Author

Caitlin M. Kehoe

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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Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alex DésautelsiD· 1 shared Cheryl WatersiD· 1 shared Dan SpiegelmaniD· 1 shared Edward A. FoniD· 1 shared Gilad YahalomiD· 1 shared Guy Armand RouleauiD· 1 shared Jacques Yves MontplaisiriD· 1 shared Jennifer A. RuskeyiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Alex DésautelsORCID

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1 paper

Recent·Most cited

Analysis of common and rare VPS13C variants in late onset Parkinson disease

Uladzislau Rudakou, Jennifer A. Ruskey, Lynne Krohn, Sandra B. Laurent, Dan Spiegelman, Lior Greenbaum, Gilad Yahalom, Alex Désautels, Jacques Yves Montplaisir, Stanley Fahn, Cheryl Waters, Oren Levy, Caitlin M. Kehoe, Sushma Narayan, Yves A Dauvilliers, , Ziv Gan‐Or

The paper investigates the role of VPS13C variants in late-onset Parkinson disease, finding no significant association with rare variants but a nominal association with a haplotype.

Neurology Genetics · Jan 9, 2020Peer-reviewedGenetics