Turku Hypertension Center
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L. Kallio
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NTHL1 is a recessive cancer susceptibility gene
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
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
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
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
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
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