-
1
-
-
1842506281
-
Asymptomatic peripheral arterial occlusive disease predicted cardiovascular morbidity and mortality in a 7-year follow-up study
-
Hooi JD, Kester AD, Stoffers HE, Rinkens PE, Knottnerus JA, van Ree JW: Asymptomatic peripheral arterial occlusive disease predicted cardiovascular morbidity and mortality in a 7-year follow-up study. J Clin Epidemiol, 2004; 57: 294-300
-
(2004)
J Clin Epidemiol
, vol.57
, pp. 294-300
-
-
Hooi, J.D.1
Kester, A.D.2
Stoffers, H.E.3
Rinkens, P.E.4
Knottnerus, J.A.5
van Ree, J.W.6
-
2
-
-
0026501734
-
Mortality over a period of 10 years in patients with peripheral arterial disease
-
Criqui MH, Langer RD, Fronek A, Feigelson HS, Klauber MR, McCann TJ, Browner D: Mortality over a period of 10 years in patients with peripheral arterial disease. N Engl J Med, 1992; 326: 381-386
-
(1992)
N Engl J Med
, vol.326
, pp. 381-386
-
-
Criqui, M.H.1
Langer, R.D.2
Fronek, A.3
Feigelson, H.S.4
Klauber, M.R.5
McCann, T.J.6
Browner, D.7
-
3
-
-
0142243263
-
Peripheral arterial disease: Identification and implications
-
Mohler ER, 3rd: Peripheral arterial disease: identification and implications. Arch Intern Med, 2003; 163: 2306-2314
-
(2003)
Arch Intern Med
, vol.163
, pp. 2306-2314
-
-
Mohler III, E.R.1
-
4
-
-
0033655477
-
The Framingham Study: ITS 50-year legacy and future promise
-
Kannel WB: The Framingham Study: ITS 50-year legacy and future promise. J Atheroscler Thromb, 2000; 6: 60-66
-
(2000)
J Atheroscler Thromb
, vol.6
, pp. 60-66
-
-
Kannel, W.B.1
-
5
-
-
0035913589
-
Peripheral arterial disease detection, awareness, and treatment in primary care
-
Hirsch AT, Criqui MH, Treat-Jacobson D, Regensteiner JG, Creager MA, Olin JW, Krook SH, Hunninghake DB, Comerota AJ, Walsh ME, McDermott MM, Hiatt WR: Peripheral arterial disease detection, awareness, and treatment in primary care. JAMA, 2001; 286: 1317-1324
-
(2001)
JAMA
, vol.286
, pp. 1317-1324
-
-
Hirsch, A.T.1
Criqui, M.H.2
Treat-Jacobson, D.3
Regensteiner, J.G.4
Creager, M.A.5
Olin, J.W.6
Krook, S.H.7
Hunninghake, D.B.8
Comerota, A.J.9
Walsh, M.E.10
McDermott, M.M.11
Hiatt, W.R.12
-
6
-
-
26844542906
-
The morbidity and mortality following a diagnosis of peripheral arterial disease: Long-term follow-up of a large database
-
Caro J, Migliaccio-Walle K, Ishak KJ, Proskorovsky I: The morbidity and mortality following a diagnosis of peripheral arterial disease: long-term follow-up of a large database. BMC Cardiovasc Disord, 2005; 5: 14
-
(2005)
BMC Cardiovasc Disord
, vol.5
, pp. 14
-
-
Caro, J.1
Migliaccio-Walle, K.2
Ishak, K.J.3
Proskorovsky, I.4
-
7
-
-
35148875935
-
Genetic susceptibility to peripheral arterial disease: A dark corner in vascular biology
-
Knowles JW, Assimes TL, Li J, Quertermous T, Cooke JP: Genetic susceptibility to peripheral arterial disease: a dark corner in vascular biology. Arterioscler Thromb Vasc Biol, 2007; 27: 2068-2078
-
(2007)
Arterioscler Thromb Vasc Biol
, vol.27
, pp. 2068-2078
-
-
Knowles, J.W.1
Assimes, T.L.2
Li, J.3
Quertermous, T.4
Cooke, J.P.5
-
8
-
-
0034159774
-
Contribution of genetic and environmental influences to ankle-brachial blood pressure index in the NHLBI Twin Study. National Heart, Lung, and Blood Institute
-
Carmelli D, Fabsitz RR, Swan GE, Reed T, Miller B, Wolf PA: Contribution of genetic and environmental influences to ankle-brachial blood pressure index in the NHLBI Twin Study. National Heart, Lung, and Blood Institute. Am J Epidemiol, 2000; 151: 452-458
-
(2000)
Am J Epidemiol
, vol.151
, pp. 452-458
-
-
Carmelli, D.1
Fabsitz, R.R.2
Swan, G.E.3
Reed, T.4
Miller, B.5
Wolf, P.A.6
-
9
-
-
33745510306
-
A genome-wide linkage scan for anklebrachial index in African American and non-Hispanic white subjects participating in the GENOA study
-
Kullo IJ, Turner ST, Kardia SL, Mosley TH Jr, Boerwinkle E, de Andrade M: A genome-wide linkage scan for anklebrachial index in African American and non-Hispanic white subjects participating in the GENOA study. Atherosclerosis, 2006; 187: 433-438
-
(2006)
Atherosclerosis
, vol.187
, pp. 433-438
-
-
Kullo, I.J.1
Turner, S.T.2
Kardia, S.L.3
Mosley Jr., T.H.4
Boerwinkle, E.5
de Andrade, M.6
-
10
-
-
33750919796
-
Heritability of the ankle-brachial index: The Framingham Offspring study
-
Murabito JM, Guo CY, Fox CS, D'Agostino RB: Heritability of the ankle-brachial index: the Framingham Offspring study. Am J Epidemiol, 2006; 164: 963-968
-
(2006)
Am J Epidemiol
, vol.164
, pp. 963-968
-
-
Murabito, J.M.1
Guo, C.Y.2
Fox, C.S.3
D'agostino, R.B.4
-
11
-
-
0036956227
-
Gene-based SNP discovery as part of the Japanese Millennium Genome Project: Identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism
-
Haga H, Yamada R, Ohnishi Y, Nakamura Y, Tanaka T: Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism. J Hum Genet, 2002; 47: 605-610
-
(2002)
J Hum Genet
, vol.47
, pp. 605-610
-
-
Haga, H.1
Yamada, R.2
Ohnishi, Y.3
Nakamura, Y.4
Tanaka, T.5
-
12
-
-
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, 2007; 449: 851-861
-
(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
Tanaka, T.99
more..
-
13
-
-
0034885541
-
A high-throughput SNP typing system for genome-wide association studies
-
Ohnishi Y, Tanaka T, Ozaki K, Yamada R, Suzuki H, Nakamura Y: A high-throughput SNP typing system for genome-wide association studies. J Hum Genet, 2001; 46: 471-477
-
(2001)
J Hum Genet
, vol.46
, pp. 471-477
-
-
Ohnishi, Y.1
Tanaka, T.2
Ozaki, K.3
Yamada, R.4
Suzuki, H.5
Nakamura, Y.6
-
14
-
-
0029150074
-
A comparison of linkage disequilibrium measures for fine-scale mapping
-
Devlin B, Risch N: A comparison of linkage disequilibrium measures for fine-scale mapping. Genomics, 1995; 29: 311-322
-
(1995)
Genomics
, vol.29
, pp. 311-322
-
-
Devlin, B.1
Risch, N.2
-
16
-
-
38949137379
-
Characteristics of oxysterol binding proteins
-
Yan D, Olkkonen VM: Characteristics of oxysterol binding proteins. Int Rev Cytol, 2008; 265: 253-285
-
(2008)
Int Rev Cytol
, vol.265
, pp. 253-285
-
-
Yan, D.1
Olkkonen, V.M.2
-
17
-
-
33745477974
-
The OSBP-related proteins (ORPs): Global sterol sensors for co-ordination of cellular lipid metabolism, membrane trafficking and signalling processes?
-
Olkkonen VM, Johansson M, Suchanek M, Yan D, Hynynen R, Ehnholm C, Jauhiainen M, Thiele C, Lehto M: The OSBP-related proteins (ORPs): global sterol sensors for co-ordination of cellular lipid metabolism, membrane trafficking and signalling processes? Biochem Soc Trans, 2006; 34: 389-391
-
(2006)
Biochem Soc Trans
, vol.34
, pp. 389-391
-
-
Olkkonen, V.M.1
Johansson, M.2
Suchanek, M.3
Yan, D.4
Hynynen, R.5
Ehnholm, C.6
Jauhiainen, M.7
Thiele, C.8
Lehto, M.9
-
18
-
-
0038558194
-
A conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAP
-
Loewen CJ, Roy A, Levine TP: A conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAP. EMBO J, 2003; 22: 2025-2035
-
(2003)
EMBO J
, vol.22
, pp. 2025-2035
-
-
Loewen, C.J.1
Roy, A.2
Levine, T.P.3
-
19
-
-
70349263990
-
OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism
-
Perttila J, Merikanto K, Naukkarinen J, Surakka I, Martin NW, Tanhuanpaa K, Grimard V, Taskinen MR, Thiele C, Salomaa V, Jula A, Perola M, Virtanen I, Peltonen L, Olkkonen VM: OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism. J Mol Med, 2009; 87: 825-835
-
(2009)
J Mol Med
, vol.87
, pp. 825-835
-
-
Perttila, J.1
Merikanto, K.2
Naukkarinen, J.3
Surakka, I.4
Martin, N.W.5
Tanhuanpaa, K.6
Grimard, V.7
Taskinen, M.R.8
Thiele, C.9
Salomaa, V.10
Jula, A.11
Perola, M.12
Virtanen, I.13
Peltonen, L.14
Olkkonen, V.M.15
-
20
-
-
33646021647
-
CSMD1 is a novel multiple domain complementregulatory protein highly expressed in the central nervous system and epithelial tissues
-
Kraus DM, Elliott GS, Chute H, Horan T, Pfenninger KH, Sanford SD, Foster S, Scully S, Welcher AA, Holers VM: CSMD1 is a novel multiple domain complementregulatory protein highly expressed in the central nervous system and epithelial tissues. J Immunol, 2006; 176: 4419-4430
-
(2006)
J Immunol
, vol.176
, pp. 4419-4430
-
-
Kraus, D.M.1
Elliott, G.S.2
Chute, H.3
Horan, T.4
Pfenninger, K.H.5
Sanford, S.D.6
Foster, S.7
Scully, S.8
Welcher, A.A.9
Holers, V.M.10
-
21
-
-
59249099537
-
A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease
-
Burgner D, Davila S, Breunis WB, Ng SB, Li Y, Bonnard C, Ling L, Wright VJ, Thalamuthu A, Odam M, Shimizu C, Burns JC, Levin M, Kuijpers TW, Hibberd ML: A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease. PLoS Genet, 2009; 5: e1000319
-
(2009)
PLoS Genet
, vol.5
-
-
Burgner, D.1
Davila, S.2
Breunis, W.B.3
Ng, S.B.4
Li, Y.5
Bonnard, C.6
Ling, L.7
Wright, V.J.8
Thalamuthu, A.9
Odam, M.10
Shimizu, C.11
Burns, J.C.12
Levin, M.13
Kuijpers, T.W.14
Hibberd, M.L.15
-
22
-
-
71249107630
-
Defining genetic determinants of the Metabolic Syndrome in the Framingham Heart Study using association and structural equation modeling methods
-
Nock NL, Wang X, Thompson CL, Song Y, Baechle D, Raska P, Stein CM, Gray-McGuire C: Defining genetic determinants of the Metabolic Syndrome in the Framingham Heart Study using association and structural equation modeling methods. BMC Proc, 2009; 3 Suppl 7: S50
-
(2009)
BMC Proc
, vol.3
, Issue.SUPPL. 7
-
-
Nock, N.L.1
Wang, X.2
Thompson, C.L.3
Song, Y.4
Baechle, D.5
Raska, P.6
Stein, C.M.7
Gray-McGuire, C.8
-
23
-
-
78249256470
-
Genetic variations in ATP2B1, CSK, ARSG and CSMD1 loci are related to blood pressure and/or hypertension in two Korean cohorts
-
Hong KW, Go MJ, Jin HS, Lim JE, Lee JY, Han BG, Hwang SY, Lee SH, Park HK, Cho YS, Oh B: Genetic variations in ATP2B1, CSK, ARSG and CSMD1 loci are related to blood pressure and/or hypertension in two Korean cohorts. J Hum Hypertens, 2009
-
(2009)
J Hum Hypertens
-
-
Hong, K.W.1
Go, M.J.2
Jin, H.S.3
Lim, J.E.4
Lee, J.Y.5
Han, B.G.6
Hwang, S.Y.7
Lee, S.H.8
Park, H.K.9
Cho, Y.S.10
Oh, B.11
-
24
-
-
0035844876
-
Intracellular retention of newly synthesized insulin in yeast is caused by endoproteolytic processing in the Golgi complex
-
Zhang B, Chang A, Kjeldsen TB, Arvan P: Intracellular retention of newly synthesized insulin in yeast is caused by endoproteolytic processing in the Golgi complex. J Cell Biol, 2001; 153: 1187-1198
-
(2001)
J Cell Biol
, vol.153
, pp. 1187-1198
-
-
Zhang, B.1
Chang, A.2
Kjeldsen, T.B.3
Arvan, P.4
-
25
-
-
3843101623
-
Analysis of the human VPS13 gene family
-
Velayos-Baeza A, Vettori A, Copley RR, Dobson-Stone C, Monaco AP: Analysis of the human VPS13 gene family. Genomics, 2004; 84: 536-549
-
(2004)
Genomics
, vol.84
, pp. 536-549
-
-
Velayos-Baeza, A.1
Vettori, A.2
Copley, R.R.3
Dobson-Stone, C.4
Monaco, A.P.5
-
26
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K: The future of genetic studies of complex human diseases. Science, 1996; 273: 1516-1517
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
27
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn JN, Daly MJ: Genome-wide association studies for common diseases and complex traits. Nat Rev Genet, 2005; 6: 95-108
-
(2005)
Nat Rev Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
|