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1
A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

von Walsh, R ; Mauleekoonphairoj, J ; Mengarelli, I ; et al.
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2
Device-related Complications in Transvenous Versus Subcutaneous Defibrillator Therapy During Long-term Follow-up: the PRAETORIAN-XL Trial.

von Olde Nordkamp, LRA ; de Veld, JA ; Ghani, A ; et al.
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3
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

von Tadros, R ; Zheng, SL ; Grace, C ; et al.
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4
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings

von Zheng, SL ; Jurgens, SJ ; Mcgurk, KA ; et al.
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5
Predictive value of the PRAETORIAN score for defibrillation test success in patients with subcutaneous ICD: A subanalysis of the PRAETORIAN-DFT trial

von Knops, RE ; El-Chami, MF ; Marquie, C ; et al.

Heart Rhythm (2024) (In press).

Schlagworte: Defibrillation testing; PRAETORIAN score; Subcutaneous ICD; Transvenous ICD; Ventricular arrhythmia
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6
Influence of stressful life events and personality traits on PLN cardiomyopathy severity: an exploratory study

von van Drie, E ; Taal, SEL ; Schmidt, AF ; et al.

EP Europace , 26 (1) , Article euad368. (2024)

Schlagworte: Arrhythmogenic cardiomyopathy; Distressed personality; Personality traits; Phospholamban; Stressful life events; Humans; Personality; Stress; Psychological; Cardiomyopathies
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7
Recreational and Occupational Physical Activity and Risk of Adverse Events in Truncating MYBPC3 Founder Variant Carriers

von Hassanzada, F ; Jansen, M ; Van Lint, FHM ; et al.

Circulation: Genomic and Precision Medicine , 17 (6) , Article e004561. (2024)

Schlagworte: Arrhythmias; cardiac; cardiomyopathy; hypertrophic; heart failure; hypertrophy; left ventricular; stroke volume
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8
Inappropriate Therapy and Shock Rates Between the Subcutaneous and Transvenous Implantable Cardiac Defibrillator: A Secondary Analysis of the PRAETORIAN Trial.

von Olde Nordkamp, LRA ; Pepplinkhuizen, S ; Ghani, A ; et al.
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9
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience.

von Jurgens, SJ ; Rämö, JT ; Kramarenko, DR ; et al.
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10
aTrial arrhythmias in inhEriTed aRrhythmIa Syndromes: results from the TETRIS study.

von Conte, G ; Bergonti, M ; Probst, V ; et al.
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11
Quality of Life in Subcutaneous or Transvenous Implantable Cardioverter-Defibrillator Patients: A Secondary Analysis of the PRAETORIAN Trial.

von Knops, RE ; de Veld, JA ; Ghani, A ; et al.
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12
Mitral annular disjunction in idiopathic ventricular fibrillation patients: just a bystander or a potential cause?

von Verheul, LM ; Guglielmo, M ; Groeneveld, SA ; et al.
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13
Insights into adherence to medication and lifestyle recommendations in an international cohort of patients with catecholaminergic polymorphic ventricular tachycardia.

von Peltenburg, PJ ; van den Heuvel, LM ; Kallas, D ; et al.
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14
Maturation of hiPSC-derived cardiomyocytes promotes adult alternative splicing of SCN5A and reveals changes in sodium current associated with cardiac arrhythmia

von Campostrini G ; Kosmidis G ; Ward-van Oostwaard D ; et al.
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15
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance

von Copier, JS ; Bootsma, M ; Ng, CA ; et al.

urn:ISSN:0964-6906 ; urn:ISSN:1460-2083 ; Human Molecular Genetics, 32, 7, 1072-1082

Schlagworte: 31 Biological Sciences; 3105 Genetics; Genetics; Pediatric Research Initiative; Heart Disease; Congenital Heart Disease; Rare Diseases; Cardiovascular; Humans; Long QT Syndrome; Ether-A-Go-Go Potassium Channels; HEK293 Cells; Penetrance; Heart; ERG1 Potassium Channel; anzsrc-for: 31 Biological Sciences; anzsrc-for: 3105 Genetics; anzsrc-for: 06 Biological Sciences; anzsrc-for: 11 Medical and Health Sciences
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16
Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy

von Muller, SA ; Gasperetti, A ; Bosman, LP ; et al.

Journal of the American College of Cardiology , 82 (3) pp. 214-225. (2023)

Schlagworte: ARVC; family screening; predictors; screening interval; ventricular arrhythmia
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17
Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathy

von van Lint, FHM ; Hassanzada, F ; Verstraelen, TE ; et al.

Netherlands Heart Journal , 31 (7-8) pp. 291-299. (2023)
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18
A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients

von Nagyova, E ; Hoorntje, ET ; Rijdt, WPT ; et al.

Journal of Cardiovascular Translational Research (2023) (In press).

Schlagworte: ARVC; Arrhythmia; Composite endpoint; Desmosomal genes; Genetics; Multiple variants
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19
Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers

von Jansen, Mark ; Schmidt, AF ; Jans, JJM ; et al.

Journal of Cardiovascular Translational Research , 16 pp. 1267-1275. (2023)

Schlagworte: Acylcarnitine; Biomarker; Hypertrophic Cardiomyopathy; MYBPC3; Metabolism
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20
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.

von Crotti, L ; Spazzolini, C ; Nyegaard, M ; et al.
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21
Subepicardial Cardiomyopathy: A Disease Underlying J-Wave Syndromes and Idiopathic Ventricular Fibrillation.

von Miles, C ; Boukens, BJ ; Scrocco, C ; et al.
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22
Long-Term Outcomes of Brugada Substrate Ablation: A Report from BRAVO (Brugada Ablation of VF Substrate Ongoing Multicenter Registry).

von Nademanee, K ; Chung, F-P ; Sacher, F ; et al.
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23
Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy

von Roudijk, RW ; Verheul, L ; Bosman, LP ; et al.

JACC: Clinical Electrophysiology , 8 (3) pp. 306-318. (2022)

Schlagworte: Science & Technology; Life Sciences & Biomedicine; Cardiac & Cardiovascular Systems; Cardiovascular System & Cardiology; arrhythmogenic right ventricular cardiomyopathy; cascade screening; genetics; heart failure; pediatric-onset; sudden cardiac death; ventricular tachycardia; TASK-FORCE CRITERIA; CHILDREN; DIAGNOSIS; RISK; ADOLESCENTS; AGE
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24
Device-related complications in subcutaneous versus transvenous ICD: a secondary analysis of the PRAETORIAN trial

von Knops, RE ; Pepplinkhuizen, S ; Delnoy, PPHM ; et al.
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25
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.

von Wilde, AAM ; Semsarian, C ; Márquez, MF ; et al.
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