Wilbert van Workum
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Explore the profile of Wilbert van Workum including associated specialties, affiliations and a list of published articles.
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11
Citations
462
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Recent Articles
1.
Hoogstrate Y, Komor M, Bottcher R, van Riet J, van de Werken H, van Lieshout S, et al.
Gigascience
. 2021 Dec;
10(12).
PMID: 34891161
Background: Fusion genes are typically identified by RNA sequencing (RNA-seq) without elucidating the causal genomic breakpoints. However, non-poly(A)-enriched RNA-seq contains large proportions of intronic reads that also span genomic breakpoints....
2.
Finkers R, van Kaauwen M, Ament K, Burger-Meijer K, Egging R, Huits H, et al.
G3 (Bethesda)
. 2021 Sep;
11(9).
PMID: 34544132
Onion is an important vegetable crop with an estimated genome size of 16 Gb. We describe the de novo assembly and ab initio annotation of the genome of a doubled...
3.
Vrijenhoek T, Kraaijeveld K, Elferink M, de Ligt J, Kranendonk E, Santen G, et al.
Eur J Hum Genet
. 2015 Aug;
23(9):1270.
PMID: 26269248
No abstract available.
4.
Begemann M, Zirn B, Santen G, Wirthgen E, Soellner L, Buttel H, et al.
N Engl J Med
. 2015 Jul;
373(4):349-56.
PMID: 26154720
In humans, mutations in IGF1 or IGF1R cause intrauterine and postnatal growth restriction; however, data on mutations in IGF2, encoding insulin-like growth factor (IGF) II, are lacking. We report an...
5.
Goossens-Beumer I, Oosting J, Corver W, Janssen M, Janssen B, van Workum W, et al.
BMC Genomics
. 2015 Jun;
16:438.
PMID: 26048403
Background: In rectal cancer, total mesorectal excision surgery combined with preoperative (chemo)radiotherapy reduces local recurrence rates but does not improve overall patient survival, a result that may be due to...
6.
Vrijenhoek T, Kraaijeveld K, Elferink M, de Ligt J, Kranendonk E, Santen G, et al.
Eur J Hum Genet
. 2015 Jan;
23(9):1142-50.
PMID: 25626705
Implementation of next-generation DNA sequencing (NGS) technology into routine diagnostic genome care requires strategic choices. Instead of theoretical discussions on the consequences of such choices, we compared NGS-based diagnostic practices...
7.
Barrett J, Taylor J, Bright C, Harland M, Dunning A, Akslen L, et al.
Int J Cancer
. 2014 Aug;
136(6):1351-60.
PMID: 25077817
At least 17 genomic regions are established as harboring melanoma susceptibility variants, in most instances with genome-wide levels of significance and replication in independent samples. Based on genome-wide single nucleotide...
8.
Polko J, Temanni M, van Zanten M, van Workum W, Iburg S, Pierik R, et al.
Mol Plant
. 2012 Mar;
5(4):948-50.
PMID: 22461665
No abstract available.
9.
Hestand M, Klingenhoff A, Scherf M, Ariyurek Y, Ramos Y, van Workum W, et al.
Nucleic Acids Res
. 2010 Jul;
38(16):e165.
PMID: 20615900
Next-generation sequencing is excellently suited to evaluate the abundance of mRNAs to study gene expression. Here we compare two alternative technologies, cap analysis of gene expression (CAGE) and serial analysis...
10.
Bishop D, Demenais F, Iles M, Harland M, Taylor J, Corda E, et al.
Nat Genet
. 2009 Jul;
41(8):920-5.
PMID: 19578364
We report a genome-wide association study of melanoma conducted by the GenoMEL consortium based on 317K tagging SNPs for 1,650 selected cases and 4,336 controls, with replication in an additional...