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26 results on '"Bourassa CV"'

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1. Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?

2. Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome.

3. Evolution of a Human-Specific Tandem Repeat Associated with ALS.

4. Genetic and epidemiological characterization of restless legs syndrome in Québec.

5. Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease.

6. Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations.

7. Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males.

8. Genetic architecture and adaptations of Nunavik Inuit.

9. Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases.

10. Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.

11. Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population.

12. No rare deleterious variants from STK32B , PPARGC1A , and CTNNA3 are associated with essential tremor.

13. Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population.

14. Genome-wide association study in essential tremor identifies three new loci.

15. RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population.

16. Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals.

17. The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder.

18. De novo variants in sporadic cases of childhood onset schizophrenia.

20. Mutation burden of rare variants in schizophrenia candidate genes.

21. Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population.

22. C9orf72 repeat expansions in rapid eye movement sleep behaviour disorder.

23. SYNE1 mutations in autosomal recessive cerebellar ataxia.

24. VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families.

25. Exome sequencing identifies FUS mutations as a cause of essential tremor.

26. LINGO1 variants in the French-Canadian population.

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