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

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenetic EpidemiologyPeer-reviewedJan 6, 2026

Archipelago method for variant set association test statistics.

Dylan Lawless, Saadat Ali, Mariam Ait Oumelloul…·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.

DOI 10.1002/gepi.70025

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJun 12, 2025

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

Dylan Lawless, Pauline Rogg, Manon Bouzereau…·Luregn Jan Schlapbach

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

DOI 10.1101/2025.06.12.25329504

humanwhole-exome sequencing

𝕏 PostBluesky