJ, Wacholder S, Wijsman EM, Winn DM, Collins FS. Replicating genotype-phenotype associations. Nature 447: 655-660, 2007.
-
(2007)
Nature
, vol.447
, pp. 655-660
-
-
Chanock, S.J.1
Manolio, T.2
Boehnke, M.3
Boerwinkle, E.4
Hunter, D.J.5
Thomas, G.6
Hirschhorn, J.N.7
Abecasis, G.8
Altshuler, D.9
Bailey-Wilson, J.E.10
Brooks, L.D.11
Cardon, L.R.12
Daly, M.13
Donnelly, P.14
Fraumeni Jr., J.F.15
Freimer, N.B.16
Gerhard, D.S.17
Gunter, C.18
Guttmacher, A.E.19
Guyer, M.S.20
Harris, E.L.21
Hoh, J.22
Hoover, R.23
Kong, C.A.24
Merikangas, K.R.25
Morton, C.C.26
Palmer, L.J.27
Phimister, E.G.28
Rice, J.P.29
Roberts, J.30
Rotimi, C.31
Tucker, M.A.32
Vogan, K.J.33
Wacholder, S.34
Wijsman, E.M.35
Winn, D.M.36
Collins, F.S.37
more..
-
16
-
-
67349188883
-
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
-
Cho YS, Go MJ, Kim YJ, Heo JY, Oh JH, Ban HJ, Yoon D, Lee MH, Kim DJ, Park M, Cha SH, Kim JW, Han BG, Min H, Ahn Y, Park MS, Han HR, Jang HY, Cho EY, Lee JE, Cho NH, Shin C, Park T, Park JW, Lee JK, Cardon L, Clarke G, McCarthy MI, Lee JY, Oh B, Kim HL. A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Nat Genet 41: 527-534, 2009.
-
(2009)
Nat Genet
, vol.41
, pp. 527-534
-
-
Cho, Y.S.1
Go, M.J.2
Kim, Y.J.3
Heo, J.Y.4
Oh, J.H.5
Ban, H.J.6
Yoon, D.7
Lee, M.H.8
Kim, D.J.9
Park, M.10
Cha, S.H.11
Kim, J.W.12
Han, B.G.13
Min, H.14
Ahn, Y.15
Park, M.S.16
Han, H.R.17
Jang, H.Y.18
Cho, E.Y.19
Lee, J.E.20
Cho, N.H.21
Shin, C.22
Park, T.23
Park, J.W.24
Lee, J.K.25
Cardon, L.26
Clarke, G.27
McCarthy, M.I.28
Lee, J.Y.29
Oh, B.30
Kim, H.L.31
more..
-
17
-
-
0027416241
-
Linkage of 11 beta-hydroxylase mutations with altered steroid biosynthesis and blood pressure in the Dahl rat
-
Cicila GT, Rapp JP, Wang JM, St Lezin E, Ng SC, Kurtz TW. Linkage of 11 beta-hydroxylase mutations with altered steroid biosynthesis and blood pressure in the Dahl rat. Nat Genet 3: 346-353, 1993.
-
(1993)
Nat Genet
, vol.3
, pp. 346-353
-
-
Cicila, G.T.1
Rapp, J.P.2
Wang, J.M.3
St Lezin, E.4
Ng, S.C.5
Kurtz, T.W.6
-
18
-
-
79951678251
-
Normotension in Lewis and Dahl salt-resistant rats is governed by different genes
-
Crespo K, Chauvet C, Blain M, Menard A, Roy J, Deng AY. Normotension in Lewis and Dahl salt-resistant rats is governed by different genes. J Hypertens 29: 460-465, 2011.
-
(2011)
J Hypertens
, vol.29
, pp. 460-465
-
-
Crespo, K.1
Chauvet, C.2
Blain, M.3
Menard, A.4
Roy, J.5
Deng, A.Y.6
-
19
-
-
0030898258
-
Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertension
-
Cusi D, Barlassina C, Azzani T, Casari G, Citterio L, Devoto M, Glorioso N, Lanzani C, Manunta P, Righetti M, Rivera R, Stella P, Troffa C, Zagato L, Bianchi G. Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertension. Lancet 349: 1353-1357, 1997.
-
(1997)
Lancet
, vol.349
, pp. 1353-1357
-
-
Cusi, D.1
Barlassina, C.2
Azzani, T.3
Casari, G.4
Citterio, L.5
Devoto, M.6
Glorioso, N.7
Lanzani, C.8
Manunta, P.9
Righetti, M.10
Rivera, R.11
Stella, P.12
Troffa, C.13
Zagato, L.14
Bianchi, G.15
-
20
-
-
0016733244
-
Primary role of renal homografts in setting chronic blood pressure levels in rats
-
Dahl LK, Heine M. Primary role of renal homografts in setting chronic blood pressure levels in rats. Circ Res 36: 692-696, 1975.
-
(1975)
Circ Res
, vol.36
, pp. 692-696
-
-
Dahl, L.K.1
Heine, M.2
-
21
-
-
59449104674
-
Angiotensin converting enzyme gene polymorphism (insertion/deletion) and hypertension in adult Asian Indians: A population-based study from Calcutta, India
-
Das M, Pal S, Ghosh A. Angiotensin converting enzyme gene polymorphism (insertion/deletion) and hypertension in adult Asian Indians: a population-based study from Calcutta, India. Hum Biol 80: 303-312, 2008.
-
(2008)
Hum Biol
, vol.80
, pp. 303-312
-
-
Das, M.1
Pal, S.2
Ghosh, A.3
-
22
-
-
77958614358
-
Genetics of hypertension: From experimental animals to humans
-
Delles C, McBride MW, Graham D, Padmanabhan S, Dominiczak AF. Genetics of hypertension: from experimental animals to humans. Biochim Biophys Acta 1802: 1299-1308, 2010.
-
(2010)
Biochim Biophys Acta
, vol.1802
, pp. 1299-1308
-
-
Delles, C.1
McBride, M.W.2
Graham, D.3
Padmanabhan, S.4
Dominiczak, A.F.5
-
23
-
-
53649091022
-
Glutathione S-transferase variants and hypertension
-
Delles C, Padmanabhan S, Lee WK, Miller WH, McBride MW, McClure JD, Brain NJ, Wallace C, Marcano AC, Schmieder RE, Brown MJ, Caulfield MJ, Munroe PB, Farrall M, Webster J, Connell JM, Dominiczak AF. Glutathione S-transferase variants and hypertension. J Hypertens 26: 1343-1352, 2008.
-
(2008)
J Hypertens
, vol.26
, pp. 1343-1352
-
-
Delles, C.1
Padmanabhan, S.2
Lee, W.K.3
Miller, W.H.4
McBride, M.W.5
McClure, J.D.6
Brain, N.J.7
Wallace, C.8
Marcano, A.C.9
Schmieder, R.E.10
Brown, M.J.11
Caulfield, M.J.12
Munroe, P.B.13
Farrall, M.14
Webster, J.15
Connell, J.M.16
Dominiczak, A.F.17
-
24
-
-
37349125527
-
A high-density admixture scan in 1,670 African Americans with hypertension
-
Deo RC, Patterson N, Tandon A, McDonald GJ, Haiman CA, Ardlie K, Henderson BE, Henderson SO, Reich D. A high-density admixture scan in 1,670 African Americans with hypertension. PLoS Genet 3: e196, 2007.
-
(2007)
PLoS Genet
, vol.3
-
-
Deo, R.C.1
Patterson, N.2
Tandon, A.3
McDonald, G.J.4
Haiman, C.A.5
Ardlie, K.6
Henderson, B.E.7
Henderson, S.O.8
Reich, D.9
-
25
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
Dickson SP, Wang K, Krantz I, Hakonarson H, Goldstein DB. Rare variants create synthetic genome-wide associations. PLoS Biol 8: e1000294, 2010.
-
(2010)
PLoS Biol
, vol.8
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
26
-
-
0029933535
-
Angiotensinogen polymorphism M235T, hypertension, and nephropathy in insulin-dependent diabetes
-
Doria A, Onuma T, Gearin G, Freire MB, Warram JH, Krolewski AS. Angiotensinogen polymorphism M235T, hypertension, and nephropathy in insulin-dependent diabetes. Hypertension 27: 1134-1139, 1996.
-
(1996)
Hypertension
, vol.27
, pp. 1134-1139
-
-
Doria, A.1
Onuma, T.2
Gearin, G.3
Freire, M.B.4
Warram, J.H.5
Krolewski, A.S.6
-
27
-
-
84865790047
-
An integrated encyclopedia of DNA elements in the human genome
-
Dunham I, Kundaje A, Aldred SF, Collins PJ, Davis CA, Doyle F, Epstein CB, Frietze S, Harrow J, Kaul R, Khatun J, Lajoie BR, Landt SG, Lee BK, Pauli F, Rosenbloom KR, Sabo P, Safi A, Sanyal A, Shoresh N, Simon JM, Song L, Trinklein ND, Altshuler RC, Birney E, Brown JB, Cheng C, Djebali S, Dong X, Ernst J, Furey TS, Gerstein M, Giardine B, Greven M, Hardison RC, Harris RS, Herrero J, Hoffman MM, Iyer S, Kelllis M, Kheradpour P, Lassmann T, Li Q, Lin X, Marinov GK, Merkel A, Mortazavi A, Parker SC, Reddy TE, Rozowsky J, Schlesinger F, Thurman RE, Wang J, Ward LD, Whitfield TW, Wilder SP, Wu W, Xi HS, Yip KY, Zhuang J, Bernstein BE, Green ED, Gunter C, Snyder M, Pazin MJ, Lowdon RF, Dillon LA, Adams LB, Kelly CJ, Zhang J, Wexler JR, Good PJ, Feingold EA, Crawford GE, Dekker J, Elinitski L, Farnham PJ, Giddings MC, Gingeras TR, Guigo R, Hubbard TJ, Kellis M, Kent WJ, Lieb JD, Margulies EH, Myers RM, Starnatoyannopoulos JA, Tennebaum SA, Weng Z, White KP, Wold B, Yu Y, Wrobel J, Risk BA, Gunawardena HP, Kuiper HC, Maier CW, Xie L, Chen X, Mikkelsen TS, Gillespie S, Goren A, Ram O, Zhang X, Wang L, Issner R, Coyne MJ, Durham T, Ku M, Truong T, Eaton ML, Dobin A, Tanzer A, Lagarde J, Lin W, Xue C, Williams BA, Zaleski C, Roder M, Kokocinski F, Abdelhamid RF, Alioto T, Antoshechkin I, Baer MT, Batut P, Bell I, Bell K, Chakrabortty S, Chrast J, Curado J, Derrien T, Drenkow J, Dumais E, Dumais J, Duttagupta R, Fastuca M, Fejes-Toth K, Ferreira P, Foissac S, Fullwood MJ, Gao H, Gonzalez D, Gordon A, Howald C, Jha S, Johnson R, Kapranov P, King B, Kingswood C, Li G, Luo OJ, Park E, Preall JB, Presaud K, Ribeca P, Robyr D, Ruan X, Sammeth M, Sandu KS, Schaeffer L, See LH, Shahab A, Skancke J, Suzuki AM, Takahashi H, Tilgner H, Trout D, Walters N, Wang H, Hayashizaki Y, Reymond A, Antonarakis SE, Hannon GJ, Ruan Y, Carninci P, Sloan CA, Learned K, Malladi VS, Wong MC, Barber GP, Cline MS, Dreszer TR, Heitner SG, Karolchik D, Kirkup VM, Meyer LR, Long JC, Maddren M, Raney BJ, Grasfeder LL, Giresi PG, Battenhouse A, Sheffield NC, Showers KA, London D, Bhinge AA, Shestak C, Schaner MR, Kim SK, Zhang ZZ, Mieczkowski PA, Mieczkowska JO, Liu Z, McDaniell RM, Ni Y, Rashid NU, Kim MJ, Adar S, Zhang Z, Wang T, Winter D, Keefe D, Iyer VR, Sandhu KS, Zheng M, Wang P, Gertz J, Vielmetter J, Partridge EC, Varley KE, Gasper C, Bansal A, Pepke S, Jain P, Amrhein H, Bowling KM, Anaya M, Cross MK, Muratet MA, Newberry KM, McCue K, Nesmith AS, Fisher-Aylor KI, Pusey B, DeSalvo G, Parker SL, Balasubramanian S, Davis NS, Meadows SK, Eggleston T, Newberry JS, Levy SE, Absher DM, Wong WH, Blow MJ, Visel A, Pennachio LA, Elnitski L, Petrykowska HM, Abyzov A, Aken B, Barrell D, Barson G, Berry A, Bignell A, Boychenko V, Bussotti G, Davidson C, Despacio-Reyes G, Diekhans M, Ezkurdia I, Frankish A, Gilbert J, Gonzalez JM, Griffiths E, Harte R, Hendrix DA, Hunt T, Jungreis I, Kay M, Khurana E, Leng J, Lin MF, Loveland J, Lu Z, Manthravadi D, Mariotti M, Mudge J, Mukherjee G, Notredame C, Pei B, Rodriguez JM, Saunders G, Sboner A, Searle S, Sisu C, Snow C, Steward C, Tapanari E, Tress ML, van Baren MJ, Washieti S, Wilming L, Zadissa A, Zhengdong Z, Brent M, Haussler D, Valencia A, Raymond A, Addleman N, Alexander RP, Auerbach RK, Bettinger K, Bhardwaj N, Boyle AP, Cao AR, Cayting P, Charos A, Cheng Y, Eastman C, Euskirchen G, Fleming JD, Grubert F, Habegger L, Hariharan M, Harmanci A, Iyenger S, Jin VX, Karczewski KJ, Kasowski M, Lacroute P, Lam H, Larnarre-Vincent N, Lian J, Lindahl-Allen M, Min R, Miotto B, Monahan H, Moqtaderi Z, Mu XJ, O'Geen H, Ouyang Z, Patacsil D, Raha D, Ramirez L, Reed B, Shi M, Slifer T, Witt H, Wu L, Xu X, Yan KK, Yang X, Struhl K, Weissman SM, Tenebaum SA, Penalva LO, Karmakar S, Bhanvadia RR, Choudhury A, Domanus M, Ma L, Moran J, Victorsen A, Auer T, Centarin L, Eichenlaub M, Gruhl F, Heerman S, Hoeckendorf B, Inoue D, Kellner T, Kirchmaier S, Mueller C, Reinhardt R, Schertel L, Schneider S, Sinn R, Wittbrodt B, Wittbrodt J, Jain G, Balasundaram G, Bates DL, Byron R, Canfield TK, Diegel MJ, Dunn D, Ebersol AK, Frum T, Garg K, Gist E, Hansen RS, Boatman L, Haugen E, Humbert R, Johnson AK, Johnson EM, Kutyavin TM, Lee K, Lotakis D, Maurano MT, Neph SJ, Neri FV, Nguyen ED, Qu H, Reynolds AP, Roach V, Rynes E, Sanchez ME, Sandstrom RS, Shafer AO, Stergachis AB, Thomas S, Vernot B, Vierstra J, Vong S, Weaver MA, Yan Y, Zhang M, Akey JA, Bender M, Dorschner MO, Groudine M, MacCoss MJ, Navas P, Stamatoyannopoulos G, Stamatoyannopoulos JA, Beal K, Brazma A, Flicek P, Johnson N, Lukk M, Luscombe NM, Sobral D, Vaquerizas JM, Batzoglou S, Sidow A, Hussami N, Kyriazopoulou-Panagiotopoulou S, Libbrecht MW, Schaub MA, Miller W, Bickel PJ, Banfai B, Boley NP, Huang H, Li JJ, Noble WS, Bilmes JA, Buske OJ, Sahu AO, Kharchenko PV, Park PJ, Baker D, Taylor J, Lochovsky L. An integrated encyclopedia of DNA elements in the human genome. Nature 489: 57-74, 2012.
-
(2012)
Nature
, vol.489
, pp. 57-74
-
-
Dunham, I.1
Kundaje, A.2
Aldred, S.F.3
Collins, P.J.4
Davis, C.A.5
Doyle, F.6
Epstein, C.B.7
Frietze, S.8
Harrow, J.9
Kaul, R.10
Khatun, J.11
Lajoie, B.R.12
Landt, S.G.13
Lee, B.K.14
Pauli, F.15
Rosenbloom, K.R.16
Sabo, P.17
Safi, A.18
Sanyal, A.19
Shoresh, N.20
Simon, J.M.21
Song, L.22
Trinklein, N.D.23
Altshuler, R.C.24
Birney, E.25
Brown, J.B.26
Cheng, C.27
Djebali, S.28
Dong, X.29
Ernst, J.30
Furey, T.S.31
Gerstein, M.32
Giardine, B.33
Greven, M.34
Hardison, R.C.35
Harris, R.S.36
Herrero, J.37
Hoffman, M.M.38
Iyer, S.39
Kelllis, M.40
Kheradpour, P.41
Lassmann, T.42
Li, Q.43
Lin, X.44
Marinov, G.K.45
Merkel, A.46
Mortazavi, A.47
Parker, S.C.48
Reddy, T.E.49
Rozowsky, J.50
Schlesinger, F.51
Thurman, R.E.52
Wang, J.53
Ward, L.D.54
Whitfield, T.W.55
Wilder, S.P.56
Wu, W.57
Xi, H.S.58
Yip, K.Y.59
Zhuang, J.60
Bernstein, B.E.61
Green, E.D.62
Gunter, C.63
Snyder, M.64
Pazin, M.J.65
Lowdon, R.F.66
Dillon, L.A.67
Adams, L.B.68
Kelly, C.J.69
Zhang, J.70
Wexler, J.R.71
Good, P.J.72
Feingold, E.A.73
Crawford, G.E.74
Dekker, J.75
Elinitski, L.76
Farnham, P.J.77
Giddings, M.C.78
Gingeras, T.R.79
Guigo, R.80
Hubbard, T.J.81
Kellis, M.82
Kent, W.J.83
Lieb, J.D.84
Margulies, E.H.85
Myers, R.M.86
Starnatoyannopoulos, J.A.87
Tennebaum, S.A.88
Weng, Z.89
White, K.P.90
Wold, B.91
Yu, Y.92
Wrobel, J.93
Risk, B.A.94
Gunawardena, H.P.95
Kuiper, H.C.96
Maier, C.W.97
Xie, L.98
more..
-
28
-
-
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, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sober S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjogren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimaki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kahonen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Kottgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grassler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stancakova A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT Jr, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikainen LP, Soininen P, Tukiainen T, Wurtz P, Ong RT, Dorr M, Kroemer HK, Volker U, Volzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Jarvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, and Johnson T. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 478: 103-109, 2011.
-
(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
Smith, A.V.7
Tobin, M.D.8
Verwoert, G.C.9
Hwang, S.J.10
Pihur, V.11
Vollenweider, P.12
O'Reilly, P.F.13
Amin, N.14
Bragg-Gresham, J.L.15
Teumer, A.16
Glazer, N.L.17
Launer, L.18
Zhao, J.H.19
Aulchenko, Y.20
Heath, S.21
Sober, S.22
Parsa, A.23
Luan, J.24
Arora, P.25
Dehghan, A.26
Zhang, F.27
Lucas, G.28
Hicks, A.A.29
Jackson, A.U.30
Peden, J.F.31
Tanaka, T.32
Wild, S.H.33
Rudan, I.34
Igl, W.35
Milaneschi, Y.36
Parker, A.N.37
Fava, C.38
Chambers, J.C.39
Fox, E.R.40
Kumari, M.41
Go, M.J.42
van der Harst, P.43
Kao, W.H.44
Sjogren, M.45
Vinay, D.G.46
Alexander, M.47
Tabara, Y.48
Shaw-Hawkins, S.49
Whincup, P.H.50
Liu, Y.51
Shi, G.52
Kuusisto, J.53
Tayo, B.54
Seielstad, M.55
Sim, X.56
Nguyen, K.D.57
Lehtimaki, T.58
Matullo, G.59
Wu, Y.60
Gaunt, T.R.61
Onland-Moret, N.C.62
Cooper, M.N.63
Platou, C.G.64
Org, E.65
Hardy, R.66
Dahgam, S.67
Palmen, J.68
Vitart, V.69
Braund, P.S.70
Kuznetsova, T.71
Uiterwaal, C.S.72
Adeyemo, A.73
Palmas, W.74
Campbell, H.75
Ludwig, B.76
Tomaszewski, M.77
Tzoulaki, I.78
Palmer, N.D.79
Aspelund, T.80
Garcia, M.81
Chang, Y.P.82
O'Connell, J.R.83
Steinle, N.I.84
Grobbee, D.E.85
Arking, D.E.86
Kardia, S.L.87
Morrison, A.C.88
Hernandez, D.89
Najjar, S.90
McArdle, W.L.91
Hadley, D.92
Brown, M.J.93
Connell, J.M.94
Hingorani, A.D.95
Day, I.N.96
Lawlor, D.A.97
Beilby, J.P.98
more..
-
29
-
-
0033905618
-
Nov gene encodes adhesion factor for vascular smooth muscle cells and is dynamically regulated in response to vascular injury
-
Ellis PD, Chen Q, Barker PJ, Metcalfe JC, Kemp PR. Nov gene encodes adhesion factor for vascular smooth muscle cells and is dynamically regulated in response to vascular injury. Arterioscler Thromb Vasc Biol 20: 1912-1919, 2000.
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 1912-1919
-
-
Ellis, P.D.1
Chen, Q.2
Barker, P.J.3
Metcalfe, J.C.4
Kemp, P.R.5
-
30
-
-
0038205688
-
The Chronic Renal Insufficiency Cohort (CRIC) Study: Design and Methods
-
Feldman HI, Appel LJ, Chertow GM, Cifelli D, Cizman B, Daugirdas J, Fink JC, Franklin-Becker ED, Go AS, Hamm LL, He J, Hostetter T, Hsu CY, Jamerson K, Joffe M, Kusek JW, Landis JR, Lash JP, Miller ER, Mohler ER, 3rd Muntner P, Ojo AO, Rahman M, Townsend RR, Wright JT. The Chronic Renal Insufficiency Cohort (CRIC) Study: Design and Methods. J Am Soc Nephrol 14: S148-S153, 2003.
-
(2003)
J Am Soc Nephrol
, vol.14
-
-
Feldman, H.I.1
Appel, L.J.2
Chertow, G.M.3
Cifelli, D.4
Cizman, B.5
Daugirdas, J.6
Fink, J.C.7
Franklin-Becker, E.D.8
Go, A.S.9
Hamm, L.L.10
He, J.11
Hostetter, T.12
Hsu, C.Y.13
Jamerson, K.14
Joffe, M.15
Kusek, J.W.16
Landis, J.R.17
Lash, J.P.18
Miller, E.R.19
Mohler III, E.R.20
Muntner, P.21
Ojo, A.O.22
Rahman, M.23
Townsend, R.R.24
Wright, J.T.25
more..
-
31
-
-
17744406760
-
+-ATPase: Relation to genetic hypertension
-
+-ATPase: relation to genetic hypertension. Am J Physiol Heart Circ Physiol 277: H1338-H1349, 1999.
-
(1999)
Am J Physiol Heart Circ Physiol
, vol.277
-
-
Ferrandi, M.1
Salardi, S.2
Tripodi, G.3
Barassi, P.4
Rivera, R.5
Manunta, P.6
Goldshleger, R.7
Ferrari, P.8
Bianchi, G.9
Karlish, S.J.10
-
32
-
-
79956051525
-
Association of genetic variation with systolic and diastolic blood pressure among African Americans: The Candidate Gene Association Resource study
-
Fox ER, Young JH, Li Y, Dreisbach AW, Keating BJ, Musani SK, Liu K, Morrison AC, Ganesh S, Kutlar A, Ramachandran VS, Polak JF, Fabsitz RR, Dries DL, Farlow DN, Redline S, Adeyemo A, Hirschorn JN, Sun YV, Wyatt SB, Penman AD, Palmas W, Rotter JI, Townsend RR, Doumatey AP, Tayo BO, Mosley TH Jr, Lyon HN, Kang SJ, Rotimi CN, Cooper RS, Franceschini N, Curb JD, Martin LW, Eaton CB, Kardia SL, Taylor HA, Caulfield MJ, Ehret GB, Johnson T, Chakravarti A, Zhu X, Levy D. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Hum Mol Genet 20: 2273-2284, 2011.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2273-2284
-
-
Fox, E.R.1
Young, J.H.2
Li, Y.3
Dreisbach, A.W.4
Keating, B.J.5
Musani, S.K.6
Liu, K.7
Morrison, A.C.8
Ganesh, S.9
Kutlar, A.10
Ramachandran, V.S.11
Polak, J.F.12
Fabsitz, R.R.13
Dries, D.L.14
Farlow, D.N.15
Redline, S.16
Adeyemo, A.17
Hirschorn, J.N.18
Sun, Y.V.19
Wyatt, S.B.20
Penman, A.D.21
Palmas, W.22
Rotter, J.I.23
Townsend, R.R.24
Doumatey, A.P.25
Tayo, B.O.26
Mosley Jr., T.H.27
Lyon, H.N.28
Kang, S.J.29
Rotimi, C.N.30
Cooper, R.S.31
Franceschini, N.32
Curb, J.D.33
Martin, L.W.34
Eaton, C.B.35
Kardia, S.L.36
Taylor, H.A.37
Caulfield, M.J.38
Ehret, G.B.39
Johnson, T.40
Chakravarti, A.41
Zhu, X.42
Levy, D.43
more..
-
33
-
-
84883824600
-
Genomewide 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, Tayo BO, Sun YV, Gottesman O, Adeyemo A, Johnson AD, Young JH, Rice K, Duan Q, Chen F, Li Y, Tang H, Fornage M, Keene KL, Andrews JS, Smith JA, Faul JD, Guangfa Z, Guo W, Liu Y, Murray SS, Musani SK, Srinivasan S, Velez Edwards DR, Wang H, Becker LC, Bovet P, Bochud M, Broeckel U, Burnier M, Carty C, Chasman DI, Ehret G, Chen WM, Chen G, Chen W, Ding J, Dreisbach AW, Evans MK, Guo X, Garcia ME, Jensen R, Keller MF, Lettre G, Lotay V, Martin LW, Moore JH, Morrison AC, Mosley TH, Ogunniyi A, Palmas W, Papanicolaou G, Penman A, Polak JF, Ridker PM, Salako B, Singleton AB, Shriner D, Taylor KD, Vasan R, Wiggins K, Williams SM, Yanek LR, Zhao W, Zonderman AB, Becker DM, Berenson G, Boerwinkle E, Bottinger E, Cushman M, Eaton C, Nyberg F, Heiss G, Hirschhron JN, Howard VJ, Karczewsk KJ, Lanktree MB, Liu K, Loos R, Margolis K, Snyder M, Psaty BM, Schork NJ, Weir DR, Rotimi CN, Sale MM, Harris T, Kardia SL, Hunt SC, Arnett D, Redline S, Cooper RS, Risch NJ, Rao DC, Rotter JI, Chakravarti A, Reiner AP, Levy D, Keating BJ, Zhu X. Genomewide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet 93: 545-554, 2013.
-
(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
Tayo, B.O.7
Sun, Y.V.8
Gottesman, O.9
Adeyemo, A.10
Johnson, A.D.11
Young, J.H.12
Rice, K.13
Duan, Q.14
Chen, F.15
Li, Y.16
Tang, H.17
Fornage, M.18
Keene, K.L.19
Andrews, J.S.20
Smith, J.A.21
Faul, J.D.22
Guangfa, Z.23
Guo, W.24
Liu, Y.25
Murray, S.S.26
Musani, S.K.27
Srinivasan, S.28
Velez Edwards, D.R.29
Wang, H.30
Becker, L.C.31
Bovet, P.32
Bochud, M.33
Broeckel, U.34
Burnier, M.35
Carty, C.36
Chasman, D.I.37
Ehret, G.38
Chen, W.M.39
Chen, G.40
Chen, W.41
Ding, J.42
Dreisbach, A.W.43
Evans, M.K.44
Guo, X.45
Garcia, M.E.46
Jensen, R.47
Keller, M.F.48
Lettre, G.49
Lotay, V.50
Martin, L.W.51
Moore, J.H.52
Morrison, A.C.53
Mosley, T.H.54
Ogunniyi, A.55
Palmas, W.56
Papanicolaou, G.57
Penman, A.58
Polak, J.F.59
Ridker, P.M.60
Salako, B.61
Singleton, A.B.62
Shriner, D.63
Taylor, K.D.64
Vasan, R.65
Wiggins, K.66
Williams, S.M.67
Yanek, L.R.68
Zhao, W.69
Zonderman, A.B.70
Becker, D.M.71
Berenson, G.72
Boerwinkle, E.73
Bottinger, E.74
Cushman, M.75
Eaton, C.76
Nyberg, F.77
Heiss, G.78
Hirschhron, J.N.79
Howard, V.J.80
Karczewsk, K.J.81
Lanktree, M.B.82
Liu, K.83
Loos, R.84
Margolis, K.85
Snyder, M.86
Psaty, B.M.87
Schork, N.J.88
Weir, D.R.89
Rotimi, C.N.90
Sale, M.M.91
Harris, T.92
Kardia, S.L.93
Hunt, S.C.94
Arnett, D.95
Redline, S.96
Cooper, R.S.97
Risch, N.J.98
more..
-
34
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, Yang H, Zeng C, Gao Y, Hu H, Hu W, Li C, Lin W, Liu S, Pan H, Tang X, Wang J, Wang W, Yu J, Zhang B, Zhang Q, Zhao H, Zhou J, Gabriel SB, Barry R, Blumenstiel B, Camargo A, Defelice M, Faggart M, Goyette M, Gupta S, Moore J, Nguyen H, Onofrio RC, Parkin M, Roy J, Stahl E, Winchester E, Ziaugra L, Altshuler D, Shen Y, Yao Z, Huang W, Chu X, He Y, Jin L, Liu Y, Sun W, Wang H, Wang Y, Xiong X, Xu L, Waye MM, Tsui SK, Xue H, Wong JT, Galver LM, Fan JB, Gunderson K, Murray SS, Oliphant AR, Chee MS, Montpetit A, Chagnon F, Ferretti V, Leboeuf M, Olivier JF, Phillips MS, Roumy S, Sallee C, Verner A, Hudson TJ, Kwok PY, Cai D, Koboldt DC, Miller RD, Pawlikowska L, Taillon-Miller P, Xiao M, Tsui LC, Mak W, Song YQ, Tam PK, Nakamura Y, Kawaguchi T, Kitamoto T, Morizono T, Nagashima A, Ohnishi Y, Sekine A, Tanaka T, Tsunoda T, Deloukas P, Bird CP, Delgado M, Dermitzakis ET, Gwilliam R, Hunt S, Morrison J, Powell D, Stranger BE, Whittaker P, Bentley DR, Daly MJ, de Bakker PI, Barrett J, Chretien YR, Maller J, McCarroll S, Patterson N, Pe'er I, Price A, Purcell S, Richter DJ, Sabeti P, Saxena R, Schaffner SF, Sham PC, Varilly P, Stein LD, Krishnan L, Smith AV, Tello-Ruiz MK, Thorisson GA, Chakravarti A, Chen PE, Cutler DJ, Kashuk CS, Lin S, Abecasis GR, Guan W, Li Y, Munro HM, Qin ZS, Thomas DJ, McVean G, Auton A, Bottolo L, Cardin N, Eyheramendy S, Freeman C, Marchini J, Myers S, Spencer C, Stephens M, Donnelly P, Cardon LR, Clarke G, Evans DM, Morris AP, Weir BS, Mullikin JC, Sherry ST, Feolo M, Skol A, Zhang H, Matsuda I, Fukushima Y, Macer DR, Suda E, Rotimi CN, Adebamowo CA, Ajayi I, Aniagwu T, Marshall PA, Nkwodimmah C, Royal CD, Leppert MF, Dixon M, Peiffer A, Qiu R, Kent A, Kato K, Niikawa N, Adewole IF, Knoppers BM, Foster MW, Clayton EW, Watkin J, Muzny D, Nazareth L, Sodergren E, Weinstock GM, Yakub I, Birren BW, Wilson RK, Fulton LL, Rogers J, Burton J, Carter NP, Clee CM, Griffiths M, Jones MC, McLay K, Plumb RW, Ross MT, Sims SK, Willey DL, Chen Z, Han H, Kang L, Godbout M, Wallenburg JC, L'Archeveque P, Bellemare G, Saeki K, An D, Fu H, Li Q, Wang Z, Wang R, Holden AL, Brooks LD, McEwen JE, Guyer MS, Wang VO, Peterson JL, Shi M, Spiegel J, Sung LM, Zacharia LF, Collins FS, Kennedy K, Jamieson R, Stewart J. A second generation human haplotype map of over 3.1 million SNPs. Nature 449: 851-861, 2007.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
Pasternak, S.11
Wheeler, D.A.12
Willis, T.D.13
Yu, F.14
Yang, H.15
Zeng, C.16
Gao, Y.17
Hu, H.18
Hu, W.19
Li, C.20
Lin, W.21
Liu, S.22
Pan, H.23
Tang, X.24
Wang, J.25
Wang, W.26
Yu, J.27
Zhang, B.28
Zhang, Q.29
Zhao, H.30
Zhou, J.31
Gabriel, S.B.32
Barry, R.33
Blumenstiel, B.34
Camargo, A.35
Defelice, M.36
Faggart, M.37
Goyette, M.38
Gupta, S.39
Moore, J.40
Nguyen, H.41
Onofrio, R.C.42
Parkin, M.43
Roy, J.44
Stahl, E.45
Winchester, E.46
Ziaugra, L.47
Altshuler, D.48
Shen, Y.49
Yao, Z.50
Huang, W.51
Chu, X.52
He, Y.53
Jin, L.54
Liu, Y.55
Sun, W.56
Wang, H.57
Wang, Y.58
Xiong, X.59
Xu, L.60
Waye, M.M.61
Tsui, S.K.62
Xue, H.63
Wong, J.T.64
Galver, L.M.65
Fan, J.B.66
Gunderson, K.67
Murray, S.S.68
Oliphant, A.R.69
Chee, M.S.70
Montpetit, A.71
Chagnon, F.72
Ferretti, V.73
Leboeuf, M.74
Olivier, J.F.75
Phillips, M.S.76
Roumy, S.77
Sallee, C.78
Verner, A.79
Hudson, T.J.80
Kwok, P.Y.81
Cai, D.82
Koboldt, D.C.83
Miller, R.D.84
Pawlikowska, L.85
Taillon-Miller, P.86
Xiao, M.87
Tsui, L.C.88
Mak, W.89
Song, Y.Q.90
Tam, P.K.91
Nakamura, Y.92
Kawaguchi, T.93
Kitamoto, T.94
Morizono, T.95
Nagashima, A.96
Ohnishi, Y.97
Sekine, A.98
more..
-
35
-
-
12144285594
-
Assessing the impact of population stratification on genetic association studies
-
Freedman ML, Reich D, Penney KL, McDonald GJ, Mignault AA, Patterson N, Gabriel SB, Topol EJ, Smoller JW, Pato CN, Pato MT, Petryshen TL, Kolonel LN, Lander ES, Sklar P, Henderson B, Hirschhorn JN, Altshuler D. Assessing the impact of population stratification on genetic association studies. Nat Genet 36: 388-393, 2004.
-
(2004)
Nat Genet
, vol.36
, pp. 388-393
-
-
Freedman, M.L.1
Reich, D.2
Penney, K.L.3
McDonald, G.J.4
Mignault, A.A.5
Patterson, N.6
Gabriel, S.B.7
Topol, E.J.8
Smoller, J.W.9
Pato, C.N.10
Pato, M.T.11
Petryshen, T.L.12
Kolonel, L.N.13
Lander, E.S.14
Sklar, P.15
Henderson, B.16
Hirschhorn, J.N.17
Altshuler, D.18
-
36
-
-
34250653301
-
Fatal gastrointestinal obstruction and hypertension in mice lacking nitric oxide-sensitive guanylyl cyclase
-
Friebe A, Mergia E, Dangel O, Lange A, Koesling D. Fatal gastrointestinal obstruction and hypertension in mice lacking nitric oxide-sensitive guanylyl cyclase. Proc Natl Acad Sci USA 104: 7699-7704, 2007.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 7699-7704
-
-
Friebe, A.1
Mergia, E.2
Dangel, O.3
Lange, A.4
Koesling, D.5
-
37
-
-
84875781416
-
Loci influencing blood pressure identified using a cardiovascular gene-centric array
-
Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, Gaunt TR, Gho JM, Gieger C, Gong Y, Isaacs A, Kleber ME, Mateo Leach I, McDonough CW, Meijs MF, Mellander O, Molony CM, Nolte IM, Padmanabhan S, Price TS, Rajagopalan R, Shaffer J, Shah S, Shen H, Soranzo N, van der Most PJ, Van Iperen EP, Van Setten JA, Vonk JM, Zhang L, Beitelshees AL, Berenson GS, Bhatt DL, Boer JM, Boerwinkle E, Burkley B, Burt A, Chakravarti A, Chen W, Cooper-Dehoff RM, Curtis SP, Dreisbach A, Duggan D, Ehret GB, Fabsitz RR, Fornage M, Fox E, Furlong CE, Gansevoort RT, Hofker MH, Hovingh GK, Kirkland SA, Kottke-Marchant K, Kutlar A, Lacroix AZ, Langaee TY, Li YR, Lin H, Liu K, Maiwald S, Malik R, Murugesan G, Newton-Cheh C, O'Connell JR, Onland-Moret NC, Ouwehand WH, Palmas W, Penninx BW, Pepine CJ, Pettinger M, Polak JF, Ramachandran VS, Ranchalis J, Redline S, Ridker PM, Rose LM, Scharnag H, Schork NJ, Shimbo D, Shuldiner AR, Srinivasan SR, Stolk RP, Taylor HA, Thorand B, Trip MD, van Duijn CM, Verschuren WM, Wijmenga C, Winkelmann BR, Wyatt S, Young JH, Boehm BO, Caulfield MJ, Chasman DI, Davidson KW, Doevendans PA, Fitzgerald GA, Gums JG, Hakonarson H, Hillege HL, Illig T, Jarvik GP, Johnson JA, Kastelein JJ, Koenig W, Marz W, Mitchell BD, Murray SS, Oldehinkel AJ, Rader DJ, Reilly MP, Reiner AP, Schadt EE, Silverstein RL, Snieder H, Stanton AV, Uitterlinden AG, van der Harst P, van der Schouw YT, Samani NJ, Johnson AD, Munroe PB, de Bakker PI, Zhu X, Levy D, Keating BJ, Asselbergs FW. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum Mol Genet 22: 1663-1678, 2013.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 1663-1678
-
-
Ganesh, S.K.1
Tragante, V.2
Guo, W.3
Guo, Y.4
Lanktree, M.B.5
Smith, E.N.6
Johnson, T.7
Castillo, B.A.8
Barnard, J.9
Baumert, J.10
Chang, Y.P.11
Elbers, C.C.12
Farrall, M.13
Fischer, M.E.14
Franceschini, N.15
Gaunt, T.R.16
Gho, J.M.17
Gieger, C.18
Gong, Y.19
Isaacs, A.20
Kleber, M.E.21
Mateo Leach, I.22
McDonough, C.W.23
Meijs, M.F.24
Mellander, O.25
Molony, C.M.26
Nolte, I.M.27
Padmanabhan, S.28
Price, T.S.29
Rajagopalan, R.30
Shaffer, J.31
Shah, S.32
Shen, H.33
Soranzo, N.34
van der Most, P.J.35
Van Iperen, E.P.36
Van Setten, J.A.37
Vonk, J.M.38
Zhang, L.39
Beitelshees, A.L.40
Berenson, G.S.41
Bhatt, D.L.42
Boer, J.M.43
Boerwinkle, E.44
Burkley, B.45
Burt, A.46
Chakravarti, A.47
Chen, W.48
Cooper-Dehoff, R.M.49
Curtis, S.P.50
Dreisbach, A.51
Duggan, D.52
Ehret, G.B.53
Fabsitz, R.R.54
Fornage, M.55
Fox, E.56
Furlong, C.E.57
Gansevoort, R.T.58
Hofker, M.H.59
Hovingh, G.K.60
Kirkland, S.A.61
Kottke-Marchant, K.62
Kutlar, A.63
Lacroix, A.Z.64
Langaee, T.Y.65
Li, Y.R.66
Lin, H.67
Liu, K.68
Maiwald, S.69
Malik, R.70
Murugesan, G.71
Newton-Cheh, C.72
O'Connell, J.R.73
Onland-Moret, N.C.74
Ouwehand, W.H.75
Palmas, W.76
Penninx, B.W.77
Pepine, C.J.78
Pettinger, M.79
Polak, J.F.80
Ramachandran, V.S.81
Ranchalis, J.82
Redline, S.83
Ridker, P.M.84
Rose, L.M.85
Scharnag, H.86
Schork, N.J.87
Shimbo, D.88
Shuldiner, A.R.89
Srinivasan, S.R.90
Stolk, R.P.91
Taylor, H.A.92
Thorand, B.93
Trip, M.D.94
van Duijn, C.M.95
Verschuren, W.M.96
Wijmenga, C.97
Winkelmann, B.R.98
more..
-
38
-
-
0037385533
-
Defining the blood pressure QTL on chromosome 7 in Dahl rats by a 177-kb congenic segment containing Cyp11b1
-
Garrett MR, Rapp JP. Defining the blood pressure QTL on chromosome 7 in Dahl rats by a 177-kb congenic segment containing Cyp11b1. Mamm Genome 14: 268-273, 2003.
-
(2003)
Mamm Genome
, vol.14
, pp. 268-273
-
-
Garrett, M.R.1
Rapp, J.P.2
-
39
-
-
84872054233
-
Executive summary: Heart disease and stroke statistics-2013 update: A report from the American Heart Association
-
Go AS, Mozaffarian D, Roger VL, Benjamin EJ, Berry JD, Borden WB, Bravata DM, Dai S, Ford ES, Fox CS, Franco S, Fullerton HJ, Gillespie C, Hailpern SM, Heit JA, Howard VJ, Huffman MD, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Magid D, Marcus GM, Marelli A, Matchar DB, McGuire DK, Mohler ER, Moy CS, Mussolino ME, Nichol G, Paynter NP, Schreiner PJ, Sorlie PD, Stein J, Turan TN, Virani SS, Wong ND, Woo D, Turner MB. Executive summary: heart disease and stroke statistics-2013 update: a report from the American Heart Association. Circulation 127: 143-152, 2013.
-
(2013)
Circulation
, vol.127
, pp. 143-152
-
-
Go, A.S.1
Mozaffarian, D.2
Roger, V.L.3
Benjamin, E.J.4
Berry, J.D.5
Borden, W.B.6
Bravata, D.M.7
Dai, S.8
Ford, E.S.9
Fox, C.S.10
Franco, S.11
Fullerton, H.J.12
Gillespie, C.13
Hailpern, S.M.14
Heit, J.A.15
Howard, V.J.16
Huffman, M.D.17
Kissela, B.M.18
Kittner, S.J.19
Lackland, D.T.20
Lichtman, J.H.21
Lisabeth, L.D.22
Magid, D.23
Marcus, G.M.24
Marelli, A.25
Matchar, D.B.26
McGuire, D.K.27
Mohler, E.R.28
Moy, C.S.29
Mussolino, M.E.30
Nichol, G.31
Paynter, N.P.32
Schreiner, P.J.33
Sorlie, P.D.34
Stein, J.35
Turan, T.N.36
Virani, S.S.37
Wong, N.D.38
Woo, D.39
Turner, M.B.40
more..
-
40
-
-
0027968723
-
Lack of association between the I/D polymorphism of the angiotensin-converting enzyme gene and essential hypertension in a Belgian population
-
Gu XX, Spaepen M, Guo C, Fagard R, Amery A, Lijnen P, Cassiman JJ. Lack of association between the I/D polymorphism of the angiotensin-converting enzyme gene and essential hypertension in a Belgian population. J Hum Hypertens 8: 683-685, 1994.
-
(1994)
J Hum Hypertens
, vol.8
, pp. 683-685
-
-
Gu, X.X.1
Spaepen, M.2
Guo, C.3
Fagard, R.4
Amery, A.5
Lijnen, P.6
Cassiman, J.J.7
-
41
-
-
0025011680
-
Long-term arterial pressure control: An analysis from animal experiments and computer and graphic models
-
Guyton AC. Long-term arterial pressure control: an analysis from animal experiments and computer and graphic models. Am J Physiol Regul Integr Comp Physiol 259: R865-R877, 1990.
-
(1990)
Am J Physiol Regul Integr Comp Physiol
, vol.259
-
-
Guyton, A.C.1
-
42
-
-
0015338161
-
Arterial pressure regulation overriding dominance of the kidneys in long-term regulation and in hypertension
-
Guyton AC, Coleman TG, Cowley AV Jr, Scheel KW, Manning RD Jr, Norman RA Jr. Arterial pressure regulation overriding dominance of the kidneys in long-term regulation and in hypertension. Am J Med 52: 584-594, 1972.
-
(1972)
Am J Med
, vol.52
, pp. 584-594
-
-
Guyton, A.C.1
Coleman, T.G.2
Cowley Jr., A.V.3
Scheel, K.W.4
Manning Jr., R.D.5
Norman Jr., R.A.6
-
43
-
-
0038690424
-
Trends in prevalence, awareness, treatment, and control of hypertension in the United States, 1988-2000
-
Hajjar I, Kotchen TA. Trends in prevalence, awareness, treatment, and control of hypertension in the United States, 1988-2000. JAMA 290: 199-206, 2003.
-
(2003)
JAMA
, vol.290
, pp. 199-206
-
-
Hajjar, I.1
Kotchen, T.A.2
-
44
-
-
0037952930
-
Historical perspective of the renin-angiotensin system
-
Hall JE. Historical perspective of the renin-angiotensin system. Mol Biotechnol 24: 27-39, 2003.
-
(2003)
Mol Biotechnol
, vol.24
, pp. 27-39
-
-
Hall, J.E.1
-
45
-
-
58049217860
-
-
[Online], [06/09/]
-
Hindorff LA, MacArthur J, Morales J, Junkins HA, Hall PN, Klemm AK, Manolio TA. A Catalog of Published Genome-Wide Association Studies. [Online]. www.genome.gov/gwastudies. [06/09/2013].
-
(2013)
A Catalog of Published Genome-Wide Association Studies
-
-
Hindorff, L.A.1
McArthur, J.2
Morales, J.3
Junkins, H.A.4
Hall, P.N.5
Klemm, A.K.6
Manolio, T.A.7
-
46
-
-
78650802616
-
Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study
-
Ho JE, Levy D, Rose L, Johnson AD, Ridker PM, Chasman DI. Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study. J Hypertens 29: 62-69, 2011.
-
(2011)
J Hypertens
, vol.29
, pp. 62-69
-
-
Ho, J.E.1
Levy, D.2
Rose, L.3
Johnson, A.D.4
Ridker, P.M.5
Chasman, D.I.6
-
47
-
-
0344271798
-
Genetics of hypertension
-
Hopkins PN, Hunt SC. Genetics of hypertension. Genet Med 5: 413-429, 2003.
-
(2003)
Genet Med
, vol.5
, pp. 413-429
-
-
Hopkins, P.N.1
Hunt, S.C.2
-
48
-
-
17644378057
-
Elevated blood pressure and risk of end-stage renal disease in subjects without baseline kidney disease
-
Hsu CY, McCulloch CE, Darbinian J, Go AS, Iribarren C. Elevated blood pressure and risk of end-stage renal disease in subjects without baseline kidney disease. Arch Intern Med 165: 923-928, 2005.
-
(2005)
Arch Intern Med
, vol.165
, pp. 923-928
-
-
Hsu, C.Y.1
McCulloch, C.E.2
Darbinian, J.3
Go, A.S.4
Iribarren, C.5
-
49
-
-
84873085571
-
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion
-
Huyghe JR, Jackson AU, Fogarty MP, Buchkovich ML, Stancakova A, Stringham HM, Sim X, Yang L, Fuchsberger C, Cederberg H, Chines PS, Teslovich TM, Romm JM, Ling H, McMullen I, Ingersoll R, Pugh EW, Doheny KF, Neale BM, Daly MJ, Kuusisto J, Scott LJ, Kang HM, Collins FS, Abecasis GR, Watanabe RM, Boehnke M, Laakso M, Mohlke KL. Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nat Genet 45: 197-201, 2013.
-
(2013)
Nat Genet
, vol.45
, pp. 197-201
-
-
Huyghe, J.R.1
Jackson, A.U.2
Fogarty, M.P.3
Buchkovich, M.L.4
Stancakova, A.5
Stringham, H.M.6
Sim, X.7
Yang, L.8
Fuchsberger, C.9
Cederberg, H.10
Chines, P.S.11
Teslovich, T.M.12
Romm, J.M.13
Ling, H.14
McMullen, I.15
Ingersoll, R.16
Pugh, E.W.17
Doheny, K.F.18
Neale, B.M.19
Daly, M.J.20
Kuusisto, J.21
Scott, L.J.22
Kang, H.M.23
Collins, F.S.24
Abecasis, G.R.25
Watanabe, R.M.26
Boehnke, M.27
Laakso, M.28
Mohlke, K.L.29
more..
-
50
-
-
0030893575
-
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro
-
Inoue I, Nakajima T, Williams CS, Quackenbush J, Puryear R, Powers M, Cheng T, Ludwig EH, Sharma AM, Hata A, Jeunemaitre X, Lalouel JM. A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro. J Clin Invest 99: 1786-1797, 1997.
-
(1997)
J Clin Invest
, vol.99
, pp. 1786-1797
-
-
Inoue, I.1
Nakajima, T.2
Williams, C.S.3
Quackenbush, J.4
Puryear, R.5
Powers, M.6
Cheng, T.7
Ludwig, E.H.8
Sharma, A.M.9
Hata, A.10
Jeunemaitre, X.11
Lalouel, J.M.12
-
51
-
-
0021717196
-
The sympathoadrenal system in the maintenance of elevated arterial pressure
-
Izzo JL Jr. The sympathoadrenal system in the maintenance of elevated arterial pressure. J Cardiovasc Pharmacol 6, Suppl 3: S514-S521, 1984.
-
(1984)
J Cardiovasc Pharmacol
, vol.6
, Issue.SUPPL. 3
-
-
Izzo Jr., J.L.1
-
52
-
-
0033966178
-
Applicability of a "speed" congenic strategy to dissect blood pressure quantitative trait loci on rat chromosome 2
-
Jeffs B, Negrin CD, Graham D, Clark JS, Anderson NH, Gauguier D, Dominiczak AF. Applicability of a "speed" congenic strategy to dissect blood pressure quantitative trait loci on rat chromosome 2. Hypertension 35: 179-187, 2000.
-
(2000)
Hypertension
, vol.35
, pp. 179-187
-
-
Jeffs, B.1
Negrin, C.D.2
Graham, D.3
Clark, J.S.4
Anderson, N.H.5
Gauguier, D.6
Dominiczak, A.F.7
-
53
-
-
0026669336
-
Molecular basis of human hypertension: Role of angiotensinogen
-
Jeunemaitre X, Soubrier F, Kotelevtsev YV, Lifton RP, Williams CS, Charru A, Hunt SC, Hopkins PN, Williams RR, Lalouel JM, Corvol P. Molecular basis of human hypertension: role of angiotensinogen. Cell 71: 169-180, 1992.
-
(1992)
Cell
, vol.71
, pp. 169-180
-
-
Jeunemaitre, X.1
Soubrier, F.2
Kotelevtsev, Y.V.3
Lifton, R.P.4
Williams, C.S.5
Charru, A.6
Hunt, S.C.7
Hopkins, P.N.8
Williams, R.R.9
Lalouel, J.M.10
Corvol, P.11
-
54
-
-
77149140136
-
Association of angiotensinogen gene M235T and angiotensin-converting enzyme gene I/D polymorphisms with essential hypertension in Han Chinese population: A meta-analysis
-
Ji LD, Zhang LN, Shen P, Wang P, Zhang YM, Xing WH, Xu J. Association of angiotensinogen gene M235T and angiotensin-converting enzyme gene I/D polymorphisms with essential hypertension in Han Chinese population: a meta-analysis. J Hypertens 28: 419-428, 2010.
-
(2010)
J Hypertens
, vol.28
, pp. 419-428
-
-
Ji, L.D.1
Zhang, L.N.2
Shen, P.3
Wang, P.4
Zhang, Y.M.5
Xing, W.H.6
Xu, J.7
-
55
-
-
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, Newton-Cheh C, State MW, Levy D, Lifton RP. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet 40: 592-599, 2008.
-
(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
Newton-Cheh, C.7
State, M.W.8
Levy, D.9
Lifton, R.P.10
-
56
-
-
83555162484
-
Blood pressure loci identified with a gene-centric array
-
Johnson T, Gaunt TR, Newhouse SJ, Padmanabhan S, Tomaszewski M, Kumari M, Morris RW, Tzoulaki I, O'Brien ET, Poulter NR, Sever P, Shields DC, Thom S, Wannamethee SG, Whincup PH, Brown MJ, Connell JM, Dobson RJ, Howard PJ, Mein CA, Onipinla A, Shaw-Hawkins S, Zhang Y, Davey Smith G, Day IN, Lawlor DA, Goodall AH, Fowkes FG, Abecasis GR, Elliott P, Gateva V, Braund PS, Burton PR, Nelson CP, Tobin MD, van der Harst P, Glorioso N, Neuvrith H, Salvi E, Staessen JA, Stucchi A, Devos N, Jeunemaitre X, Plouin PF, Tichet J, Juhanson P, Org E, Putku M, Sober S, Veldre G, Viigimaa M, Levinsson A, Rosengren A, Thelle DS, Hastie CE, Hedner T, Lee WK, Melander O, Wahlstrand B, Hardy R, Wong A, Cooper JA, Palmen J, Chen L, Stewart AF, Wells GA, Westra HJ, Wolfs MG, Clarke R, Franzosi MG, Goel A, Hamsten A, Lathrop M, Peden JF, Seedorf U, Watkins H, Ouwehand WH, Sambrook J, Stephens J, Casas JP, Drenos F, Holmes MV, Kivimaki M, Shah S, Shah T, Talmud PJ, Whittaker J, Wallace C, Delles C, Laan M, Kuh D, Humphries SE, Nyberg F, Cusi D, Roberts R, Newton-Cheh C, Franke L, Stanton AV, Dominiczak AF, Farrall M, Hingorani AD, Samani NJ, Caulfield MJ, Munroe PB. Blood pressure loci identified with a gene-centric array. Am J Hum Genet 89: 688-700, 2011.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 688-700
-
-
Johnson, T.1
Gaunt, T.R.2
Newhouse, S.J.3
Padmanabhan, S.4
Tomaszewski, M.5
Kumari, M.6
Morris, R.W.7
Tzoulaki, I.8
O'Brien, E.T.9
Poulter, N.R.10
Sever, P.11
Shields, D.C.12
Thom, S.13
Wannamethee, S.G.14
Whincup, P.H.15
Brown, M.J.16
Connell, J.M.17
Dobson, R.J.18
Howard, P.J.19
Mein, C.A.20
Onipinla, A.21
Shaw-Hawkins, S.22
Zhang, Y.23
Davey Smith, G.24
Day, I.N.25
Lawlor, D.A.26
Goodall, A.H.27
Fowkes, F.G.28
Abecasis, G.R.29
Elliott, P.30
Gateva, V.31
Braund, P.S.32
Burton, P.R.33
Nelson, C.P.34
Tobin, M.D.35
van der Harst, P.36
Glorioso, N.37
Neuvrith, H.38
Salvi, E.39
Staessen, J.A.40
Stucchi, A.41
Devos, N.42
Jeunemaitre, X.43
Plouin, P.F.44
Tichet, J.45
Juhanson, P.46
Org, E.47
Putku, M.48
Sober, S.49
Veldre, G.50
Viigimaa, M.51
Levinsson, A.52
Rosengren, A.53
Thelle, D.S.54
Hastie, C.E.55
Hedner, T.56
Lee, W.K.57
Melander, O.58
Wahlstrand, B.59
Hardy, R.60
Wong, A.61
Cooper, J.A.62
Palmen, J.63
Chen, L.64
Stewart, A.F.65
Wells, G.A.66
Westra, H.J.67
Wolfs, M.G.68
Clarke, R.69
Franzosi, M.G.70
Goel, A.71
Hamsten, A.72
Lathrop, M.73
Peden, J.F.74
Seedorf, U.75
Watkins, H.76
Ouwehand, W.H.77
Sambrook, J.78
Stephens, J.79
Casas, J.P.80
Drenos, F.81
Holmes, M.V.82
Kivimaki, M.83
Shah, S.84
Shah, T.85
Talmud, P.J.86
Whittaker, J.87
Wallace, C.88
Delles, C.89
Laan, M.90
Kuh, D.91
Humphries, S.E.92
Nyberg, F.93
Cusi, D.94
Roberts, R.95
Newton-Cheh, C.96
Franke, L.97
Stanton, A.V.98
more..
-
58
-
-
0024344616
-
Adducin: Ca++-dependent association with sites of cell-cell contact
-
Kaiser HW, O'Keefe E, Bennett V. Adducin: Ca++-dependent association with sites of cell-cell contact. J Cell Biol 109: 557-569, 1989.
-
(1989)
J Cell Biol
, vol.109
, pp. 557-569
-
-
Kaiser, H.W.1
O'Keefe, E.2
Bennett, V.3
-
59
-
-
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, Tay WT, Chen CH, Zhang Y, Yamamoto K, Katsuya T, Yokota M, Kim YJ, Ong RT, Nabika T, Gu D, Chang LC, Kokubo Y, Huang W, Ohnaka K, Yamori Y, Nakashima E, Jaquish CE, Lee JY, Seielstad M, Isono M, Hixson JE, Chen YT, Miki T, Zhou X, Sugiyama T, Jeon JP, Liu JJ, Takayanagi R, Kim SS, Aung T, Sung YJ, Zhang X, Wong TY, Han BG, Kobayashi S, Ogihara T, Zhu D, Iwai N, Wu JY, Teo YY, Tai ES, Cho YS, He J. Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat Genet 43: 531-538, 2011.
-
(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
Tay, W.T.7
Chen, C.H.8
Zhang, Y.9
Yamamoto, K.10
Katsuya, T.11
Yokota, M.12
Kim, Y.J.13
Ong, R.T.14
Nabika, T.15
Gu, D.16
Chang, L.C.17
Kokubo, Y.18
Huang, W.19
Ohnaka, K.20
Yamori, Y.21
Nakashima, E.22
Jaquish, C.E.23
Lee, J.Y.24
Seielstad, M.25
Isono, M.26
Hixson, J.E.27
Chen, Y.T.28
Miki, T.29
Zhou, X.30
Sugiyama, T.31
Jeon, J.P.32
Liu, J.J.33
Takayanagi, R.34
Kim, S.S.35
Aung, T.36
Sung, Y.J.37
Zhang, X.38
Wong, T.Y.39
Han, B.G.40
Kobayashi, S.41
Ogihara, T.42
Zhu, D.43
Iwai, N.44
Wu, J.Y.45
Teo, Y.Y.46
Tai, E.S.47
Cho, Y.S.48
He, J.49
more..
-
60
-
-
82455172153
-
Rare variants, common markers: Synthetic association and beyond
-
Kent JW Jr. Rare variants, common markers: synthetic association and beyond. Genet Epidemiol 35, Suppl 1: S80-S84, 2011.
-
(2011)
Genet Epidemiol
, vol.35
, Issue.SUPPL. 1
-
-
Kent Jr., J.W.1
-
61
-
-
0028944631
-
Genetic control of blood pressure and the angiotensinogen locus
-
Kim HS, Krege JH, Kluckman KD, Hagaman JR, Hodgin JB, Best CF, Jennette JC, Coffman TM, Maeda N, Smithies O. Genetic control of blood pressure and the angiotensinogen locus. Proc Natl Acad Sci USA 92: 2735-2739, 1995.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 2735-2739
-
-
Kim, H.S.1
Krege, J.H.2
Kluckman, K.D.3
Hagaman, J.R.4
Hodgin, J.B.5
Best, C.F.6
Jennette, J.C.7
Coffman, T.M.8
Maeda, N.9
Smithies, O.10
-
62
-
-
84858699473
-
Mice lacking hypertension candidate gene ATP2B1 in vascular smooth muscle cells show significant blood pressure elevation
-
Kobayashi Y, Hirawa N, Tabara Y, Muraoka H, Fujita M, Miyazaki N, Fujiwara A, Ichikawa Y, Yamamoto Y, Ichihara N, Saka S, Wakui H, Yoshida S, Yatsu K, Toya Y, Yasuda G, Kohara K, Kita Y, Takei K, Goshima Y, Ishikawa Y, Ueshima H, Miki T, Umemura S. Mice lacking hypertension candidate gene ATP2B1 in vascular smooth muscle cells show significant blood pressure elevation. Hypertension 59: 854-860, 2012.
-
(2012)
Hypertension
, vol.59
, pp. 854-860
-
-
Kobayashi, Y.1
Hirawa, N.2
Tabara, Y.3
Muraoka, H.4
Fujita, M.5
Miyazaki, N.6
Fujiwara, A.7
Ichikawa, Y.8
Yamamoto, Y.9
Ichihara, N.10
Saka, S.11
Wakui, H.12
Yoshida, S.13
Yatsu, K.14
Toya, Y.15
Yasuda, G.16
Kohara, K.17
Kita, Y.18
Takei, K.19
Goshima, Y.20
Ishikawa, Y.21
Ueshima, H.22
Miki, T.23
Umemura, S.24
more..
-
63
-
-
34147116715
-
Most rare missense alleles are deleterious in humans: Implications for complex disease and association studies
-
Kryukov GV, Pennacchio LA, Sunyaev SR. Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. Am J Hum Genet 80: 727-739, 2007.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 727-739
-
-
Kryukov, G.V.1
Pennacchio, L.A.2
Sunyaev, S.R.3
-
64
-
-
43049097195
-
Global burden of bloodpressure-related disease, 2001
-
Lawes CM, Vander Hoorn S, Rodgers A. Global burden of bloodpressure-related disease, 2001. Lancet 371: 1513-1518, 2008.
-
(2008)
Lancet
, vol.371
, pp. 1513-1518
-
-
Lawes, C.M.1
Vander Hoorn, S.2
Rodgers, A.3
-
65
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Kottgen A, Vasan RS, Rivadeneira F, Eiriksdottir G, Guo X, Arking DE, Mitchell GF, Mattace-Raso FU, Smith AV, Taylor K, Scharpf RB, Hwang SJ, Sijbrands EJ, Bis J, Harris TB, Ganesh SK, O'Donnell CJ, Hofman A, Rotter JI, Coresh J, Benjamin EJ, Uitterlinden AG, Heiss G, Fox CS, Witteman JC, Boerwinkle E, Wang TJ, Gudnason V, Larson MG, Chakravarti A, Psaty BM, van Duijn CM. Genome-wide association study of blood pressure and hypertension. Nat Genet 41: 677-687, 2009.
-
(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
Glazer, N.L.7
Morrison, A.C.8
Johnson, A.D.9
Aspelund, T.10
Aulchenko, Y.11
Lumley, T.12
Kottgen, A.13
Vasan, R.S.14
Rivadeneira, F.15
Eiriksdottir, G.16
Guo, X.17
Arking, D.E.18
Mitchell, G.F.19
Mattace-Raso, F.U.20
Smith, A.V.21
Taylor, K.22
Scharpf, R.B.23
Hwang, S.J.24
Sijbrands, E.J.25
Bis, J.26
Harris, T.B.27
Ganesh, S.K.28
O'Donnell, C.J.29
Hofman, A.30
Rotter, J.I.31
Coresh, J.32
Benjamin, E.J.33
Uitterlinden, A.G.34
Heiss, G.35
Fox, C.S.36
Witteman, J.C.37
Boerwinkle, E.38
Wang, T.J.39
Gudnason, V.40
Larson, M.G.41
Chakravarti, A.42
Psaty, B.M.43
van Duijn, C.M.44
more..
-
66
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Kottgen A, Vasan RS, Rivadeneira F, Eiriksdottir G, Guo X, Arking DE, Mitchell GF, Mattace-Raso FU, Smith AV, Taylor K, Scharpf RB, Hwang SJ, Sijbrands EJ, Bis J, Harris TB, Ganesh SK, O'Donnell CJ, Hofman A, Rotter JI, Coresh J, Benjamin EJ, Uitterlinden AG, Heiss G, Fox CS, Witteman JC, Boerwinkle E, Wang TJ, Gudnason V, Larson MG, Chakravarti A, Psaty BM, van Duijn CM. Genome-wide association study of blood pressure and hypertension. Nat Genet 41: 677-687, 2009.
-
(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
Glazer, N.L.7
Morrison, A.C.8
Johnson, A.D.9
Aspelund, T.10
Aulchenko, Y.11
Lumley, T.12
Kottgen, A.13
Vasan, R.S.14
Rivadeneira, F.15
Eiriksdottir, G.16
Guo, X.17
Arking, D.E.18
Mitchell, G.F.19
Mattace-Raso, F.U.20
Smith, A.V.21
Taylor, K.22
Scharpf, R.B.23
Hwang, S.J.24
Sijbrands, E.J.25
Bis, J.26
Harris, T.B.27
Ganesh, S.K.28
O'Donnell, C.J.29
Hofman, A.30
Rotter, J.I.31
Coresh, J.32
Benjamin, E.J.33
Uitterlinden, A.G.34
Heiss, G.35
Fox, C.S.36
Witteman, J.C.37
Boerwinkle, E.38
Wang, T.J.39
Gudnason, V.40
Larson, M.G.41
Chakravarti, A.42
Psaty, B.M.43
van Duijn, C.M.44
more..
-
67
-
-
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. 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 360: 1903-1913, 2002.
-
(2002)
Lancet
, vol.360
, pp. 1903-1913
-
-
Lewington, S.1
Clarke, R.2
Qizilbash, N.3
Peto, R.4
Collins, R.5
-
68
-
-
0026580019
-
A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton RP, Dluhy RG, Powers M, Rich GM, Cook S, Ulick S, Lalouel JM. A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature 355: 262-265, 1992.
-
(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
-
69
-
-
0026919361
-
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase
-
Lifton RP, Dluhy RG, Powers M, Rich GM, Gutkin M, Fallo F, Gill JR Jr, Feld L, Ganguly A, Laidlaw JC, Murnaghan DJ, Kaufman C, Stockigt JR, Ulick S, Lalouel JM Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase. Nat Genet 2: 66-74, 1992.
-
(1992)
Nat Genet
, vol.2
, pp. 66-74
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, G.M.4
Gutkin, M.5
Fallo, F.6
Gill Jr., J.R.7
Feld, L.8
Ganguly, A.9
Laidlaw, J.C.10
Murnaghan, D.J.11
Kaufman, C.12
Stockigt, J.R.13
Ulick, S.14
Lalouel, J.M.15
-
70
-
-
0035936780
-
Molecular mechanisms of human hypertension
-
Lifton RP, Gharavi AG, Geller DS. Molecular mechanisms of human hypertension. Cell 104: 545-556, 2001.
-
(2001)
Cell
, vol.104
, pp. 545-556
-
-
Lifton, R.P.1
Gharavi, A.G.2
Geller, D.S.3
-
71
-
-
84859120701
-
Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative
-
Liu EY, Buyske S, Aragaki AK, Peters U, Boerwinkle E, Carlson C, Carty C, Crawford DC, Haessler J, Hindorff LA, Marchand LL, Manolio TA, Matise T, Wang W, Kooperberg C, North KE, Li Y. Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative. Genet Epidemiol 36: 107-117, 2012.
-
(2012)
Genet Epidemiol
, vol.36
, pp. 107-117
-
-
Liu, E.Y.1
Buyske, S.2
Aragaki, A.K.3
Peters, U.4
Boerwinkle, E.5
Carlson, C.6
Carty, C.7
Crawford, D.C.8
Haessler, J.9
Hindorff, L.A.10
Marchand, L.L.11
Manolio, T.A.12
Matise, T.13
Wang, W.14
Kooperberg, C.15
North, K.E.16
Li, Y.17
-
72
-
-
76349121984
-
Defining and setting national goals for cardiovascular health promotion and disease reduction: The American Heart Association's strategic Impact Goal through 2020 and beyond
-
Lloyd-Jones DM, Hong Y, Labarthe D, Mozaffarian D, Appel LJ, Van Horn L, Greenlund K, Daniels S, Nichol G, Tomaselli GF, Arnett DK, Fonarow GC, Ho PM, Lauer MS, Masoudi FA, Robertson RM, Roger V, Schwamm LH, Sorlie P, Yancy CW, Rosamond WD. Defining and setting national goals for cardiovascular health promotion and disease reduction: the American Heart Association's strategic Impact Goal through 2020 and beyond. Circulation 121: 586-613, 2010.
-
(2010)
Circulation
, vol.121
, pp. 586-613
-
-
Lloyd-Jones, D.M.1
Hong, Y.2
Labarthe, D.3
Mozaffarian, D.4
Appel, L.J.5
Van Horn, L.6
Greenlund, K.7
Daniels, S.8
Nichol, G.9
Tomaselli, G.F.10
Arnett, D.K.11
Fonarow, G.C.12
Ho, P.M.13
Lauer, M.S.14
Masoudi, F.A.15
Robertson, R.M.16
Roger, V.17
Schwamm, L.H.18
Sorlie, P.19
Yancy, C.W.20
Rosamond, W.D.21
more..
-
73
-
-
80053549439
-
Clan genomics and the complex architecture of human disease
-
Lupski JR, Belmont JW, Boerwinkle E, Gibbs RA. Clan genomics and the complex architecture of human disease. Cell 147: 32-43, 2011.
-
(2011)
Cell
, vol.147
, pp. 32-43
-
-
Lupski, J.R.1
Belmont, J.W.2
Boerwinkle, E.3
Gibbs, R.A.4
-
74
-
-
80052825195
-
The functional spectrum of low-frequency coding variation
-
Marth GT, Yu F, Indap AR, Garimella K, Gravel S, Leong WF, Tyler-Smith C, Bainbridge M, Blackwell T, Zheng-Bradley X, Chen Y, Challis D, Clarke L, Ball EV, Cibulskis K, Cooper DN, Fulton B, Hartl C, Koboldt D, Muzny D, Smith R, Sougnez C, Stewart C, Ward A, Yu J, Xue Y, Altshuler D, Bustamante CD, Clark AG, Daly M, DePristo M, Flicek P, Gabriel S, Mardis E, Palotie A, Gibbs R. The functional spectrum of low-frequency coding variation. Genome Biol 12: R84, 2011.
-
(2011)
Genome Biol
, vol.12
-
-
Marth, G.T.1
Yu, F.2
Indap, A.R.3
Garimella, K.4
Gravel, S.5
Leong, W.F.6
Tyler-Smith, C.7
Bainbridge, M.8
Blackwell, T.9
Zheng-Bradley, X.10
Chen, Y.11
Challis, D.12
Clarke, L.13
Ball, E.V.14
Cibulskis, K.15
Cooper, D.N.16
Fulton, B.17
Hartl, C.18
Koboldt, D.19
Muzny, D.20
Smith, R.21
Sougnez, C.22
Stewart, C.23
Ward, A.24
Yu, J.25
Xue, Y.26
Altshuler, D.27
Bustamante, C.D.28
Clark, A.G.29
Daly, M.30
DePristo, M.31
Flicek, P.32
Gabriel, S.33
Mardis, E.34
Palotie, A.35
Gibbs, R.36
more..
-
75
-
-
20144373060
-
Reduction of Gstm1 expression in the stroke-prone spontaneously hypertension rat contributes to increased oxidative stress
-
McBride MW, Brosnan MJ, Mathers J, McLellan LI, Miller WH, Graham D, Hanlon N, Hamilton CA, Polke JM, Lee WK, Dominiczak AF. Reduction of Gstm1 expression in the stroke-prone spontaneously hypertension rat contributes to increased oxidative stress. Hypertension 45: 786-792, 2005.
-
(2005)
Hypertension
, vol.45
, pp. 786-792
-
-
McBride, M.W.1
Brosnan, M.J.2
Mathers, J.3
McLellan, L.I.4
Miller, W.H.5
Graham, D.6
Hanlon, N.7
Hamilton, C.A.8
Polke, J.M.9
Lee, W.K.10
Dominiczak, A.F.11
-
76
-
-
14644404384
-
Polymorphisms of the insertion/deletion ACE and M235T AGT genes and hypertension: Surprising new findings and meta-analysis of data
-
Mondry A, Loh M, Liu P, Zhu A, Nagel M. Polymorphisms of the insertion/deletion ACE and M235T AGT genes and hypertension: surprising new findings and meta-analysis of data. Bio Med Central Nephrol 6: 1, 2005.
-
(2005)
Bio Med Central Nephrol
, vol.6
, pp. 1
-
-
Mondry, A.1
Loh, M.2
Liu, P.3
Zhu, A.4
Nagel, M.5
-
77
-
-
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, Najjar SS, Zhao JH, Heath SC, Eyheramendy S, Papadakis K, Voight BF, Scott LJ, Zhang F, Farrall M, Tanaka T, Wallace C, Chambers JC, Khaw KT, Nilsson P, van der Harst P, Polidoro S, Grobbee DE, Onland-Moret NC, Bots ML, Wain LV, Elliott KS, Teumer A, Luan J, Lucas G, Kuusisto J, Burton PR, Hadley D, McArdle WL, Brown M, Dominiczak A, Newhouse SJ, Samani NJ, Webster J, Zeggini E, Beckmann JS, Bergmann S, Lim N, Song K, Vollenweider P, Waeber G, Waterworth DM, Yuan X, Groop L, Orho-Melander M, Allione A, Di Gregorio A, Guarrera S, Panico S, Ricceri F, Romanazzi V, Sacerdote C, Vineis P, Barroso I, Sandhu MS, Luben RN, Crawford GJ, Jousilahti P, Perola M, Boehnke M, Bonnycastle LL, Collins FS, Jackson AU, Mohlke KL, Stringham HM, Valle TT, Willer CJ, Bergman RN, Morken MA, Doring A, Gieger C, Illig T, Meitinger T, Org E, Pfeufer A, Wichmann HE, Kathiresan S, Marrugat J, O'Donnell CJ, Schwartz SM, Siscovick DS, Subirana I, Freimer NB, Hartikainen AL, McCarthy MI, O'Reilly PF, Peltonen L, Pouta A, de Jong PE, Snieder H, van Gilst WH, Clarke R, Goel A, Hamsten A, Peden JF, Seedorf U, Syvanen AC, Tognoni G, Lakatta EG, Sanna S, Scheet P, Schlessinger D, Scuteri A, Dorr M, Ernst F, Felix SB, Homuth G, Lorbeer R, Reffelmann T, Rettig R, Volker U, Galan P, Gut IG, Hercberg S, Lathrop GM, Zelenika D, Deloukas P, Soranzo N, Williams FM, Zhai G, Salomaa V, Laakso M, Elosua R, Forouhi NG, Volzke H, Uiterwaal CS, van der Schouw YT, Numans ME, Matullo G, Navis G, Berglund G, Bingham SA, Kooner JS, Connell JM, Bandinelli S, Ferrucci L, Watkins H, Spector TD, Tuomilehto J, Altshuler D, Strachan DP, Laan M, Meneton P, Wareham NJ, Uda M, Jarvelin MR, Mooser V, Melander O, Loos RJ, Elliott P, Abecasis GR, Caulfield M, Munroe PB. Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 41: 666-676, 2009.
-
(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
Najjar, S.S.7
Zhao, J.H.8
Heath, S.C.9
Eyheramendy, S.10
Papadakis, K.11
Voight, B.F.12
Scott, L.J.13
Zhang, F.14
Farrall, M.15
Tanaka, T.16
Wallace, C.17
Chambers, J.C.18
Khaw, K.T.19
Nilsson, P.20
van der Harst, P.21
Polidoro, S.22
Grobbee, D.E.23
Onland-Moret, N.C.24
Bots, M.L.25
Wain, L.V.26
Elliott, K.S.27
Teumer, A.28
Luan, J.29
Lucas, G.30
Kuusisto, J.31
Burton, P.R.32
Hadley, D.33
McArdle, W.L.34
Brown, M.35
Dominiczak, A.36
Newhouse, S.J.37
Samani, N.J.38
Webster, J.39
Zeggini, E.40
Beckmann, J.S.41
Bergmann, S.42
Lim, N.43
Song, K.44
Vollenweider, P.45
Waeber, G.46
Waterworth, D.M.47
Yuan, X.48
Groop, L.49
Orho-Melander, M.50
Allione, A.51
Di Gregorio, A.52
Guarrera, S.53
Panico, S.54
Ricceri, F.55
Romanazzi, V.56
Sacerdote, C.57
Vineis, P.58
Barroso, I.59
Sandhu, M.S.60
Luben, R.N.61
Crawford, G.J.62
Jousilahti, P.63
Perola, M.64
Boehnke, M.65
Bonnycastle, L.L.66
Collins, F.S.67
Jackson, A.U.68
Mohlke, K.L.69
Stringham, H.M.70
Valle, T.T.71
Willer, C.J.72
Bergman, R.N.73
Morken, M.A.74
Doring, A.75
Gieger, C.76
Illig, T.77
Meitinger, T.78
Org, E.79
Pfeufer, A.80
Wichmann, H.E.81
Kathiresan, S.82
Marrugat, J.83
O'Donnell, C.J.84
Schwartz, S.M.85
Siscovick, D.S.86
Subirana, I.87
Freimer, N.B.88
Hartikainen, A.L.89
McCarthy, M.I.90
O'Reilly, P.F.91
Peltonen, L.92
Pouta, A.93
de Jong, P.E.94
Snieder, H.95
van Gilst, W.H.96
Clarke, R.97
Goel, A.98
more..
-
78
-
-
61349089775
-
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
-
Newton-Cheh C, Larson MG, Vasan RS, Levy D, Bloch KD, Surti A, Guiducci C, Kathiresan S, Benjamin EJ, Struck J, Morgenthaler NG, Bergmann A, Blankenberg S, Kee F, Nilsson P, Yin X, Peltonen L, Vartiainen E, Salomaa V, Hirschhorn JN, Melander O, Wang TJ. Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure. Nat Genet 41: 348-353, 2009.
-
(2009)
Nat Genet
, vol.41
, pp. 348-353
-
-
Newton-Cheh, C.1
Larson, M.G.2
Vasan, R.S.3
Levy, D.4
Bloch, K.D.5
Surti, A.6
Guiducci, C.7
Kathiresan, S.8
Benjamin, E.J.9
Struck, J.10
Morgenthaler, N.G.11
Bergmann, A.12
Blankenberg, S.13
Kee, F.14
Nilsson, P.15
Yin, X.16
Peltonen, L.17
Vartiainen, E.18
Salomaa, V.19
Hirschhorn, J.N.20
Melander, O.21
Wang, T.J.22
more..
-
79
-
-
70249111091
-
Targeted capture and massively parallel sequencing of 12 human exomes
-
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J. Targeted capture and massively parallel sequencing of 12 human exomes. Nature 461: 272-276, 2009.
-
(2009)
Nature
, vol.461
, pp. 272-276
-
-
Ng, S.B.1
Turner, E.H.2
Robertson, P.D.3
Flygare, S.D.4
Bigham, A.W.5
Lee, C.6
Shaffer, T.7
Wong, M.8
Bhattacharjee, A.9
Eichler, E.E.10
Bamshad, M.11
Nickerson, D.A.12
Shendure, J.13
-
80
-
-
0001113072
-
Cardiovascular diseases in the spontaneously hypertensive Rat
-
Okamoto K, Aoki K, Nosaka S, Fukushima M. Cardiovascular diseases in the spontaneously hypertensive Rat. Jpn Circ J 28: 943-952, 1964.
-
(1964)
Jpn Circ J
, vol.28
, pp. 943-952
-
-
Okamoto, K.1
Aoki, K.2
Nosaka, S.3
Fukushima, M.4
-
81
-
-
0242381308
-
Phosphoinositide 3-kinase gammadeficient mice are protected from isoproterenol-induced heart failure
-
Oudit GY, Crackower MA, Eriksson U, Sarao R, Kozieradzki I, Sasaki T, Irie-Sasaki J, Gidrewicz D, Rybin VO, Wada T, Steinberg SF, Backx PH, Penninger JM. Phosphoinositide 3-kinase gammadeficient mice are protected from isoproterenol-induced heart failure. Circulation 108: 2147-2152, 2003.
-
(2003)
Circulation
, vol.108
, pp. 2147-2152
-
-
Oudit, G.Y.1
Crackower, M.A.2
Eriksson, U.3
Sarao, R.4
Kozieradzki, I.5
Sasaki, T.6
Irie-Sasaki, J.7
Gidrewicz, D.8
Rybin, V.O.9
Wada, T.10
Steinberg, S.F.11
Backx, P.H.12
Penninger, J.M.13
-
82
-
-
78449233580
-
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension
-
Padmanabhan S, Melander O, Johnson T, Di Blasio AM, Lee WK, Gentilini D, Hastie CE, Menni C, Monti MC, Delles C, Laing S, Corso B, Navis G, Kwakernaak AJ, van der Harst P, Bochud M, Maillard M, Burnier M, Hedner T, Kjeldsen S, Wahlstrand B, Sjogren M, Fava C, Montagnana M, Danese E, Torffvit O, Hedblad B, Snieder H, Connell JM, Brown M, Samani NJ, Farrall M, Cesana G, Mancia G, Signorini S, Grassi G, Eyheramendy S, Wichmann HE, Laan M, Strachan DP, Sever P, Shields DC, Stanton A, Vollenweider P, Teumer A, Volzke H, Rettig R, Newton-Cheh C, Arora P, Zhang F, Soranzo N, Spector TD, Lucas G, Kathiresan S, Siscovick DS, Luan J, Loos RJ, Wareham NJ, Penninx BW, Nolte IM, McBride M, Miller WH, Nicklin SA, Baker AH, Graham D, McDonald RA, Pell JP, Sattar N, Welsh P, Munroe P, Caulfield MJ, Zanchetti A, Dominiczak AF. Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. PLoS Genet 6: e1001177, 2010.
-
(2010)
PLoS Genet
, vol.6
-
-
Padmanabhan, S.1
Melander, O.2
Johnson, T.3
Di Blasio, A.M.4
Lee, W.K.5
Gentilini, D.6
Hastie, C.E.7
Menni, C.8
Monti, M.C.9
Delles, C.10
Laing, S.11
Corso, B.12
Navis, G.13
Kwakernaak, A.J.14
van der Harst, P.15
Bochud, M.16
Maillard, M.17
Burnier, M.18
Hedner, T.19
Kjeldsen, S.20
Wahlstrand, B.21
Sjogren, M.22
Fava, C.23
Montagnana, M.24
Danese, E.25
Torffvit, O.26
Hedblad, B.27
Snieder, H.28
Connell, J.M.29
Brown, M.30
Samani, N.J.31
Farrall, M.32
Cesana, G.33
Mancia, G.34
Signorini, S.35
Grassi, G.36
Eyheramendy, S.37
Wichmann, H.E.38
Laan, M.39
Strachan, D.P.40
Sever, P.41
Shields, D.C.42
Stanton, A.43
Vollenweider, P.44
Teumer, A.45
Volzke, H.46
Rettig, R.47
Newton-Cheh, C.48
Arora, P.49
Zhang, F.50
Soranzo, N.51
Spector, T.D.52
Lucas, G.53
Kathiresan, S.54
Siscovick, D.S.55
Luan, J.56
Loos, R.J.57
Wareham, N.J.58
Penninx, B.W.59
Nolte, I.M.60
McBride, M.61
Miller, W.H.62
Nicklin, S.A.63
Baker, A.H.64
Graham, D.65
McDonald, R.A.66
Pell, J.P.67
Sattar, N.68
Welsh, P.69
Munroe, P.70
Caulfield, M.J.71
Zanchetti, A.72
Dominiczak, A.F.73
more..
-
83
-
-
34247867956
-
Molecular genetics of experimental hypertension and the metabolic syndrome: From gene pathways to new therapies
-
Pravenec M, Kurtz TW. Molecular genetics of experimental hypertension and the metabolic syndrome: from gene pathways to new therapies. Hypertension 49: 941-952, 2007.
-
(2007)
Hypertension
, vol.49
, pp. 941-952
-
-
Pravenec, M.1
Kurtz, T.W.2
-
84
-
-
0035134739
-
Transgenic rescue of defective Cd36 ameliorates insulin resistance in spontaneously hypertensive rats
-
Pravenec M, Landa V, Zidek V, Musilova A, Kren V, Kazdova L, Aitman TJ, Glazier AM, Ibrahimi A, Abumrad NA, Qi N, Wang JM, St Lezin EM, Kurtz TW. Transgenic rescue of defective Cd36 ameliorates insulin resistance in spontaneously hypertensive rats. Nat Genet 27: 156-158, 2001.
-
(2001)
Nat Genet
, vol.27
, pp. 156-158
-
-
Pravenec, M.1
Landa, V.2
Zidek, V.3
Musilova, A.4
Kren, V.5
Kazdova, L.6
Aitman, T.J.7
Glazier, A.M.8
Ibrahimi, A.9
Abumrad, N.A.10
Qi, N.11
Wang, J.M.12
St. Lezin, E.M.13
Kurtz, T.W.14
-
85
-
-
43749105013
-
Genetic variation in the renal expression of CD36 regulates blood pressure in the sponteneously hypertensive rat
-
Abstract 56
-
Pravenec M, Zidek V, Landa V, Viklicky O, Sugimoto K, Qi N, Kurtz TW. Genetic variation in the renal expression of CD36 regulates blood pressure in the sponteneously hypertensive rat. Proceedings of the 21st Scientific Meeting of the International Society of Hypertension. Abstract 56, 2006.
-
(2006)
Proceedings of the 21st Scientific Meeting of the International Society of Hypertension
-
-
Pravenec, M.1
Zidek, V.2
Landa, V.3
Viklicky, O.4
Sugimoto, K.5
Qi, N.6
Kurtz, T.W.7
-
86
-
-
77953811255
-
New approaches to population stratification in genome-wide association studies
-
Price AL, Zaitlen NA, Reich D, Patterson N. New approaches to population stratification in genome-wide association studies. Nat Rev Genet 11: 459-463, 2010.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 459-463
-
-
Price, A.L.1
Zaitlen, N.A.2
Reich, D.3
Patterson, N.4
-
87
-
-
18344377665
-
A polymorphism in the beta1 adrenergic receptor is associated with resting heart rate
-
Ranade K, Jorgenson E, Sheu WH, Pei D, Hsiung CA, Chiang FT, Chen YD, Pratt R, Olshen RA, Curb D, Cox DR, Botstein D, Risch N. A polymorphism in the beta1 adrenergic receptor is associated with resting heart rate. Am J Hum Genet 70: 935-942, 2002.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 935-942
-
-
Ranade, K.1
Jorgenson, E.2
Sheu, W.H.3
Pei, D.4
Hsiung, C.A.5
Chiang, F.T.6
Chen, Y.D.7
Pratt, R.8
Olshen, R.A.9
Curb, D.10
Cox, D.R.11
Botstein, D.12
Risch, N.13
-
88
-
-
25444506231
-
The kidney as a determinant of genetic hypertension: Evidence from renal transplantation studies
-
Rettig R, Grisk O. The kidney as a determinant of genetic hypertension: evidence from renal transplantation studies. Hypertension 46: 463-468, 2005.
-
(2005)
Hypertension
, vol.46
, pp. 463-468
-
-
Rettig, R.1
Grisk, O.2
-
89
-
-
0025165779
-
An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels
-
Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest 86: 1343-1346, 1990.
-
(1990)
J Clin Invest
, vol.86
, pp. 1343-1346
-
-
Rigat, B.1
Hubert, C.2
Alhenc-Gelas, F.3
Cambien, F.4
Corvol, P.5
Soubrier, F.6
-
90
-
-
84856261411
-
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase
-
Salvi E, Kutalik Z, Glorioso N, Benaglio P, Frau F, Kuznetsova T, Arima H, Hoggart C, Tichet J, Nikitin YP, Conti C, Seidlerova J, Tikhonoff V, Stolarz-Skrzypek K, Johnson T, Devos N, Zagato L, Guarrera S, Zaninello R, Calabria A, Stancanelli B, Troffa C, Thijs L, Rizzi F, Simonova G, Lupoli S, Argiolas G, Braga D, D'Alessio MC, Ortu MF, Ricceri F, Mercurio M, Descombes P, Marconi M, Chalmers J, Harrap S, Filipovsky J, Bochud M, Iacoviello L, Ellis J, Stanton AV, Laan M, Padmanabhan S, Dominiczak AF, Samani NJ, Melander O, Jeunemaitre X, Manunta P, Shabo A, Vineis P, Cappuccio FP, Caulfield MJ, Matullo G, Rivolta C, Munroe PB, Barlassina C, Staessen JA, Beckmann JS, Cusi D. Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase. Hypertension 59: 248-255, 2012.
-
(2012)
Hypertension
, vol.59
, pp. 248-255
-
-
Salvi, E.1
Kutalik, Z.2
Glorioso, N.3
Benaglio, P.4
Frau, F.5
Kuznetsova, T.6
Arima, H.7
Hoggart, C.8
Tichet, J.9
Nikitin, Y.P.10
Conti, C.11
Seidlerova, J.12
Tikhonoff, V.13
Stolarz-Skrzypek, K.14
Johnson, T.15
Devos, N.16
Zagato, L.17
Guarrera, S.18
Zaninello, R.19
Calabria, A.20
Stancanelli, B.21
Troffa, C.22
Thijs, L.23
Rizzi, F.24
Simonova, G.25
Lupoli, S.26
Argiolas, G.27
Braga, D.28
D'Alessio, M.C.29
Ortu, M.F.30
Ricceri, F.31
Mercurio, M.32
Descombes, P.33
Marconi, M.34
Chalmers, J.35
Harrap, S.36
Filipovsky, J.37
Bochud, M.38
Iacoviello, L.39
Ellis, J.40
Stanton, A.V.41
Laan, M.42
Padmanabhan, S.43
Dominiczak, A.F.44
Samani, N.J.45
Melander, O.46
Jeunemaitre, X.47
Manunta, P.48
Shabo, A.49
Vineis, P.50
Cappuccio, F.P.51
Caulfield, M.J.52
Matullo, G.53
Rivolta, C.54
Munroe, P.B.55
Barlassina, C.56
Staessen, J.A.57
Beckmann, J.S.58
Cusi, D.59
more..
-
91
-
-
0037305164
-
Genome scans for hypertension and blood pressure regulation
-
Samani NJ. Genome scans for hypertension and blood pressure regulation. Am J Hypertens 16: 167-171, 2003.
-
(2003)
Am J Hypertens
, vol.16
, pp. 167-171
-
-
Samani, N.J.1
-
92
-
-
77950868711
-
CCN3 inhibits neointimal hyperplasia through modulation of smooth muscle cell growth and migration
-
Shimoyama T, Hiraoka S, Takemoto M, Koshizaka M, Tokuyama H, Tokuyama T, Watanabe A, Fujimoto M, Kawamura H, Sato S, Tsurutani Y, Saito Y, Perbal B, Koseki H, Yokote K. CCN3 inhibits neointimal hyperplasia through modulation of smooth muscle cell growth and migration. Arterioscler Thromb Vasc Biol 30: 675-682, 2010.
-
(2010)
Arterioscler Thromb Vasc Biol
, vol.30
, pp. 675-682
-
-
Shimoyama, T.1
Hiraoka, S.2
Takemoto, M.3
Koshizaka, M.4
Tokuyama, H.5
Tokuyama, T.6
Watanabe, A.7
Fujimoto, M.8
Kawamura, H.9
Sato, S.10
Tsurutani, Y.11
Saito, Y.12
Perbal, B.13
Koseki, H.14
Yokote, K.15
-
93
-
-
82555194123
-
Two-marker association tests yield new disease associations for coronary artery disease and hypertension
-
Slavin TP, Feng T, Schnell A, Zhu X, Elston RC. Two-marker association tests yield new disease associations for coronary artery disease and hypertension. Hum Genet 130: 725-733, 2011.
-
(2011)
Hum Genet
, vol.130
, pp. 725-733
-
-
Slavin, T.P.1
Feng, T.2
Schnell, A.3
Zhu, X.4
Elston, R.C.5
-
94
-
-
0028354218
-
Targeted gene duplication and disruption for analyzing quantitative genetic traits in mice
-
Smithies O, Kim HS. Targeted gene duplication and disruption for analyzing quantitative genetic traits in mice. Proc Natl Acad Sci USA 91: 3612-3615, 1994.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3612-3615
-
-
Smithies, O.1
Kim, H.S.2
-
95
-
-
78049531165
-
Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: The Japanese Millennium Genome Project
-
Tabara Y, Kohara K, Kita Y, Hirawa N, Katsuya T, Ohkubo T, Hiura Y, Tajima A, Morisaki T, Miyata T, Nakayama T, Takashima N, Nakura J, Kawamoto R, Takahashi N, Hata A, Soma M, Imai Y, Kokubo Y, Okamura T, Tomoike H, Iwai N, Ogihara T, Inoue I, Tokunaga K, Johnson T, Caulfield M, Munroe P, Umemura S, Ueshima H, Miki T. Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project. Hypertension 56: 973-980, 2010.
-
(2010)
Hypertension
, vol.56
, pp. 973-980
-
-
Tabara, Y.1
Kohara, K.2
Kita, Y.3
Hirawa, N.4
Katsuya, T.5
Ohkubo, T.6
Hiura, Y.7
Tajima, A.8
Morisaki, T.9
Miyata, T.10
Nakayama, T.11
Takashima, N.12
Nakura, J.13
Kawamoto, R.14
Takahashi, N.15
Hata, A.16
Soma, M.17
Imai, Y.18
Kokubo, Y.19
Okamura, T.20
Tomoike, H.21
Iwai, N.22
Ogihara, T.23
Inoue, I.24
Tokunaga, K.25
Johnson, T.26
Caulfield, M.27
Munroe, P.28
Umemura, S.29
Ueshima, H.30
Miki, T.31
more..
-
96
-
-
80053383403
-
Genomewide 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, Bochud M, Rice KM, Henneman P, Smith AV, Ehret GB, Amin N, Larson MG, Mooser V, Hadley D, Dorr M, Bis JC, Aspelund T, Esko T, Janssens AC, Zhao JH, Heath S, Laan M, Fu J, Pistis G, Luan J, Arora P, Lucas G, Pirastu N, Pichler I, Jackson AU, Webster RJ, Zhang F, Peden JF, Schmidt H, Tanaka T, Campbell H, Igl W, Milaneschi Y, Hottenga JJ, Vitart V, Chasman DI, Trompet S, Bragg-Gresham JL, Alizadeh BZ, Chambers JC, Guo X, Lehtimaki T, Kuhnel B, Lopez LM, Polasek O, Boban M, Nelson CP, Morrison AC, Pihur V, Ganesh SK, Hofman A, Kundu S, Mattace-Raso FU, Rivadeneira F, Sijbrands EJ, Uitterlinden AG, Hwang SJ, Vasan RS, Wang TJ, Bergmann S, Vollenweider P, Waeber G, Laitinen J, Pouta A, Zitting P, McArdle WL, Kroemer HK, Volker U, Volzke H, Glazer NL, Taylor KD, Harris TB, Alavere H, Haller T, Keis A, Tammesoo ML, Aulchenko Y, Barroso I, Khaw KT, Galan P, Hercberg S, Lathrop M, Eyheramendy S, Org E, Sober S, Lu X, Nolte IM, Penninx BW, Corre T, Masciullo C, Sala C, Groop L, Voight BF, Melander O, O'Donnell CJ, Salomaa V, d'Adamo AP, Fabretto AFaletra F, Ulivi S, Del Greco F, Facheris M, Collins FS, Bergman RN, Beilby JP, Hung J, Musk AW, Mangino M, Shin SY, Soranzo N, Watkins H, Goel A, Hamsten A, Gider P, Loitfelder M, Zeginigg M, Hernandez D, Najjar SS, Navarro P, Wild SH, Corsi AM, Singleton A, de Geus EJ, Willemsen G, Parker AN, Rose LM, Buckley B, Stott D, Orru M, Uda M, van der Klauw MM, Zhang W, Li X, Scott J, Chen YD, Burke GL, Kahonen M, Viikari J, Doring A, Meitinger T, Davies G, Starr JM, Emilsson V, Plump A, Lindeman JH, Hoen PA, Konig IR, Felix JF, Clarke R, Hopewell JC, Ongen H, Breteler M, Debette S, Destefano AL, Fornage M, Mitchell GF, Smith NL, Holm H, Stefansson K, Thorleifsson G, Thorsteinsdottir U, Samani NJ, Preuss M, Rudan I, Hayward C, Deary IJ, Wichmann HE, Raitakari OT, Palmas W, Kooner JS, Stolk RP, Jukema JW, Wright AF, Boomsma DI, Bandinelli S, Gyllensten UB, Wilson JF, Ferrucci L, Schmidt R, Farrall M, Spector TD, Palmer LJ, Tuomilehto J, Pfeufer A, Gasparini P, Siscovick D, Altshuler D, Loos RJ, Toniolo D, Snieder H, Gieger C, Meneton P, Wareham NJ, Oostra BA, Metspalu A, Launer L, Rettig R, Strachan DP, Beckmann JS, Witteman JC, Erdmann J, van Dijk KW, Boerwinkle E, Boehnke M, Ridker PM, Jarvelin MR, Chakravarti A, Abecasis GR, Gudnason V, Newton-Cheh C, Levy D, Munroe PB, Psaty BM, Caulfield MJ, Rao DC, Tobin MD, Elliott P, van Duijn CM. Genomewide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet 43: 1005-1011, 2011.
-
(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
Bochud, M.7
Rice, K.M.8
Henneman, P.9
Smith, A.V.10
Ehret, G.B.11
Amin, N.12
Larson, M.G.13
Mooser, V.14
Hadley, D.15
Dorr, M.16
Bis, J.C.17
Aspelund, T.18
Esko, T.19
Janssens, A.C.20
Zhao, J.H.21
Heath, S.22
Laan, M.23
Fu, J.24
Pistis, G.25
Luan, J.26
Arora, P.27
Lucas, G.28
Pirastu, N.29
Pichler, I.30
Jackson, A.U.31
Webster, R.J.32
Zhang, F.33
Peden, J.F.34
Schmidt, H.35
Tanaka, T.36
Campbell, H.37
Igl, W.38
Milaneschi, Y.39
Hottenga, J.J.40
Vitart, V.41
Chasman, D.I.42
Trompet, S.43
Bragg-Gresham, J.L.44
Alizadeh, B.Z.45
Chambers, J.C.46
Guo, X.47
Lehtimaki, T.48
Kuhnel, B.49
Lopez, L.M.50
Polasek, O.51
Boban, M.52
Nelson, C.P.53
Morrison, A.C.54
Pihur, V.55
Ganesh, S.K.56
Hofman, A.57
Kundu, S.58
Mattace-Raso, F.U.59
Rivadeneira, F.60
Sijbrands, E.J.61
Uitterlinden, A.G.62
Hwang, S.J.63
Vasan, R.S.64
Wang, T.J.65
Bergmann, S.66
Vollenweider, P.67
Waeber, G.68
Laitinen, J.69
Pouta, A.70
Zitting, P.71
McArdle, W.L.72
Kroemer, H.K.73
Volker, U.74
Volzke, H.75
Glazer, N.L.76
Taylor, K.D.77
Harris, T.B.78
Alavere, H.79
Haller, T.80
Keis, A.81
Tammesoo, M.L.82
Aulchenko, Y.83
Barroso, I.84
Khaw, K.T.85
Galan, P.86
Hercberg, S.87
Lathrop, M.88
Eyheramendy, S.89
Org, E.90
Sober, S.91
Lu, X.92
Nolte, I.M.93
Penninx, B.W.94
Corre, T.95
Masciullo, C.96
Sala, C.97
Groop, L.98
more..
-
97
-
-
78549251736
-
Analysing biological pathways in genome-wide association studies
-
Wang K, Li M, Hakonarson H. Analysing biological pathways in genome-wide association studies. Nat Rev Genet 11: 843-854, 2010.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 843-854
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
98
-
-
0029847663
-
Inherited forms of mineralocorticoid hypertension
-
White PC. Inherited forms of mineralocorticoid hypertension. Hypertension 28: 927-936, 1996.
-
(1996)
Hypertension
, vol.28
, pp. 927-936
-
-
White, P.C.1
-
99
-
-
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 JM, 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 293: 1107-1112, 2001.
-
(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
-
100
-
-
84859043741
-
Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study
-
Yang HC, Liang YJ, Chen JW, Chiang KM, Chung CM, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Leu HB, Yin WH, Chiu TY, Chern CL, Lin SJ, Tomlinson B, Guo Y, Sham PC, Cherny SS, Lam TH, Thomas GN, Pan WH. Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. PLoS One 7: e32907, 2012.
-
(2012)
PLoS One
, vol.7
-
-
Yang, H.C.1
Liang, Y.J.2
Chen, J.W.3
Chiang, K.M.4
Chung, C.M.5
Ho, H.Y.6
Ting, C.T.7
Lin, T.H.8
Sheu, S.H.9
Tsai, W.C.10
Chen, J.H.11
Leu, H.B.12
Yin, W.H.13
Chiu, T.Y.14
Chern, C.L.15
Lin, S.J.16
Tomlinson, B.17
Guo, Y.18
Sham, P.C.19
Cherny, S.S.20
Lam, T.H.21
Thomas, G.N.22
Pan, W.H.23
more..
-
101
-
-
73349118815
-
Glutathione S-transferase-micro1 regulates vascular smooth muscle cell proliferation, migration, and oxidative stress
-
Yang Y, Parsons KK, Chi L, Malakauskas SM, Le TH. Glutathione S-transferase-micro1 regulates vascular smooth muscle cell proliferation, migration, and oxidative stress. Hypertension 54: 1360-1368, 2009.
-
(2009)
Hypertension
, vol.54
, pp. 1360-1368
-
-
Yang, Y.1
Parsons, K.K.2
Chi, L.3
Malakauskas, S.M.4
Le, T.H.5
-
102
-
-
79955989635
-
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: Contributions from the CARe consortium
-
Zhu X, Young JH, Fox E, Keating BJ, Franceschini N, Kang S, Tayo B, Adeyemo A, Sun YV, Li Y, Morrison A, Newton-Cheh C, Liu K, Ganesh SK, Kutlar A, Vasan RS, Dreisbach A, Wyatt S, Polak J, Palmas W, Musani S, Taylor H, Fabsitz R, Townsend RR, Dries D, Glessner J, Chiang CW, Mosley T, Kardia S, Curb D, Hirschhorn JN, Rotimi C, Reiner A, Eaton C, Rotter JI, Cooper RS, Redline S, Chakravarti A, Levy D. Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium. Hum Mol Genet 20: 2285-2295, 2011.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2285-2295
-
-
Zhu, X.1
Young, J.H.2
Fox, E.3
Keating, B.J.4
Franceschini, N.5
Kang, S.6
Tayo, B.7
Adeyemo, A.8
Sun, Y.V.9
Li, Y.10
Morrison, A.11
Newton-Cheh, C.12
Liu, K.13
Ganesh, S.K.14
Kutlar, A.15
Vasan, R.S.16
Dreisbach, A.17
Wyatt, S.18
Polak, J.19
Palmas, W.20
Musani, S.21
Taylor, H.22
Fabsitz, R.23
Townsend, R.R.24
Dries, D.25
Glessner, J.26
Chiang, C.W.27
Mosley, T.28
Kardia, S.29
Curb, D.30
Hirschhorn, J.N.31
Rotimi, C.32
Reiner, A.33
Eaton, C.34
Rotter, J.I.35
Cooper, R.S.36
Redline, S.37
Chakravarti, A.38
Levy, D.39
more..
|