Rouleau GA - Search Results

1

De novo truncating mutation in Kinesin 17 associated with schizophrenia.

Tarabeux J, Champagne N, Brustein E, Hamdan FF, Gauthier J, Lapointe M, Maios C, Piton A, Spiegelman D, Henrion E; Synapse to Disease Team; Millet B, Rapoport JL, Delisi LE, Joober R, Fathalli F, Fombonne E, Mottron L, Forget-Dubois N, Boivin M, Michaud JL, Lafrenière RG, Drapeau P, Krebs MO, Rouleau GA. Tarabeux J, et al. Among authors: rouleau ga. Biol Psychiatry. 2010 Oct 1;68(7):649-56. doi: 10.1016/j.biopsych.2010.04.018. Epub 2010 Jun 19. Biol Psychiatry. 2010. PMID: 20646681

2

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

3

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

4

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

5

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

6

A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family.

Rivière JB, Verlaan DJ, Shekarabi M, Lafrenière RG, Bénard M, Der Kaloustian VM, Shbaklo Z, Rouleau GA. Rivière JB, et al. Among authors: rouleau ga. Ann Neurol. 2004 Oct;56(4):572-5. doi: 10.1002/ana.20237. Ann Neurol. 2004. PMID: 15455397

7

CAA insertion polymorphism in the 3'UTR of Nogo gene on 2p14 is not associated with schizophrenia.

Xiong L, Rouleau GA, Delisi LE, St-Onge J, Najafee R, Rivière JB, Benkelfat C, Tabbane K, Fathalli F, Danics Z, Labelle A, Lal S, Joober R. Xiong L, et al. Among authors: rouleau ga. Brain Res Mol Brain Res. 2005 Jan 5;133(1):153-6. doi: 10.1016/j.molbrainres.2004.08.024. Brain Res Mol Brain Res. 2005. PMID: 15661375

8

Increased prevalence of schizophrenia spectrum disorders in relatives of neuroleptic-nonresponsive schizophrenic patients.

Joober R, Rouleau GA, Lal S, Bloom D, Lalonde P, Labelle A, Benkelfat C. Joober R, et al. Among authors: rouleau ga. Schizophr Res. 2005 Sep 1;77(1):35-41. doi: 10.1016/j.schres.2005.01.008. Schizophr Res. 2005. PMID: 16005383

9

Clinical stringency greatly improves mutation detection in Rett syndrome.

Gauthier J, de Amorim G, Mnatzakanian GN, Saunders C, Vincent JB, Toupin S, Kauffman D, St-Onge J, Laurent S, Macleod PM, Minassian BA, Rouleau GA. Gauthier J, et al. Among authors: rouleau ga. Can J Neurol Sci. 2005 Aug;32(3):321-6. doi: 10.1017/s0317167100004200. Can J Neurol Sci. 2005. PMID: 16225173

10

Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.

Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz M, Reid E, Dion PA, Drapeau P, Rouleau GA. Valdmanis PN, et al. Among authors: rouleau ga. Am J Hum Genet. 2007 Jan;80(1):152-61. doi: 10.1086/510782. Epub 2006 Dec 1. Am J Hum Genet. 2007. PMID: 17160902 Free PMC article.

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