A. Malarstig | Turku Hypertension Center

Latest

Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
FinnGen provides genetic insights from a well-phenotyped isolated population
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
The genomics of heart failure: design and rationale of the HERMES consortium
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
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
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
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Genetic architecture of human plasma lipidome and its link to cardiovascular disease