Brisebois K - Search Results

1

Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophrenia.

Joober R, Benkelfat C, Brisebois K, Toulouse A, Lafrenière RG, Turecki G, Lal S, Bloom D, Labelle A, Lalonde P, Fortin D, Alda M, Palmour R, Rouleau GA. Joober R, et al. Among authors: brisebois k. Am J Med Genet. 1999 Apr 16;88(2):154-7. Am J Med Genet. 1999. PMID: 10206235

2

T102C polymorphism in the 5HT2A gene and schizophrenia: relation to phenotype and drug response variability.

Joober R, Benkelfat C, Brisebois K, Toulouse A, Turecki G, Lal S, Bloom D, Labelle A, Lalonde P, Fortin D, Alda M, Palmour R, Rouleau GA. Joober R, et al. Among authors: brisebois k. J Psychiatry Neurosci. 1999 Mar;24(2):141-6. J Psychiatry Neurosci. 1999. PMID: 10212557 Free PMC article.

3

CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2).

Hayes S, Turecki G, Brisebois K, Lopes-Cendes I, Gaspar C, Riess O, Ranum LP, Pulst SM, Rouleau GA. Hayes S, et al. Among authors: brisebois k. Hum Mol Genet. 2000 Jul 22;9(12):1753-8. doi: 10.1093/hmg/9.12.1753. Hum Mol Genet. 2000. PMID: 10915763

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: brisebois k. Neurology. 2002 Jul 23;59(2):215-9. doi: 10.1212/wnl.59.2.215. Neurology. 2002. PMID: 12136060

5

Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment.

Pramatarova A, Laganière J, Roussel J, Brisebois K, Rouleau GA. Pramatarova A, et al. Among authors: brisebois k. J Neurosci. 2001 May 15;21(10):3369-74. doi: 10.1523/JNEUROSCI.21-10-03369.2001. J Neurosci. 2001. PMID: 11331366 Free PMC article.

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: brisebois k. Sleep. 2003 Dec 15;26(8):1055-7. doi: 10.1093/sleep/26.8.1055. Sleep. 2003. PMID: 14746390

7

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: brisebois k. Nat Genet. 2002 Jun;31(2):184-9. doi: 10.1038/ng885. Epub 2002 May 6. Nat Genet. 2002. PMID: 11992121

8

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: brisebois k. Arch Neurol. 2005 Apr;62(4):591-6. doi: 10.1001/archneur.62.4.591. Arch Neurol. 2005. PMID: 15824258

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