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Detecting recent positive selection in the human genome from haplotype structure.
Sabeti PC, Reich DE, Higgins JM, Levine HZ, Richter DJ, Schaffner SF, Gabriel SB, Platko JV, Patterson NJ, McDonald GJ, Ackerman HC, Campbell SJ, Altshuler D, Cooper R, Kwiatkowski D, Ward R, Lander ES. Sabeti PC, et al. Among authors: platko jv. Nature. 2002 Oct 24;419(6909):832-7. doi: 10.1038/nature01140. Epub 2002 Oct 9. Nature. 2002. PMID: 12397357
Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension.
Hamet P, Merlo E, Seda O, Broeckel U, Tremblay J, Kaldunski M, Gaudet D, Bouchard G, Deslauriers B, Gagnon F, Antoniol G, Pausová Z, Labuda M, Jomphe M, Gossard F, Tremblay G, Kirova R, Tonellato P, Orlov SN, Pintos J, Platko J, Hudson TJ, Rioux JD, Kotchen TA, Cowley AW Jr. Hamet P, et al. Am J Hum Genet. 2005 May;76(5):815-32. doi: 10.1086/430133. Epub 2005 Mar 30. Am J Hum Genet. 2005. PMID: 15800845 Free PMC article.
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
Engert JC, Lemire M, Faith J, Brisson D, Fujiwara TM, Roslin NM, Brewer CG, Montpetit A, Darmond-Zwaig C, Renaud Y, Doré C, Bailey SD, Verner A, Tremblay G, St-Pierre J, Bétard C, Platko J, Rioux JD, Morgan K, Hudson TJ, Gaudet D. Engert JC, et al. Eur J Hum Genet. 2008 Jan;16(1):105-14. doi: 10.1038/sj.ejhg.5201920. Epub 2007 Sep 5. Eur J Hum Genet. 2008. PMID: 17805225
Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.
Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B, Jenike E, Stewart SE, Pauls DL; Tourette Syndrome International Consortium for Genetics. Scharf JM, et al. Among authors: platko jv. Neurology. 2008 Apr 15;70(16 Pt 2):1495-6. doi: 10.1212/01.wnl.0000296833.25484.bb. Neurology. 2008. PMID: 18413575 Free PMC article. No abstract available.
28 results