Author

Marianna Niemi

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· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

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 Anu LoukolaiD· 1 shared Aoxing LiuiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abdelrahman G. ElnahasORCID

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Author profile →

1 paper

Recent·Most cited

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