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• Development and clinical validation of a miniaturized finger probe for bedside hemodynamic monitoring
• NTHL1 is a recessive cancer susceptibility gene
• A FinnGen pilot clinical recall study for Alzheimer's disease
• Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry)
• Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
• The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
• Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals
• Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
• Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study
• Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
• Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity
• Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity
• Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
• FinnGen provides genetic insights from a well-phenotyped isolated population
• Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen
• Association between arterial hypertension and liver outcomes using polygenic risk scores: a population-based study
• Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis
• Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis