Nina Hutri‐Kähönen

X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

Whole blood microRNA levels associate with glycemic status and correlate with target mRNAs in pathways important to type 2 diabetes

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

Vitamin D and cognitive function: A Mendelian randomisation study

Blood hsa-miR-122-5p and hsa-miR-885-5p levels associate with fatty liver and related lipoprotein metabolism—The Young Finns Study

Effect of birth weight on life-course blood pressure levels among children born premature

Continuous and Dichotomous Metabolic Syndrome Definitions in Youth Predict Adult Type 2 Diabetes and Carotid Artery Intima Media Thickness: The Cardiovascular Risk in Young Finns Study

A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure

Blood microRNA profile associates with the levels of serum lipids and metabolites associated with glucose metabolism and insulin resistance and pinpoints pathways underlying metabolic syndrome