Author

Lauri Ryyppö

Tampere 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

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Cancer Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Hanna Selin· 1 shared Jukka‐Pekka MeckliniD· 1 shared Jussi NikkolaiD· 1 shared Juuso Vuorinen· 1 shared Kirsi PylvänäineniD· 1 shared Lauri MoilaneniD· 1 shared Maarit AhtiaineniD· 1 shared Matti AnnalaiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperCancer Biology

Hanna Selin

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1 paper

Recent·Most cited

Constrained hypermutation and absence of TERT promoter mutations in Lynch syndrome-associated urothelial cancer

Jussi Nikkola, Lauri Ryyppö, Juuso Vuorinen, Lauri Moilanen, Maarit Ahtiainen, Kirsi Pylvänäinen, Hanna Selin, Tuomo Virtanen, Matti Nykter, Thea Veitonmäki, Jukka‐Pekka Mecklin, Toni T. Seppälä, Matti Annala

This study analyzes the somatic mutation landscape of Lynch syndrome-associated urothelial cancer and finds a lack of TERT promoter mutations and a distinct mutation profile.

Cell Reports · Oct 1, 2025Peer-reviewedCancer Biology