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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 1
2012 2
2013 1
2014 1
2015 4
2016 5
2017 2
2018 4
2019 4
2020 3
2022 2
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26 results
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Page 1
Genetic architecture and adaptations of Nunavik Inuit.
Zhou S, Xie P, Quoibion A, Ambalavanan A, Dionne-Laporte A, Spiegelman D, Bourassa CV, Xiong L, Dion PA, Rouleau GA. Zhou S, et al. Among authors: bourassa cv. Proc Natl Acad Sci U S A. 2019 Aug 6;116(32):16012-16017. doi: 10.1073/pnas.1810388116. Epub 2019 Jul 22. Proc Natl Acad Sci U S A. 2019. PMID: 31332017 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.
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.
SYNE1 mutations in autosomal recessive cerebellar ataxia.
Noreau A, Bourassa CV, Szuto A, Levert A, Dobrzeniecka S, Gauthier J, Forlani S, Durr A, Anheim M, Stevanin G, Brice A, Bouchard JP, Dion PA, Dupré N, Rouleau GA. Noreau A, et al. Among authors: bourassa cv. JAMA Neurol. 2013 Oct;70(10):1296-31. doi: 10.1001/jamaneurol.2013.3268. JAMA Neurol. 2013. PMID: 23959263
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.
Mutation burden of rare variants in schizophrenia candidate genes.
Girard SL, Dion PA, Bourassa CV, Geoffroy S, Lachance-Touchette P, Barhdadi A, Langlois M, Joober R, Krebs MO, Dubé MP, Rouleau GA. Girard SL, et al. Among authors: bourassa cv. PLoS One. 2015 Jun 3;10(6):e0128988. doi: 10.1371/journal.pone.0128988. eCollection 2015. PLoS One. 2015. PMID: 26039597 Free PMC article.
C9orf72 repeat expansions in rapid eye movement sleep behaviour disorder.
Daoud H, Postuma RB, Bourassa CV, Rochefort D, Gauthier MT, Montplaisir J, Gagnon JF, Arnulf I, Dauvilliers Y, Charley CM, Inoue Y, Sasai T, Högl B, Desautels A, Frauscher B, Cochen De Cock V, Rouleau GA, Dion PA. Daoud H, et al. Among authors: bourassa cv. Can J Neurol Sci. 2014 Nov;41(6):759-62. doi: 10.1017/cjn.2014.39. Epub 2014 Nov 4. Can J Neurol Sci. 2014. PMID: 25377888
26 results