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Results: 1-25 |
Results: 25
GAW12: Simulated genome scan, sequence, and family data for a common disease
Authors: Almasy, L Terwilliger, JD Nielsen, D Dyer, TD Zaykin, D Blangero, J
Citation: L. Almasy et al., GAW12: Simulated genome scan, sequence, and family data for a common disease, GENET EPID, 21, 2001, pp. S332-S338
A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22
Authors: Liu, JJ Juo, SH Terwilliger, JD Grunn, A Tong, XM Brito, M Loth, JE Kanyas, K Lerer, B Endicott, J Penchaszadeh, G Gilliam, TC Baron, M
Citation: Jj. Liu et al., A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22, AM J MED G, 105(2), 2001, pp. 189-194
Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth
Authors: Lupu, F Terwilliger, JD Lee, K Segre, GV Efstratiadis, A
Citation: F. Lupu et al., Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth, DEVELOP BIO, 229(1), 2001, pp. 141-162
Large upward bias in estimation of locus-specific effects from genomewide scans
Authors: Goring, HHH Terwilliger, JD Blangero, J
Citation: Hhh. Goring et al., Large upward bias in estimation of locus-specific effects from genomewide scans, AM J HU GEN, 69(6), 2001, pp. 1357-1369
How many diseases does it take to map a gene with SNPs?
Authors: Weiss, KM Terwilliger, JD
Citation: Km. Weiss et Jd. Terwilliger, How many diseases does it take to map a gene with SNPs?, NAT GENET, 26(2), 2000, pp. 151-157
Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo
Authors: Varilo, T Laan, M Hovatta, I Wiebe, V Terwilliger, JD Peltonen, L
Citation: T. Varilo et al., Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo, EUR J HUM G, 8(8), 2000, pp. 604-612
A likelihood-based extended admixture model of oligogenic inheritance in 'model-based' and 'model-free' analysis
Authors: Terwilliger, JD
Citation: Jd. Terwilliger, A likelihood-based extended admixture model of oligogenic inheritance in 'model-based' and 'model-free' analysis, EUR J HUM G, 8(6), 2000, pp. 399-406
Genome-wide scan for schizophrenia in the Finnish population: evidence fora locus on chromosome 7q22
Authors: Ekelund, J Lichtermann, D Hovatta, L Ellonen, P Suvisaari, J Terwilliger, JD Juvonen, H Varilo, T Arajarvi, R Kokko-Sahin, ML Lonnqvist, J Peltonen, L
Citation: J. Ekelund et al., Genome-wide scan for schizophrenia in the Finnish population: evidence fora locus on chromosome 7q22, HUM MOL GEN, 9(7), 2000, pp. 1049-1057
A susceptibility locus for human systemic lupus erythematosus (hSLE1) on chromosome 2q
Authors: Lindqvist, AKB Steinsson, K Johanneson, B Kristjansdottir, H Arnasson, A Grondal, G Jonasson, I Magnusson, V Sturfelt, G Truedsson, L Svenungsson, E Lundberg, I Terwilliger, JD Gyllensten, UB Alarcon-Riquelme, ME
Citation: Akb. Lindqvist et al., A susceptibility locus for human systemic lupus erythematosus (hSLE1) on chromosome 2q, J AUTOIMMUN, 14(2), 2000, pp. 169-178
Fine mapping of the SLEB2 locus involved in susceptibility to systemic lupus erythematosus
Authors: Magnusson, V Lindqvist, AKB Castillejo-Lopez, C Kristjansdottir, H Steinsson, K Grondal, G Sturfelt, G Truedsson, L Svenungsson, E Lundberg, I Gunnarsson, I Bolstad, AI Haga, HJ Jonsson, R Klareskog, L Alcocer-Varela, J Alarcon-Segovia, D Terwilliger, JD Gyllensten, UB Alarcon-Riquelme, ME
Citation: V. Magnusson et al., Fine mapping of the SLEB2 locus involved in susceptibility to systemic lupus erythematosus, GENOMICS, 70(3), 2000, pp. 307-314
Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings
Authors: Perola, M Kainulainen, K Pajukanta, P Terwilliger, JD Hiekkalinna, T Ellonen, P Kaprio, J Koskenvuo, M Kontula, K Peltonen, L
Citation: M. Perola et al., Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings, J HYPERTENS, 18(11), 2000, pp. 1579-1585
Gene mapping in the 20th and 21st centuries: Statistical methods, data analysis, and experimental design
Authors: Terwilliger, JD Goring, HHH
Citation: Jd. Terwilliger et Hhh. Goring, Gene mapping in the 20th and 21st centuries: Statistical methods, data analysis, and experimental design, HUMAN BIOL, 72(1), 2000, pp. 63-132
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland
Authors: Pajukanta, P Cargill, M Viitanen, L Nuotio, I Kareinen, A Perola, M Terwilliger, JD Kempas, E Day, M Lilja, H Rioux, JD Brettin, T Viikari, JSA Ronnemaa, T Laakso, M Lander, ES Peltonen, L
Citation: P. Pajukanta et al., Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland, AM J HU GEN, 67(6), 2000, pp. 1481-1493
A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2
Authors: Moses, EK Lade, JA Guo, GL Wilton, AN Grehan, M Freed, K Borg, A Terwilliger, JD North, R Cooper, DW Brennecke, SP
Citation: Ek. Moses et al., A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2, AM J HU GEN, 67(6), 2000, pp. 1581-1585
Inflated false-positive rates in Hardy-Weinberg and linkage-equilibrium tests are due to sampling on the basis of rare familial phenotypes in finite populations
Authors: Terwilliger, JD
Citation: Jd. Terwilliger, Inflated false-positive rates in Hardy-Weinberg and linkage-equilibrium tests are due to sampling on the basis of rare familial phenotypes in finite populations, AM J HU GEN, 67(1), 2000, pp. 258-259
QTL fine mapping, in extreme samples of finite populations, for complex traits with familial correlation due to polygenes - Reply
Authors: Terwilliger, JD
Citation: Jd. Terwilliger, QTL fine mapping, in extreme samples of finite populations, for complex traits with familial correlation due to polygenes - Reply, AM J HU GEN, 67(1), 2000, pp. 261-262
Linkage analysis in the presence of errors III: Marker loci and their map as nuisance parameters
Authors: Goring, HHH Terwilliger, JD
Citation: Hhh. Goring et Jd. Terwilliger, Linkage analysis in the presence of errors III: Marker loci and their map as nuisance parameters, AM J HU GEN, 66(4), 2000, pp. 1298-1309
Linkage analysis in the presence of errors IV: Joint pseudomarker analysisof linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified
Authors: Goring, HHH Terwilliger, JD
Citation: Hhh. Goring et Jd. Terwilliger, Linkage analysis in the presence of errors IV: Joint pseudomarker analysisof linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified, AM J HU GEN, 66(4), 2000, pp. 1310-1327
Linkage analysis in the presence of errors I: Complex-valued recombinationfractions and complex phenotypes
Authors: Goring, HHH Terwilliger, JD
Citation: Hhh. Goring et Jd. Terwilliger, Linkage analysis in the presence of errors I: Complex-valued recombinationfractions and complex phenotypes, AM J HU GEN, 66(3), 2000, pp. 1095-1106
Linkage analysis in the presence of errors II: Marker-locus genotyping errors modeled with hypercomplex recombination fractions
Authors: Goring, HHH Terwilliger, JD
Citation: Hhh. Goring et Jd. Terwilliger, Linkage analysis in the presence of errors II: Marker-locus genotyping errors modeled with hypercomplex recombination fractions, AM J HU GEN, 66(3), 2000, pp. 1107-1118
Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: Evidence for a locus on 2q
Authors: Leppavuori, J Kujala, U Kinnunen, J Kaprio, J Nissila, M Heliovaara, M Klinger, N Partanen, J Terwilliger, JD Peltonen, L
Citation: J. Leppavuori et al., Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: Evidence for a locus on 2q, AM J HU GEN, 65(4), 1999, pp. 1060-1067
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
Authors: Hovatta, I Varilo, T Suvisaari, J Terwilliger, JD Ollikainen, V Arajarvi, R Juvonen, H Kokko-Sahin, ML Vaisanen, L Mannila, H Lonnqvist, J Peltonen, L
Citation: I. Hovatta et al., A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci, AM J HU GEN, 65(4), 1999, pp. 1114-1124
Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
Authors: 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
Citation: P. Pajukanta et al., Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels, AM J HU GEN, 64(5), 1999, pp. 1453-1463
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus
Authors: Aita, VM Liu, JJ Knowles, JA Terwilliger, JD Baltazar, R Grunn, A Loth, JE Kanyas, K Lerer, B Endicott, J Wang, ZY Penchaszadeh, G Gilliam, TC Baron, M
Citation: Vm. Aita et al., A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus, AM J HU GEN, 64(1), 1999, pp. 210-217
Linkage disequilibrium mapping of complex disease: fantasy or reality?
Authors: Terwilliger, JD Weiss, KM
Citation: Jd. Terwilliger et Km. Weiss, Linkage disequilibrium mapping of complex disease: fantasy or reality?, CURR OPIN B, 9(6), 1998, pp. 578-594
Risultati: 1-25 |