Author

Kai Kaarniranta

Radboud University NijmegenORCID 0000-0003-2600-8679Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Organism:human· 2 Approach:statistical model· 2 Approach:Bayesian inference· 1 Research Focus:database / resource· 1 Assay:electronic health records· 1 Research Focus:fine-mapping· 1

Frequent Co-Authors

Joel T RämöiD· 2 shared Aarno V. PalotieiD· 1 shared Abdelrahman G. ElnahasiD· 1 shared Adriana Huertas‐Vázquez· 1 shared Anders MälarstigiD· 1 shared Andrea GannaiD· 1 shared Antti A. MäkitieiD· 1 shared Antti HakaneniD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Joel T RämöORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 8, 2024

Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma

Joel T Rämö, Bryan R. Gorman, Lu-Chen C Weng…·Elizabeth J. Rossin

The paper identifies a rare variant in VE-PTP associated with CSC, varicose veins, and glaucoma using genome-wide data from multiple cohorts.

1 citation

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintMar 3, 2022

✦ In-depth digest

FinnGen: Unique genetic insights from combining isolated population and national health register data

Mitja Kurki, Juha M Karjalainen, Priit Palta…·Marianna Niemi

Finnish-enriched low-frequency variants, often coding, underlie many GWAS signals across 1,932 register endpoints in 218,792 Finns; a 15-disease meta-analysis with Estonian and UK biobanks adds 30 unreported associations.

404 citations

humanelectronic health records

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