Author

Vincent Llorens

University of Helsinki

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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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:GWAS summary statistics· 2 Approach:statistical model· 2 Approach:Bayesian inference· 1 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:electronic health records· 1 Approach:experimental assay· 1

Frequent Co-Authors

Mary Pat ReeveiD· 3 shared Mervi AavikkoiD· 3 shared Mitja KurkiiD· 3 shared Pietro Della Briotta Parolo· 3 shared Timo Petteri SipilaiD· 3 shared Andrea GannaiD· 2 shared Aoxing LiuiD· 2 shared Arto LehistöiD· 2 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Mary Pat ReeveORCID

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3 papers

Recent·Most cited

PGS Browser: a public platform for personalized polygenic score interpretation

Nikita Kolosov, Mary Pat Reeve, Pietro Della Briotta Parolo, Mitja Kurki, Vincent Llorens, FinnGen, Timo Petteri Sipila, Adam Herman, Иван Игоревич Молотков, Mervi Aavikko, Samuli Ripatti, Aarno V. Palotie, Mark J. Daly, Mykyta Artomov

The paper benchmarks polygenic scores in a large cohort, identifies top-performing models, and provides a public platform for PGS analysis and interpretation.

medRxiv · Jul 3, 2025 · PreprintGenetic & Genomic Medicine

A FinnGen pilot clinical recall study for Alzheimer's disease

Valtteri Julkunen, Claudia Schwarz, Juho Kalapudas, Merja Hallikainen, Aino‐Kaisa Piironen, Arto Mannermaa, Hanna Kujala, T. Laitinen, Veli‐Matti Kosma, Teemu I. Paajanen, Reetta K. Kälviäinen, Mikko Hiltunen, Sanna‐Kaisa Herukka, Sari Kärkkäinen, Tarja Kokkola, , Zhihao Ding

The paper demonstrates the feasibility of conducting clinical recall studies from the FinnGen biobank to collect customized clinical data from participants with Alzheimer's disease or mild cognitive disorder.

Scientific Reports · Aug 3, 2023Peer-reviewedGenetic & Genomic Medicine

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

Mitja Kurki, Juha M Karjalainen, Priit Palta, Timo Petteri Sipila, Kati Kristiansson, Kati M. Donner, Mary Pat Reeve, Hannele M. Laivuori, Mervi Aavikko, Mari Anneli Kaunisto, Anu Loukola, Elisa Lahtela, Hannele Mattsson, Päivi Laiho, Pietro Della Briotta Parolo, , 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.

medRxiv · Mar 3, 2022 · PreprintGenetic & Genomic Medicine✦ In-depth digest