Author

Saana Eskelinen

University of HelsinkiORCID 0000-0002-6324-3291Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:synaptic & neural circuits· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Aiden Peter CorviniD· 1 shared Alan F. SchatzbergiD· 1 shared Alessia FiorentinoiD· 1 shared Ana Maria OlivaresiD· 1 shared Anders Dupont BørglumiD· 1 shared Andrea GannaiD· 1 shared Andrew Mark McIntoshiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aarno V. PalotieORCID

Mutual co-authors in cluster

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1 paper

Recent·Most cited

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam M. AlEissa, Jack D. Barchas, Nicholas James Bass, Tim B. Bigdeli, Gerome D. Breen, Evelyn J. Bromet, P.F. Buckley, William E. Bunney, Jonas Bybjerg‐Grauholm, William Byerley, Sinéad B. Chapman, , David St Clair

Exomes of 24,248 schizophrenia cases and 97,322 controls implicate ultra-rare damaging variants in 10 genes, including GRIN2A and GRIA3, with odds ratios of 3 to 50.

Nature · Apr 8, 2022Peer-reviewedGenetic & Genomic Medicine✦ In-depth digest