Area of research
Genetics · Cardiology and Cardiovascular Medicine
Research interest
Research interests include Genetic Associations and Epidemiology, Cardiac electrophysiology and arrhythmias, Genomics and Rare Diseases, and Atrial Fibrillation Management and Outcomes.
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization
<i>ABO</i> O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease
Association of <i>FADS1/2</i> Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis
Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome
Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants
Comparison of HLA allelic imputation programs
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough
CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies