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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: rioux 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.
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.
Wang DG, Fan JB, Siao CJ, Berno A, Young P, Sapolsky R, Ghandour G, Perkins N, Winchester E, Spencer J, Kruglyak L, Stein L, Hsie L, Topaloglou T, Hubbell E, Robinson E, Mittmann M, Morris MS, Shen N, Kilburn D, Rioux J, Nusbaum C, Rozen S, Hudson TJ, Lipshutz R, Chee M, Lander ES. Wang DG, et al. Science. 1998 May 15;280(5366):1077-82. doi: 10.1126/science.280.5366.1077. Science. 1998. PMID: 9582121
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: rioux 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.
259 results