Author

Milla M. Laarne

University of HelsinkiORCID 0000-0001-5690-4779Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

A. ZygmuntiD· 1 shared Alan H. BeggsiD· 1 shared Andoni Echaniz‐LagunaiD· 1 shared Anna LaGroon· 1 shared Carina Wallgren‐PetterssoniD· 1 shared Carsten G. BönnemanniD· 1 shared Casie A. GenettiiD· 1 shared Curtis R. RogersiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. ZygmuntORCID

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2 papers

Recent·Most cited

Molecular BiologySTAR ProtocolsPeer-reviewedFeb 6, 2026

Rapid tRNA Isolation and Chemiluminescent Northern Blot Detection of tRNA and tRNA-Derived Fragments

Pavlína Gregorová, Minna-Maria K. Heinonen, Milla M. Laarne, L. Peter Sarin

The paper describes a rapid tRNA isolation method and a non-radioactive chemiluminescent Northern blotting technique for detecting tRNA and tRNA-derived fragments.

4 citationstop 3%

experimental assay

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Genetic & Genomic MedicinemedRxivPreprintOct 4, 2024

Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions

Lydia Sagath, K. Kiiski, Kireshnee Naidu…·Vilma‐Lotta Lehtokari

The paper identifies structural variants in the NEB gene across 35 families, showing large deletions cause dominant distal myopathy while recessive variants show no severity correlation.

DOI 10.1101/2024.10.04.24313542

humanwhole-exome sequencing

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