-
1
-
-
0033770421
-
Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study
-
1:CAS:528:DC%2BD3cXnslChu78%3D 11040222
-
D Levy AL DeStefano MG Larson, et al. 2000 Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study Hypertension 36 4 477 483 1:CAS:528:DC%2BD3cXnslChu78%3D 11040222
-
(2000)
Hypertension
, vol.36
, Issue.4
, pp. 477-483
-
-
Levy, D.1
Destefano, A.L.2
Larson, M.G.3
-
2
-
-
33748039452
-
Heritability of cardiovascular and personality traits in 6,148 Sardinians
-
DOI 10.1371/journal.pgen.0020132
-
G Pilia WM Chen A Scuteri, et al. 2006 Heritability of cardiovascular and personality traits in 6, 148 Sardinians PLoS Genetics 2 8 e132 10.1371/journal.pgen.0020132 16934002 (Pubitemid 44298495)
-
(2006)
PLoS Genetics
, vol.2
, Issue.8
, pp. 1207-1223
-
-
Pilia, G.1
Chen, W.-M.2
Scuteri, A.3
Orru, M.4
Albai, G.5
Dei, M.6
Lai, S.7
Usala, G.8
Lai, M.9
Loi, P.10
Mameli, C.11
Vacca, L.12
Deiana, M.13
Olla, N.14
Masala, M.15
Cao, A.16
Najjar, S.S.17
Terracciano, A.18
Nedorezov, T.19
Sharov, A.20
Zonderman, A.B.21
Abecasis, G.R.22
Costa, P.23
Lakatta, E.24
Schlessinger, D.25
more..
-
3
-
-
33846786802
-
Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes
-
DOI 10.1097/HJH.0b013e32801449fb, PII 0000487220070300000013
-
MJ van Rijn AF Schut YS Aulchenko, et al. 2007 Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes J Hypertens 25 3 565 570 10.1097/HJH.0b013e32801449fb 17278972 (Pubitemid 46213794)
-
(2007)
Journal of Hypertension
, vol.25
, Issue.3
, pp. 565-570
-
-
Van Rijn, M.J.E.1
Schut, A.F.2
Aulchenko, Y.S.3
Deinum, J.4
Sayed-Tabatabaei, F.A.5
Yazdanpanah, M.6
Isaacs, A.7
Axenovich, T.I.8
Zorkoltseva, I.V.9
Zillikens, M.C.10
Pols, H.A.11
Witteman, J.C.12
Oostra, B.A.13
Van Duijn, C.M.14
-
4
-
-
33644874530
-
Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general population
-
DOI 10.1161/CIRCULATIONAHA.105.555474, PII 0000301720051129000012
-
MD Tobin SM Raleigh S Newhouse, et al. 2005 Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general population Circulation 112 22 3423 3429 10.1161/CIRCULATIONAHA.105.555474 1:CAS:528:DC%2BD2MXht1Cqt7zN 16301342 (Pubitemid 43739557)
-
(2005)
Circulation
, vol.112
, Issue.22
, pp. 3423-3429
-
-
Tobin, M.D.1
Raleigh, S.M.2
Newhouse, S.3
Braund, P.4
Bodycote, C.5
Ogleby, J.6
Cross, D.7
Gracey, J.8
Hayes, S.9
Smith, T.10
Ridge, C.11
Caulfield, M.12
Sheehan, N.A.13
Munroe, P.B.14
Burton, P.R.15
Samani, N.J.16
-
5
-
-
0035936780
-
Molecular mechanisms of human hypertension
-
DOI 10.1016/S0092-8674(01)00241-0
-
RP Lifton AG Gharavi DS Geller 2001 Molecular mechanisms of human hypertension Cell 104 4 545 556 10.1016/S0092-8674(01)00241-0 1:CAS:528:DC%2BD3MXis1Kks7w%3D 11239411 (Pubitemid 32201949)
-
(2001)
Cell
, vol.104
, Issue.4
, pp. 545-556
-
-
Lifton, R.P.1
Gharavi, A.G.2
Geller, D.S.3
-
6
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
10.1126/science.273.5281.1516 1:CAS:528:DyaK28Xls1Wqs7o%3D 8801636
-
N Risch K Merikangas 1996 The future of genetic studies of complex human diseases Science 273 5281 1516 1517 10.1126/science.273.5281.1516 1:CAS:528:DyaK28Xls1Wqs7o%3D 8801636
-
(1996)
Science
, vol.273
, Issue.5281
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
7
-
-
0001732173
-
On the sphygmographic evidence of arterio-capillary fibrosis
-
FA Mahomed 1877 On the sphygmographic evidence of arterio-capillary fibrosis Trans Path Soc 28 394 397
-
(1877)
Trans Path Soc
, vol.28
, pp. 394-397
-
-
Mahomed, F.A.1
-
8
-
-
0001252770
-
The nature of essential hypertension
-
10.1016/S0140-6736(59)91496-5
-
GW Pickering H Keen G Rose A Smith 1959 The nature of essential hypertension Lancet 274 7110 1027 1030 10.1016/S0140-6736(59)91496-5
-
(1959)
Lancet
, vol.274
, Issue.7110
, pp. 1027-1030
-
-
Pickering, G.W.1
Keen, H.2
Rose, G.3
Smith, A.4
-
9
-
-
0000790103
-
Genetics and the nature of essential hypertension
-
VA McKusick 1960 Genetics and the nature of essential hypertension Circulation 22 5 857 863
-
(1960)
Circulation
, vol.22
, Issue.5
, pp. 857-863
-
-
McKusick, V.A.1
-
10
-
-
0033936872
-
Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays
-
DOI 10.1101/gr.10.6.853
-
JB Fan X Chen MK Halushka, et al. 2000 Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays Genome Res 10 6 853 860 10.1101/gr.10.6.853 1:CAS:528:DC%2BD3cXkt1eisb8%3D 10854416 (Pubitemid 30433358)
-
(2000)
Genome Research
, vol.10
, Issue.6
, pp. 853-860
-
-
Fan, J.-B.1
Chen, X.2
Halushka, M.K.3
Berno, A.4
Huang, X.5
Ryder, T.6
Lipshutz, R.J.7
Lockhart, D.J.8
Chakravarti, A.9
-
11
-
-
0036275126
-
BeadArray technology: Enabling an accurate, cost-effective approach to high-throughput genotyping
-
Suppl:56-58
-
Oliphant A, Barker DL, Stuelpnagel JR, Chee MS: BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping. BioTechniques 2002, Suppl:56-58, 60-61.
-
(2002)
BioTechniques
, pp. 60-61
-
-
Oliphant, A.1
Barker, D.L.2
Stuelpnagel, J.R.3
Chee, M.S.4
-
12
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
DOI 10.1038/35057062
-
ES Lander LM Linton B Birren, et al. 2001 Initial sequencing and analysis of the human genome Nature 409 6822 860 921 10.1038/35057062 1:CAS:528:DC%2BD3MXhsFCjtLc%3D 11237011 (Pubitemid 32165345)
-
(2001)
Nature
, vol.409
, Issue.6822
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
Devon, K.7
Dewar, K.8
Doyle, M.9
Fitzhugh, W.10
Funke, R.11
Gage, D.12
Harris, K.13
Heaford, A.14
Howland, J.15
Kann, L.16
Lehoczky, J.17
Levine, R.18
McEwan, P.19
McKernan, K.20
Meldrim, J.21
Mesirov, J.P.22
Miranda, C.23
Morris, W.24
Naylor, J.25
Raymond, C.26
Rosetti, M.27
Santos, R.28
Sheridan, A.29
Sougnez, C.30
Stange-Thomann, N.31
Stojanovic, N.32
Subramanian, A.33
Wyman, D.34
Rogers, J.35
Sulston, J.36
Ainscough, R.37
Beck, S.38
Bentley, D.39
Burton, J.40
Clee, C.41
Carter, N.42
Coulson, A.43
Deadman, R.44
Deloukas, P.45
Dunham, A.46
Dunham, I.47
Durbin, R.48
French, L.49
Grafham, D.50
Gregory, S.51
Hubbard, T.52
Humphray, S.53
Hunt, A.54
Jones, M.55
Lloyd, C.56
McMurray, A.57
Matthews, L.58
Mercer, S.59
Milne, S.60
Mullikin, J.C.61
Mungall, A.62
Plumb, R.63
Ross, M.64
Shownkeen, R.65
Sims, S.66
Waterston, R.H.67
Wilson, R.K.68
Hillier, L.W.69
McPherson, J.D.70
Marra, M.A.71
Mardis, E.R.72
Fulton, L.A.73
Chinwalla, A.T.74
Pepin, K.H.75
Gish, W.R.76
Chissoe, S.L.77
Wendl, M.C.78
Delehaunty, K.D.79
Miner, T.L.80
Delehaunty, A.81
Kramer, J.B.82
Cook, L.L.83
Fulton, R.S.84
Johnson, D.L.85
Minx, P.J.86
Clifton, S.W.87
Hawkins, T.88
Branscomb, E.89
Predki, P.90
Richardson, P.91
Wenning, S.92
Slezak, T.93
Doggett, N.94
Cheng, J.-F.95
Olsen, A.96
Lucas, S.97
Elkin, C.98
Uberbacher, E.99
more..
-
13
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
DOI 10.1038/nature06258, PII NATURE06258
-
KA Frazer DG Ballinger DR Cox, et al. 2007 A second generation human haplotype map of over 3.1 million SNPs Nature 449 7164 851 861 10.1038/nature06258 1:CAS:528:DC%2BD2sXhtFOjt7jL 17943122 This is a report of phase 2 of the HapMap project, a large collaborative effort to identify common variation in the human genome. (Pubitemid 47598626)
-
(2007)
Nature
, vol.449
, Issue.7164
, 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
Zhao, H.31
Zhou, J.32
Gabriel, S.B.33
Barry, R.34
Blumenstiel, B.35
Camargo, A.36
Defelice, M.37
Faggart, M.38
Goyette, M.39
Gupta, S.40
Moore, J.41
Nguyen, H.42
Onofrio, R.C.43
Parkin, M.44
Roy, J.45
Stahl, E.46
Winchester, E.47
Ziaugra, L.48
Altshuler, D.49
Shen, Y.50
Yao, Z.51
Huang, W.52
Chu, X.53
He, Y.54
Jin, L.55
Liu, Y.56
Shen, Y.57
Sun, W.58
Wang, H.59
Wang, Y.60
Wang, Y.61
Xiong, X.62
Xu, L.63
Waye, M.M.Y.64
Tsui, S.K.W.65
Xue, H.66
Wong, J.T.-F.67
Galver, L.M.68
Fan, J.-B.69
Gunderson, K.70
Murray, S.S.71
Oliphant, A.R.72
Chee, M.S.73
Montpetit, A.74
Chagnon, F.75
Ferretti, V.76
Leboeuf, M.77
Olivier, J.-F.78
Phillips, M.S.79
Roumy, S.80
Sallee, C.81
Verner, A.82
Hudson, T.J.83
Kwok, P.-Y.84
Cai, D.85
Koboldt, D.C.86
Miller, R.D.87
Pawlikowska, L.88
Taillon-Miller, P.89
Xiao, M.90
Tsui, L.-C.91
Mak, W.92
You, Q.S.93
Tam, P.K.H.94
Nakamura, Y.95
Kawaguchi, T.96
Kitamoto, T.97
Morizono, T.98
Nagashima, A.99
more..
-
14
-
-
42349112088
-
Genome-wide association studies for complex traits: Consensus, uncertainty and challenges
-
DOI 10.1038/nrg2344, PII NRG2344
-
MI McCarthy GR Abecasis LR Cardon, et al. 2008 Genome-wide association studies for complex traits: consensus, uncertainty and challenges Nat Rev 9 5 356 369 10.1038/nrg2344 1:CAS:528:DC%2BD1cXkvVOhs7Y%3D This is a review of the genetic challenges and opportunities of GWAS. (Pubitemid 351556063)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.5
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
Goldstein, D.B.4
Little, J.5
Ioannidis, J.P.A.6
Hirschhorn, J.N.7
-
15
-
-
84984932946
-
Population genetics - Making sense out of sequence
-
DOI 10.1038/4482
-
A Chakravarti 1999 Population genetics-making sense out of sequence Nat Genet 21 1 Suppl 56 60 10.1038/4482 1:CAS:528:DyaK1MXltlWhuw%3D%3D 9915503 (Pubitemid 29031494)
-
(1999)
Nature Genetics
, vol.21
, pp. 56-60
-
-
Chakravarti, A.1
-
16
-
-
0029805706
-
The new genomics: Global views of biology
-
DOI 10.1126/science.274.5287.536
-
ES Lander 1996 The new genomics: global views of biology Science 274 5287 536 539 10.1126/science.274.5287.536 1:CAS:528:DyaK28XmsVWlsb4%3D 8928008 (Pubitemid 26360427)
-
(1996)
Science
, vol.274
, Issue.5287
, pp. 536-539
-
-
Lander, E.S.1
-
17
-
-
77249121375
-
The identification of over 135 loci involved in adult height variation provides important insights into the contribution of common variation to a model complex trait [abstract]
-
Honolulu, HI; October 20-24
-
Lango Allen H, Lettre G, Estrada K, et al.: The identification of over 135 loci involved in adult height variation provides important insights into the contribution of common variation to a model complex trait [abstract]. Presentation at the 59th Annual Meeting of the American Society of Human Genetics. Honolulu, HI; October 20-24, 2009.
-
(2009)
Presentation at the 59th Annual Meeting of the American Society of Human Genetics
-
-
Lango Allen, H.1
Lettre, G.2
Estrada, K.3
-
18
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
1:CAS:528:DC%2BD1MXotVSgtLg%3D 19571811
-
SM Purcell NR Wray JL Stone, et al. 2009 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Nature 460 7256 748 752 1:CAS:528:DC%2BD1MXotVSgtLg%3D 19571811
-
(2009)
Nature
, vol.460
, Issue.7256
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
-
19
-
-
33745237158
-
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
-
DOI 10.1038/ng1790, PII N1790
-
DE Arking A Pfeufer W Post, et al. 2006 A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization Nat Genet 38 6 644 651 10.1038/ng1790 1:CAS:528:DC%2BD28XltVOhtbs%3D 16648850 (Pubitemid 43927305)
-
(2006)
Nature Genetics
, vol.38
, Issue.6
, pp. 644-651
-
-
Arking, D.E.1
Pfeufer, A.2
Post, W.3
Kao, W.H.L.4
Newton-Cheh, C.5
Ikeda, M.6
West, K.7
Kashuk, C.8
Akyol, M.9
Perz, S.10
Jalilzadeh, S.11
Illig, T.12
Gieger, C.13
Guo, C.-Y.14
Larson, M.G.15
Wichmann, H.E.16
Marban, E.17
O'Donnell, C.J.18
Hirschhorn, J.N.19
Kaab, S.20
Spooner, P.M.21
Meitinger, T.22
Chakravarti, A.23
more..
-
20
-
-
56749149825
-
Replication of the Wellcome Trust genome-wide association study of essential hypertension: The Family Blood Pressure Program
-
10.1038/ejhg.2008.102 1:CAS:528:DC%2BD1cXhsVSjs7jL 18523456
-
GB Ehret AC Morrison AA O'Connor, et al. 2008 Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program Eur J Hum Genet 16 12 1507 1511 10.1038/ejhg.2008.102 1:CAS:528:DC%2BD1cXhsVSjs7jL 18523456
-
(2008)
Eur J Hum Genet
, vol.16
, Issue.12
, pp. 1507-1511
-
-
Ehret, G.B.1
Morrison, A.C.2
O'Connor, A.A.3
-
21
-
-
70450227480
-
Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study
-
10.1038/ejhg.2009.94 1:CAS:528:DC%2BD1MXhsVensbjO 19536175
-
GB Ehret AA O'Connor A Weder, et al. 2009 Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study Eur J Hum Genet 17 12 1650 1657 10.1038/ejhg.2009.94 1:CAS:528:DC%2BD1MXhsVensbjO 19536175
-
(2009)
Eur J Hum Genet
, vol.17
, Issue.12
, pp. 1650-1657
-
-
Ehret, G.B.1
O'Connor, A.A.2
Weder, A.3
-
22
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
10.1038/ng.384 1:CAS:528:DC%2BD1MXls1Cmurk%3D This reference and reference [23••] are the largest published GWAS. Collectively, they identify more than a dozen blood pressure and hypertension genes.
-
D Levy GB Ehret K Rice, et al. 2009 Genome-wide association study of blood pressure and hypertension Nat Genet 41 6 677 687 10.1038/ng.384 1:CAS:528:DC%2BD1MXls1Cmurk%3D This reference and reference [23••] are the largest published GWAS. Collectively, they identify more than a dozen blood pressure and hypertension genes.
-
(2009)
Nat Genet
, vol.41
, Issue.6
, pp. 677-687
-
-
Levy, D.1
Ehret, G.B.2
Rice, K.3
-
23
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
10.1038/ng.361 1:CAS:528:DC%2BD1MXls1CmsbY%3D This reference and reference [22••] are the largest published GWAS on blood pressure traits so far. Collectively, they identify more than a dozen blood pressure and hypertension genes.
-
C Newton-Cheh T Johnson V Gateva, et al. 2009 Genome-wide association study identifies eight loci associated with blood pressure Nat Genet 41 6 666 676 10.1038/ng.361 1:CAS:528:DC%2BD1MXls1CmsbY%3D This reference and reference [22••] are the largest published GWAS on blood pressure traits so far. Collectively, they identify more than a dozen blood pressure and hypertension genes.
-
(2009)
Nat Genet
, vol.41
, Issue.6
, pp. 666-676
-
-
Newton-Cheh, C.1
Johnson, T.2
Gateva, V.3
-
24
-
-
58549108489
-
Whole-genome association study identifies STK39 as a hypertension susceptibility gene
-
10.1073/pnas.0808358106 1:CAS:528:DC%2BD1MXltF2ksQ%3D%3D 19114657
-
Y Wang JR O'Connell PF McArdle, et al. 2009 Whole-genome association study identifies STK39 as a hypertension susceptibility gene Proc Natl Acad Sci U S A 106 1 226 231 10.1073/pnas.0808358106 1:CAS:528:DC%2BD1MXltF2ksQ%3D%3D 19114657
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, Issue.1
, pp. 226-231
-
-
Wang, Y.1
O'Connell, J.R.2
McArdle, P.F.3
-
25
-
-
67349188883
-
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
-
10.1038/ng.357 1:CAS:528:DC%2BD1MXltValt7k%3D 19396169
-
YS Cho MJ Go YJ Kim, et al. 2009 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Nat Genet 41 5 527 534 10.1038/ng.357 1:CAS:528: DC%2BD1MXltValt7k%3D 19396169
-
(2009)
Nat Genet
, vol.41
, Issue.5
, pp. 527-534
-
-
Cho, Y.S.1
Go, M.J.2
Kim, Y.J.3
-
26
-
-
0025234906
-
Blood pressure, stroke, and coronary heart disease. Part 1, prolonged differences in blood pressure: Prospective observational studies corrected for the regression dilution bias
-
DOI 10.1016/0140-6736(90)90878-9
-
S MacMahon R Peto J Cutler, et al. 1990 Blood pressure, stroke, and coronary heart disease. Part 1, Prolonged differences in blood pressure: prospective observational studies corrected for the regression dilution bias Lancet 335 8692 765 774 10.1016/0140-6736(90)90878-9 1:STN:280: DyaK3c3gsFegug%3D%3D 1969518 (Pubitemid 20106689)
-
(1990)
Lancet
, vol.335
, Issue.8692
, pp. 765-774
-
-
MacMahon, S.1
Peto, R.2
Cutler, J.3
Collins, R.4
Sorlie, P.5
Neaton, J.6
Abbott, R.7
Godwin, J.8
Dyer, A.9
Stamler, J.10
-
27
-
-
0035209177
-
Large upward bias in estimation of locus-specific effects from genomewide scans
-
DOI 10.1086/324471
-
HH Goring JD Terwilliger J Blangero 2001 Large upward bias in estimation of locus-specific effects from genomewide scans Am J Hum Genet 69 6 1357 1369 10.1086/324471 1:STN:280:DC%2BD3Mnlt1Sjtg%3D%3D 11593451 (Pubitemid 33124216)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.6
, pp. 1357-1369
-
-
Goring, H.H.H.1
Terwilliger, J.D.2
Blangero, J.3
-
28
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
10.1038/nature08494 1:CAS:528:DC%2BD1MXht1CisbrF 19812666 This meeting report on the "missing heritability" of complex genetic traits discusses in detail possible reasons why only little heritability can be explained so far.
-
TA Manolio FS Collins NJ Cox, et al. 2009 Finding the missing heritability of complex diseases Nature 461 7265 747 753 10.1038/nature08494 1:CAS:528:DC%2BD1MXht1CisbrF 19812666 This meeting report on the "missing heritability" of complex genetic traits discusses in detail possible reasons why only little heritability can be explained so far.
-
(2009)
Nature
, vol.461
, Issue.7265
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
-
29
-
-
65549171064
-
Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan
-
10.1371/journal.pone.0005459 19421330
-
HC Yang YJ Liang YL Wu, et al. 2009 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan PloS One 4 5 e5459 10.1371/journal.pone.0005459 19421330
-
(2009)
PloS One
, vol.4
, Issue.5
, pp. 5459
-
-
Yang, H.C.1
Liang, Y.J.2
Wu, Y.L.3
-
30
-
-
38849098917
-
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project
-
DOI 10.1093/hmg/ddm335
-
N Kato T Miyata Y Tabara, et al. 2008 High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project Hum Mol Genet 17 4 617 627 10.1093/hmg/ddm335 1:CAS:528: DC%2BD1cXhsVSnt7k%3D 18003638 (Pubitemid 351201773)
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.4
, pp. 617-627
-
-
Kato, N.1
Miyata, T.2
Tabara, Y.3
Katsuya, T.4
Yanai, K.5
Hanada, H.6
Kamide, K.7
Nakura, J.8
Kohara, K.9
Takeuchi, F.10
Mano, H.11
Yasunami, M.12
Kimura, A.13
Kita, Y.14
Ueshima, H.15
Nakayama, T.16
Soma, M.17
Hata, A.18
Fujioka, A.19
Kawano, Y.20
Nakao, K.21
Sekine, A.22
Yoshida, T.23
Nakamura, Y.24
Saruta, T.25
Ogihara, T.26
Sugano, S.27
Miki, T.28
Tomoike, H.29
more..
-
31
-
-
68249107559
-
A genome-wide association study of hypertension and blood pressure in African Americans
-
10.1371/journal.pgen.1000564 19609347 This is the only GWAS on hypertension in African American individuals published to date.
-
A Adeyemo N Gerry G Chen, et al. 2009 A genome-wide association study of hypertension and blood pressure in African Americans PLoS Genet 5 7 e1000564 10.1371/journal.pgen.1000564 19609347 This is the only GWAS on hypertension in African American individuals published to date.
-
(2009)
PLoS Genet
, vol.5
, Issue.7
, pp. 1000564
-
-
Adeyemo, A.1
Gerry, N.2
Chen, G.3
-
32
-
-
35748962317
-
Framingham Heart Study 100K Project: Genome-wide associations for blood pressure and arterial stiffness
-
DOI 10.1186/1471-2350-8-S1-S3
-
D Levy MG Larson EJ Benjamin, et al. 2007 Framingham Heart Study 100 K Project: genome-wide associations for blood pressure and arterial stiffness BMC Med Genet 8 Suppl 1 S3 10.1186/1471-2350-8-S1-S3 17903302 (Pubitemid 351958756)
-
(2007)
BMC Medical Genetics
, vol.8
, Issue.SUPPL. 1
-
-
Levy, D.1
Larson, M.G.2
Benjamin, E.J.3
Newton-Cheh, C.4
Wang, T.J.5
Hwang, S.-J.6
Vasan, R.S.7
Mitchell, G.F.8
-
33
-
-
66149105886
-
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations
-
10.1093/hmg/ddp135 1:CAS:528:DC%2BD1MXmtlWnt7s%3D 19304780
-
E Org S Eyheramendy P Juhanson, et al. 2009 Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations Hum Mol Genet 18 12 2288 2296 10.1093/hmg/ddp135 1:CAS:528:DC%2BD1MXmtlWnt7s%3D 19304780
-
(2009)
Hum Mol Genet
, vol.18
, Issue.12
, pp. 2288-2296
-
-
Org, E.1
Eyheramendy, S.2
Juhanson, P.3
-
34
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
DOI 10.1038/nature05911, PII NATURE05911
-
Wellcome Trust Case Control Consortium 2007 Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls Nature 447 7145 661 678 10.1038/nature05911 This report describes the first large GWAS on seven complex genetic traits. (Pubitemid 46889737)
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 661-678
-
-
Burton, P.R.1
Clayton, D.G.2
Cardon, L.R.3
Craddock, N.4
Deloukas, P.5
Duncanson, A.6
Kwiatkowski, D.P.7
McCarthy, M.I.8
Ouwehand, W.H.9
Samani, N.J.10
Todd, J.A.11
Donnelly, P.12
Barrett, J.C.13
Davison, D.14
Easton, D.15
Evans, D.16
Leung, H.-T.17
Marchini, J.L.18
Morris, A.P.19
Spencer, C.C.A.20
Tobin, M.D.21
more..
-
35
-
-
58149159573
-
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
-
10.1038/ng.271 1:CAS:528:DC%2BD1cXhsVKlt7zO 19060910
-
C Sabatti SK Service AL Hartikainen, et al. 2009 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Nat Genet 41 1 35 46 10.1038/ng.271 1:CAS:528:DC%2BD1cXhsVKlt7zO 19060910
-
(2009)
Nat Genet
, vol.41
, Issue.1
, pp. 35-46
-
-
Sabatti, C.1
Service, S.K.2
Hartikainen, A.L.3
-
36
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
DOI 10.1126/science.1142358
-
R Saxena BF Voight V Lyssenko, et al. 2007 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Science 316 5829 1331 1336 10.1126/science.1142358 1:CAS:528:DC%2BD2sXmtVyitrk%3D 17463246 (Pubitemid 46871653)
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1331-1336
-
-
Saxena, R.1
Voight, B.F.2
Lyssenko, V.3
Burtt, N.P.4
De Bakker, P.I.W.5
Chen, H.6
Roix, J.J.7
Kathiresan, S.8
Hirschhorn, J.N.9
Daly, M.J.10
Hughes, T.E.11
Groop, L.12
Altshuler, D.13
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