Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
8 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
Nat Genet. 2002 Jun;31(2):184-9. doi: 10.1038/ng885. Epub 2002 May 6.
Nat Genet. 2002.
PMID: 11992121
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.
Item in Clipboard
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
Item in Clipboard
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
Item in Clipboard
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
Item in Clipboard
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
Item in Clipboard
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
Item in Clipboard
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.
Item in Clipboard
Cite
Cite