Roy Straver
Overview
Explore the profile of Roy Straver including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
15
Citations
369
Followers
0
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Recent Articles
1.
Marcozzi A, Jager M, Elferink M, Straver R, van Ginkel J, Peltenburg B, et al.
NPJ Genom Med
. 2023 Jun;
8(1):12.
PMID: 37286583
No abstract available.
2.
Marcozzi A, Jager M, Elferink M, Straver R, van Ginkel J, Peltenburg B, et al.
NPJ Genom Med
. 2021 Dec;
6(1):106.
PMID: 34887408
Levels of circulating tumor DNA (ctDNA) in liquid biopsies may serve as a sensitive biomarker for real-time, minimally-invasive tumor diagnostics and monitoring. However, detecting ctDNA is challenging, as much fewer...
3.
Mes S, Brink A, Sistermans E, Straver R, Oudejans C, Poell J, et al.
Oral Oncol
. 2020 Jun;
109:104852.
PMID: 32590298
Introduction: Tumor-specific genetic aberrations in cell-free DNA (cfDNA) from plasma are promising biomarkers for diagnosis of recurrent head and neck squamous cell carcinoma (HNSCC). However, the sensitivity when using somatic...
4.
Vermeulen C, Allahyar A, Bouwman B, Krijger P, Verstegen M, Geeven G, et al.
Nat Protoc
. 2020 Jan;
15(2):364-397.
PMID: 31932773
We present the experimental protocol and data analysis toolbox for multi-contact 4C (MC-4C), a new proximity ligation method tailored to study the higher-order chromatin contact patterns of selected genomic sites....
5.
Nieboer M, Dorssers L, Straver R, Looijenga L, de Ridder J
PLoS One
. 2018 Nov;
13(11):e0208002.
PMID: 30496231
Most tumors are composed of a heterogeneous population of subclones. A more detailed insight into the subclonal evolution of these tumors can be helpful to study progression and treatment response....
6.
Allahyar A, Vermeulen C, Bouwman B, Krijger P, Verstegen M, Geeven G, et al.
Nat Genet
. 2018 Jul;
50(8):1151-1160.
PMID: 29988121
Chromatin folding contributes to the regulation of genomic processes such as gene activity. Existing conformation capture methods characterize genome topology through analysis of pairwise chromatin contacts in populations of cells...
7.
Amsterdam K, Straver R, van Maarle M, Knegt A, Van Opstal D, Sleutels F, et al.
Genet Med
. 2018 Mar;
20(11):1472-1476.
PMID: 29493577
Purpose: Using genome-wide noninvasive prenatal screening (NIPS), we detected a 20-megabase specific deletion starting at 10q25 in eight pregnancies. The deletion could not be confirmed by invasive testing. Since all...
8.
van Beek D, Straver R, Weiss M, Boon E, Amsterdam K, Oudejans C, et al.
Prenat Diagn
. 2017 Dec;
37(12):1266-1267.
PMID: 29271028
No abstract available.
9.
Straver R, Weiss M, Waisfisz Q, Sistermans E, Reinders M
Eur J Hum Genet
. 2017 Dec;
25(12):1354-1363.
PMID: 29255179
In clinical genetics, detection of single nucleotide polymorphisms (SNVs) as well as copy number variations (CNVs) is essential for patient genotyping. Obtaining both CNV and SNV information from WES data...
10.
Van Opstal D, van Maarle M, Lichtenbelt K, Weiss M, Schuring-Blom H, Bhola S, et al.
Genet Med
. 2017 Nov;
20(5):480-485.
PMID: 29121006
PurposeNoninvasive prenatal screening (NIPS) using cell-free DNA in maternal blood is highly sensitive for detecting fetal trisomies 21, 18, and 13. Using a genome-wide approach, other chromosome anomalies can also...