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.

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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

Genetic & Genomic MedicinemedRxivPreprintAug 11, 2022

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

Jay P. Ross, Fulya Akçimen, Calwing Liao…·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.

DOI 10.1101/2022.08.11.22278628

humanwhole-exome sequencing

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