Area of research
Cardiology and Cardiovascular Medicine · Pulmonary and Respiratory Medicine
Research interest
Research interests include Medicine, Internal medicine, Biology, Genetics, Cardiology, and Hypertrophic cardiomyopathy.
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants
Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients
Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies
Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants
Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population
Evaluation of the cardiac amyloidosis clinical pathway implementation: a real-world experience
Blood-Based Biomarkers for the Prediction of Hypertrophic Cardiomyopathy Prognosis: A Systematic Review and Meta-Analysis
Automatic Identification of Patients With Unexplained Left Ventricular Hypertrophy in Electronic Health Record Data to Improve Targeted Treatment and Family Screening
Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification
Automatic multilabel detection of ICD10 codes in Dutch cardiology discharge letters using neural networks
Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations
Diagnosis and Risk Prediction of Dilated Cardiomyopathy in the Era of Big Data and Genomics
Genotype-phenotype correlation in pseudoxanthoma elasticum
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)
A mutation update for the <i>FLNC</i> gene in myopathies and cardiomyopathies
UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking
A mutation update on the LDS-associated genes<i>TGFB2/3</i>and<i>SMAD2/3</i>
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations
Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders
The prevalence of pseudoxanthoma elasticum: Revised estimations based on genotyping in a high vascular risk cohort
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases
Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring
Familial Ehlers‐Danlos syndrome with lethal arterial events caused by a mutation in <i>COL5A1</i>
STRAD pseudokinases regulate axogenesis and LKB1 stability
Statin therapy is associated with improved survival after endovascular and open aneurysm repair
Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism