Author

Tuuli Metsvaht

Tartu University HospitalORCID 0000-0003-3206-3092Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Tuuli Metsvaht2 papers

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Andres SalumetsiD· 1 shared Aspasia DestouniiD· 1 shared Benelote UuskülaiD· 1 shared Cristina Rodríguez‐AntonaiD· 1 shared Hindrek TederiD· 1 shared Javier LanillosiD· 1 shared Kaarel KrjutškoviD· 1 shared Priit PaluojaiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andres SalumetsORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJan 6, 2026

Non-invasive Prenatal MT-RNR1 Pharmacogenetic Testing for the Prevention of Aminoglycoside-Induced Profound Hearing Loss

Aspasia Destouni, Benelote Uusküla, Javier Lanillos…·Kaarel Krjutškov

The paper develops a prenatal pharmacogenetic test using non-invasive prenatal testing data to identify variants in MT-RNR1 that predict risk of aminoglycoside-induced hearing loss with high accuracy.

2 citations

humanbulk RNA-seq

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