Linkage of familial combined hyperlipidaemia to chromosome 1q21–q23
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T. Lehtimäki | L. Peltonen | M. Laakso | J. Terwilliger | J. Viikari | M. Taskinen | A. Syvänen | P. Pajukanta | J. Pihlajamäki | K. Porkka | C. Ehnholm | I. Nuotio | K. Ylitalo | Ak Suomalainen
[1] A. Lusis,et al. Mapping a gene for combined hyperlipidaemia in a mutant mouse strain , 1998, Nature Genetics.
[2] L. Peltonen,et al. No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families. , 1997, Arteriosclerosis, thrombosis, and vascular biology.
[3] J. Rotter,et al. Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes. , 1997, The Journal of clinical investigation.
[4] Leena Peltonen,et al. A putative vulnerability locus to multiple sclerosis maps to 5p14–p12 in a region syntenic to the murine locus Eae2 , 1996, Nature Genetics.
[5] M. Hayden,et al. Lack of association of the apolipoprotein A-I-C-III-A-IV gene XmnI and SstI polymorphisms and of the lipoprotein lipase gene mutations in familial combined hyperlipoproteinemia in French Canadian subjects. , 1996, Journal of lipid research.
[6] D. Kromhout,et al. A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia. , 1995, Human molecular genetics.
[7] J. Terwilliger. A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. , 1995, American journal of human genetics.
[8] E. Wijsman,et al. Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype. , 1994, Arteriosclerosis and thrombosis : a journal of vascular biology.
[9] J. Viikari,et al. Age and gender specific serum lipid and apolipoprotein fractiles of Finnish children and young adults. The Cardiovascular Risk in Young Finns Study , 1994, Acta paediatrica.
[10] M. Farrall,et al. Complex segregation analysis provides evidence for a major gene acting on serum triglyceride levels in 55 British families with familial combined hyperlipidemia. , 1994, Arteriosclerosis and thrombosis : a journal of vascular biology.
[11] A A Schäffer,et al. Avoiding recomputation in linkage analysis. , 1994, Human heredity.
[12] E. Vartiainen,et al. Twenty-year trends in coronary risk factors in north Karelia and in other areas of Finland. , 1994, International journal of epidemiology.
[13] J. Terwilliger. Genetic Variation and Human Disease: Principles and Evolutionary Approaches , 1997 .
[14] A. Chapelle,et al. Disease gene mapping in isolated human populations: the example of Finland. , 1993, Journal of medical genetics.
[15] A A Schäffer,et al. Faster sequential genetic linkage computations. , 1993, American journal of human genetics.
[16] P. Kwiterovich. Genetics and molecular biology of familial combined hyperlipidemia , 1993 .
[17] J D Terwilliger,et al. A novel polylocus method for linkage analysis using the lod‐score or affected sib‐pair method , 1993, Genetic epidemiology.
[18] A Sajantila,et al. Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing. , 1993, American journal of human genetics.
[19] S. Hodge,et al. Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods. , 1992, American journal of human genetics.
[20] Richard H. Myers,et al. Familial Lipoprotein Disorders in Patients With Premature Coronary Artery Disease , 1992, Circulation.
[21] R. Krauss,et al. Linkage of atherogenic lipoprotein phenotype to the low density lipoprotein receptor locus on the short arm of chromosome 19. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[22] N Risch,et al. Model misspecification and multipoint linkage analysis. , 1992, Human heredity.
[23] M. Farrall,et al. Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24 , 1991, Nature.
[24] R. Krauss,et al. Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia. , 1990, Arteriosclerosis.
[25] M. E. Ramirez,et al. Apolipoprotein, Low Density Lipoprotein Subtraction, and Insulin Associations with Familial Combined Hyperlipidemia: Study of Utah Patients with Familial Dyslipidemic Hypertension , 1989, Arteriosclerosis.
[26] S. Grundy,et al. Familial combined hyperlipidemia workshop , 1989 .
[27] A. Lusis,et al. Ath-1, a gene determining atherosclerosis susceptibility and high density lipoprotein levels in mice. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[28] P. Lipsky,et al. Detection of familial hypercholesterolemia by assaying functional low-density-lipoprotein receptors on lymphocytes. , 1986, The New England journal of medicine.
[29] J. Ott. Analysis of Human Genetic Linkage , 1985 .
[30] J. Ott,et al. Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[31] R. Deitch. Commentary from Westminster , 1981, The Lancet.
[32] A. Motulsky,et al. Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia. , 1973, The Journal of clinical investigation.
[33] A. Aro,et al. Family study of serum lipids and lipoproteins in coronary heart-disease. , 1973, Lancet.
[34] Joseph L. Goldstein,et al. Hyperlipidemia in Coronary Heart Disease , 1973 .