Maarten P van den Berg
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Explore the profile of Maarten P van den Berg including associated specialties, affiliations and a list of published articles.
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Recent Articles
11.
de Winter J, Bouman K, Strom J, Methawasin M, Jongbloed J, van der Roest W, et al.
Hum Mutat
. 2022 Nov;
43(12):1860-1865.
PMID: 36335629
KBTBD13 variants cause nemaline myopathy type 6 (NEM6). The majority of NEM6 patients harbors the Dutch founder variant, c.1222C>T, p.Arg408Cys (KBTBD13 p.R408C). Although KBTBD13 is expressed in cardiac muscle, cardiac...
12.
Carrick R, Te Riele A, Gasperetti A, Bosman L, Muller S, Pendleton C, et al.
Circ Arrhythm Electrophysiol
. 2022 Oct;
15(11):e011207.
PMID: 36315818
Background: The arrhythmogenic right ventricular cardiomyopathy (ARVC) risk calculator stratifies risk for incident sustained ventricular arrhythmias (VA) at the time of ARVC diagnosis. However, included risk factors change over time,...
13.
Gasperetti A, Carrick R, Costa S, Compagnucci P, Bosman L, Chivulescu M, et al.
Circulation
. 2022 Oct;
146(19):1434-1443.
PMID: 36205131
Background: A novel risk calculator based on clinical characteristics and noninvasive tests that predicts the onset of clinical sustained ventricular arrhythmias (VA) in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC)...
14.
Vermeer M, Andrei D, Marsili L, van Tintelen J, Sillje H, van den Berg M, et al.
Int J Mol Sci
. 2022 Sep;
23(18).
PMID: 36142674
Genetic variants in gene-encoding proteins involved in cell−cell connecting structures, such as desmosomes and gap junctions, may cause a skin and/or cardiac phenotype, of which the combination is called cardiocutaneous...
15.
van Andel M, Graaumans K, Groenink M, Zwinderman A, Van Kimmenade R, Scholte A, et al.
Clin Genet
. 2022 Sep;
102(5):404-413.
PMID: 36059006
Marfan syndrome (MFS) is a connective tissue disorder affecting the cardiovascular, ocular, and skeletal system, which may be accompanied by psychological features. This study aimed to determine the prevalence of...
16.
de Brouwer R, Bosman L, Gripenstedt S, Wilde A, van den Berg M, van Tintelen J, et al.
Heart Rhythm
. 2022 Jun;
19(10):1659-1665.
PMID: 35688345
Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by risk of malignant ventricular arrhythmia (VA). ARVC is diagnosed using an array of clinical tests in the consensus-based Task Force Criteria...
17.
Cadrin-Tourigny J, Bosman L, Nozza A, Wang W, Tadros R, Bhonsale A, et al.
Eur Heart J
. 2022 Apr;
43(32):e1-e9.
PMID: 35441664
Aims: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC) is characterized by ventricular arrhythmias (VAs) and sudden cardiac death (SCD). We aimed to develop a model for individualized prediction of incident VA/SCD in...
18.
Roudijk R, Verheul L, Bosman L, Bourfiss M, Breur J, Slieker M, et al.
JACC Clin Electrophysiol
. 2022 Mar;
8(3):306-318.
PMID: 35331425
Objectives: The goal of this study was to describe characteristics, cascade screening results, and predictors of adverse outcome in pediatric-onset arrhythmogenic right ventricular cardiomyopathy (ARVC). Background: Although ARVC is increasingly...
19.
Vermeer M, Andrei D, Kramer D, Nijenhuis A, Hoedemaekers Y, Westers H, et al.
Exp Dermatol
. 2022 Mar;
31(6):970-979.
PMID: 35325485
Desmoplakin (DP) is an important component of desmosomes, essential in cell-cell connecting structures in stress-bearing tissues. Over the years, many hundreds of pathogenic variants in DSP have been associated with...
20.
van Andel M, Groenink M, van den Berg M, Timmermans J, Scholte A, Mulder B, et al.
Clin Epigenetics
. 2021 Dec;
13(1):217.
PMID: 34895303
Background: Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in the Fibrillin-1 gene (FBN1). Here, we undertook the first epigenome-wide association study (EWAS) in patients with MFS...