Arthur van den Wijngaard
Overview
Explore the profile of Arthur van den Wijngaard including associated specialties, affiliations and a list of published articles.
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64
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1518
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Recent Articles
1.
Hops W, Weiss M, Derks R, Galbany J, Ouden A, van den Heuvel S, et al.
Am J Hum Genet
. 2025 Jan;
112(2):450-456.
PMID: 39809270
Clinical short-read exome and genome sequencing approaches have positively impacted diagnostic testing for rare diseases. Yet, technical limitations associated with short reads challenge their use for the detection of disease-associated...
2.
Stroeks S, Henkens M, Dominguez F, Merlo M, Hellebrekers D, Gonzalez-Lopez E, et al.
JACC Heart Fail
. 2024 Oct;
13(1):133-145.
PMID: 39425739
Background: Systemic immune-mediated diseases (SIDs) are a well-known cause of dilated cardiomyopathy (DCM), a cardiac phenotype influenced by genetic predispositions and environmental factors. Objectives: This study sought to examine if...
3.
Janssen A, Koeck R, Essers R, Cao P, van Dijk W, Drusedau M, et al.
Nat Commun
. 2024 Sep;
15(1):7164.
PMID: 39223156
High-throughput sequencing technologies have increasingly led to discovery of disease-causing genetic variants, primarily in postnatal multi-cell DNA samples. However, applying these technologies to preimplantation genetic testing (PGT) in nuclear or...
4.
Loid M, Obukhova D, Kask K, Apostolov A, Meltsov A, Tserpelis D, et al.
Hum Reprod Open
. 2024 Aug;
2024(3):hoae048.
PMID: 39185250
Study Question: What changes occur in the endometrium during aging, and do they impact fertility? Summary Answer: Both the transcriptome and cellular composition of endometrial samples from women of advanced...
5.
Verdonschot J, Hellebrekers D, van Empel V, Heijligers M, de Munnik S, Coonen E, et al.
Circ Genom Precis Med
. 2024 Mar;
17(2):e004416.
PMID: 38516780
Background: Preimplantation genetic testing (PGT) is a reproductive technology that selects embryos without (familial) genetic variants. PGT has been applied in inherited cardiac disease and is included in the latest...
6.
Schobers G, Derks R, Ouden A, Swinkels H, van Reeuwijk J, Bosgoed E, et al.
Genome Med
. 2024 Feb;
16(1):32.
PMID: 38355605
Background: To diagnose the full spectrum of hereditary and congenital diseases, genetic laboratories use many different workflows, ranging from karyotyping to exome sequencing. A single generic high-throughput workflow would greatly...
7.
Essers R, Lebedev I, Kurg A, Fonova E, Stevens S, Koeck R, et al.
Nat Med
. 2023 Nov;
29(12):3233-3242.
PMID: 37996709
Pregnancy loss is often caused by chromosomal abnormalities of the conceptus. The prevalence of these abnormalities and the allocation of (ab)normal cells in embryonic and placental lineages during intrauterine development...
8.
Sikking M, Stroeks S, Henkens M, Raafs A, Cossins B, van Deuren R, et al.
JACC Heart Fail
. 2023 Aug;
12(5):905-914.
PMID: 37638520
Background: Clonal hematopoiesis (CH) gives rise to mutated leukocyte clones that induce cardiovascular inflammation and thereby impact the disease course in atherosclerosis and ischemic heart failure. CH of indeterminate potential...
9.
Stroeks S, Hellebrekers D, Claes G, Krapels I, Henkens M, Sikking M, et al.
Eur J Hum Genet
. 2023 May;
31(7):776-783.
PMID: 37198425
It was previously suggested that increasing the number of genes on diagnostic gene panels could increase the genetic yield in patient with dilated cardiomyopathy (DCM). We explored the diagnostic and...
10.
Verdonschot J, Wang P, Derks K, Adriaens M, Stroeks S, Henkens M, et al.
JACC Basic Transl Sci
. 2023 May;
8(4):406-418.
PMID: 37138803
Dilated cardiomyopathy is a heterogeneous disease characterized by multiple genetic and environmental etiologies. The majority of patients are treated the same despite these differences. The cardiac transcriptome provides information on...