Bernard Thienpont
Bernard Thienpont
Laboratory of Functional Epigenetics - KULeuven, Belgium
Verified email at kuleuven.be - Homepage
TitleCited byYear
The dynamics of genome-wide DNA methylation reprogramming in mouse primordial germ cells
S Seisenberger, S Andrews, F Krueger, J Arand, J Walter, F Santos, ...
Molecular cell 48 (6), 849-862, 2012
6072012
Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of …
B Menten, N Maas, B Thienpont, K Buysse, J Vandesompele, C Melotte, ...
Journal of medical genetics 43 (8), 625-633, 2006
4272006
Single-cell chromosomal imbalances detection by array CGH
C Le Caignec, C Spits, K Sermon, M De Rycke, B Thienpont, S Debrock, ...
Nucleic acids research 34 (9), e68-e68, 2006
2342006
Tumour hypoxia causes DNA hypermethylation by reducing TET activity
B Thienpont, J Steinbacher, H Zhao, F D’Anna, A Kuchnio, A Ploumakis, ...
Nature 537 (7618), 63-68, 2016
2042016
Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients
B Thienpont, L Mertens, T de Ravel, B Eyskens, D Boshoff, N Maas, ...
European heart journal 28 (22), 2778-2784, 2007
1902007
Inhibition of the glycolytic activator PFKFB3 in endothelium induces tumor vessel normalization, impairs metastasis, and improves chemotherapy
AR Cantelmo, LC Conradi, A Brajic, J Goveia, J Kalucka, A Pircher, ...
Cancer cell 30 (6), 968-985, 2016
1472016
Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)
NMC Maas, G Van Buggenhout, F Hannes, B Thienpont, D Sanlaville, ...
Journal of medical genetics 45 (2), 71-80, 2008
1192008
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
A Sifrim, MP Hitz, A Wilsdon, J Breckpot, SH Al Turki, B Thienpont, ...
Nature genetics 48 (9), 1060-1065, 2016
1142016
Phenotype molding of stromal cells in the lung tumor microenvironment
D Lambrechts, E Wauters, B Boeckx, S Aibar, D Nittner, O Burton, ...
Nature medicine 24 (8), 1277, 2018
952018
Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1
KB Meyer, M O’Reilly, K Michailidou, S Carlebur, SL Edwards, JD French, ...
The American Journal of Human Genetics 93 (6), 1046-1060, 2013
932013
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
S Al Turki, AK Manickaraj, CL Mercer, SS Gerety, MP Hitz, S Lindsay, ...
The American Journal of Human Genetics 94 (4), 574-585, 2014
922014
The role of fatty acid β-oxidation in lymphangiogenesis
BW Wong, X Wang, A Zecchin, B Thienpont, I Cornelissen, J Kalucka, ...
Nature 542 (7639), 49-54, 2017
882017
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
M Ghoussaini, SL Edwards, K Michailidou, S Nord, R Cowper-Sal, ...
Nature communications 4, 2014
822014
Subtelomeric imbalances in phenotypically normal individuals
I Balikova, B Menten, T de Ravel, C Le Caignec, B Thienpont, M Urbina, ...
Human mutation 28 (10), 958-967, 2007
772007
A single-cell transcriptome atlas of the aging Drosophila brain
K Davie, J Janssens, D Koldere, M De Waegeneer, U Pech, Ł Kreft, ...
Cell, 2018
762018
Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects
J Breckpot, B Thienpont, H Peeters, T de Ravel, A Singer, M Rayyan, ...
The Journal of pediatrics 156 (5), 810-817. e4, 2010
762010
Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects
J Breckpot, B Thienpont, Y Arens, LC Tranchevent, JR Vermeesch, ...
Cytogenetic and genome research 135 (3-4), 251-259, 2011
642011
Network analysis of differential expression for the identification of disease-causing genes
D Nitsch, LC Tranchevent, B Thienpont, L Thorrez, H Van Esch, ...
PloS one 4 (5), e5526, 2009
622009
Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome
I Balikova, AE Lehesjoki, TJL De Ravel, B Thienpont, KE Chandler, ...
Human mutation 30 (9), E845-E854, 2009
602009
Duplications of the critical Rubinstein–Taybi deletion region on chromosome 16p13. 3 cause a novel recognisable syndrome
B Thienpont, F Béna, J Breckpot, N Philip, B Menten, H Van Esch, ...
Journal of medical genetics 47 (3), 155-161, 2010
552010
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