Author

Jonna Komulainen‐Ebrahim

Oulu University HospitalORCID 0000-0002-3876-9830Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Activity by Year

2018-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetics

Aarno V. PalotieORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

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, Padhraig Gormley, Dennis Lal, Sini Kerminen, Minna Torniainen‐Holm, Eija Hämäläinen, Elisa Rahikkala, Riikka Keski‐Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen‐Ebrahim, Heli M. Helander, Päivi Vieira, , 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.

bioRxiv · May 28, 2018 · PreprintGenetics