F. Vaura | Turku Hypertension Center

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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
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
Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis
Multi-Trait Genetic Analysis Reveals Clinically Interpretable Hypertension Subtypes
Genetic, Molecular, and Cellular Determinants of Sex-Specific Cardiovascular Traits
Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes
Polygenic Risk Scores for Predicting Adverse Outcomes After Coronary Revascularization
Sex Differences in Genetic Risk for Hypertension
The genomics of heart failure: design and rationale of the HERMES consortium
mutation carriers
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection