Author

Miro Viitala

University of TurkuORCID 0000-0002-0951-0168Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Immunology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:experimental assay· 1 Research Focus:host-pathogen & immune response· 1 Assay:proteomics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Maija HollméniD· 2 shared Ábris Ádám BendesiD· 1 shared Alberto PipernoiD· 1 shared Alessio Di FonzoiD· 1 shared Arno YlitaloiD· 1 shared Carlos R. FigueiredoiD· 1 shared Daniel A. PatteniD· 1 shared Edoardo MonfriniiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersImmunology

Maija HollménORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

ImmunologyTheranosticsPeer-reviewedJun 23, 2025

Secreted Clever-1 Modulates T Cell Responses and Impacts Cancer Immunotherapy Efficacy

Stuart Prince, Miro Viitala, Riikka Sjöroos…·Maija Hollmén

This study identifies a secreted form of Clever-1 that suppresses T cell responses and reduces anti-PD-1 efficacy in cancer, suggesting it as a therapeutic target and biomarker.

9 citations

humanproteomics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintNov 24, 2022

Biallelic STAB1 pathogenic variants cause hereditary hyperferritinemia

Edoardo Monfrini, Sara Pelucchi, Maija Hollmén…·Alberto Piperno

The paper identifies biallelic STAB1 mutations as a genetic cause of inherited hyperferritinemia without iron overload.

DOI 10.1101/2022.11.24.22282670

humanwhole-exome sequencing

𝕏 PostBluesky