Marja W Wessels
Overview
Explore the profile of Marja W Wessels including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
64
Citations
2095
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Richer J, Velchev J, Goobie S, Boswell-Patterson C, van de Laar I, Verhagen J, et al.
J Med Genet
. 2025 Jan;
62(3):199-205.
PMID: 39746778
Background: Individuals harbouring pathogenic variants are at risk for aneurysms/dissections throughout the arterial tree. Based on prior reports of sex differences in thoracic aortic aneurysm/dissection, we investigated the sexual dimorphism...
2.
van den Bersselaar L, Verhagen J, Bekkers J, Kempers M, Houweling A, Baars M, et al.
Genet Med
. 2023 Dec;
26(2):101024.
PMID: 38085215
No abstract available.
3.
Schoonvelde S, Ruijmbeek C, Hirsch A, van Slegtenhorst M, Wessels M, von der Thusen J, et al.
Heart Rhythm
. 2023 Aug;
20(11):1512-1521.
PMID: 37562486
Background: Dilated cardiomyopathy (DCM) can be caused by truncating variants in the filamin C gene (FLNC). A new pathogenic FLNC variant, c.6864_6867dup, p.(Val2290Argfs∗23), was recently identified in Dutch patients with...
4.
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)...
5.
ONeill M, Chen S, Rumping L, Johnson R, van Slegtenhorst M, Glazer A, et al.
Heart Rhythm
. 2023 May;
20(8):1158-1166.
PMID: 37164047
Background: Truncating variants in filamin C (FLNC) can cause arrhythmogenic cardiomyopathy (ACM) through haploinsufficiency. Noncanonical splice-altering variants may contribute to this phenotype. Objective: The purpose of this study was to...
6.
Huang Y, Lemire G, Briere L, Liu F, Wessels M, Wang X, et al.
Am J Hum Genet
. 2022 Nov;
109(11):2092.
PMID: 36332614
No abstract available.
7.
Huang Y, Lemire G, Briere L, Liu F, Wessels M, Wang X, et al.
Am J Hum Genet
. 2022 Sep;
109(10):1923-1931.
PMID: 36067766
MTSS2, also known as MTSS1L, binds to plasma membranes and modulates their bending. MTSS2 is highly expressed in the central nervous system (CNS) and appears to be involved in activity-dependent...
8.
van den Bersselaar L, Verhagen J, Bekkers J, Kempers M, Houweling A, Baars M, et al.
Genet Med
. 2022 Sep;
24(10):2112-2122.
PMID: 36053285
Purpose: Heterozygous pathogenic/likely pathogenic (P/LP) variants in the ACTA2 gene confer a high risk for thoracic aortic aneurysms and aortic dissections. This retrospective multicenter study elucidates the clinical outcome of...
9.
The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations
van Woerden G, Senden R, de Konink C, Trezza R, Baban A, Bassetti J, et al.
Hum Mutat
. 2022 Jun;
43(10):1377-1395.
PMID: 35730652
Mitogen-activated protein 3 kinase 7 (MAP3K7) encodes the ubiquitously expressed transforming growth factor β-activated kinase 1, which plays a crucial role in many cellular processes. Mutationsin the MAP3K7 gene have...
10.
Scala M, Drouot N, MacLennan S, Wessels M, Krygier M, Pavinato L, et al.
Hum Mutat
. 2022 May;
43(9):1299-1313.
PMID: 35607920
Alternative splicing (AS) is crucial for cell-type-specific gene transcription and plays a critical role in neuronal differentiation and synaptic plasticity. De novo frameshift variants in NOVA2, encoding a neuron-specific key...