Daniela Q C M Barge-Schaapveld

Claudia A L Ruivenkamp 6 collaborations

Arthur A M Wilde 6 collaborations

Annette F Baas 5 collaborations

Tamara T Koopmann 5 collaborations

Marianne Bootsma 5 collaborations

Elisabeth M Lodder 5 collaborations

Imke Christiaans 5 collaborations

J Peter van Tintelen 5 collaborations

Emmelien Aten 4 collaborations

Cacha M P C D Peeters-Scholte 4 collaborations

Jan D H Jongbloed 4 collaborations

Ingrid P C Krapels 4 collaborations

Connie R Bezzina 4 collaborations

Arjan C Houweling 4 collaborations

Dennis Dooijes 4 collaborations

Emilia K Bijlsma 3 collaborations

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Yvonne Hilhorst-Hofstee 3 collaborations

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Leander Beekman 3 collaborations

None None 3 collaborations

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Thomas H Sharp 1 collaboration

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Victoria Harrison 1 collaboration

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Daniela Q C M Barge-Schaapveld

Affiliations

Publications (31)

Correction: Putting genome-wide sequencing in neonates into perspective.

Case series, chemotherapy-induced cardiomyopathy: mind the family history!

Distinct Metabolomic Signatures in Preclinical and Obstructive Hypertrophic Cardiomyopathy.

Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.

Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service.

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardia.

Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants.

Identification of known and unknown genes associated with mitral valve prolapse using an exome slice methodology.

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome?

Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification.

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

The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant.

Germline variant affecting p53β isoforms predisposes to familial cancer.

Mortality Risk Associated With Truncating Founder Mutations in Titin.

Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.

Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort.

Genetic Burden of

The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview.

Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (

Atypical Progeria Primarily Manifesting as Premature Cardiac Valvular Disease Segregates with

Pathogenic effect of a TGFBR1 mutation in a family with Loeys-Dietz syndrome.

GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum.

Putting genome-wide sequencing in neonates into perspective.

Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant.

A mutation update for the FLNC gene in myopathies and cardiomyopathies.

Characterization of Degenerative Mitral Valve Disease: Differences between Fibroelastic Deficiency and Barlow's Disease.

Consolidation of the clinical and genetic definition of a

Case report: challenges in monitoring and treatment of anthracycline induced cardiotoxicity in young adults with osteosarcoma.

Genetic variant in the

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