J Peter van Tintelen
Overview
Explore the profile of J Peter van Tintelen including associated specialties, affiliations and a list of published articles.
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206
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6127
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Recent Articles
1.
Ebert M, de Riva M, Wijnmaalen A, Barge-Schaapveld D, Bootsma M, Hoogendoorn J, et al.
JACC Clin Electrophysiol
. 2025 Mar;
PMID: 40088216
Background: Truncating titin variants (TTNtvs) are the most prevalent cause of inherited dilated cardiomyopathy. Occurrence of different ventricular arrhythmia (VA) subtypes, including premature ventricular complexes (PVCs), nonsustained ventricular tachycardia (NSVT),...
2.
Gigli M, Stolfo D, Barbati G, Graw S, Chen S, Merlo M, et al.
JAMA Cardiol
. 2025 Feb;
PMID: 39937464
Importance: Filamin C truncating variants (FLNCtv) are a rare cause of cardiomyopathy with heterogeneous phenotypic presentations. Despite a high incidence of life-threatening ventricular arrhythmias and sudden cardiac death (SCD), reliable...
3.
Thierry I, Muller S, Baas A, Dooijes D, van Loon R, Schoemaker A, et al.
Neth Heart J
. 2025 Jan;
33(2):46-54.
PMID: 39833651
Introduction: Current family screening approaches in dilated cardiomyopathy (DCM) depend on the presence or absence of a familial genetic variant, in which variant pathogenicity (i.e. benign or pathogenic) classification drives...
4.
Hassanzada F, Jansen M, van Lint F, Bosman L, Schmidt A, Dooijes D, et al.
Circ Genom Precis Med
. 2024 Dec;
17(6):e004561.
PMID: 39689185
Background: founder variants cause hypertrophic cardiomyopathy leading to heart failure and malignant ventricular arrhythmias. Exercise is typically regarded as a risk factor for disease expression although evidence is conflicting. Stratifying...
5.
Muller S, Asatryan B, Murray B, Tichnell C, Cox M, Amin A, et al.
Circ Arrhythm Electrophysiol
. 2024 Dec;
18(1):e013144.
PMID: 39670315
No abstract available.
6.
Salavati A, van der Wilt C, Calore M, van Es R, Rampazzo A, van der Harst P, et al.
Curr Heart Fail Rep
. 2024 Dec;
22(1):5.
PMID: 39661213
Purpose Of Review: This review aims to explore the emerging potential of artificial intelligence (AI) in refining risk prediction, clinical diagnosis, and treatment stratification for cardiomyopathies, with a specific emphasis...
7.
Muller S, Bertoli G, Wang J, Gasperetti A, Cox M, Calkins H, et al.
J Cardiovasc Electrophysiol
. 2024 Dec;
PMID: 39623588
Arrhythmogenic cardiomyopathy (ACM) is a genetically heterogeneous inherited cardiomyopathy with an estimated prevalence of 1:5000-10 000 that predisposes patients to life-threatening ventricular arrhythmias (VA) and sudden cardiac death (SCD). ACM...
8.
Rekker L, Renkema E, Hilverda F, van Laake L, Doevendans P, Sluijter J, et al.
Heart Rhythm O2
. 2024 Nov;
5(10):747-749.
PMID: 39524059
No abstract available.
9.
Tuijnenburg F, Proost V, Thollet A, Barc J, Groffen A, Veerman C, et al.
Heart Rhythm
. 2024 Nov;
PMID: 39491571
Background: The long-term prognosis of patients with a loss-of-function variant in the cardiac sodium channel gene SCN5A is unknown. Objective: This study aimed to evaluate the long-term arrhythmic risk in...
10.
Gasperetti A, Carrick R, Protonotarios A, Murray B, Laredo M, van der Schaaf I, et al.
Eur Heart J
. 2024 Sep;
46(4):362-376.
PMID: 39288222
Background And Aims: Pathogenic variants in the desmoplakin (DSP) gene are associated with the development of a distinct arrhythmogenic cardiomyopathy phenotype not fully captured by either dilated cardiomyopathy (DCM), non-dilated...