Author

Päivi Laiho

Finnish Institute for Health and WelfareORCID 0009-0004-3302-4321Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Kati M. DonneriD· 2 shared Aarno V. PalotieiD· 1 shared Abdelrahman G. ElnahasiD· 1 shared Adriana Huertas‐Vázquez· 1 shared Alena G. DushinaiD· 1 shared Alexander Loboda· 1 shared Alexey SergushicheviD· 1 shared Alina Yu. BabenkoiD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetics

Kati M. DonnerORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintMar 23, 2023

Understanding Complex Trait Susceptibilities and Ethnical Diversity in a Sample of 4,145 Russians Through Analysis of Clinical and Genetic Data

Dmitrii Usoltsev, Nikita Kolosov, Oxana Rotar…·Mykyta Artomov

The paper analyzes genetic and phenotypic data from 4,145 Russians to explore ethnic diversity and genetic associations, finding enrichment of Finnish-specific variants and providing a GWAS database.

5 citations

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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