Author
University of Helsinki
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
Mutual co-authors in cluster
5 papers
Recent·Most cited
Anni A. Antikainen, Jani K. Haukka, Anmol Kumar…·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.
Valtteri Julkunen, Claudia Schwarz, Juho Kalapudas…·Zhihao Ding
The paper demonstrates the feasibility of conducting clinical recall studies from the FinnGen biobank to collect customized clinical data from participants with Alzheimer's disease or mild cognitive disorder.
Niina Sandholm, Ronja Hotakainen, Jani K. Haukka…·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.
Mitja Kurki, Juha M Karjalainen, Priit Palta…·Marianna Niemi
Finnish-enriched low-frequency variants, often coding, underlie many GWAS signals across 1,932 register endpoints in 218,792 Finns; a 15-disease meta-analysis with Estonian and UK biobanks adds 30 unreported associations.
Dorothée Diogo, Chao Tian, Christopher S. Franklin…·Heiko Runz
The paper uses PheWAS across large cohorts to identify genetic associations with drug targets and predict drug safety and efficacy.