Author

Martine Cools

Ghent University HospitalORCID 0000-0002-9552-4899Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:spatial domain detection· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Hannes SyryniD· 2 shared Julie Van De VeldeiD· 2 shared Aaron Verplancke· 1 shared Alison Ross· 1 shared Andrea Louise VincentiD· 1 shared Andrew Neil ShellingiD· 1 shared Annelies DheedeneiD· 1 shared Cathérine CassimaniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenomics

Hannes SyrynORCID

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2 papers

Recent·Most cited

A laser capture microdissection-based method for high-sensitivity transcriptomics from archived FFPE tissue slides with single-cell resolution using LCM-FFPEseq

Elise Callens, Hannes Syryn, Koen Deserranno, Guillaume Cattebeke, Henri Couckuyt, Julie Van De Velde, Danique Berrevoet, Aaron Verplancke, Dieter L. D. Deforce, Ward De Spiegelaere, Koen K Van de Vijver, Martine Cools, Filip Van Nieuwerburgh

LCM-FFPEseq enables high-sensitivity transcriptomics from FFPE tissues with single-cell resolution, detecting over 14,000 genes per sample using as few as 30 cells.

Scientific Reports · Sep 1, 2026Peer-reviewedGenomics

Variant curation of the largest compendium of FOXL2 coding and non-coding sequence and structural variants in BPES

Charlotte Matton, Julie Van De Velde, Marieke De Bruyne, Stijn Van de Sompele, Sally Hooghe, Hannes Syryn, Miriam Bauwens, Eva D’haene, Annelies Dheedene, Martine Cools, Shoko Komatsuzaki, Ewelina Preizner-Rzucidło, Alison Ross, Christine Armstrong, Wendy Watkins, , Elfride B. W. De Baere

The paper curates and classifies the largest compendium of FOXL2 sequence and structural variants in BPES, identifying key mutational patterns and improving diagnostic and genetic counseling.

Human Mutation · Jan 1, 2026Peer-reviewedGenetic & Genomic Medicine