Suzanne Vanhauwaert
Overview
Explore the profile of Suzanne Vanhauwaert 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
18
Citations
938
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Vanhauwaert S, Decaesteker B, De Brouwer S, Leonelli C, Durinck K, Mestdagh P, et al.
Sci Rep
. 2018 Dec;
8(1):17468.
PMID: 30504901
Chemotherapy resistance is responsible for high mortality rates in neuroblastoma. MYCN, an oncogenic driver in neuroblastoma, controls pluripotency genes including LIN28B. We hypothesized that enhanced embryonic stem cell (ESC) gene...
12.
Decaesteker B, Denecker G, Van Neste C, Dolman E, Van Loocke W, Gartlgruber M, et al.
Nat Commun
. 2018 Nov;
9(1):4866.
PMID: 30451831
Chromosome 17q gains are almost invariably present in high-risk neuroblastoma cases. Here, we perform an integrative epigenomics search for dosage-sensitive transcription factors on 17q marked by H3K27ac defined super-enhancers and...
13.
Renard M, Vanhauwaert S, Vanhomwegen M, Rihani A, Vandamme N, Goossens S, et al.
Sci Rep
. 2018 May;
8(1):7642.
PMID: 29769563
Reverse transcription quantitative PCR (RT-qPCR) is the gold standard method for gene expression analysis on mRNA level. To remove experimental variation, expression levels of the gene of interest are typically...
14.
Van Deun J, Mestdagh P, Agostinis P, Akay O, Anand S, Anckaert J, et al.
Nat Methods
. 2017 Mar;
14(3):228-232.
PMID: 28245209
We argue that the field of extracellular vesicle (EV) biology needs more transparent reporting to facilitate interpretation and replication of experiments. To achieve this, we describe EV-TRACK, a crowdsourcing knowledgebase...
15.
Durinck K, Wallaert A, Van de Walle I, Van Loocke W, Volders P, Vanhauwaert S, et al.
Haematologica
. 2014 Oct;
99(12):1808-16.
PMID: 25344525
Genetic studies in T-cell acute lymphoblastic leukemia have uncovered a remarkable complexity of oncogenic and loss-of-function mutations. Amongst this plethora of genetic changes, NOTCH1 activating mutations stand out as the...
16.
Vanhauwaert S, Van Peer G, Rihani A, Janssens E, Rondou P, Lefever S, et al.
PLoS One
. 2014 Oct;
9(10):e109091.
PMID: 25310091
The selection and validation of stably expressed reference genes is a critical issue for proper RT-qPCR data normalization. In zebrafish expression studies, many commonly used reference genes are not generally...
17.
De Rocker N, Vergult S, Koolen D, Jacobs E, Hoischen A, Zeesman S, et al.
Genet Med
. 2014 Sep;
17(6):460-6.
PMID: 25232846
Purpose: Submicroscopic deletions of chromosome band 2p25.3 are associated with intellectual disability and/or central obesity. Although MYT1L is believed to be a critical gene responsible for intellectual disability, so far...
18.
Malfait F, Kariminejad A, Van Damme T, Gauche C, Syx D, Merhi-Soussi F, et al.
Am J Hum Genet
. 2013 May;
92(6):935-45.
PMID: 23664118
Proteoglycans are important components of cell plasma membranes and extracellular matrices of connective tissues. They consist of glycosaminoglycan chains attached to a core protein via a tetrasaccharide linkage, whereby the...