Researcher
Bernard Thienpont
- Disciplines:Epigenetics, Epigenomics
Affiliations
- Laboratory for Functional Epigenetics (Division)
Responsible
From1 Oct 2017 → Today - Department of Human Genetics (Department)
Member
From1 Oct 2017 → Today - Laboratory of Translational Genetics (VIB-KU Leuven) (Division)
Member
From1 Jul 2012 → 30 Sep 2015 - Laboratory for Genetics of Human Development (Division)
Member
From1 Apr 2009 → 31 Dec 2009
Projects
1 - 10 of 32
- Nuclear metabolism in the control of cancer cells methylome under hypoxia.From1 Oct 2023 → TodayFunding: BOF - postdoctoral mandates
- High-throughput multiplex quantitative PCRFrom1 Jan 2023 → TodayFunding: BOF - scientific equipment program
- Single-cell and spatial multi-omics for biomedicineFrom1 Oct 2022 → TodayFunding: IOF - mandates
- Methylome analysis of cfDNA: novel applicationsFrom1 Oct 2022 → TodayFunding: FWO Strategic Basic Research Grant
- Unraveling the epigenetic mechanisms behind epithelial cell plasticity in metaplastic colorectal cancerFrom19 Sep 2022 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Mapping gene regulatory networks in the era of single-cell multi-omicsFrom1 Sep 2022 → TodayFunding: BOF - doctoral mandates
- Remote allograft rejection diagnosis by epigenetic changes in circulating cell-free DNA in kidney transplanted patients.From1 Feb 2022 → TodayFunding: FWO Strategic Basic Research Grant
- Novel Diagnostics through Methylation Profiling of Cell-free DNAFrom1 Jan 2022 → TodayFunding: FWO research project (including WEAVE projects)
- Multiomic Integration of cell-free DNA profiles to Advance Disease OutcomeFrom1 Oct 2021 → TodayFunding: FWO Strategic Basic Research (SBO)
- The neurovascular link: an unexpectedly important role of metabolism.From1 Oct 2021 → TodayFunding: BOF - Methusalem
Publications
81 - 90 of 105
- Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1(2012)
Authors: Jeroen Breckpot, Bernard Thienpont, Marijke Bauters, Léon-Charles Tranchevent, Marc Gewillig, Karel Allegaert, Joris Vermeesch, Yves Moreau, Koenraad Devriendt
Pages: 574 - 580 - Differences in Copy Number Variation between Discordant Monozygotic Twins as a Model for Exploring Chromosomal Mosaicism in Congenital Heart Defects(2012)
Authors: Jeroen Breckpot, Bernard Thienpont, Marc Gewillig, Karel Allegaert, Joris Vermeesch, Koenraad Devriendt
Pages: 81 - 87 - BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome(2012)
Authors: Jeroen Breckpot, Léon-Charles Tranchevent, Bernard Thienpont, Marijke Bauters, Marc Gewillig, Joris Vermeesch, Yves Moreau, Koenraad Devriendt, Hilde Van Esch
Pages: 12 - 16 - The Dynamics of Genome-wide DNA Methylation Reprogramming in Mouse Primordial Germ Cells(2012)
Authors: Bernard Thienpont
Pages: 849 - 862 - Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects(2011)
Authors: Jeroen Breckpot, Bernard Thienpont, Léon-Charles Tranchevent, Joris Vermeesch, Yves Moreau, Marc Gewillig, Koenraad Devriendt
Pages: 251 - 259 - High Frequency Of Submicroscopic Chromosomal Deletions in Patients with Idiopathic Congenital Eye Malformations(2011)
Authors: Irina Balikova, Thomy de Ravel de l'Argentière, Bernard Thienpont, Ingele Casteels, Koenraad Devriendt, Jean-Pierre Frijns, Joris Vermeesch
Pages: 1087 - 1094 - Haplo-insufficiency of TAB2 causes congenital heart defects in humans(2010)
Authors: Bernard Thienpont, Jeroen Breckpot, Léon-Charles Tranchevent, Peter Van Loo, Geert Mortier, Marc Gewillig, Yves Moreau, Koenraad Devriendt
Pages: 839 - 849 - Array Comparative Genomic Hybridization as a Diagnostic Tool for Syndromic Heart Defects(2010)
Authors: Jeroen Breckpot, Bernard Thienpont, Hilde Peeters, Thomy de Ravel de l'Argentière, Maissa Rayyan, Karel Allegaert, Christine Vanhole, Benedicte Eyskens, Joris Vermeesch, Marc Gewillig, et al.
Pages: 810 - 817 - A second patient with Tsukahara syndrome: type A1 brachydactyly, short stature, hearing loss, microcephaly, mental retardation and ptosis(2010)
Authors: Jeroen Breckpot, Bernard Thienpont, Koenraad Devriendt
Pages: 947 - 9 - Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome(2010)
Authors: Bernard Thienpont, Jeroen Breckpot, Hilde Van Esch, Jean-Pierre Frijns, Geert Mortier, Joris Vermeesch, Koenraad Devriendt
Pages: 155 - 161
Patents
1 - 3 of 3
- Preeclampsia diagnosis (Inventor)
- Markers for determining tumor hypoxia (Inventor)
- Markers for determining tumor hypoxia (Inventor)