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Page 1
RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population.
Zhou S, Ambalavanan A, Rochefort D, Xie P, Bourassa CV, Hince P, Dionne-Laporte A, Spiegelman D, Gan-Or Z, Mirarchi C, Zaharieva V, Dupré N, Kobayashi H, Hitomi T, Harada K, Koizumi A, Xiong L, Dion PA, Rouleau GA. Zhou S, et al. Among authors: bourassa cv. Am J Hum Genet. 2016 Nov 3;99(5):1072-1085. doi: 10.1016/j.ajhg.2016.09.001. Epub 2016 Oct 13. Am J Hum Genet. 2016. PMID: 27745834 Free PMC article.
No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremor.
Houle G, Ambalavanan A, Schmouth JF, Leblond CS, Spiegelman D, Laurent SB, Bourassa CV, Grayson C, Panisset M, Chouinard S, Dupré N, Vilariño-Güell C, Rajput A, Girard SL, Dion PA, Rouleau GA. Houle G, et al. Among authors: bourassa cv. Neurol Genet. 2017 Oct 19;3(5):e195. doi: 10.1212/NXG.0000000000000195. eCollection 2017 Oct. Neurol Genet. 2017. PMID: 30584593 Free PMC article.
Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease.
Akçimen F, Martins S, Liao C, Bourassa CV, Catoire H, Nicholson GA, Riess O, Raposo M, França MC, Vasconcelos J, Lima M, Lopes-Cendes I, Saraiva-Pereira ML, Jardim LB, Sequeiros J, Dion PA, Rouleau GA. Akçimen F, et al. Among authors: bourassa cv. Aging (Albany NY). 2020 Mar 23;12(6):4742-4756. doi: 10.18632/aging.102825. Epub 2020 Mar 23. Aging (Albany NY). 2020. PMID: 32205469 Free PMC article.
Evolution of a Human-Specific Tandem Repeat Associated with ALS.
Course MM, Gudsnuk K, Smukowski SN, Winston K, Desai N, Ross JP, Sulovari A, Bourassa CV, Spiegelman D, Couthouis J, Yu CE, Tsuang DW, Jayadev S, Kay MA, Gitler AD, Dupre N, Eichler EE, Dion PA, Rouleau GA, Valdmanis PN. Course MM, et al. Among authors: bourassa cv. Am J Hum Genet. 2020 Sep 3;107(3):445-460. doi: 10.1016/j.ajhg.2020.07.004. Epub 2020 Aug 3. Am J Hum Genet. 2020. PMID: 32750315 Free PMC article.
LINGO1 variants in the French-Canadian population.
Bourassa CV, Rivière JB, Dion PA, Bernard G, Diab S, Panisset M, Chouinard S, Dupré N, Fournier H, Raelson J, Belouchi M, Rouleau GA. Bourassa CV, et al. PLoS One. 2011 Jan 11;6(1):e16254. doi: 10.1371/journal.pone.0016254. PLoS One. 2011. PMID: 21264305 Free PMC article.
Exome sequencing identifies FUS mutations as a cause of essential tremor.
Merner ND, Girard SL, Catoire H, Bourassa CV, Belzil VV, Rivière JB, Hince P, Levert A, Dionne-Laporte A, Spiegelman D, Noreau A, Diab S, Szuto A, Fournier H, Raelson J, Belouchi M, Panisset M, Cossette P, Dupré N, Bernard G, Chouinard S, Dion PA, Rouleau GA. Merner ND, et al. Among authors: bourassa cv. Am J Hum Genet. 2012 Aug 10;91(2):313-9. doi: 10.1016/j.ajhg.2012.07.002. Epub 2012 Aug 2. Am J Hum Genet. 2012. PMID: 22863194 Free PMC article.
VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families.
Bourassa CV, Meijer IA, Merner ND, Grewal KK, Stefanelli MG, Hodgkinson K, Ives EJ, Pryse-Phillips W, Jog M, Boycott K, Grimes DA, Goobie S, Leckey R, Dion PA, Rouleau GA. Bourassa CV, et al. Am J Hum Genet. 2012 Sep 7;91(3):548-52. doi: 10.1016/j.ajhg.2012.07.018. Am J Hum Genet. 2012. PMID: 22958904 Free PMC article.
32 results