Author

Hannes Syryn

Ghent University HospitalORCID 0000-0002-0914-2676Unclaimed 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

Julie Van De VeldeiD· 2 shared Martine CoolsiD· 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

Julie Van De VeldeORCID

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2 papers

Recent·Most cited

GenomicsScientific ReportsPeer-reviewedSep 1, 2026

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…·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.

1 citation

humanbulk RNA-seq

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Genetic & Genomic MedicineHuman MutationPeer-reviewedJan 1, 2026

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…·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.

DOI 10.1155/humu/8478740

humanwhole-exome sequencing

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