Author

Simon Fournier

Université de MontréalORCID 0000-0003-4972-9030Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Simon Fournier1 paper · Setec (France)

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alex DésautelsiD· 1 shared Antonio L. ZadraiD· 1 shared Lucie BarateauiD· 1 shared Marjorie LabrecqueiD· 1 shared Martine TétreaultiD· 1 shared Régis LopeziD· 1 shared Saiyet Baez LlovioiD· 1 shared Simon C. WarbyiD· 1 shared

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2025-2025 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alex DésautelsORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 17, 2025

Genetics of Sleepwalking: Insights from whole exome sequencing.

Saiyet Baez Llovio, Yves A Dauvilliers, Valérie Triassi…·Martine Tétreault

This study uses whole-exome sequencing to identify rare genetic variants associated with sleepwalking in two cohorts, finding 99 genes enriched in patients and 31 shared genes with rare variants.

1 citation

humanwhole-exome sequencing

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