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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, Pihlajamäki J, Porkka K, Laakso M, Viikari J, Ehnholm C, Taskinen MR, Peltonen L. Pajukanta P, et al. Among authors: terwilliger jd. Am J Hum Genet. 1999 May;64(5):1453-63. doi: 10.1086/302365. Am J Hum Genet. 1999. PMID: 10205279 Free PMC article.
Genomewide scan of multiple sclerosis in Finnish multiplex families.
Kuokkanen S, Gschwend M, Rioux JD, Daly MJ, Terwilliger JD, Tienari PJ, Wikström J, Palo J, Stein LD, Hudson TJ, Lander ES, Peltonen L. Kuokkanen S, et al. Among authors: terwilliger jd. Am J Hum Genet. 1997 Dec;61(6):1379-87. doi: 10.1086/301637. Am J Hum Genet. 1997. PMID: 9399895 Free PMC article.
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.
Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamäki J, Suomalainen AJ, Syvänen AC, Lehtimäki T, Viikari JS, Laakso M, Taskinen MR, Ehnholm C, Peltonen L. Pajukanta P, et al. Among authors: terwilliger jd. Nat Genet. 1998 Apr;18(4):369-73. doi: 10.1038/ng0498-369. Nat Genet. 1998. PMID: 9537421
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
Pajukanta P, Cargill M, Viitanen L, Nuotio I, Kareinen A, Perola M, Terwilliger JD, Kempas E, Daly M, Lilja H, Rioux JD, Brettin T, Viikari JS, Rönnemaa T, Laakso M, Lander ES, Peltonen L. Pajukanta P, et al. Among authors: terwilliger jd. Am J Hum Genet. 2000 Dec;67(6):1481-93. doi: 10.1086/316902. Epub 2000 Nov 13. Am J Hum Genet. 2000. PMID: 11078477 Free PMC article.
124 results