Author

Anni A. Antikainen

University of HelsinkiORCID 0000-0003-2488-6830Unclaimed 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· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Aarno V. PalotieiD· 2 shared Anastasia Kytölä· 2 shared Anna SyreeniiD· 2 shared Elina Kilpeläinen· 2 shared Jani K. HaukkaiD· 2 shared Niina SandholmiD· 2 shared Per‐Henrik GroopiD· 2 shared Valma HarjutsaloiD· 2 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aarno V. PalotieORCID

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2 papers

Recent·Most cited

Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes

Anni A. Antikainen, Jani K. Haukka, Anmol Kumar, Anna Syreeni, Stefanie Hägg-Holmberg, Anni Ylinen, Elina Kilpeläinen, Anastasia Kytölä, Aarno V. Palotie, Jukka Putaala A, Lena M. Thorn, Valma Harjutsalo, Per‐Henrik Groop, Niina Sandholm, the FinnDiane Study Group

The paper uses whole-genome sequencing to identify genetic variants associated with stroke in type 1 diabetes and finds replication evidence for several loci in both diabetic and non-diabetic populations.

Scientific Reports · Jun 11, 2024Peer-reviewedGenetic & Genomic Medicine

Novel protein-altering variants associated with serum apolipoprotein and lipid levels

Niina Sandholm, Ronja Hotakainen, Jani K. Haukka, Fanny Jansson Sigfrids, Emma H. Dahlström, Anni A. Antikainen, Erkka Valo, Anna Syreeni, Elina Kilpeläinen, Anastasia Kytölä, Aarno V. Palotie, Valma Harjutsalo, Carol M. Forsblom, Per‐Henrik Groop, on behalf of the FinnDiane Study Group

The paper identifies novel protein-altering variants associated with serum apolipoprotein and lipid levels using whole-exome and whole-genome sequencing data from individuals with type 1 diabetes.

Genome Medicine · Nov 23, 2022Peer-reviewedGenetic & Genomic Medicine