Author

Klavs Jermakovs

University of Cambridge

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biophysics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:proteomics· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alejandro Díaz-BarreiroiD· 1 shared Anastasiia AlekseienkoiD· 1 shared Antonio Jose Costa-FilhoiD· 1 shared Anu ReigoiD· 1 shared Emanuel KavaiD· 1 shared Erik AbneriD· 1 shared Ewa Andrzejewska· 1 shared Fabian SvaraiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBiophysics

Alejandro Díaz-BarreiroORCID

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2 papers

Recent·Most cited

Mapping high resolution, multidimensional phase diagrams of physiological protein condensates

Tanushree Agarwal, Tomas Šneideris, Fabian Svara, Klavs Jermakovs, Helena Coyle, Seema Qamar, Emanuel Kava, Rob M. Scrutton, Nicole Pleschka, Priyanka Peres, Gea Cereghetti, Ewa Andrzejewska, Alejandro Díaz-Barreiro, Gaby Palmer, Antonio Jose Costa-Filho, , Jonathon Nixon‐Abell

This study introduces ExVivo PhaseScan to generate high-resolution phase diagrams of physiological protein condensates and reveals how FUS mutations cause liquid-to-solid transitions in stress granules and nucleoli.

bioRxiv · Jun 5, 2026Biophysics

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

Erik Abner, Anastasiia Alekseienko, Kanwal Batool, Klavs Jermakovs, Mihkel Jesse, Hele Haapaniemi, Satu J. Strausz, Lehte Türk, Sviatoslav-Oleh Savchak, FinnGen, Anu Reigo, Teele Palumaa, Hanna Maria Ollila, Jaanika Kronberg, Urmo Võsa, , 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.

medRxiv · Mar 18, 2025 · PreprintGenetic & Genomic Medicine