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Page 1
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height.
Hirschhorn JN, Lindgren CM, Daly MJ, Kirby A, Schaffner SF, Burtt NP, Altshuler D, Parker A, Rioux JD, Platko J, Gaudet D, Hudson TJ, Groop LC, Lander ES. Hirschhorn JN, et al. Among authors: platko j. Am J Hum Genet. 2001 Jul;69(1):106-16. doi: 10.1086/321287. Epub 2001 Jun 15. Am J Hum Genet. 2001. PMID: 11410839 Free PMC article.
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects.
Dastani Z, Pajukanta P, Marcil M, Rudzicz N, Ruel I, Bailey SD, Lee JC, Lemire M, Faith J, Platko J, Rioux J, Hudson TJ, Gaudet D, Engert JC, Genest J. Dastani Z, et al. Among authors: platko j. Eur J Hum Genet. 2010 Mar;18(3):342-7. doi: 10.1038/ejhg.2009.157. Epub 2009 Oct 21. Eur J Hum Genet. 2010. PMID: 19844255 Free PMC article.
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. Among authors: platko j. 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. Among authors: platko j. 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
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
The familial association of tourette's disorder and ADHD: the impact of OCD symptoms.
O'Rourke JA, Scharf JM, Platko J, Stewart SE, Illmann C, Geller DA, King RA, Leckman JF, Pauls DL. O'Rourke JA, et al. Among authors: platko j. Am J Med Genet B Neuropsychiatr Genet. 2011 Jul;156B(5):553-60. doi: 10.1002/ajmg.b.31195. Epub 2011 May 6. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21557467 Free PMC article.
Family-based genetic association study of DLGAP3 in Tourette Syndrome.
Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM; Tourette Syndrome International Consortium for Genetics (TSAICG). Crane J, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):108-14. doi: 10.1002/ajmg.b.31134. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184590 Free PMC article.
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.
34 results