Author

Kirmo Wartiovaara

University of HelsinkiORCID 0000-0002-5677-1117Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Biochemistry· 1 Developmental Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Organism:human· 3 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1

Frequent Co-Authors

Rocio Sartori-MaldonadoiD· 2 shared Athina Balatsou· 1 shared Dario BoffelliiD· 1 shared David I. K. Martin· 1 shared Henna TyynismaaiD· 1 shared Jacob E. CorniD· 1 shared Jennifer E. ChungiD· 1 shared Jonathan T. VuiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 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 papersDevelopmental Biology

Rocio Sartori-MaldonadoORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Developmental BiologybioRxivPreprintMay 29, 2026

Human models of GLE1 associated LCCS1 reveal neural crest deficiency and multisystem developmental failure accompanied by altered RNA metabolism

Tomáš Zárybnický, O. Mäkelä, Athina Balatsou…·Satu Kuure

This study uses human stem cells and tissues to investigate LCCS1, revealing impaired RNA metabolism and developmental defects in neural crest and neuromuscular systems.

DOI 10.64898/2026.05.28.726124

humanbulk RNA-seq

𝕏 PostBluesky

BiochemistrybioRxivPreprintMay 13, 2024

Finnish gyrate atrophy mutation OAT;c.1205C>T leads to accumulation of intracellular GABA

Rocio Sartori-Maldonado, Kirmo Wartiovaara

The paper investigates the metabolic effects of a Finnish gyrate atrophy mutation in patient-derived cells, identifying GABA accumulation as a potential contributor to retinal degeneration.

DOI 10.1101/2024.05.13.593857

humanmetabolomics

𝕏 PostBluesky

GeneticsPLoS ONEPeer-reviewedJan 15, 2019

CRISPR-Cas9 interrogation of a putative fetal globin repressor in human erythroid cells.

Jennifer E. Chung, Wendy Magis, Jonathan T. Vu…·Mark A. DeWitt

This study uses CRISPR-Cas9 to test a putative fetal globin repressor region, finding it does not autonomously silence gamma-globin, suggesting it is not a therapeutic target for beta-hemoglobinopathies.

25 citations

humanexperimental assay

𝕏 PostBluesky