Jaap I. Van Waning
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant.
Journal: Circulation. Genomic and precision medicine
Published: December 29, 2022
State-of-the art review: Noncompaction cardiomyopathy in pediatric patients.
Journal: Heart failure reviews
Published: February 15, 2021
A mutation update for the FLNC gene in myopathies and cardiomyopathies.
Journal: Human mutation
Published: December 20, 2019
Diagnostic Cardiovascular Magnetic Resonance Imaging Criteria in Noncompaction Cardiomyopathy and the Yield of Genetic Testing.
Journal: The Canadian journal of cardiology
Published: December 07, 2019
Systematic Review of Genotype-Phenotype Correlations in Noncompaction Cardiomyopathy.
Journal: Journal of the American Heart Association
Published: November 28, 2019
Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy.
Journal: Journal of the American College of Cardiology
Published: July 01, 2018
Reply: Different Outcomes and Additional Gene Testing.
Journal: Journal of the American College of Cardiology
Published: April 03, 2018
Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.
Journal: Journal of the American College of Cardiology
Published: November 22, 2017
A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects.
Journal: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Published: March 02, 2017
Postnatal Outcome of Fetal Left Ventricular Hypertrabeculation/Noncompaction.
Journal: Pediatric cardiology
Published: January 20, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026