H. Laivuori | 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)
Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry)
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
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
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
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
Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals
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
New insights into the genetic etiology of Alzheimer's disease and related dementias
Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes
mutation carriers
mutation carriers
mutation carriers
Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease
Sleep apnoea is a risk factor for severe COVID-19
The role of polygenic risk and susceptibility genes in breast cancer over the course of life
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers
Genetic architecture of human plasma lipidome and its link to cardiovascular disease