Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Metabolomics and Mass Spectrometry Studies, Diet and metabolism studies, and Diabetes, Cardiovascular Risks, and Lipoproteins.
FinnGen provides genetic insights from a well-phenotyped isolated population
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
OTTERS: a powerful TWAS framework leveraging summary-level reference data
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
DNA methylation and lipid metabolism: an EWAS of 226 metabolic measures
Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke: Meta-analysis From 7 Prospective Cohorts.
A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease
A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase
Mergeomics: multidimensional data integration to identify pathogenic perturbations to biological systems
Metabolic Characterization of a Rare Genetic Variation Within <i>APOC3</i> and Its Lipoprotein Lipase–Independent Effects
Insomnia does not mediate or modify the association between MTNR1B risk variant rs10830963 and glucose levels
The impact of low-frequency and rare variants on lipid levels
Cell Specific eQTL Analysis without Sorting Cells
Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty
High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms
Genetic Determinants of Circulating Interleukin-1 Receptor Antagonist Levels and Their Association With Glycemic Traits
Systematic identification of trans eQTLs as putative drivers of known disease associations
Identification of seven loci affecting mean telomere length and their association with disease