Author

Janick St-Cyr

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

Click to filter author papers

Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 2 Research Focus:variant calling· 2 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Vincent MooseriD· 3 shared Claude BhéreriD· 2 shared Daniel TaliuniD· 2 shared Danielle S. Perley· 2 shared François LefebvreiD· 2 shared Guillaume BourqueiD· 2 shared Jiannis RagoussisiD· 2 shared Katerina TrajanoskaiD· 2 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Vincent MooserORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genome-wide Association Study of Long COVID

Vilma Lammi, Tomoko Nakanishi, Samuel E. Jones, Shea J. Andrews, Juha M Karjalainen, Beatriz Cortés, Heath O’Brien, Ana Ochoa-Guzmán, Brian Fulton‐Howard, Martin E. Broberg, Hele Haapaniemi, Masahiro Kanai, Matti Pirinen, Axel Schmidt, Ruth E. Mitchell, , Sergi Papiol

This study performs a genome-wide association study for Long COVID, identifying a significant association with the FOXP4 locus and highlighting the role of pulmonary dysfunction and COVID-19 severity.

Nature Genetics · May 21, 2025Peer-reviewedGenetic & Genomic Medicine

WEGS: a cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome

Claude Bhérer, Robert J. M. Eveleigh, Katerina Trajanoska, Janick St-Cyr, Antoine Paccard, Praveen Nadukkalam Ravindran, Elizabeth A. Caron, Nimara Bader Asbah, Peyton McClelland, Clare Wei, Iris Baumgärtner, Marc Schindewolf, Yvonne Döring, Danielle S. Perley, François Lefebvre, , Daniel Taliun

WEGS combines low-depth whole genome and high-depth whole exome sequencing to reduce costs while maintaining variant detection accuracy in genetic studies.

npj Genomic Medicine · Feb 7, 2024Peer-reviewedGenomics

Rare splice and missense variants with evidence of pathogenicity in consanguineous families with autosomal recessive intellectual disability from Pakistan

Abdul Waheed, Robert J. M. Eveleigh, Danielle S. Perley, Janick St-Cyr, François Lefebvre, Abdul Hameed Khan, Zarqash Majeed, Abrish Majeed, Katerina Trajanoska, Raquel Cuella-Martin, Claude Bhérer, Ghazanfar Ali, Vincent Mooser, Daniel Taliun

medRxiv · Jan 8, 2024 · PreprintGenetic & Genomic Medicine