Author

Kayla Horowitz

McGill University Health CentreORCID 0000-0002-8319-2188Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 1

Frequent Co-Authors

Alana J. Mistry· 1 shared Allison Ann DilliottiD· 1 shared Angela L. GengeiD· 1 shared Emily DwoshiD· 1 shared Guy Armand RouleauiD· 1 shared Isabela Dall Oglio BuccoiD· 1 shared Justin SimoiD· 1 shared Kristiana SalmoniD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alana J. Mistry

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2 papers

Recent·Most cited

Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care Centre

Kayla Horowitz, Nellie H. Fotopoulos, Alana J. Mistry, Justin Simo, Miranda Medeiros, Isabela Dall Oglio Bucco, Mia Ginsberg, Emily Dwosh, Roberta La Piana, Guy Armand Rouleau, Allison Ann Dilliott, Sali M.K. Farhan

The paper describes how multidisciplinary VUS Rounds help classify and manage variants of uncertain significance in neurogenetics patients.

Journal of Medical Genetics · Nov 15, 2024Peer-reviewedGenetic & Genomic Medicine

How the prospect of a clinical trial impacts decision-making for predictive genetic testing in amyotrophic lateral sclerosis

Myriam Fontaine, Kayla Horowitz, Nancy Anoja, Angela L. Genge, Kristiana Salmon

This study examines how the prospect of a clinical trial influences decision-making for predictive genetic testing in individuals at-risk for familial ALS, highlighting the role of genetic counseling.

medRxiv · Sep 30, 2024 · PreprintGenetic & Genomic Medicine