Mitja Kurki

Research interests

Publications

• Proteomic aging clock predicts mortality and risk of common age-related diseases in diverse populations

  Nature Medicine · 2024 · 10.1038/s41591-024-03164-7

• FinnGen provides genetic insights from a well-phenotyped isolated population

  Nature · 2023 · https://doi.org/10.1038/s41586-022-05473-8

• Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses

  Nature Medicine · 2023 · 10.1038/s41591-023-02352-1

• Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population

  Nature · 2023 · https://doi.org/10.1038/s41586-023-05837-8

• Genetic associations of protein-coding variants in human disease

  Nature · 2022 · 10.1038/s41586-022-04394-w

• Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

  Cell Genomics · 2022 · 10.1016/j.xgen.2022.100192

• FinnGen: Unique genetic insights from combining isolated population and national health register data

  medRxiv · 2022 · 10.1101/2022.03.03.22271360

• Genetic associations of protein-coding variants in human disease

  Nature · 2022 · 10.1038/s41586-022-04394-w

• A cross-population atlas of genetic associations for 220 human phenotypes

  Nature Genetics · 2021 · https://doi.org/10.1038/s41588-021-00931-x

• Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers

  Nature Medicine · 2020 · https://doi.org/10.1038/s41591-020-0800-0

• The role of polygenic risk and susceptibility genes in breast cancer over the course of life

  Nature Communications · 2020 · 10.1038/s41467-020-19966-5

• Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health

  European Respiratory Journal · 2020 · https://doi.org/10.1183/13993003.03091-2020

• Genetic architecture of human plasma lipidome and its link to cardiovascular disease

  Nature Communications · 2019 · https://doi.org/10.1038/s41467-019-11954-8

• Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

  Molecular Psychiatry · 2018 · 10.1038/s41380-018-0112-7

• Analysis of protein-coding genetic variation in 60,706 humans

  Nature · 2016 · https://doi.org/10.1038/nature19057

• Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

  Nature Neuroscience · 2016 · 10.1038/nn.4267

• Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

  Nature Genetics · 2016 · https://doi.org/10.1038/ng.3598

Current projects

No projects listed.