Author

Jessica Charlebois

Montreal Neurological Institute and Hospital

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Alfredo BruscoiD· 1 shared Bianca E. RusselliD· 1 shared Brett TrostiD· 1 shared Carole Shum· 1 shared Clarrisa A. BradleyiD· 1 shared Claudio GrazianoiD· 1 shared Emilie D. DouineiD· 1 shared Evdokia A. AnagnostouiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alfredo BruscoORCID

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1 paper

Recent·Most cited

Genetic variants in DDX53 contribute to Autism Spectrum Disorder associated with the Xp22.11 locus

Marcello Scala, Clarrisa A. Bradley, Jennifer Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum, Marla Mendes de Aquino, Miriam S. Reuter, Evdokia A. Anagnostou, Jeffrey R. MacDonald, Sangyoon Y. Ko, Paul W. Frankland, Jessica Charlebois, Mayada Elsabbagh, Leslie Granger, , Stephen W. Scherer

The paper identifies DDX53 genetic variants in individuals with ASD, showing a link between DDX53 and ASD, and highlights implications for genetic testing and mouse modeling.

The American Journal of Human Genetics · Dec 19, 2024Peer-reviewedGenetic & Genomic Medicine