Rouleau GA - Search Results

1

Mutations in the calcium-related gene IL1RAPL1 are associated with autism.

Piton A, Michaud JL, Peng H, Aradhya S, Gauthier J, Mottron L, Champagne N, Lafrenière RG, Hamdan FF; S2D team; Joober R, Fombonne E, Marineau C, Cossette P, Dubé MP, Haghighi P, Drapeau P, Barker PA, Carbonetto S, Rouleau GA. Piton A, et al. Among authors: rouleau ga. Hum Mol Genet. 2008 Dec 15;17(24):3965-74. doi: 10.1093/hmg/ddn300. Epub 2008 Sep 18. Hum Mol Genet. 2008. PMID: 18801879

2

Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.

Meijer IA, Hand CK, Cossette P, Figlewicz DA, Rouleau GA. Meijer IA, et al. Among authors: rouleau ga. Arch Neurol. 2002 Feb;59(2):281-6. doi: 10.1001/archneur.59.2.281. Arch Neurol. 2002. PMID: 11843700

3

Krit1 missense mutations lead to splicing errors in cerebral cavernous malformation.

Verlaan DJ, Siegel AM, Rouleau GA. Verlaan DJ, et al. Among authors: rouleau ga. Am J Hum Genet. 2002 Jun;70(6):1564-7. doi: 10.1086/340604. Epub 2002 Apr 8. Am J Hum Genet. 2002. PMID: 11941540 Free PMC article.

4

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.

Cossette P, Liu L, Brisebois K, Dong H, Lortie A, Vanasse M, Saint-Hilaire JM, Carmant L, Verner A, Lu WY, Wang YT, Rouleau GA. Cossette P, et al. Among authors: rouleau ga. Nat Genet. 2002 Jun;31(2):184-9. doi: 10.1038/ng885. Epub 2002 May 6. Nat Genet. 2002. PMID: 11992121

5

Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population.

Howard HC, Dubé MP, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Howard HC, et al. Among authors: rouleau ga. Eur J Hum Genet. 2002 Jul;10(7):406-12. doi: 10.1038/sj.ejhg.5200815. Eur J Hum Genet. 2002. PMID: 12107814

6

Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS).

Cossette P, Loukas A, Lafrenière RG, Rochefort D, Harvey-Girard E, Ragsdale DS, Dunn RJ, Rouleau GA. Cossette P, et al. Among authors: rouleau ga. Epilepsy Res. 2003 Feb;53(1-2):107-17. doi: 10.1016/s0920-1211(02)00259-0. Epilepsy Res. 2003. PMID: 12576172

7

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

8

Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia.

Toulouse A, Rochefort D, Roussel J, Joober R, Rouleau GA. Toulouse A, et al. Among authors: rouleau ga. Genomics. 2003 Aug;82(2):162-71. doi: 10.1016/s0888-7543(03)00101-0. Genomics. 2003. PMID: 12837267

9

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.

Lafreniere RG, MacDonald ML, Dube MP, MacFarlane J, O'Driscoll M, Brais B, Meilleur S, Brinkman RR, Dadivas O, Pape T, Platon C, Radomski C, Risler J, Thompson J, Guerra-Escobio AM, Davar G, Breakefield XO, Pimstone SN, Green R, Pryse-Phillips W, Goldberg YP, Younghusband HB, Hayden MR, Sherrington R, Rouleau GA, Samuels ME. Lafreniere RG, et al. Among authors: rouleau ga. Am J Hum Genet. 2004 May;74(5):1064-73. doi: 10.1086/420795. Epub 2004 Apr 1. Am J Hum Genet. 2004. PMID: 15060842 Free PMC article.

10

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

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