University of Helsinki
Raynaud's Syndrome Genetics, Biology Uncovered in GWAS, Functional Study
A large genome-wide association study and meta-analysis identified eight Raynaud's syndrome-related loci, pointing to multiple proposed disease mechanisms.
Study Finds Genetic, Nongenetic Ties to Nonresponse Behavior in Surveys
Using UK Biobank and other data, researchers unearthed factors coinciding with nonresponse to behavioral survey questions, providing nuance to genetic association analyses.
Uterine Leiomyoma Risk Linked to Inherited SRCAP Complex Mutations
After identifying uterine leiomyoma-associated germline variants in SRCAP complex genes in UK Biobank participants, researchers tracked down similar risk variants in Finnish individuals.
Study Traces Maternal Impacts on Developing Infant Gut Microbe, Metabolite Features
Researchers identified horizontal gene transfer between maternal and infant microbiomes, as well as other factors contributing to infant gut microbiome development.
Genetic Risk Factors for Disease Contribute to Decrease in Healthy Life Years
A team led by researchers at the University of Helsinki examined the contribution of rare and common genetic variants to changes in disability-adjusted life years.