Author

Samuli Eldfors

University of HelsinkiORCID 0000-0001-5056-4750Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Assay:DNA methylation· 1 Organism:mouse· 1

Frequent Co-Authors

Amy M. Bertino· 1 shared Angelique Gilbert· 1 shared Caroline Akemi HeckmaniD· 1 shared Claudia C. PastranaiD· 1 shared Esa PitkäneniD· 1 shared Kimmo PorkkaiD· 1 shared Markus J. V. Vähä-KoskelaiD· 1 shared Matthew J. WalteriD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 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

1 shared paperCancer Biology

Amy M. Bertino

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Cancer BiologyLeukemiaPeer-reviewedOct 6, 2026

Sensitivity to ATR-CHK1 pathway inhibition in AML/MDS is enhanced by SRSF2 mutations and reduced by RUNX1 loss

Samuli Eldfors, Sumit Rai, Vineet Sharma…·Timothy Aaron Graubert

This study identifies SRSF2 and U2AF1 mutations as biomarkers of sensitivity to ATR-CHK1 pathway inhibitors and RUNX1 mutations as a mechanism of resistance in MDS/AML.

DOI 10.1038/s41375-026-03142-7

humanmouse

𝕏 PostBluesky

GenomicsComputational and Structural Biotechnology JournalPeer-reviewedJan 1, 2025

Whole Exome Sequencing and Single-Cell DNA Sequencing for Assessment of Clonal Heterogeneity and Evolution in Acute Myeloid Leukemia

Sadiksha Adhikari, Samuli Eldfors, Esa Pitkänen…·Caroline Akemi Heckman

The paper compares whole exome sequencing and single-cell DNA sequencing in AML to assess clonal heterogeneity and evolution, finding both methods have strengths and limitations in variant detection and clonal analysis.

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky