Christiaan C Veerman
Overview
Explore the profile of Christiaan C Veerman 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
14
Citations
459
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
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...
2.
Krijger Juarez C, Sequeira V, van den Boogaard M, Veerman C, Hoetjes N, Poel E, et al.
Heart Rhythm
. 2024 Feb;
21(7):1173-1175.
PMID: 38382684
No abstract available.
3.
Marchal G, Jouni M, Chiang D, Perez-Hernandez M, Podliesna S, Yu N, et al.
Circ Res
. 2021 Jun;
129(3):349-365.
PMID: 34092082
[Figure: see text].
4.
Veerman C, Mengarelli I, Koopman C, Wilders R, van Amersfoorth S, Bakker D, et al.
Dis Model Mech
. 2019 Jun;
12(7).
PMID: 31208990
Mutations in , encoding the G-protein β5 subunit (Gβ5), have recently been linked to a multisystem disorder that includes severe bradycardia. Here, we investigated the mechanism underlying bradycardia caused by...
5.
Verkerk A, Veerman C, Zegers J, Mengarelli I, Bezzina C, Wilders R
Int J Mol Sci
. 2017 Sep;
18(9).
PMID: 28867785
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) hold great promise for studying inherited cardiac arrhythmias and developing drug therapies to treat such arrhythmias. Unfortunately, until now, action potential (AP) measurements...
6.
Veerman C, Wilders R, Wilde A, Coronel R, Remme C, Verkerk A, et al.
Circ Res
. 2017 Aug;
121(5):e21.
PMID: 28819042
No abstract available.
7.
Veerman C, Mengarelli I, Lodder E, Kosmidis G, Bellin M, Zhang M, et al.
J Am Heart Assoc
. 2017 Jul;
6(7).
PMID: 28739862
Background: Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) can recapitulate features of ion channel mutations causing inherited rhythm disease. However, the lack of maturity of these cells is considered a...
8.
Veerman C, Podliesna S, Tadros R, Lodder E, Mengarelli I, de Jonge B, et al.
Circ Res
. 2017 Jun;
121(5):537-548.
PMID: 28637782
Rationale: Genome-wide association studies previously identified an association of rs9388451 at chromosome 6q22.3 (near ) with Brugada syndrome. The causal gene and underlying mechanism remain unresolved. Objective: We used an...
9.
Kosmidis G, Veerman C, Casini S, Verkerk A, van de Pas S, Bellin M, et al.
Circ Arrhythm Electrophysiol
. 2016 Oct;
9(11).
PMID: 27784737
Background: Several compounds have been reported to induce translational readthrough of premature stop codons resulting in the production of full-length protein by interfering with ribosomal proofreading. Here we examined the...
10.
Veerman C, Mengarelli I, Guan K, Stauske M, Barc J, Tan H, et al.
Sci Rep
. 2016 Aug;
6:30967.
PMID: 27485484
Brugada syndrome (BrS) is a rare cardiac rhythm disorder associated with sudden cardiac death. Mutations in the sodium channel gene SCN5A are found in ~20% of cases while mutations in...