-
2
-
-
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
-
3
-
-
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
-
4
-
-
0030897631
-
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy
-
(1997)
Diabetes
, vol.46
, pp. 882-886
-
-
Bowden, D.W.1
Sale, M.2
Howard, T.D.3
Qadri, A.4
Spray, B.J.5
Rothschild, C.B.6
Akots, G.7
Rich, S.S.8
Freedman, B.I.9
-
5
-
-
0032813808
-
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
-
(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
Brewer, C.8
Collins, J.A.9
Molhuizen, H.O.10
Loubser, O.11
Ouelette, B.F.12
Fichter, K.13
Ashbourne-Excoffon, K.J.14
Sensen, C.W.15
Scherer, S.16
Mott, S.17
Denis, M.18
Martindale, D.19
Frohlich, J.20
Morgan, K.21
Koop, B.22
Pimstone, S.23
Kastelein, J.J.24
Hayden, M.R.25
more..
-
6
-
-
0035814958
-
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
-
(2001)
Circulation
, vol.103
, pp. 1198-1205
-
-
Clee, S.M.1
Zwinderman, A.H.2
Engert, J.C.3
Zwarts, K.Y.4
Molhuizen, H.O.5
Roomp, K.6
Jukema, J.W.7
Van Wijland, M.8
Van Dam, M.9
Hudson, T.J.10
Brooks-Wilson, A.11
Genest, J.12
Kastelein, J.J.13
Hayden, M.R.14
-
9
-
-
0026762806
-
Familial lipoprotein disorders in patients with premature coronary artery disease
-
(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
Wilson, P.W.8
Salem, D.N.9
Schaefer, E.J.10
-
10
-
-
0033764737
-
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2, diabetes
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1174-1185
-
-
Ghosh, S.1
Watanabe, R.M.2
Valle, T.T.3
Hauser, E.R.4
Magnuson, V.L.5
Langefeld, C.D.6
Ally, D.S.7
-
12
-
-
0034164617
-
Linkage analysis in the presence of errors. III. Marker loci and their map as nuisance parameters
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1298-1309
-
-
-
13
-
-
0030017175
-
A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2
-
(1996)
Nat Genet
, vol.13
, pp. 477-480
-
-
Kuokkanen, S.1
Sundvall, M.2
Terwilliger, J.D.3
Tienari, P.J.4
Wikstrom, J.5
Holmdahl, R.6
Pettersson, U.7
Peltonen, L.8
-
15
-
-
1842292786
-
Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q
-
(1997)
J Clin Invest
, vol.100
, pp. 1240-1247
-
-
Lembertas, A.V.1
Perusse, L.2
Chagnon, Y.C.3
Fisler, J.S.4
Warden, C.H.5
Purcell-Huynh, D.A.6
Dionne, F.T.7
Gagnon, J.8
Nadeau, A.9
Lusis, A.J.10
Bouchard, C.11
-
16
-
-
85001739876
-
A candidate gene study in low HDL-cholesterol families provides evidence for the involvement of the apoA2 gene and the ApoA1C3A4 gene cluster
-
in press
-
Atherosclerosis
-
-
Lilja, H.E.1
Soro, A.2
Ylitalo, K.3
Nuotio, I.4
Viikari, J.S.A.5
Salomaa, V.6
Vartiainen, E.7
Taskinen, M.-R.8
Peltonen, L.9
Pajukanta, P.10
-
19
-
-
0031918837
-
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
-
(1998)
Nat Genet
, vol.18
, pp. 369-373
-
-
Pajukanta, P.1
Nuotio, I.2
Terwilliger, J.D.3
Porkka, K.V.4
Ylitalo, K.5
Pihlajamaki, J.6
Suomalainen, A.J.7
Syvanen, A.C.8
Lehtimaki, T.9
Viikari, J.S.10
Laakso, M.11
Taskinen, M.R.12
Ehnholm, C.13
Peltonen, L.14
-
20
-
-
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
Porkka, K.11
Laakso, M.12
Viikari, J.13
Ehnholm, C.14
Taskinen, M.R.15
Peltonen, L.16
-
24
-
-
0032813660
-
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
-
(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
Brewer, H.B.8
Duverger, N.9
Denefle, P.10
Assmann, G.11
-
26
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
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