Rouleau GA - Search Results

1

Analysis of common and rare VPS13C variants in late-onset Parkinson disease.

Rudakou U, Ruskey JA, Krohn L, Laurent SB, Spiegelman D, Greenbaum L, Yahalom G, Desautels A, Montplaisir JY, Fahn S, Waters CH, Levy O, Kehoe CM, Narayan S, Dauvilliers Y, Dupré N, Hassin-Baer S, Alcalay RN, Rouleau GA, Fon EA, Gan-Or Z. Rudakou U, et al. Among authors: rouleau ga. Neurol Genet. 2020 Jan 9;6(1):385. doi: 10.1212/NXG.0000000000000385. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32042909 Free PMC article.

2

Mutation screening of FOXP2 in individuals diagnosed with autistic disorder.

Gauthier J, Joober R, Mottron L, Laurent S, Fuchs M, De Kimpe V, Rouleau GA. Gauthier J, et al. Among authors: rouleau ga. Am J Med Genet A. 2003 Apr 15;118A(2):172-5. doi: 10.1002/ajmg.a.10105. Am J Med Genet A. 2003. PMID: 12655497

3

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.

Dupré N, Verlaan DJ, Hand CK, Laurent SB, Turecki G, Davenport WJ, Acciarri N, Dichgans J, Ohkuma A, Siegel AM, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Can J Neurol Sci. 2003 May;30(2):122-8. doi: 10.1017/s0317167100053385. Can J Neurol Sci. 2003. PMID: 12774951

4

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum.

Dupré N, Howard HC, Mathieu J, Karpati G, Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Ann Neurol. 2003 Jul;54(1):9-18. doi: 10.1002/ana.77777. Ann Neurol. 2003. PMID: 12838516 Review.

5

Mutational analysis of neurotensin in familial restless legs syndrome.

Desautels A, Turecki G, Xiong L, Rochefort D, Montplaisir J, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Mov Disord. 2004 Jan;19(1):90-4. doi: 10.1002/mds.10617. Mov Disord. 2004. PMID: 14743366

6

Analysis of CAG repeat expansions in restless legs syndrome.

Desautels A, Turecki G, Montplaisir J, Brisebois K, Desautels AK, Adam B, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Sleep. 2003 Dec 15;26(8):1055-7. doi: 10.1093/sleep/26.8.1055. Sleep. 2003. PMID: 14746390

7

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: rouleau ga. Ann Neurol. 2004 Jun;55(6):887-91. doi: 10.1002/ana.20140. Ann Neurol. 2004. PMID: 15174026

8

A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.

Gros-Louis F, Larivière R, Gowing G, Laurent S, Camu W, Bouchard JP, Meininger V, Rouleau GA, Julien JP. Gros-Louis F, et al. Among authors: rouleau ga. J Biol Chem. 2004 Oct 29;279(44):45951-6. doi: 10.1074/jbc.M408139200. Epub 2004 Aug 17. J Biol Chem. 2004. PMID: 15322088 Free article.

9

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population.

Gauthier J, Bonnel A, St-Onge J, Karemera L, Laurent S, Mottron L, Fombonne E, Joober R, Rouleau GA. Gauthier J, et al. Among authors: rouleau ga. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):74-5. doi: 10.1002/ajmg.b.30066. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15389766

10

Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.

Desautels A, Turecki G, Montplaisir J, Xiong L, Walters AS, Ehrenberg BL, Brisebois K, Desautels AK, Gingras Y, Johnson WG, Lugaresi E, Coccagna G, Picchietti DL, Lazzarini A, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Arch Neurol. 2005 Apr;62(4):591-6. doi: 10.1001/archneur.62.4.591. Arch Neurol. 2005. PMID: 15824258

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