Area of research
Hematology · Genetics
Research interest
Research interests include Genetic Associations and Epidemiology, Blood Coagulation and Thrombosis Mechanisms, Venous Thromboembolism Diagnosis and Management, and Protease and Inhibitor Mechanisms.
Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes
Multipopulation GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels
Integrative Multiomics in the Lung Reveals a Protective Role of Asporin in Pulmonary Arterial Hypertension
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Post-transcriptional control of haemostatic genes: mechanisms and emerging therapeutic concepts in thrombo-inflammatory disorders
Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomization analysis
Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomisation analysis
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis
Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus
Stroke genetics informs drug discovery and risk prediction across ancestries
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
Cerebral small vessel disease genomics and its implications across the lifespan
Single-Cell Study of Two Rat Models of Pulmonary Arterial Hypertension Reveals Connections to Human Pathobiology and Drug Repositioning
Whole-Blood RNA Profiles Associated with Pulmonary Arterial Hypertension and Clinical Outcome
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease
Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation
Genome wide association analysis in dilated cardiomyopathy reveals two new key players in systolic heart failure on chromosome 3p25.1 and 22q11.23
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen