-
1
-
-
0001117051
-
Familial aggregation of morbid obesity
-
Adams TD, Hunt SC, Mason LA, Ramirez ME, Fisher AG, Williams RR (1993) Familial aggregation of morbid obesity. Obes Res 1:261-270
-
(1993)
Obes Res
, vol.1
, pp. 261-270
-
-
Adams, T.D.1
Hunt, S.C.2
Mason, L.A.3
Ramirez, M.E.4
Fisher, A.G.5
Williams, R.R.6
-
2
-
-
0033032512
-
Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population
-
Acton S, Osgood D, Donoghue M, Corella D, Pocovi M, Cenarro A, Mozas P, et al (1999) Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population. Arterioscler Thromb Vasc Biol 19:1734-1743
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 1734-1743
-
-
Acton, S.1
Osgood, D.2
Donoghue, M.3
Corella, D.4
Pocovi, M.5
Cenarro, A.6
Mozas, P.7
-
3
-
-
0033361796
-
Human pedigree-based quantitative-trait-locus mapping: Localization of two genes influencing HDL-cholesterol metabolism
-
Almasy L, Hixson JE, Rainwater DL, Cole S, Williams JT, Mahaney MC, VandeBerg JL, et al (1999) Human pedigree-based quantitative-trait-locus mapping: localization of two genes influencing HDL-cholesterol metabolism. Am J Hum Genet 64:1686-1693
-
(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
-
4
-
-
0032813809
-
The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
-
Bodzioch M, Orso E, Klucken J, Langmann T, Bottcher A, Diederich W, Drobnik W, et al (1999) The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat Genet 22:347-351
-
(1999)
Nat Genet
, vol.22
, pp. 347-351
-
-
Bodzioch, M.1
Orso, E.2
Klucken, J.3
Langmann, T.4
Bottcher, A.5
Diederich, W.6
Drobnik, W.7
-
5
-
-
0032127075
-
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites
-
Boright AP, Connelly PW, Brunt JH, Scherer SW, Tsui LC, Hegele RA (1998) Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites. Atherosclerosis 139:131-136
-
(1998)
Atherosclerosis
, vol.139
, pp. 131-136
-
-
Boright, A.P.1
Connelly, P.W.2
Brunt, J.H.3
Scherer, S.W.4
Tsui, L.C.5
Hegele, R.A.6
-
6
-
-
0001474759
-
Familial disorders of high-density lipoprotein metabolism
-
Scriver CR, Beaudet AL, Sly WS, Valle D (eds). McGraw Hill, New York
-
Breslow JL (1995) Familial disorders of high-density lipoprotein metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular basis of inherited disease. McGraw Hill, New York, vol 2, pp 2031-2052
-
(1995)
The Metabolic and Molecular Basis of Inherited Disease
, vol.2
, pp. 2031-2052
-
-
Breslow, J.L.1
-
7
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman KW, Murray JC, Sheffield VC, White RL, Weber JL (1998) Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am J Hum Genet 63:861-869
-
(1998)
Am J Hum Genet
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
8
-
-
0032813808
-
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
-
Brooks-Wilson A, Marcil M, Clee SM, Zhang L-H, Roomp K, van Dam M, Yu L, et al (1999) Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat Genet 22:336-345
-
(1999)
Nat Genet
, vol.22
, pp. 336-345
-
-
Brooks-Wilson, A.1
Marcil, M.2
Clee, S.M.3
Zhang, L.-H.4
Roomp, K.5
Van Dam, M.6
Yu, L.7
-
9
-
-
0001506104
-
Modulation of non-templated nucleotide addition by Taq polymerase: Primer modifications that facilitate genotyping
-
Brownstein MJ, Carpten JD, Smith JR (1996) Modulation of non-templated nucleotide addition by Taq polymerase: primer modifications that facilitate genotyping. Biotechniques 20:1004-1010
-
(1996)
Biotechniques
, vol.20
, pp. 1004-1010
-
-
Brownstein, M.J.1
Carpten, J.D.2
Smith, J.R.3
-
10
-
-
0028228359
-
Linkage analysis of the genetic determinants of high density lipoprotein concentrations and composition: Evidence for involvement of the apolipoprotein A-II and cholesteryl ester transfer protein loci
-
Bu X, Warden CH, Xia Y-R, DeMeester C, Puppione DL, Teruya S, Lokens B, et al (1994) Linkage analysis of the genetic determinants of high density lipoprotein concentrations and composition: evidence for involvement of the apolipoprotein A-II and cholesteryl ester transfer protein loci. Hum Genet 93:639-648
-
(1994)
Hum Genet
, vol.93
, pp. 639-648
-
-
Bu, X.1
Warden, C.H.2
Xia, Y.-R.3
DeMeester, C.4
Puppione, D.L.5
Teruya, S.6
Lokens, B.7
-
11
-
-
0022728801
-
Effects of misspecifying genetic parameters in lod score analysis
-
Clerget-Darpoux F, Bonaïti-Pellié C (1986) Effects of misspecifying genetic parameters in lod score analysis. Biometrics 42:393-399
-
(1986)
Biometrics
, vol.42
, pp. 393-399
-
-
Clerget-Darpoux, F.1
Bonaïti-Pellié, C.2
-
12
-
-
0028037134
-
Variation at the hepatic lipase and apolipoprotein AI/CIII/ AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels
-
Cohen JC, Wang Z, Grundy SM, Stoesz MR, Guerra R (1994) Variation at the hepatic lipase and apolipoprotein AI/CIII/ AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels. J Clin Invest 94: 2377-2384
-
(1994)
J Clin Invest
, vol.94
, pp. 2377-2384
-
-
Cohen, J.C.1
Wang, Z.2
Grundy, S.M.3
Stoesz, M.R.4
Guerra, R.5
-
13
-
-
0022194309
-
Report of the committee on methods of linkage analysis and reporting
-
Conneally PM, Edwards JH, Kidd KK, Lalouel J-M, Morton NE, Ott J, White R (1985) Report of the committee on methods of linkage analysis and reporting. Cytogenet Cell Genet 40:356-359
-
(1985)
Cytogenet Cell Genet
, vol.40
, pp. 356-359
-
-
Conneally, P.M.1
Edwards, J.H.2
Kidd, K.K.3
Lalouel, J.-M.4
Morton, N.E.5
Ott, J.6
White, R.7
-
16
-
-
0008533111
-
Evidence of a gene at 6q for high levels of high density lipoprotein cholesterol: The Framingham study
-
abstract 78
-
Cupples, LA, Ordovas JM, Rao VS, Harmon MD, Wilson PWF, Schaefer EJ, Myers RH (1998) Evidence of a gene at 6q for high levels of high density lipoprotein cholesterol: the Framingham study. Am J Hum Genet 63 Suppl:A16 (abstract 78)
-
(1998)
Am J Hum Genet
, vol.63
, Issue.SUPPL.
-
-
Cupples, L.A.1
Ordovas, J.M.2
Rao, V.S.3
Harmon, M.D.4
Wilson, P.W.F.5
Schaefer, E.J.6
Myers, R.H.7
-
17
-
-
0027223301
-
An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3′ untranslated region polymorphisms
-
Dammerman M, Sandkuul LA, Halaas JL, Chung W, Breslow JL (1993) An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3′ untranslated region polymorphisms. Proc Natl Acad Sci USA 90:4562-4566
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 4562-4566
-
-
Dammerman, M.1
Sandkuul, L.A.2
Halaas, J.L.3
Chung, W.4
Breslow, J.L.5
-
18
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Fauré, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
-
19
-
-
0031470430
-
Common variation in the lipoprotein lipase gene: Effects on plasma lipids and risk of atherosclerosis
-
Fisher RM, Humphries SE, Talmud PJ (1997) Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis. Atherosclerosis 135:145-159
-
(1997)
Atherosclerosis
, vol.135
, pp. 145-159
-
-
Fisher, R.M.1
Humphries, S.E.2
Talmud, P.J.3
-
20
-
-
0019226420
-
A-I Milano apoprotein: Decreased high density lipoprotein cholesterol levels with significant lipoprotein modifications and without clinical atherosclerosis in an Italian family
-
Franceschini G, Sirtori CR, Capurso A, Weisgraber KH, Mahley RW (1980) A-I Milano apoprotein: decreased high density lipoprotein cholesterol levels with significant lipoprotein modifications and without clinical atherosclerosis in an Italian family. J Clin Invest 66:892-900
-
(1980)
J Clin Invest
, vol.66
, pp. 892-900
-
-
Franceschini, G.1
Sirtori, C.R.2
Capurso, A.3
Weisgraber, K.H.4
Mahley, R.W.5
-
21
-
-
0022485722
-
Biological and environmental sources of variation in plasma lipids and lipoproteins: The Jerusalem Lipid Research Clinic
-
Friedlander Y, Kark JD, Stein Y (1986) Biological and environmental sources of variation in plasma lipids and lipoproteins: the Jerusalem Lipid Research Clinic. Hum Hered 36:143-153
-
(1986)
Hum Hered
, vol.36
, pp. 143-153
-
-
Friedlander, Y.1
Kark, J.D.2
Stein, Y.3
-
22
-
-
0026101257
-
A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin:Cholesterol acyltransferase deficiency, and corneal opacities
-
Funke H, von Eckardstein A, Pritchard PH, Karas M, Albers JJ, Assmann G (1991) A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin:cholesterol acyltransferase deficiency, and corneal opacities. J Clin Invest 87:371-376
-
(1991)
J Clin Invest
, vol.87
, pp. 371-376
-
-
Funke, H.1
Von Eckardstein, A.2
Pritchard, P.H.3
Karas, M.4
Albers, J.J.5
Assmann, G.6
-
23
-
-
0026762806
-
Familial lipoprotein disorders in patients with premature coronary artery disease
-
Genest JJ, Martin-Munley SS, McNamara JR, Ordovas JM, Jenner J, Myers RH, Silberman SR, et al (1992) Familial lipoprotein disorders in patients with premature coronary artery disease. Circulation 85:2025-2033
-
(1992)
Circulation
, vol.85
, pp. 2025-2033
-
-
Genest, J.J.1
Martin-Munley, S.S.2
McNamara, J.R.3
Ordovas, J.M.4
Jenner, J.5
Myers, R.H.6
Silberman, S.R.7
-
24
-
-
0015796295
-
Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia
-
Goldstein JL, Schrott HG, Hazzard WR, Bierman EL, Motulsky AG (1973) Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia. J Clin Invest 52:1544-1568
-
(1973)
J Clin Invest
, vol.52
, pp. 1544-1568
-
-
Goldstein, J.L.1
Schrott, H.G.2
Hazzard, W.R.3
Bierman, E.L.4
Motulsky, A.G.5
-
25
-
-
0032231322
-
An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians
-
Hanson RL, Ehm MG, Pettitt DJ, Prochazka M, Thompson DB, Timberlake D, Foroud T, et al (1998) An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians. Am J Hum Genet 63: 1130-1138
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1130-1138
-
-
Hanson, R.L.1
Ehm, M.G.2
Pettitt, D.J.3
Prochazka, M.4
Thompson, D.B.5
Timberlake, D.6
Foroud, T.7
-
26
-
-
17344374012
-
A novel homozygous missense mutation in the Apo A-I gene with Apo A-I deficiency
-
Huang W, Sasaki J, Matsunaga A, Nanimatsu H, Moriyama K, Han H, Kugi M, et al (1998) A novel homozygous missense mutation in the Apo A-I gene with Apo A-I deficiency. Arterioscler Thromb Vasc Biol 18:389-396
-
(1998)
Arterioscler Thromb Vasc Biol
, vol.18
, pp. 389-396
-
-
Huang, W.1
Sasaki, J.2
Matsunaga, A.3
Nanimatsu, H.4
Moriyama, K.5
Han, H.6
Kugi, M.7
-
27
-
-
0024556170
-
Genetic heritability and common environmental components of resting and stressed blood pressures, lipids, and body mass index in Utah pedigrees and twins
-
Hunt SC, Hasstedt SJ, Kuida H, Stults BM, Hopkins PN, Williams RR (1989) Genetic heritability and common environmental components of resting and stressed blood pressures, lipids, and body mass index in Utah pedigrees and twins. Am J Epidemiol 129:625-638
-
(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
-
28
-
-
85031579156
-
Genome-wide searches for genes influencing serum lipid concentrations in Pima Indians
-
abstract 1695
-
Imperatore G, Hanson RL, Pettitt DJ, Kobes S, Bennett PH, Knowler WC (1998) Genome-wide searches for genes influencing serum lipid concentrations in Pima Indians. Am J Hum Genet 63 Suppl:A293 (abstract 1695)
-
(1998)
Am J Hum Genet
, vol.63
, Issue.SUPPL.
-
-
Imperatore, G.1
Hanson, R.L.2
Pettitt, D.J.3
Kobes, S.4
Bennett, P.H.5
Knowler, W.C.6
-
29
-
-
4243385085
-
A genome scan for quantitative trait loci influencing adiposity in the Framingham heart study
-
abstract 1905
-
Jaquish CE, Fabsitz RR, Larson MG, Cupples LA, Myers RH, Levy D (1998) A genome scan for quantitative trait loci influencing adiposity in the Framingham heart study. Am J Hum Genet 63 Suppl:A329 (abstract 1905)
-
(1998)
Am J Hum Genet
, vol.63
, Issue.SUPPL.
-
-
Jaquish, C.E.1
Fabsitz, R.R.2
Larson, M.G.3
Cupples, L.A.4
Myers, R.H.5
Levy, D.6
-
30
-
-
0032961228
-
Genetic association of five apolipoprotein polymorphisms with serum lipoprotein-lipid levels in African blacks
-
Kamboh MI, Bunker CH, Aston CE, Nestlerode CS, McAllister AE, Ukoli FA (1999) Genetic association of five apolipoprotein polymorphisms with serum lipoprotein-lipid levels in African blacks. Genet Epidemiol 16:205-222
-
(1999)
Genet Epidemiol
, vol.16
, pp. 205-222
-
-
Kamboh, M.I.1
Bunker, C.H.2
Aston, C.E.3
Nestlerode, C.S.4
McAllister, A.E.5
Ukoli, F.A.6
-
31
-
-
0025815683
-
Effects of polymorphisms in apolipoproteins E, A-IV, and H on quantitative traits related to risk for cardiovascular disease
-
Kaprio J, Ferrell RE, Kottke BA, Kamboh MI, Sing CF (1991) Effects of polymorphisms in apolipoproteins E, A-IV, and H on quantitative traits related to risk for cardiovascular disease. Arterioscler Thromb 11:1330-1348
-
(1991)
Arterioscler Thromb
, vol.11
, pp. 1330-1348
-
-
Kaprio, J.1
Ferrell, R.E.2
Kottke, B.A.3
Kamboh, M.I.4
Sing, C.F.5
-
32
-
-
0030933460
-
The molecular pathology of lecithin:Cholesterol acyltransferase (LCAT) deficiency syndromes
-
Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J (1997) The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes. J Lipid Res 38:191-205
-
(1997)
J Lipid Res
, vol.38
, pp. 191-205
-
-
Kuivenhoven, J.A.1
Pritchard, H.2
Hill, J.3
Frohlich, J.4
Assmann, G.5
Kastelein, J.6
-
33
-
-
0000803318
-
Construction of multilocus genetic linkage maps in humans
-
Lander E, Green P (1987) Construction of multilocus genetic linkage maps in humans. Proc Natl Acad Sci USA 84: 2363-2367
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 2363-2367
-
-
Lander, E.1
Green, P.2
-
34
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L (1995) Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11:241-247
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
35
-
-
0021344005
-
Easy calculations of LOD scores and genetic risks on small computers
-
Lathrop GM, Lalouel J-M (1984) Easy calculations of LOD scores and genetic risks on small computers. Am J Hum Genet 36:460-465
-
(1984)
Am J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.-M.2
-
37
-
-
0022646961
-
Construction of human genetic linkage maps: Likelihood calculations for multilocus analysis
-
Lathrop GM, Lalouel J-M, White RL (1986) Construction of human genetic linkage maps: likelihood calculations for multilocus analysis. Genet Epidemiol 3:39-52
-
(1986)
Genet Epidemiol
, vol.3
, pp. 39-52
-
-
Lathrop, G.M.1
Lalouel, J.-M.2
White, R.L.3
-
38
-
-
0032725185
-
The tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway
-
Lawn RM, Wade DP, Garvin MR, Wang X, Schwartz K, Porter JG, Seilhamer JJ, et al (1999) The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway. J Clin Invest 104:R25-R31
-
(1999)
J Clin Invest
, vol.104
-
-
Lawn, R.M.1
Wade, D.P.2
Garvin, M.R.3
Wang, X.4
Schwartz, K.5
Porter, J.G.6
Seilhamer, J.J.7
-
39
-
-
0028997460
-
The CEPH consortium linkage map of human chromosome 11
-
Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, et al (1995) The CEPH consortium linkage map of human chromosome 11. Genomics 27:101-112
-
(1995)
Genomics
, vol.27
, pp. 101-112
-
-
Litt, M.1
Kramer, P.2
Kort, E.3
Fain, P.4
Cox, S.5
Root, D.6
White, R.7
-
40
-
-
85031592226
-
-
NIH publication no. 80-1527, US Department of Health and Human Services, Washington, DC
-
Lipid Research Clinics (1980) Population studies data book. Vol I: the prevalence study. NIH publication no. 80-1527, US Department of Health and Human Services, Washington, DC
-
(1980)
Population Studies Data Book. Vol I: the Prevalence Study
, vol.1
-
-
-
41
-
-
0029098706
-
A major locus influencing plasma high-density lipoprotein cholesterol levels in the San Antonio family heart study
-
Maheny MC, Blangero J, Rainwater DL, Comuzzie AG, VandeBerg JL, Stern MP MacCluer JW, et al (1995) A major locus influencing plasma high-density lipoprotein cholesterol levels in the San Antonio family heart study. Arterioscler Thromb Vasc Biol 15:1730-1739
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 1730-1739
-
-
Maheny, 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
-
42
-
-
0033118761
-
Apolipoprotein J polymorphisms and serum HDL cholesterol levels in African blacks
-
Nestlerode CS, Bunker CH, Sanghera DK, Aston CE, Ukoli FA, Kamboh MI (1999) Apolipoprotein J polymorphisms and serum HDL cholesterol levels in African blacks. Hum Biol 71:197-218
-
(1999)
Hum Biol
, vol.71
, pp. 197-218
-
-
Nestlerode, C.S.1
Bunker, C.H.2
Sanghera, D.K.3
Aston, C.E.4
Ukoli, F.A.5
Kamboh, M.I.6
-
43
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilites in linkage analysis
-
O'Connell JR, Weeks DE (1998) PedCheck: a program for identification of genotype incompatibilites in linkage analysis. Am J Hum Genet 63:259-266
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
44
-
-
0017724094
-
Linkage analysis with misclassification at one locus
-
Ott J (1977) Linkage analysis with misclassification at one locus. Clin Genet 12:119-124
-
(1977)
Clin Genet
, vol.12
, pp. 119-124
-
-
Ott, J.1
-
45
-
-
0021064786
-
Linkage analysis and family classification under heterogeneity
-
-(1983) Linkage analysis and family classification under heterogeneity. Ann Hum Genet 47:311-320
-
(1983)
Ann Hum Genet
, vol.47
, pp. 311-320
-
-
-
46
-
-
0033362160
-
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol and apolipoprotein B levels
-
Pajukanta P, Terwilliger JD, Perola M, Hiekkalinna T, Nuotio I, Ellonen P, Parkkonen M, et al (1999) Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol and apolipoprotein B levels. Am J Hum Genet 64:1453-1463
-
(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
-
47
-
-
0027974106
-
Associations of genotypes at the apolipoprotein AI-CIII-AIV, apolipoprotein B and lipoprotein lipase gene loci with coronary atherosclerosis and high density lipoprotein subclasses
-
Peacock RE, Hamsten A, Johansson J, Nilsson-Ehle P, Humphries SE (1994) Associations of genotypes at the apolipoprotein AI-CIII-AIV, apolipoprotein B and lipoprotein lipase gene loci with coronary atherosclerosis and high density lipoprotein subclasses. Clin Genet 46:273-282
-
(1994)
Clin Genet
, vol.46
, pp. 273-282
-
-
Peacock, R.E.1
Hamsten, A.2
Johansson, J.3
Nilsson-Ehle, P.4
Humphries, S.E.5
-
48
-
-
0024392394
-
Genetic and environmental determinants of serum lipids and lipoproteins in French Canadian families
-
Perusse L, Despres JP, Tremblay A, Leblanc C, Talbot J, Allard C, Bouchard C (1989) Genetic and environmental determinants of serum lipids and lipoproteins in French Canadian families. Arteriosclerosis 9:308-318
-
(1989)
Arteriosclerosis
, vol.9
, pp. 308-318
-
-
Perusse, L.1
Despres, J.P.2
Tremblay, A.3
Leblanc, C.4
Talbot, J.5
Allard, C.6
Bouchard, C.7
-
49
-
-
0032572381
-
Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypoalpha-lipoproteinaemia
-
Pocovi M, Cenarro A, Civeira F, Torralba MA, Perez-Calvo JI, Mozas P, Giraldo P, et al (1998) Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypoalpha-lipoproteinaemia. Lancet 351:1919-1923
-
(1998)
Lancet
, vol.351
, pp. 1919-1923
-
-
Pocovi, M.1
Cenarro, A.2
Civeira, F.3
Torralba, M.A.4
Perez-Calvo, J.I.5
Mozas, P.6
Giraldo, P.7
-
50
-
-
0026781872
-
Genetic determination of high-density lipoprotein-cholesterol and apolipoprotein A-1 plasma levels in a family study of cardiac catheterization patients
-
Prenger VL, Beaty TH, Kwiterovich PO (1992) Genetic determination of high-density lipoprotein-cholesterol and apolipoprotein A-1 plasma levels in a family study of cardiac catheterization patients. Am J Hum Genet 51:1047-1057
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1047-1057
-
-
Prenger, V.L.1
Beaty, T.H.2
Kwiterovich, P.O.3
-
51
-
-
0026529005
-
Model misspecification and multipoint linkage analysis
-
Risch N, Giuffra L (1992) Model misspecification and multipoint linkage analysis. Hum Hered 42:77-92
-
(1992)
Hum Hered
, vol.42
, pp. 77-92
-
-
Risch, N.1
Giuffra, L.2
-
52
-
-
0028170617
-
A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas
-
Romling R, von Eckardstein A, Funke H, Motti C, Fragiacomo GC, Noseda G, Assmann G (1994) A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas. Arterioscler Thromb 14:1915-1922
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 1915-1922
-
-
Romling, R.1
Von Eckardstein, A.2
Funke, H.3
Motti, C.4
Fragiacomo, G.C.5
Noseda, G.6
Assmann, G.7
-
53
-
-
0032813660
-
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
-
Rust S, Rosier M, Funke H, Real J, Amoura Z, Piette J-C, Deleuze J-F, et al (1999) Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat Genet 22:352-355
-
(1999)
Nat Genet
, vol.22
, pp. 352-355
-
-
Rust, S.1
Rosier, M.2
Funke, H.3
Real, J.4
Amoura, Z.5
Piette, J.-C.6
Deleuze, J.-F.7
-
56
-
-
0001586099
-
Plasma high-density lipoproteins and atherogenesis
-
Fuster V, Ross R, Topol EJ (eds). Lippincott-Raven, Philadelphia
-
Tall AR, Breslow JL (1996) Plasma high-density lipoproteins and atherogenesis. In: Fuster V, Ross R, Topol EJ (eds) Ath erosclerosis and coronary artery disease. Lippincott-Raven, Philadelphia, pp 105-128
-
(1996)
Ath Erosclerosis and Coronary Artery Disease
, pp. 105-128
-
-
Tall, A.R.1
Breslow, J.L.2
-
58
-
-
0020335173
-
Apolipoprotein AI (Marburg): Studies of two kindreds with a mutant of human apolipoprotein AI
-
Utermann G, Steinmetz A, Paetzold R, Wilk J, Feussner G, Kaffarnik H, Mueller-Eckhardt C, et al (1982) Apolipoprotein AI (Marburg): studies of two kindreds with a mutant of human apolipoprotein AI. Hum Genet 61:329-337
-
(1982)
Hum Genet
, vol.61
, pp. 329-337
-
-
Utermann, G.1
Steinmetz, A.2
Paetzold, R.3
Wilk, J.4
Feussner, G.5
Kaffarnik, H.6
Mueller-Eckhardt, C.7
-
59
-
-
0024803138
-
Apolipoprotein A-I variants: Naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I
-
Von Eckardstein A, Funke H, Henke A, Altland K, Benninghoven A, Assman G, Welp S, et al (1989) Apolipoprotein A-I variants: naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I. J Clin Invest 84:1722-1730
-
(1989)
J Clin Invest
, vol.84
, pp. 1722-1730
-
-
Von Eckardstein, A.1
Funke, H.2
Henke, A.3
Altland, K.4
Benninghoven, A.5
Assman, G.6
Welp, S.7
-
60
-
-
0028853551
-
National cholesterol education program recommendations for measurement of high-density lipoprotein cholesterol: Executive summary
-
Warnick GR, Wood PD (1995) National cholesterol education program recommendations for measurement of high-density lipoprotein cholesterol: executive summary. Clin Chem 41: 1427-1433
-
(1995)
Clin Chem
, vol.41
, pp. 1427-1433
-
-
Warnick, G.R.1
Wood, P.D.2
-
61
-
-
0031808957
-
Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex
-
Wijsman EM, Brunzell JD, Jarvik GP, Austin MA, Motulsky AG, Deeb SS (1998) Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex. Arterioscler Thromb Vasc Biol 18:215-226
-
(1998)
Arterioscler Thromb Vasc Biol
, vol.18
, pp. 215-226
-
-
Wijsman, E.M.1
Brunzell, J.D.2
Jarvik, G.P.3
Austin, M.A.4
Motulsky, A.G.5
Deeb, S.S.6
-
62
-
-
0025266196
-
Population-based frequency of dyslipidemia syndromes in coronary-prone families in Utah
-
Williams RR, Hopkins PN, Hunt SC, Wu LL, Hasstedt SJ, Lalouel JM, Ash KO, et al (1990) Population-based frequency of dyslipidemia syndromes in coronary-prone families in Utah. Arch Intern Med 150:582-588
-
(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
-
63
-
-
0025970749
-
Familial combined hyperlipidaemia linked to the apolipoprotein AI-CIII-AIV gene cluster on chromosome 11q23-q24
-
Wojciechowski AP, Farrall M, Cullen P, Wilson TME, Bayliss JD, Farren B, Griffin BA, et al (1991) Familial combined hyperlipidaemia linked to the apolipoprotein AI-CIII-AIV gene cluster on chromosome 11q23-q24. Nature 349: 161-164
-
(1991)
Nature
, vol.349
, pp. 161-164
-
-
Wojciechowski, A.P.1
Farrall, M.2
Cullen, P.3
Wilson, T.M.E.4
Bayliss, J.D.5
Farren, B.6
Griffin, B.A.7
-
64
-
-
0024364222
-
A rapid micro-scale procedure for determination of total lipid profile
-
Wu LL, Warnick GR, Wu JT, Williams RR, Lalouel JM (1989) A rapid micro-scale procedure for determination of total lipid profile. Clin Chem 35:1486-1491
-
(1989)
Clin Chem
, vol.35
, pp. 1486-1491
-
-
Wu, L.L.1
Warnick, G.R.2
Wu, J.T.3
Williams, R.R.4
Lalouel, J.M.5
-
65
-
-
0032898483
-
Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-I gene in the population: A population-based survey
-
Yamakawa-Kobayashi K, Yanagi H, Fukayama H, Hirano C, Shimakura Y, Yamamoto N, Arinami T, et al (1999) Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-I gene in the population: a population-based survey. Hum Mol Genet 8:331-336
-
(1999)
Hum Mol Genet
, vol.8
, pp. 331-336
-
-
Yamakawa-Kobayashi, K.1
Yanagi, H.2
Fukayama, H.3
Hirano, C.4
Shimakura, Y.5
Yamamoto, N.6
Arinami, T.7
-
66
-
-
0030320433
-
Molecular disorders of cholesteryl ester transfer protein
-
Yamashita S, Arai T, Hirano K, Sakai N, Ishigami M, Nakajima N, Matsuzawa Y (1996) Molecular disorders of cholesteryl ester transfer protein. J Atheroscler Thromb 3:1-11
-
(1996)
J Atheroscler Thromb
, vol.3
, pp. 1-11
-
-
Yamashita, S.1
Arai, T.2
Hirano, K.3
Sakai, N.4
Ishigami, M.5
Nakajima, N.6
Matsuzawa, Y.7
|