Author

Karina Kwan

McGill University

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

Biology Disciplines

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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 effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Angela L. GengeiD· 1 shared Calwing LiaoiD· 1 shared Dan SpiegelmaniD· 1 shared Daniel E. PhillipsiD· 1 shared Fulya AkçimeniD· 1 shared Guy Armand RouleauiD· 1 shared Jay P. RossiD· 1 shared Nicolas DupréiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Angela L. GengeORCID

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1 paper

Recent·Most cited

Rare and common variant analyses of amyotrophic lateral sclerosis in the French-Canadian genome

Jay P. Ross, Fulya Akçimen, Calwing Liao, Karina Kwan, Daniel E. Phillips, Zoe Schmilovich, Dan Spiegelman, Angela L. Genge, Nicolas Dupré, Patrick A. Dion, Sali M.K. Farhan, Guy Armand Rouleau

This study analyzes rare and common variants in ALS using French-Canadian data, finding that PRS and rare variants independently affect risk but do not interact significantly.

medRxiv · Aug 11, 2022 · PreprintGenetic & Genomic Medicine