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Publicaties

Cascade genetic counseling and testing in hereditary syndromes: inherited cardiovascular disease as a model: a narrative review

Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers

Genetic Burden of TNNI3K in Diagnostic Testing of Patients with Dilated Cardiomyopathy and Supraventricular Arrhythmias

Lymphedema as first clinical presentation of Cantu Syndrome: reversed phenotyping after identification of gain-of-function variant in ABCC9

Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study

Predicting personal cardiovascular disease risk based on family health history: Development of expert-based family criteria for the general population

Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance

The genetic basis of apparently idiopathic ventricular fibrillation: A retrospective overview

Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants

A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial

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