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The 14q restless legs syndrome locus in the French Canadian population.
Levchenko A, Montplaisir JY, Dubé MP, Riviere JB, St-Onge J, Turecki G, Xiong L, Thibodeau P, Desautels A, Verlaan DJ, Rouleau GA. Levchenko A, et al. Among authors: thibodeau p. Ann Neurol. 2004 Jun;55(6):887-91. doi: 10.1002/ana.20140. Ann Neurol. 2004. PMID: 15174026
Canadian restless legs syndrome twin study.
Xiong L, Jang K, Montplaisir J, Levchenko A, Thibodeau P, Gaspar C, Turecki G, Rouleau GA. Xiong L, et al. Among authors: thibodeau p. Neurology. 2007 May 8;68(19):1631-3. doi: 10.1212/01.wnl.0000261016.90374.fd. Neurology. 2007. PMID: 17485653 No abstract available.
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.
Xiong L, Catoire H, Dion P, Gaspar C, Lafrenière RG, Girard SL, Levchenko A, Rivière JB, Fiori L, St-Onge J, Bachand I, Thibodeau P, Allen R, Earley C, Turecki G, Montplaisir J, Rouleau GA. Xiong L, et al. Among authors: thibodeau p. Hum Mol Genet. 2009 Mar 15;18(6):1065-74. doi: 10.1093/hmg/ddn443. Epub 2009 Jan 6. Hum Mol Genet. 2009. PMID: 19126776 Free PMC article.
CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.
Noreau A, Dion PA, Szuto A, Levert A, Thibodeau P, Brais B, Dupré N, Rioux MF, Rouleau GA. Noreau A, et al. Among authors: thibodeau p. Can J Neurol Sci. 2012 Jan;39(1):91-4. doi: 10.1017/s0317167100012774. Can J Neurol Sci. 2012. PMID: 22384504 No abstract available.
Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia.
Tarabeux J, Kebir O, Gauthier J, Hamdan FF, Xiong L, Piton A, Spiegelman D, Henrion É, Millet B; S2D team; Fathalli F, Joober R, Rapoport JL, DeLisi LE, Fombonne É, Mottron L, Forget-Dubois N, Boivin M, Michaud JL, Drapeau P, Lafrenière RG, Rouleau GA, Krebs MO. Tarabeux J, et al. Transl Psychiatry. 2011 Nov 15;1(11):e55. doi: 10.1038/tp.2011.52. Transl Psychiatry. 2011. PMID: 22833210 Free PMC article.
95 results