Bram De Wilde
Bram De Wilde
Verified email at ugent.be - Homepage
Title
Cited by
Cited by
Year
Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer
M Peifer, L Fernández-Cuesta, ML Sos, J George, D Seidel, LH Kasper, ...
Nature genetics 44 (10), 1104-1110, 2012
9342012
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
M Peifer, F Hertwig, F Roels, D Dreidax, M Gartlgruber, R Menon, ...
Nature 526 (7575), 700-704, 2015
2892015
Targeted expression of mutated ALK induces neuroblastoma in transgenic mice
LC Heukamp, T Thor, A Schramm, K De Preter, C Kumps, B De Wilde, ...
Science translational medicine 4 (141), 141ra91-141ra91, 2012
1242012
Emergence of New ALK Mutations at Relapse of Neuroblastoma
G Schleiermacher, N Javanmardi, V Bernard, Q Leroy, J Cappo, ...
Journal of clinical oncology 32 (25), 2727-2734, 2014
1232014
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis
F Coppieters, B De Wilde, S Lefever, E De Meester, N De Rocker, ...
Genetics in medicine 14 (6), 576-585, 2012
512012
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics
K De Leeneer, J De Schrijver, L Clement, M Baetens, S Lefever, ...
PLoS One 6 (9), e25531, 2011
512011
Shallow whole genome sequencing on circulating cell-free DNA allows reliable noninvasive copy-number profiling in neuroblastoma patients
N Van Roy, M Van Der Linden, B Menten, A Dheedene, C Vandeputte, ...
Clinical Cancer Research 23 (20), 6305-6314, 2017
482017
A mechanistic classification of clinical phenotypes in neuroblastoma
S Ackermann, M Cartolano, B Hero, A Welte, Y Kahlert, A Roderwieser, ...
Science 362 (6419), 1165-1170, 2018
472018
Target enrichment using parallel nanoliter quantitative PCR amplification
B De Wilde, S Lefever, W Dong, J Dunne, S Husain, S Derveaux, ...
BMC genomics 15 (1), 184, 2014
202014
CASP8 SNP D302H (rs1045485) is associated with worse survival in MYCN-amplified neuroblastoma patients
A Rihani, B De Wilde, F Zeka, G Laureys, N Francotte, GP Tonini, S Coco, ...
PloS one 9 (12), e114696, 2014
152014
Stage 4S neuroblastoma tumors show a characteristic DNA methylation portrait
A Decock, M Ongenaert, B De Wilde, B Brichard, R Noguera, F Speleman, ...
Epigenetics 11 (10), 761-771, 2016
142016
Methyl-CpG-binding domain sequencing reveals a prognostic methylation signature in neuroblastoma
A Decock, M Ongenaert, R Cannoodt, K Verniers, B De Wilde, G Laureys, ...
Oncotarget 7 (2), 1960, 2016
142016
Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients
S Vergult, AJM Hoogeboom, EK Bijlsma, T Sante, E Klopocki, B De Wilde, ...
Genetics in Medicine 15 (3), 195-202, 2013
132013
High-throughput PCR assay design for targeted resequencing using primerXL
S Lefever, F Pattyn, B De Wilde, F Coppieters, S De Keulenaer, ...
BMC bioinformatics 18 (1), 400, 2017
92017
ALK positively regulates MYCN activity through repression of HBP1 expression
S Claeys, G Denecker, K Durinck, B Decaesteker, LM Mus, S Loontiens, ...
Oncogene 38 (15), 2690-2705, 2019
72019
Lack of association between MDM2 promoter SNP309 and clinical outcome in patients with neuroblastoma
A Rihani, T Van Maerken, B De Wilde, F Zeka, G Laureys, K Norga, ...
Pediatric blood & cancer 61 (10), 1867-1870, 2014
62014
The pitfalls and promise of liquid biopsies for diagnosing and treating solid tumors in children: a review
R Van Paemel, R Vlug, K De Preter, N Van Roy, F Speleman, L Willems, ...
European Journal of Pediatrics, 1-12, 2020
32020
The mutational landscape of MYCN, Lin28b and ALKF1174L driven murine neuroblastoma mimics human disease
B De Wilde, A Beckers, S Lindner, A Kristina, K De Preter, P Depuydt, ...
Oncotarget 9 (9), 8334, 2018
32018
A versatile method for circulating cell-free DNA methylome profiling by reduced representation bisulfite sequencing
A De Koker, R Van Paemel, B De Wilde, K De Preter, N Callewaert
bioRxiv, 663195, 2019
22019
Hypotonia and delayed motor development as an early presentation of Lowe syndrome: case report and literature review
S David, K De Waele, B De Wilde, F Faes, O Vanakker, S Walraedt, ...
Acta Clinica Belgica, 2018
22018
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