Marianne Bootsma
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Explore the profile of Marianne Bootsma including associated specialties, affiliations and a list of published articles.
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62
Citations
577
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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.
Chua A, Laenens D, Sarrazyn C, Lopez-Santi M, Nabeta T, Myagmardorj R, et al.
Am J Cardiol
. 2025 Jan;
241:61-68.
PMID: 39805356
Despite arrhythmogenic right ventricular cardiomyopathy (ARVC) being predominantly a right ventricular (RV) disease, concomitant left ventricular (LV) involvement has been recognized. ARVC is diagnosed by the RV-centric 2010 Task Force...
3.
Verheul L, Hoeksema W, Groeneveld S, Mulder B, Bootsma M, Alings M, et al.
Heart Rhythm
. 2024 Mar;
21(10):1779-1786.
PMID: 38493994
Background: Current cohorts of patients with idiopathic ventricular fibrillation (IVF) primarily include adult-onset patients. Underlying causes of sudden cardiac arrest vary with age; therefore, underlying causes and disease course may...
4.
Pham C, Koopmann T, Vinocur J, Blom N, Silbiger V, Mittal K, et al.
Clin Genet
. 2024 Mar;
106(1):37-46.
PMID: 38424693
Genetic missense variants in TNNI3K, encoding troponin-I interacting kinase, have been associated with dilated cardiomyopathy (DCM) and observed in families with supraventricular tachycardias (SVT). Previously, a family harboring the TNNI3K-c.1615A ...
5.
Verheul L, van der Ree M, Groeneveld S, Mulder B, Christiaans I, Kapel G, et al.
Europace
. 2023 Nov;
25(11).
PMID: 37967257
Aims: During the diagnostic work-up of patients with idiopathic ventricular fibrillation (VF), next-generation sequencing panels can be considered to identify genotypes associated with arrhythmias. However, consensus for gene panel testing...
6.
Feijen M, Egorova A, Kuijken T, Bootsma M, Schalij M, van Erven L
J Clin Med
. 2023 Sep;
12(17).
PMID: 37685719
Implantable cardioverter defibrillators (ICDs) significantly contribute to the prevention of sudden cardiac death in selected patients. However, it is essential to identify those who are likely to not have benefit...
7.
Bos T, Piers S, Wessels M, Houweling A, Bokenkamp R, Bootsma M, et al.
Neth Heart J
. 2023 Jul;
31(7-8):315-323.
PMID: 37505369
Background: The arrhythmogenic cardiomyopathy (ACM) phenotype, with life-threatening ventricular arrhythmias and heart failure, varies according to genetic aetiology. We aimed to characterise the phenotype associated with the variant c.1211dup (p.Val406Serfs*4)...
8.
Groeneveld S, Verheul L, van der Ree M, Mulder B, Scholten M, Alings M, et al.
JACC Clin Electrophysiol
. 2023 Feb;
9(3):345-355.
PMID: 36752476
Background: Idiopathic ventricular fibrillation (iVF) is a diagnosis of exclusion. Systematic diagnostic testing is important to exclude alternative causes for VF. The early use of "high yield" testing, including cardiac...
9.
Hoorntje E, Burns C, Marsili L, Corden B, Parikh V, Meerman G, et al.
Circ Genom Precis Med
. 2022 Dec;
16(1):e003672.
PMID: 36580316
Background: Truncating variants in desmoplakin (tv) are an important cause of arrhythmogenic cardiomyopathy; however the genetic architecture and genotype-specific risk factors are incompletely understood. We evaluated phenotype, risk factors for...
10.
Copier J, Bootsma M, Ng C, Wilde A, Bertels R, Bikker H, et al.
Hum Mol Genet
. 2022 Oct;
32(7):1072-1082.
PMID: 36269083
Background: Variants in KCNH2, encoding the human ether a-go-go (hERG) channel that is responsible for the rapid component of the cardiac delayed rectifier K+ current (IKr), are causal to long...