Mitja Kurki
Broad Institute(US)University of Helsinki(FI)University of Eastern Finland(FI)Finnish Institute for Health and Welfare(FI)Massachusetts General Hospital(US)Institute for Molecular Medicine Finland(FI)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Genomics and Rare Diseases, Intracranial Aneurysms: Treatment and Complications, Genomic variations and chromosomal abnormalities, Cerebrospinal fluid and hydrocephalus
Most-Cited Works
- → Analysis of protein-coding genetic variation in 60,706 humans(2016)10,243 cited
- → FinnGen provides genetic insights from a well-phenotyped isolated population(2023)3,864 cited
- → A cross-population atlas of genetic associations for 220 human phenotypes(2021)2,289 cited
- → Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine(2016)693 cited
- → Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers(2020)535 cited
- → Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders(2016)472 cited