Author

Sviatoslav-Oleh Savchak

University of TartuORCID 0009-0000-0678-7156Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anastasiia AlekseienkoiD· 1 shared Anu ReigoiD· 1 shared Erik AbneriD· 1 shared FinnGeniD· 1 shared Hanna Maria OllilaiD· 1 shared Hele HaapaniemiiD· 1 shared Jaanika KronbergiD· 1 shared Kanwal BatooliD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anastasiia AlekseienkoORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMar 18, 2025

Leveraging nationwide health care records in Estonia to identify the genetic background of understudied disease phenotypes

Erik Abner, Anastasiia Alekseienko, Kanwal Batool…·Priit Palta

The paper uses Estonian Biobank data to identify genetic loci associated with 5,491 disease phenotypes, finding 3,222 genome-wide significant loci and 754 protein-altering variant-trait associations.

DOI 10.1101/2025.03.18.25324091

humanwhole-genome sequencing

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