Author

Arto Pietilä

Finnish Institute for Health and WelfareORCID 0000-0002-9298-0012Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Adam E. LockeiD· 1 shared Aki Samuli HavulinnaiD· 1 shared Anne JacksoniD· 1 shared Charleston WK ChiangiD· 1 shared Chiara SabattiiD· 1 shared Chul Joo KangiD· 1 shared Daniel C. KoboldtiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Aarno V. PalotieORCID

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1 paper

Recent·Most cited

GenomicsbioRxivPreprintApr 5, 2019

Exome sequencing identifies high impact trait-associated alleles enriched in Finns

Adam E. Locke, Karyn Meltz Steinberg, Charleston WK Chiang…·Nelson B Freimer

Exome sequencing in Finnish populations identifies rare trait-associated alleles with higher frequencies and geographical clustering, revealing 30 novel associations with quantitative traits.

1 citation

humanwhole-exome sequencing

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