-
1
-
-
0037013151
-
Locus for elevated apolipoprotein b levels on chromosome 1p31 in families with familial combined hyperlipidemia
-
Allayee A, Krass KL, Pajukanta P, Cantor RM, van der Kallen CJH, Mar R, Rotter JI, de Bruin TWA, Peltonen L, Lusis AJ (2002) Locus for elevated apolipoprotein b levels on chromosome 1p31 in families with familial combined hyperlipidemia. Circ Res 90:926-931
-
(2002)
Circ Res
, vol.90
, pp. 926-931
-
-
Allayee, A.1
Krass, K.L.2
Pajukanta, P.3
Cantor, R.M.4
Van Der Kallen, C.J.H.5
Mar, R.6
Rotter, J.I.7
De Bruin, T.W.A.8
Peltonen, L.9
Lusis, A.J.10
-
2
-
-
0032698344
-
Linkage of a candidate gene locus to familial combined hyperlipidemia: Lecithin:cholesterol acyltransferase on 16q
-
Aouizerat BE, Allayee H, Cantor RM, Dallinga-Thie GM, Lanning CD, de Bruin TWA, Lusis AJ, Rotter JI (1999a) Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q. Arterioscler Thromb Vasc Biol 19:2730-2736
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 2730-2736
-
-
Aouizerat, B.E.1
Allayee, H.2
Cantor, R.M.3
Dallinga-Thie, G.M.4
Lanning, C.D.5
De Bruin, T.W.A.6
Lusis, A.J.7
Rotter, J.I.8
-
3
-
-
0033362163
-
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11
-
Aouizerat BE, Allayee H, Cantor RM, Davis RC, Lanning CD, Wen PZ, Dallinga-Thie GM, de Bruin TWA, Rotter JI, Lusis AJ (1999b) A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11. Am J Hum Genet 65:397-412
-
(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.A.8
Rotter, J.I.9
Lusis, A.J.10
-
4
-
-
18544372620
-
A comprehensive linkage analysis for myocardial infarction and its related risk factors
-
Broeckel U, Hengstenberg C, Mayer B, Holmer S, Martin LJ, Comuzzie AG, Blangero J, Nurnberg P, Reis A, Riegger GA, Jacob HJ, Schunkert H (2002) A comprehensive linkage analysis for myocardial infarction and its related risk factors. Nat Genet 30:210-214
-
(2002)
Nat Genet
, vol.30
, pp. 210-214
-
-
Broeckel, U.1
Hengstenberg, C.2
Mayer, B.3
Holmer, S.4
Martin, L.J.5
Comuzzie, A.G.6
Blangero, J.7
Nurnberg, P.8
Reis, A.9
Riegger, G.A.10
Jacob, H.J.11
Schunkert, H.12
-
5
-
-
0020621407
-
Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia
-
Brunzell JD, Albers JJ, Chait A, Grundy SM, Groszek E, McDonald GB (1983) Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia. J Lipid Res 24:147-155
-
(1983)
J Lipid Res
, vol.24
, pp. 147-155
-
-
Brunzell, J.D.1
Albers, J.J.2
Chait, A.3
Grundy, S.M.4
Groszek, E.5
McDonald, G.B.6
-
6
-
-
0027171902
-
Impaired fatty acid metabolism in familial combined hyperlipidemia
-
Castro Cabezas M, de Bruin TWA, de Valk HA, Shoulders CC, Jansen H, Erkelens DW (1993) Impaired fatty acid metabolism in familial combined hyperlipidemia. J Clin Invest 92:160-168
-
(1993)
J Clin Invest
, vol.92
, pp. 160-168
-
-
Castro Cabezas, M.1
De Bruin, T.W.A.2
De Valk, H.A.3
Shoulders, C.C.4
Jansen, H.5
Erkelens, D.W.6
-
7
-
-
17944377509
-
FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance
-
Cederberg A, Gronning LM, Ahren B, Tasken K, Carlsson P, Enerback S (2001) FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance. Cell 106:563-573
-
(2001)
Cell
, vol.106
, pp. 563-573
-
-
Cederberg, A.1
Gronning, L.M.2
Ahren, B.3
Tasken, K.4
Carlsson, P.5
Enerback, S.6
-
8
-
-
0028952336
-
Linkage detection under heterogeneity and the mixture problem
-
Chiano MN, Yates JRW (1995) Linkage detection under heterogeneity and the mixture problem. Ann Hum Genet 59:83-95
-
(1995)
Ann Hum Genet
, vol.59
, pp. 83-95
-
-
Chiano, M.N.1
Yates, J.R.W.2
-
9
-
-
0033782243
-
Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus: The NHLBI Family Heart Study
-
Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF (2000) Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus: the NHLBI Family Heart Study. Arterioscler Thromb Vasc Biol 20:2275-2280
-
(2000)
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
-
11
-
-
0034821661
-
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families
-
Cox NJ, Wapelhorst B, Morrison VA, Johnson L, Pinchuk L, Spielman RS, Todd JA, Concannon P (2001) Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families. Am J Hum Genet 69:820-830
-
(2001)
Am J Hum Genet
, vol.69
, pp. 820-830
-
-
Cox, N.J.1
Wapelhorst, B.2
Morrison, V.A.3
Johnson, L.4
Pinchuk, L.5
Spielman, R.S.6
Todd, J.A.7
Concannon, P.8
-
12
-
-
0022644326
-
Detection of familial hypercholesterolemia by assaying functional low-density-lipoprotein receptors on lymphocytes
-
Cuthbert JA, East CA, Bilheimer DW (1986) Detection of familial hypercholesterolemia by assaying functional low-density-lipoprotein receptors on lymphocytes. N Engl J Med 314:879-883
-
(1986)
N Engl J Med
, vol.314
, pp. 879-883
-
-
Cuthbert, J.A.1
East, C.A.2
Bilheimer, D.W.3
-
13
-
-
0030069735
-
Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: Effects on LDL-cholesterol and apolipoproteins B and C-III
-
Dallinga-Thie GM, Bu X, van Linde-Sibenius Trip M, Rotter JI, Lusis AJ, de Bruin TWA (1996) Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III. J Lipid Res 37:136-147
-
(1996)
J Lipid Res
, vol.37
, pp. 136-147
-
-
Dallinga-Thie, G.M.1
Bu, X.2
Van Linde-Sibenius Trip, M.3
Rotter, J.I.4
Lusis, A.J.5
De Bruin, T.W.A.6
-
14
-
-
0030937346
-
Complex genetic contribution of the apoAI-CIII-AIV gene cluster to familial combined hyperlipidemia: Identification of different susceptibility haplotypes
-
Dallinga-Thie GM, van Linde-Sibenius Trip M, Rotter JI, Cantor RM, Bu X, Lusis AJ, de Bruin TWA (1997) Complex genetic contribution of the apoAI-CIII-AIV gene cluster to familial combined hyperlipidemia: identification of different susceptibility haplotypes. J Clin Invest 99:953-961
-
(1997)
J Clin Invest
, vol.99
, pp. 953-961
-
-
Dallinga-Thie, G.M.1
Van Linde-Sibenius Trip, M.2
Rotter, J.I.3
Cantor, R.M.4
Bu, X.5
Lusis, A.J.6
De Bruin, T.W.A.7
-
15
-
-
0034791035
-
High-resolution haplotype structure in the human genome
-
Daly MJ, Rioux JD, Schaffner SF, Hudson TJ, Lander ES (2001) High-resolution haplotype structure in the human genome. Nat Genet 29:229-232
-
(2001)
Nat Genet
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.F.3
Hudson, T.J.4
Lander, E.S.5
-
16
-
-
0027507885
-
Disease gene mapping in isolated human populations: The example of Finland
-
de la Chapelle A (1993) Disease gene mapping in isolated human populations: the example of Finland. J Med Genet 30:857-865
-
(1993)
J Med Genet
, vol.30
, pp. 857-865
-
-
De La Chapelle, A.1
-
17
-
-
18144434579
-
Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22
-
Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD, Juvonen H, Varilo T, Arajärvi R, Kokko-Sahin ML, Lönnqvist J, Peltonen L (2000) Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22. Hum Mol Genet 9:1049-1057
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1049-1057
-
-
Ekelund, J.1
Lichtermann, D.2
Hovatta, I.3
Ellonen, P.4
Suvisaari, J.5
Terwilliger, J.D.6
Juvonen, H.7
Varilo, T.8
Arajärvi, R.9
Kokko-Sahin, M.L.10
Lönnqvist, J.11
Peltonen, L.12
-
18
-
-
0032910599
-
A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians
-
Elbein SC, Hoffman MD, Teng K, Leppert MF, Hasstedt SJ (1999) A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians. Diabetes 48:1175-1182
-
(1999)
Diabetes
, vol.48
, pp. 1175-1182
-
-
Elbein, S.C.1
Hoffman, M.D.2
Teng, K.3
Leppert, M.F.4
Hasstedt, S.J.5
-
19
-
-
0034793988
-
Genetic dissection of familial combined hyperlipidemia
-
Eurlings PM, van der Kallen CJ, Geurts JM, van Greevenbroek MM, de Bruin TW (2001) Genetic dissection of familial combined hyperlipidemia. Mol Genet Metab 74:98-104
-
(2001)
Mol Genet Metab
, vol.74
, pp. 98-104
-
-
Eurlings, P.M.1
Van Der Kallen, C.J.2
Geurts, J.M.3
Van Greevenbroek, M.M.4
De Bruin, T.W.5
-
20
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
-
Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayan J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, Monaco AP (2002) Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet 30:86-91
-
(2002)
Nat Genet
, vol.30
, pp. 86-91
-
-
Fisher, S.E.1
Francks, C.2
Marlow, A.J.3
MacPhie, I.L.4
Newbury, D.F.5
Cardon, L.R.6
Ishikawa-Brush, Y.7
Richardson, A.J.8
Talcott, J.B.9
Gayan, J.10
Olson, R.K.11
Pennington, B.F.12
Smith, S.D.13
DeFries, J.C.14
Stein, J.F.15
Monaco, A.P.16
-
21
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D (2002) The structure of haplotype blocks in the human genome. Science 296:2225-2229
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
22
-
-
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
-
Ghosh S, Watanabe RM, Valle TT, Hauser ER, Magnuson VL, Langefeld CD, Ally DS, et al (2000) 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. Am J Hum Genet 67:1174-1185
-
(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
-
23
-
-
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
-
24
-
-
0343158231
-
Gene mapping in the 20th and 21st centuries: Statistical methods, data analysis, and experimental design
-
Göring HH, Terwilliger JD (2000a) Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design. Hum Biol 72:63-132
-
(2000)
Hum Biol
, vol.72
, pp. 63-132
-
-
Göring, H.H.1
Terwilliger, J.D.2
-
25
-
-
0034164617
-
Linkage analysis in the presence of errors III: Marker loci and their map as nuisance parameters
-
_ (2000b) Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters. Am J Hum Genet 66:1298-1309
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1298-1309
-
-
-
26
-
-
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, Kobes S, Baier L, Burns DK, Almasy L, Blangero J, Garvey WT, Bennett PH, Knowler WC (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
Kobes, S.8
Baier, L.9
Burns, D.K.10
Almasy, L.11
Blangero, J.12
Garvey, W.T.13
Bennett, P.H.14
Knowler, W.C.15
-
27
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP, Belaiche J, Almer S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, Gower-Rousseau C, Macry J, Colombel JF, Sahbatou M, Thomas G (2001) Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411:599-603
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
Lesage, S.4
Cezard, J.P.5
Belaiche, J.6
Almer, S.7
Tysk, C.8
O'Morain, C.A.9
Gassull, M.10
Binder, V.11
Finkel, Y.12
Cortot, A.13
Modigliani, R.14
Laurent-Puig, P.15
Gower-Rousseau, C.16
Macry, J.17
Colombel, J.F.18
Sahbatou, M.19
Thomas, G.20
more..
-
28
-
-
0035004413
-
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16
-
IBD International Genetics Consortium (2001) International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16. Am J Hum Genet 68:1165-1171
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1165-1171
-
-
-
29
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Sequencing Consortium (2001) Initial sequencing and analysis of the human genome. Nature 409:860-920
-
(2001)
Nature
, vol.409
, pp. 860-920
-
-
-
30
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA (2001) Haplotype tagging for the identification of common disease genes. Nat Genet 29:233-237
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
Ueda, H.7
Cordell, H.J.8
Eaves, I.A.9
Dudbridge, F.10
Twells, R.C.11
Payne, F.12
Hughes, W.13
Nutland, S.14
Stevens, H.15
Carr, P.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Gough, S.C.19
Clayton, D.G.20
Todd, J.A.21
more..
-
31
-
-
0030017175
-
A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2
-
Kuokkanen S, Sundvall M, Terwilliger JD, Tienari PJ, Wikstrom J, Holmdahl R, Pettersson U, Peltonen L (1996) A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2. Nat Genet 13:477-480
-
(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
-
32
-
-
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
-
33
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander ES, Schork NJ (1994) Genetic dissection of complex traits. Science 265:2037-2048
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
35
-
-
0035996585
-
A candidate gene study in low HDL-cholesterol families provides evidence for the involvement of the apoA2 gene and the ApoA1C3A4 gene cluster
-
Lilja HE, Soro A, Ylitalo K, Nuotio I, Viikari JSA, Salomaa V, Vartiainen E, Taskinen M-R, Peltonen L, Pajukanta P (2002) A candidate gene study in low HDL-cholesterol families provides evidence for the involvement of the apoA2 gene and the ApoA1C3A4 gene cluster. Atherosclerosis 164:103-111
-
(2002)
Atherosclerosis
, vol.164
, pp. 103-111
-
-
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
-
36
-
-
16044374799
-
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families
-
Mahtani MM, Widen E, Lehto M, Thomas J, McCarthy M, Brayer B, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyac L, Munnelly K, Parkkonen M, Reeve-Daly MP, Weaver A, Brettin T, Duyk G, Lander ES, Groop LC (1996) Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. Nat Genet 14:90-94
-
(1996)
Nat Genet
, vol.14
, pp. 90-94
-
-
Mahtani, M.M.1
Widen, E.2
Lehto, M.3
Thomas, J.4
McCarthy, M.5
Brayer, B.6
Bryant, B.7
Chan, G.8
Daly, M.9
Forsblom, C.10
Kanninen, T.11
Kirby, A.12
Kruglyac, L.13
Munnelly, K.14
Parkkonen, M.15
Reeve-Daly, M.P.16
Weaver, A.17
Brettin, T.18
Duyk, G.19
Lander, E.S.20
Groop, L.C.21
more..
-
37
-
-
0031979443
-
Significance levels in complex inheritance
-
Morton NE (1998) Significance levels in complex inheritance. Am J Hum Genet 62:690-697
-
(1998)
Am J Hum Genet
, vol.62
, pp. 690-697
-
-
Morton, N.E.1
-
38
-
-
0015914934
-
Family study of serum lipids and lipoproteins in coronary heart disease
-
Nikkilä EA, Aro A (1973) Family study of serum lipids and lipoproteins in coronary heart disease. Lancet 1:954-959
-
(1973)
Lancet
, vol.1
, pp. 954-959
-
-
Nikkilä, E.A.1
Aro, A.2
-
39
-
-
0033859732
-
All LODs are not created equal
-
Nyholt DR (2000) All LODs are not created equal. Am J Hum Genet 67:282-288.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 282-288
-
-
Nyholt, D.R.1
-
40
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE (1998) PedCheck: a program for identification of genotype incompatibilities 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
-
41
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nunez G, Cho JH (2001) A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 411:603-606
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
Nicolae, D.L.4
Chen, F.F.5
Ramos, R.6
Britton, H.7
Moran, T.8
Karaliuskas, R.9
Duerr, R.H.10
Achkar, J.P.11
Brant, S.R.12
Bayless, T.M.13
Kirschner, B.S.14
Hanauer, S.B.15
Nunez, G.16
Cho, J.H.17
-
43
-
-
0031918837
-
Linkage of familial combined hyperlipidaemia to chromosome q21-q23
-
Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamaki J, Suomalainen AJ, Syvanen AC, Lehtimaki T, Viikari JS, Laakso M, Taskinen MR, Ehnholm C, Peltonen L (1998) Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23. Nat Genet 18:369-373
-
(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
-
44
-
-
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, Hartiala J, Ylitalo K, Pihlajamaki J, Porkka K, Laakso M, Viikari J, Ehnholm C, Taskinen MR, Peltonen L (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
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
-
45
-
-
0033984185
-
Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families
-
Pei W, Baron H, Muller-Myhsok B, Knoblauch H, Al-Yahyaee SA, Hui R, Wu X, Liu L, Busjahn A, Luft FC, Schuster H (2000) Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families. Clin Genet 57:29-34
-
(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
Schuster, H.11
-
46
-
-
0034574603
-
Use of population isolates for mapping complex traits
-
Peltonen L, Palotie A, Lange K (2000) Use of population isolates for mapping complex traits. Nat Rev Genet 1:182-190
-
(2000)
Nat Rev Genet
, vol.1
, pp. 182-190
-
-
Peltonen, L.1
Palotie, A.2
Lange, K.3
-
47
-
-
0034969436
-
QTL analysis of body mass index and stature by combined analysis of five Finnish genome scans
-
Perola M, Öhman M, Hiekkalinna T, Leppävuori J, Pajukanta P, Wessman M, Koskenvuo M, Palotie A, Lange K, Kaprio J, Peltonen L (2001) QTL analysis of body mass index and stature by combined analysis of five Finnish genome scans. Am J Hum Genet 69:117-123
-
(2001)
Am J Hum Genet
, vol.69
, pp. 117-123
-
-
Perola, M.1
Öhman, M.2
Hiekkalinna, T.3
Leppävuori, J.4
Pajukanta, P.5
Wessman, M.6
Koskenvuo, M.7
Palotie, A.8
Lange, K.9
Kaprio, J.10
Peltonen, L.11
-
48
-
-
0036165284
-
Unexpectedly high allelic diversity at the KIT locus causing dominant white color in the domestic pig
-
Pielberg G, Olsson C, Syvänen A-C, Andersson L (2002) Unexpectedly high allelic diversity at the KIT locus causing dominant white color in the domestic pig. Genetics 160:305-311
-
(2002)
Genetics
, vol.160
, pp. 305-311
-
-
Pielberg, G.1
Olsson, C.2
Syvänen, A.-C.3
Andersson, L.4
-
49
-
-
0027989434
-
Age and gender specific serum lipid and apolipoprotein fractiles of Finnish children and young adults: The Cardiovascular Risk in Young Finns Study
-
Porkka KV, Viikari JS, Ronnemaa T, Marniemi J, Akerblom HK (1994) Age and gender specific serum lipid and apolipoprotein fractiles of Finnish children and young adults: the Cardiovascular Risk in Young Finns Study. Acta Paediatr 83:838-848
-
(1994)
Acta Paediatr
, vol.83
, pp. 838-848
-
-
Porkka, K.V.1
Viikari, J.S.2
Ronnemaa, T.3
Marniemi, J.4
Akerblom, H.K.5
-
50
-
-
0034977045
-
Linkage disequilibrium in humans: Models and data
-
Pritchard JK, Przeworski M (2001) Linkage disequilibrium in humans: models and data. Am J Hum Genet 69:1-14
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1-14
-
-
Pritchard, J.K.1
Przeworski, M.2
-
51
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R, Lander ES (2001) Linkage disequilibrium in the human genome. Nature 411:199-204
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
-
52
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux JD, Daly MJ, Silverberg MS, Lindblad K, Steinhart H, Cohen Z, Delmonte T, et al (2001) Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet 29:223-228
-
(2001)
Nat Genet
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.3
Lindblad, K.4
Steinhart, H.5
Cohen, Z.6
Delmonte, T.7
-
53
-
-
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
-
54
-
-
0033358661
-
Replication of linkage studies of complex traits: An examination of variation in location estimates
-
Roberts SB, MacLean CJ, Neale MC, Eaves LJ, Kendler KS (1999) Replication of linkage studies of complex traits: an examination of variation in location estimates. Am J Hum Genet 65:876-884
-
(1999)
Am J Hum Genet
, vol.65
, pp. 876-884
-
-
Roberts, S.B.1
MacLean, C.J.2
Neale, M.C.3
Eaves, L.J.4
Kendler, K.S.5
-
56
-
-
0028865860
-
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps
-
Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, Mattes G, Businga T, McClain A, Beck J, Scherpier T, Gilliam J, Zhong J, Duyk GM (1995) A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet 4:1837-1844
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1837-1844
-
-
Sheffield, V.C.1
Weber, J.L.2
Buetow, K.H.3
Murray, J.C.4
Even, D.A.5
Wiles, K.6
Gastier, J.M.7
Pulido, J.C.8
Yandava, C.9
Sunden, S.L.10
Mattes, G.11
Businga, T.12
McClain, A.13
Beck, J.14
Scherpier, T.15
Gilliam, J.16
Zhong, J.17
Duyk, G.M.18
-
58
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K (1996) Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 58:1323-1337
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
59
-
-
18344386779
-
Genome scans provide evidence for low-HDL-C loci on 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families
-
Soro A, Pajukanta P, Lilja HE, Ylitalo K, Viikari JSA, Taskinen M-R, Peltonen L (2002) Genome scans provide evidence for low-HDL-C loci on 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families. Am J Hum Genet 70:1333-1340
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1333-1340
-
-
Soro, A.1
Pajukanta, P.2
Lilja, H.E.3
Ylitalo, K.4
Viikari, J.S.A.5
Taskinen, M.-R.6
Peltonen, L.7
-
60
-
-
0027730113
-
A novel polylocus method for linkage analysis using the lod-score or affected sib-pair method
-
Terwilliger JD, Ott J (1993) A novel polylocus method for linkage analysis using the lod-score or affected sib-pair method. Genet Epidemiol 10:477-482
-
(1993)
Genet Epidemiol
, vol.10
, pp. 477-482
-
-
Terwilliger, J.D.1
Ott, J.2
-
61
-
-
0037173639
-
Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness
-
Van Eerdewegh P, Little RD, Dupuis J, Del Mastro RG, Falls K, Simon J, Torrey D, et al (2002) Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. Nature 418:426-430
-
(2002)
Nature
, vol.418
, pp. 426-430
-
-
Van Eerdewegh, P.1
Little, R.D.2
Dupuis, J.3
Del Mastro, R.G.4
Falls, K.5
Simon, J.6
Torrey, D.7
-
62
-
-
0028360266
-
Twenty-year trends in coronary risk factors in North Karelia and in other areas of Finland
-
Vartiainen E, Puska P, Jousilahti P, Korhonen HJ, Tuomilehto J, Nissinen A (1994) Twenty-year trends in coronary risk factors in North Karelia and in other areas of Finland. Int J Epidemiol 23:495-504
-
(1994)
Int J Epidemiol
, vol.23
, pp. 495-504
-
-
Vartiainen, E.1
Puska, P.2
Jousilahti, P.3
Korhonen, H.J.4
Tuomilehto, J.5
Nissinen, A.6
-
63
-
-
0035895505
-
The sequence of the human genome
-
Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, Smith HO, et al (2001) The sequence of the human genome. Science 291:1304-1350
-
(2001)
Science
, vol.291
, pp. 1304-1350
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
Smith, H.O.7
-
64
-
-
0033652271
-
Genomewide search for type 2 diabetes-susceptibility genes in French whites: Evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24
-
Vionnet N, Hani El-H, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Leprêtre F, Lecoeur C, Gallina P, Zekiri L, Dina C, Froguel P (2000) Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24. Am J Hum Genet 67:1470-1480
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1470-1480
-
-
Vionnet, N.1
Hani, E.L.-H.2
Dupont, S.3
Gallina, S.4
Francke, S.5
Dotte, S.6
De Matos, F.7
Durand, E.8
Leprêtre, F.9
Lecoeur, C.10
Gallina, P.11
Zekiri, L.12
Dina, C.13
Froguel, P.14
-
65
-
-
0033758721
-
The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci
-
Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, et al (2000) The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci. Am J Hum Genet 67:1186-1200
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1186-1200
-
-
Watanabe, R.M.1
Ghosh, S.2
Langefeld, C.D.3
Valle, T.T.4
Hauser, E.R.5
Magnuson, V.L.6
Mohlke, K.L.7
-
66
-
-
0033780104
-
How many diseases does it take to map a gene with SNPs?
-
Weiss KM, Terwilliger JD (2000) How many diseases does it take to map a gene with SNPs? Nat Genet 26:151-157
-
(2000)
Nat Genet
, vol.26
, pp. 151-157
-
-
Weiss, K.M.1
Terwilliger, J.D.2
-
67
-
-
0036842918
-
Evaluating the results of genomewide linkage scans of complex traits by locus counting
-
Wiltshire S, Cardon LR, McCarthy MI (2002) Evaluating the results of genomewide linkage scans of complex traits by locus counting. Am J Hum Genet 71:1175-1182
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1175-1182
-
-
Wiltshire, S.1
Cardon, L.R.2
McCarthy, M.I.3
-
68
-
-
0034893106
-
A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): Analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q
-
Wiltshire S, Hattersley AT, Hitman GA, Walker M, Levy JC, Sampson M, O'Rahilly S, et al (2001) A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q. Am J Hum Genet 69:553-569
-
(2001)
Am J Hum Genet
, vol.69
, pp. 553-569
-
-
Wiltshire, S.1
Hattersley, A.T.2
Hitman, G.A.3
Walker, M.4
Levy, J.C.5
Sampson, M.6
O'Rahilly, S.7
-
69
-
-
0036234398
-
A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program
-
Wu X, Cooper RS, Borecki I, Hanis C, Bray M, Lewis CE, Zhu X, Kan D, Luke A, Curb D (2002) A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program. Am J Hum Genet 70:1247-1256
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1247-1256
-
-
Wu, X.1
Cooper, R.S.2
Borecki, I.3
Hanis, C.4
Bray, M.5
Lewis, C.E.6
Zhu, X.7
Kan, D.8
Luke, A.9
Curb, D.10
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