List of works by Gabrielle Houle

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

article

Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor

scientific article published on 04 November 2020

Characterization of the phenotype with cognitive impairment and protein mislocalization in SCA34

scientific article published on 20 February 2020

Exome-wide rare variant analysis in familial essential tremor

scientific article published on 24 November 2020

Genome-wide estimates of heritability and genetic correlations in essential tremor

article

Investigating the association and causal relationship between restless legs syndrome and essential tremor

Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression

scientific article published on 14 November 2019

Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor

scientific article published on 06 April 2020

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

scientific article published on 19 October 2017

SYNE1 mutations cause autosomal-recessive ataxia with retained reflexes in Brazilian patients.

scientific article

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

scientific article published on 3 February 2017

Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor

scientific article published on 31 July 2020

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