Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Genomics and Rare Diseases, Bioinformatics and Genomic Networks, and RNA modifications and cancer.
Translational genomics of osteoarthritis in 1,962,069 individuals
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Novel loci and biomedical consequences of iron homoeostasis variation
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Variants at the Interleukin 1 Gene Locus and Pericarditis
Genetic variants associated with syncope implicate neural and autonomic processes
The sequences of 150,119 genomes in the UK Biobank
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality
rs41291957 controls miR‐143 and miR‐145 expression and impacts coronary artery disease risk
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease
Assessing thyroid cancer risk using polygenic risk scores
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank
Association of Factor V Leiden With Subsequent Atherothrombotic Events
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults
Sequence variants with large effects on cardiac electrophysiology and disease
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events
Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention
Subsequent Event Risk in Individuals With Established Coronary Heart Disease
Integrative Functional Annotation of 52 Genetic Loci Influencing Myocardial Mass Identifies Candidate Regulatory Variants and Target Genes
Genome-wide analysis yields new loci associating with aortic valve stenosis
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits