Author

Saadat Ali

École Polytechnique Fédérale de Lausanne

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· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:GWAS summary statistics· 1 Research Focus:software / tool· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Dylan LawlessiD· 2 shared Jacques FellayiD· 2 shared Luregn Jan SchlapbachiD· 2 shared Alessandro BorghesiiD· 1 shared Anita Niederer-LoheriD· 1 shared Christa RellyiD· 1 shared Christian R. KahlertiD· 1 shared Christian Wandall ThorballiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Dylan LawlessORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Archipelago method for variant set association test statistics.

Dylan Lawless, Saadat Ali, Mariam Ait Oumelloul, Luregn Jan Schlapbach, Jacques Fellay

The paper introduces the Archipelago method to visualize variant set association test statistics by assigning genomic coordinates to P values, enabling combined visualization of set-level and individual variant associations.

Genetic Epidemiology · Jan 6, 2026Peer-reviewedGenetic & Genomic Medicine

Rare variants in infection response protein pathways associated with sepsis in children.

Dylan Lawless, Pauline Rogg, Manon Bouzereau, Robin Fallegger, Zaira Seferbekova, Valeriia Timonina, Konstantin Yu. Popadin, Saadat Ali, Zhi Ming Xu, Simon Boutry, Christian Wandall Thorball, Flavia Hodel, Alessandro Borghesi, Johannes Trück, Martin Stocker, , Luregn Jan Schlapbach

The paper identifies genetic pathways and variants associated with sepsis susceptibility in children through genomic analysis of a paediatric cohort.

medRxiv · Jun 12, 2025 · PreprintGenetic & Genomic Medicine