Maarja Joeloo
Tartu, Estonia
Last Updated: 09/26/2026
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Found 9 publications
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.
Journal: medRxiv : the preprint server for health sciences
Published: June 04, 2026
Genetic influences on antidepressant side effects: a CYP2C19 gene variation and polygenic risk study in the Estonian Biobank.
Journal: European journal of human genetics : EJHG
Published: January 07, 2025
StarPhase: Comprehensive Phase-Aware Pharmacogenomic Diplotyper for Long-Read Sequencing Data.
Journal: bioRxiv : the preprint server for biology
Published: December 23, 2024
The Estonian Biobank's journey from biobanking to personalized medicine.
Journal: Nature communications
Published: August 13, 2024
Rare copy-number variants as modulators of common disease susceptibility.
Journal: Genome medicine
Published: July 17, 2023
Genetic determinants of plasma protein levels in the Estonian population.
Journal: Scientific reports
Published: June 22, 2023
Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease.
Journal: Cell reports. Medicine
Published: March 21, 2023
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.
Journal: Human molecular genetics
Published: November 21, 2022
Showing 1-9 of 9
Last Updated: 09/26/2026