Author

Mikko Niemi

University of HelsinkiORCID 0000-0003-4550-2189Unclaimed 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· 2 Approach:statistical model· 2 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 2 shared Ari Ahola‐OlliiD· 2 shared Erkki Tapio IsometsäiD· 2 shared Jaana SuvisaariiD· 2 shared Jari TiihoneniD· 2 shared Jarmo A. HietalaiD· 2 shared Jouko K LönnqvistiD· 2 shared Kaisla Lahdensuo· 2 shared

Activity by Year

2022-2023 · 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

2 shared papersGenetic & Genomic Medicine

Aarno V. PalotieORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicineMolecular PharmaceuticsPeer-reviewedFeb 13, 2023

Functional characterization of six SLCO1B1 (OATP1B1) variants observed in Finnish individuals with a psychotic disorder

Katja Häkkinen, Wilma Kiander, Heidi Kidron…·the SUPER-Finland researchers listed in the Acknowledgements

The paper investigates six rare SLCO1B1 variants in Finnish individuals with psychosis, finding one variant causes loss-of-function and reduced OATP1B1 protein expression.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineThe Pharmacogenomics JournalPeer-reviewedFeb 23, 2022

Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

Katja Häkkinen, Johanna I. Kiiski, Markku Lähteenvuo…·Ari Ahola‐Olli

The paper constructs a CYP2D6 copy-number imputation panel and reports pharmacogenetic variant frequencies in Finnish individuals with psychosis, showing high imputation accuracy but limited clinical utility.

11 citations

humanGWAS summary statistics

𝕏 PostBluesky