Author

Päivi Vieira

Oulu University HospitalORCID 0000-0002-0796-8706Unclaimed 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· 1 Research Focus:polygenic risk· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Dennis LaliD· 1 shared Eija Hämäläinen· 1 shared Elisa RahikkalaiD· 1 shared Elmo SaarentausiD· 1 shared Heli M. HelanderiD· 1 shared Jaana SuvisaariiD· 1 shared Jarmo Körkkö· 1 shared

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2018-2018 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Aarno V. PalotieORCID

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintMay 28, 2018

Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

Mitja Kurki, Elmo Saarentaus, Olli P. H. Pietiläinen…·Aarno V. Palotie

The paper investigates the genetic contributions to intellectual disability, finding rare variants are more common in severe cases and common variants contribute to all severity levels.

5 citations

humanwhole-exome sequencing

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