Author

Antti‐Pekka Sarin

University of HelsinkiORCID 0000-0002-5753-9782Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Aarno V. PalotieiD· 3 shared Samuli RipattiiD· 3 shared Veikko V SalomaaiD· 3 shared Aki Samuli HavulinnaiD· 2 shared Mark J. DalyiD· 2 shared Markus PerolaiD· 2 shared Olli Tuomas RaitakariiD· 2 shared Alicia R. MartiniD· 1 shared

Activity by Year

2016-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Aarno V. PalotieORCID

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3 papers

Recent·Most cited

Multivariate genome-wide association analysis of a cytokine network reveals variants with widespread immune, haematological and cardiometabolic pleiotropy

Artika P. Nath, Scott C. Ritchie, Nastasiya F. Grinberg, Howard H.F. Tang, Qin Huang, Shu Mei Teo, Ari Ahola‐Olli, Peter Würtz, Aki Samuli Havulinna, Kristiina Santalahti, Niina Pitkänen, Terho J. Lehtimäki, Mika A. P. Kähönen, Leo‐Pekka Lyytikäinen, Emma Raitoharju, , Michael Inouye

This study identifies genetic variants with pleiotropic effects on cytokines and related traits using a multivariate genome-wide association analysis.

The American Journal of Human Genetics · Oct 31, 2019Peer-reviewedGenomics

Haplotype sharing provides insights into fine-scale population history and disease in Finland

Alicia R. Martin, Konrad J. Karczewski, Sini Kerminen, Mitja Kurki, Antti‐Pekka Sarin, Mykyta Artomov, Johan Gunnar Eriksson, Tõnu Esko, Giulio Genovese, Aki Samuli Havulinna, Jaakko A. Kaprio, А. О. Конради, Laszlo I Koranyi, Anna Aleksandrovna Kostareva, Minna Männikkö, , Mark J. Daly

This study uses haplotype sharing among Finns to reconstruct recent population history and identify regions with increased rare disease variant sharing.

The American Journal of Human Genetics · Apr 26, 2018Peer-reviewedGenetics

The rate of false polymorphisms introduced when imputing genotypes from global imputation panels

Ida L. Surakka, Antti‐Pekka Sarin, Sanni Ruotsalainen, Richard Michael Durbin, Veikko V Salomaa, Mark J. Daly, Aarno V. Palotie, Samuli Ripatti, SISu project group

This study evaluates false polymorphism rates in imputed Finnish genotype data using global vs. population-specific reference panels, finding higher false positives with global panels.

bioRxiv · Oct 13, 2016 · PreprintGenetics