Rouleau GA - Search Results

1

Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder.

Gan-Or Z, Girard SL, Noreau A, Leblond CS, Gagnon JF, Arnulf I, Mirarchi C, Dauvilliers Y, Desautels A, Mitterling T, Cochen De Cock V, Frauscher B, Monaca C, Hogl B, Dion PA, Postuma RB, Montplaisir JY, Rouleau GA. Gan-Or Z, et al. Among authors: rouleau ga. J Mol Neurosci. 2015 Jul;56(3):617-22. doi: 10.1007/s12031-015-0569-7. Epub 2015 May 1. J Mol Neurosci. 2015. PMID: 25929833

2

Dopaminergic neurotransmission and restless legs syndrome: a genetic association analysis.

Desautels A, Turecki G, Montplaisir J, Ftouhi-Paquin N, Michaud M, Chouinard VA, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Neurology. 2001 Oct 9;57(7):1304-6. doi: 10.1212/wnl.57.7.1304. Neurology. 2001. PMID: 11591853

3

Recent advances in the genetics of distal hereditary motor neuropathy give insight to a disease mechanism involving copper homeostasis that may extend to other motor neuron disorders.

Merner ND, Dion PA, Rouleau GA. Merner ND, et al. Among authors: rouleau ga. Clin Genet. 2011 Jan;79(1):23-34. doi: 10.1111/j.1399-0004.2010.01591.x. Clin Genet. 2011. PMID: 21143467

4

Evidence for a genetic association between monoamine oxidase A and restless legs syndrome.

Desautels A, Turecki G, Montplaisir J, Brisebois K, Sequeira A, Adam B, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Neurology. 2002 Jul 23;59(2):215-9. doi: 10.1212/wnl.59.2.215. Neurology. 2002. PMID: 12136060

5

Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors.

Cruceanu C, Schmouth JF, Torres-Platas SG, Lopez JP, Ambalavanan A, Darcq E, Gross F, Breton B, Spiegelman D, Rochefort D, Hince P, Petite JM, Gauthier J, Lafrenière RG, Dion PA, Greenwood CM, Kieffer BL, Alda M, Turecki G, Rouleau GA. Cruceanu C, et al. Among authors: rouleau ga. Mol Psychiatry. 2018 Oct;23(10):2050-2056. doi: 10.1038/mp.2017.223. Epub 2017 Nov 21. Mol Psychiatry. 2018. PMID: 29158579

6

[Restless leg syndrome: clinical aspects, etiology and genetic factors].

Desautels A, Michaud M, Montplaisir J, Turecki G, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Rev Neurol (Paris). 2002 Dec;158(12 Pt 1):1225-31. Rev Neurol (Paris). 2002. PMID: 12690746 Review. French. No abstract available.

7

Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.

Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Am J Hum Genet. 2001 Dec;69(6):1266-70. doi: 10.1086/324649. Epub 2001 Nov 6. Am J Hum Genet. 2001. PMID: 11704926 Free PMC article.

8

A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.

Levchenko A, Provost S, Montplaisir JY, Xiong L, St-Onge J, Thibodeau P, Rivière JB, Desautels A, Turecki G, Dubé MP, Rouleau GA. Levchenko A, et al. Among authors: rouleau ga. Neurology. 2006 Sep 12;67(5):900-1. doi: 10.1212/01.wnl.0000233991.20410.b6. Neurology. 2006. PMID: 16966564

9

Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathway.

Abu-Baker A, Laganiere J, Gaudet R, Rochefort D, Brais B, Neri C, Dion PA, Rouleau GA. Abu-Baker A, et al. Among authors: rouleau ga. Cell Death Dis. 2013 Oct 3;4(10):e821. doi: 10.1038/cddis.2013.342. Cell Death Dis. 2013. PMID: 24091664 Free PMC article.

10

Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death.

Fan X, Dion P, Laganiere J, Brais B, Rouleau GA. Fan X, et al. Among authors: rouleau ga. Hum Mol Genet. 2001 Oct 1;10(21):2341-51. doi: 10.1093/hmg/10.21.2341. Hum Mol Genet. 2001. PMID: 11689481

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