Leena Peltonen - Selected publications#
- Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies. Komulainen K, Alanne M, Auro K, Kilpikari R, Pajukanta P, Saarela J, Ellonen P, Salminen K, Kulathinal S, Kuulasmaa K, Silander K, Salomaa V, Perola M and Peltonen L., PLoS genetics 2006;2;5;e69
- PRKCA and multiple sclerosis: association in two independent populations., Saarela J, Kallio SP, Chen D, Montpetit A, Jokiaho A, Choi E, Asselta R, Bronnikov D, Lincoln MR, Sadovnick AD, Tienari PJ, Koivisto K, Palotie A, Ebers GC, Hudson TJ and Peltonen L., PLoS genetics 2006;2;3;e42
- MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome. Kyttälä M, Tallila J, Salonen R, Kopra O, Kohlschmidt N, Paavola-Sakki P, Peltonen L and Kestilä M., Nature genetics 2006;38;2;155-7
- Classical twin studies and beyond. Boomsma D, Busjahn A and Peltonen L., Nature reviews. Genetics 2002;3;11;872-82
- Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype. Paloneva J, Manninen T, Christman G, Hovanes K, Mandelin J, Adolfsson R, Bianchin M, Bird T, Miranda R, Salmaggi A, Tranebjaerg L, Konttinen Y and Peltonen L., American journal of human genetics 2002;71;3;656-62
- Identification of a variant associated with adult-type hypolactasia. Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L and Järvelä I., Nature genetics 2002;30;2;233-7
- Genomics and medicine. Dissecting human disease in the postgenomic era. Peltonen L and McKusick VA., Science (New York, N.Y.) 2001;291;5507;1224-9
- Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts. Paloneva J, Kestilä M, Wu J, Salminen A, Böhling T, Ruotsalainen V, Hakola P, Bakker AB, Phillips JH, Pekkarinen P, Lanier LL, Timonen T and Peltonen L., Nature genetics 2000;25;3;357-61
- 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 and Peltonen L., American journal of human genetics 1999;64;5;1453-63
- 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 and Peltonen L., Nature genetics 1998;18;4;369-73
