-
1
-
-
0023865488
-
Apolipoprotein genetic variation and human disease
-
(1988)
Physiol Rev
, vol.68
, pp. 85-132
-
-
Breslow, J.1
-
5
-
-
0024556170
-
Genetic heritability and common environmental components of resting and stressed blood pressures, lipids, and body mass index in Utah pedigrees and twins
-
(1989)
Am J Epidemiol
, vol.129
, pp. 625-638
-
-
Hunt, S.C.1
Hasstedt, S.J.2
Kuida, H.3
Stults, B.M.4
Hopkins, P.N.5
Williams, R.R.6
-
6
-
-
0031456037
-
Familial resemblance of plasma lipids, lipoproteins and postheparin lipoprotein and hepatic lipases in the HERITAGE Family study
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 3263-3269
-
-
Perusse, L.1
Rice, T.2
Despres, J.P.3
Bergeron, J.4
Province, M.A.5
Gagnon, J.6
Leon, A.S.7
Rao, D.C.8
Skinner, J.S.9
Wilmore, J.H.10
-
9
-
-
0023116068
-
Complex segregation analysis of plasma lipid and lipoprotein variables in a Jerusalem sample of nuclear families
-
(1987)
Hum Hered
, vol.37
, pp. 7-19
-
-
Friedlander, Y.1
Kark, J.D.2
-
10
-
-
0027144958
-
Genetic basis of familial dyslipidemia and hypertension: 15-Year results from Utah
-
(1993)
Am J Hypertens
, vol.6
-
-
Williams, R.R.1
Hunt, S.C.2
Hopkins, P.N.3
Wu, L.L.4
Hasstedt, S.J.5
Berry, T.D.6
Barlow, G.K.7
Stults, B.M.8
Schumacher, M.C.9
Ludwig, E.H.10
-
12
-
-
0029098706
-
A major locus influencing plasma high-density lipoprotein cholesterol levels in the San Antonio Family Heart study: Segregation and linkage analyses
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 1730-1739
-
-
Mahaney, M.C.1
Blangero, J.2
Rainwater, D.L.3
Comuzzie, A.G.4
VandeBerg, J.L.5
Stern, M.P.6
MacCluer, J.W.7
Hixson, J.E.8
-
13
-
-
0033494813
-
Evidence for a major gene unlinked to the LDL receptor accounting for mild elevation in LDL cholesterol: The NHLBI Family Heart study
-
(1998)
Ann Hum Genet
, vol.63
, pp. 401-412
-
-
Coon, H.1
Leppert, M.F.2
Province, M.A.3
Myers, R.H.4
Arnett, D.K.5
Heiss, G.6
Williams, R.R.7
Hunt, S.C.8
-
14
-
-
0023890074
-
Familial dyslipidemic hypertension: Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension
-
(1988)
JAMA
, vol.259
, pp. 3579-3586
-
-
Williams, R.R.1
Hunt, S.C.2
Hopkins, P.N.3
Stults, B.M.4
Wu, L.L.5
Hasstedt, S.J.6
Barlow, G.K.7
Stephenson, S.H.8
Lalouel, J.M.9
Kuida, H.10
-
15
-
-
0025266196
-
Population-based frequency of dyslipidemia syndromes in coronary-prone families in Utah
-
(1990)
Arch Intern Med
, vol.150
, pp. 582-588
-
-
Williams, R.R.1
Hopkins, P.N.2
Hunt, S.C.3
Wu, L.L.4
Hasstedt, S.J.5
Lalouel, J.-M.6
Ash, K.O.7
Stults, B.M.8
Kuida, H.9
-
16
-
-
0029941114
-
NHLBI Family Heart study: Objectives and design
-
(1996)
Am J Epidemiol
, vol.143
, pp. 1219-1228
-
-
Higgins, M.1
Province, M.2
Heiss, G.3
Eckfeldt, J.4
Ellison, R.C.5
Folsom, A.R.6
Rao, D.C.7
Sprafka, M.8
Williams, R.9
-
17
-
-
0033846231
-
NHLBI Family Blood Pressure Program: Methodology and recruitment in the HyperGEN hypertension genetic epidemiology network
-
(2000)
Ann Epidemiol
, vol.10
, pp. 389-400
-
-
Williams, R.R.1
Rao, D.C.2
Ellison, R.C.3
Arnett, D.K.4
Heiss, G.5
Oberman, A.6
Eckfeldt, J.H.7
Leppert, M.F.8
Province, M.A.9
Mockrin, S.C.10
-
20
-
-
0000186892
-
Separation of lipoprotein (Lp) fraction by the Beckman TL-100 table-top ultracentrifuge (UC)
-
(1986)
Clin Chem
, vol.32
, pp. 1094
-
-
David, J.A.1
Naito, N.K.2
-
27
-
-
0033942570
-
A major susceptibility locus influencing plasma triglyceride concentration is located on chromosome 15q in Mexican Americans
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1237-1245
-
-
Duggirala, R.1
Blangero, J.2
Almasy, L.3
Dyer, T.D.4
Williams, K.L.5
Leach, R.J.6
O'Connell, P.7
Stern, M.8
-
28
-
-
2042546642
-
-
Deleted in press
-
-
-
-
29
-
-
0034701934
-
Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: A genome-wide scan in the Framingham study
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1315-1320
-
-
Shearman, A.M.1
Ordovas, J.M.2
Cupples, L.A.3
Schaefer, E.J.4
Harmon, M.D.5
Shao, Y.6
Keen, J.D.7
DeStafano, A.L.8
Joost, O.9
Wilson, P.W.10
-
31
-
-
0035569958
-
Genome scan for quantitative trait loci linked to high-density lipoprotein cholesterol: The NHLBI Family Heart study
-
(2001)
Arterioscler Thromb Vasc Biol
, vol.21
, pp. 1823-1828
-
-
Peacock, J.M.1
Arnett, D.K.2
Atwood, L.D.3
Myers, R.H.4
Coon, H.5
Rich, S.S.6
Province, M.A.7
Heiss, G.8
-
32
-
-
0033361796
-
Human pedigree-based quantitative-trait-locus mapping: Localization of two genes influencing HDL-cholesterol metabolism
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1686-1693
-
-
Almasy, L.1
Hixson, J.E.2
Rainwater, D.L.3
Cole, S.4
Williams, J.T.5
Mahaney, M.C.6
VandeBerg, J.L.7
Stern, M.P.8
MacCluer, J.W.9
Blangero, J.10
-
33
-
-
0033925280
-
A cholesterol-lowering gene maps to chromosome 13q
-
(2000)
Am J Hum Genet
, vol.66
, pp. 157-166
-
-
Knoblauch, H.1
Muller-Myhosok, B.2
Busjahn, A.3
Ben Avi, L.4
Bahring, S.5
Baron, H.6
Heath, S.C.7
Uhlmann, R.8
Faulhaber, H.D.9
Shpitzen, S.10
-
35
-
-
0034127788
-
Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 1089-1093
-
-
Hunt, S.C.1
Hopkins, P.N.2
Bulka, K.3
McDermott, M.T.4
Thorne, T.L.5
Wardell, B.B.6
Bowen, B.R.7
Ballinger, D.G.8
Skolnick, M.H.9
Samuels, M.E.10
-
36
-
-
0031918837
-
Linkage of familial combined hyperlipidemia to chromosome 1q21-23
-
(1998)
Nat Genet
, vol.18
, pp. 369-373
-
-
Pajukanta, P.1
Nuotio, I.2
Terwilliger, J.D.3
Porkka, K.V.K.4
Ylitalo, K.5
Pihlajamaki, J.6
Suomalainen, A.J.7
Syvanen, A.-C.8
Lehtimakii, T.9
Viikari, J.S.A.10
-
37
-
-
0033782243
-
Replication of linkage of familial combined hyperlipidemia to chromosome 1q with an additional heterogeneous effect of the apolipoprotein AI/CIII/AIV locus: The NHLBI Family Heart study
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 2275-2280
-
-
Coon, H.1
Myers, R.H.2
Borecki, I.B.3
Arnett, D.K.4
Hunt, S.C.5
Province, M.A.6
Djousse, L.7
Leppert, M.F.8
-
38
-
-
0033984185
-
Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families
-
(2000)
Clin Genet
, vol.57
, pp. 29-34
-
-
Pei, W.1
Baron, H.2
Muller-Myhsok, B.3
Knoblauch, H.4
Al-Yahyaee, S.A.5
Hui, R.6
Wu, X.7
Liu, L.8
Busjahn, A.9
Luft, F.C.10
-
39
-
-
0033362160
-
Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1453-1463
-
-
Pajukanta, P.1
Terwilliger, J.D.2
Perola, M.3
Hiekkalinna, T.4
Nuotio, I.5
Ellonen, P.6
Parkkonen, M.7
Hartiala, J.8
Ylitalo, K.9
Pihlajamaki, J.10
-
40
-
-
0033362163
-
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11
-
(1999)
Am J Hum Genet
, vol.65
, pp. 397-412
-
-
Aouizerat, B.E.1
Allayee, H.2
Cantor, R.M.3
Davis, R.C.4
Lanning, C.D.5
Wen, P.Z.6
Dallinga-Thie, G.M.7
De Bruin, T.W.8
Rotter, J.I.9
Lusis, A.J.10
-
41
-
-
0033925779
-
A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-26
-
(2000)
Am J Hum Genet
, vol.66
, pp. 453-460
-
-
Ciccarese, M.1
Pacifico, A.2
Tonolo, G.3
Pintus, P.4
Nikoshkov, A.5
Zuiani, G.6
Fellin, R.7
Luthman, H.8
Maioli, M.9
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