Author

Heidi M Hautakangas

University of HelsinkiORCID 0000-0002-5585-6856Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:GWAS summary statistics· 3 Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Research Focus:benchmarking· 1 Research Focus:fine-mapping· 1

Frequent Co-Authors

Aarno V. PalotieiD· 3 shared Matti PirineniD· 3 shared FinnGeniD· 2 shared Paavo HäppöläiD· 2 shared Samuli RipattiiD· 2 shared Aki Samuli HavulinnaiD· 1 shared Andrea Carmine BeliniD· 1 shared Andres MetspaluiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Aarno V. PalotieORCID

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3 papers

Recent·Most cited

Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants

Heidi M Hautakangas, Joonas Kartau, FinnGen, Aarno V. Palotie, Matti Pirinen

This study fine-maps genome-wide association study results for migraine, identifying 181 credible sets of candidate causal variants across 102 regions.

Nature Communications · Jan 12, 2026Peer-reviewedGenetic & Genomic Medicine

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Heidi M Hautakangas, Bendik Slagsvold Winsvold, Sanni Ruotsalainen, Gyða Björnsdóttir, Aster V. E. Harder, Lisette J. A. Kogelman, Laurent F. Thomas, Raymond Noordam, Christian Benner, Padhraig Gormley, Ville Artto, Karina Banasik, Anna Bjornsdottir, Dorret Irene Boomsma, Ben Michael Brumpton, , Matti Pirinen

This GWAS identifies 123 migraine risk loci, including subtype-specific variants and novel targets, supporting neurovascular mechanisms in migraine.

Nature Genetics · Feb 1, 2022Peer-reviewedGenetic & Genomic Medicine

Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

Joel T Rämö, Tuomo Kiiskinen, Juha M Karjalainen, Kristi Krebs, Mitja Kurki, Aki Samuli Havulinna, Eija Hämäläinen, Paavo Häppölä, Heidi M Hautakangas, FinnGen, Konrad J. Karczewski, Masahiro Kanai, Reedik Mägi, Priit Palta, Tõnu Esko, , Aarno V. Palotie

This study identifies 15 new risk loci for otosclerosis and replicates known associations, highlighting shared genetic links with skeletal structure and bone-related disorders.

medRxiv · Nov 15, 2020 · PreprintGenetic & Genomic Medicine