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Page 1
Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models.
Hum Mol Genet. 2012 May 15;21(10):2211-8. doi: 10.1093/hmg/dds036. Epub 2012 Feb 14.
Hum Mol Genet. 2012.
PMID: 22337953
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.
Piton A, Gauthier J, Hamdan FF, Lafrenière RG, Yang Y, Henrion E, Laurent S, Noreau A, Thibodeau P, Karemera L, Spiegelman D, Kuku F, Duguay J, Destroismaisons L, Jolivet P, Côté M, Lachapelle K, Diallo O, Raymond A, Marineau C, Champagne N, Xiong L, Gaspar C, Rivière JB, Tarabeux J, Cossette P, Krebs MO, Rapoport JL, Addington A, Delisi LE, Mottron L, Joober R, Fombonne E, Drapeau P, Rouleau GA.
Piton A, et al. Among authors: karemera l.
Mol Psychiatry. 2011 Aug;16(8):867-80. doi: 10.1038/mp.2010.54. Epub 2010 May 18.
Mol Psychiatry. 2011.
PMID: 20479760
Free PMC article.
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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: karemera l.
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
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HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3.
Salin-Cantegrel A, Shekarabi M, Holbert S, Dion P, Rochefort D, Laganière J, Dacal S, Hince P, Karemera L, Gaspar C, Lapointe JY, Rouleau GA.
Salin-Cantegrel A, et al. Among authors: karemera l.
Hum Mol Genet. 2008 Sep 1;17(17):2703-11. doi: 10.1093/hmg/ddn172. Epub 2008 Jun 19.
Hum Mol Genet. 2008.
PMID: 18566107
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Distal truncation of KCC3 in non-French Canadian HMSN/ACC families.
Salin-Cantegrel A, Rivière JB, Dupré N, Charron FM, Shekarabi M, Karéméra L, Gaspar C, Horst J, Tekin M, Deda G, Krause A, Lippert MM, Willemsen MA, Jarrar R, Lapointe JY, Rouleau GA.
Salin-Cantegrel A, et al. Among authors: karemera l.
Neurology. 2007 Sep 25;69(13):1350-5. doi: 10.1212/01.wnl.0000291779.35643.15.
Neurology. 2007.
PMID: 17893295
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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.
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
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Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families.
Xiong L, Dion P, Montplaisir J, Levchenko A, Thibodeau P, Karemera L, Rivière JB, St-Onge J, Gaspar C, Dubé MP, Desautels A, Turecki G, Rouleau GA.
Xiong L, et al. Among authors: karemera l.
Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):911-7. doi: 10.1002/ajmg.b.30528.
Am J Med Genet B Neuropsychiatr Genet. 2007.
PMID: 17510944
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