Researcher
Thierry Voet
- Disciplines:Analysis of next-generation sequence data, Single-cell data analysis, Cell division, Genetics, Transcription and translation
Affiliations
- Laboratory of Reproductive Genomics (Division)
Responsible
From1 Nov 2009 → Today - Laboratory for Cytogenetics and Genome Research (Division)
Member
From1 Apr 2009 → 30 Sep 2009 - Department of Human Genetics (Department)
Member
From1 Oct 1999 → Today
Projects
1 - 10 of 58
- The malignant Glioma immuno-oncology matchmaker: towards data-driven precision medicine using spatially resolved radio-multiomicsFrom1 Jan 2024 → TodayFunding: HORIZON.2.1 - Health
- TriScanner: A fluorescence microscope for high-content high-throughput 3D imaging.From1 Oct 2023 → TodayFunding: BOF - postdoctoral mandates
- Immunotherapy for childhood, adolescent, and adult Glioblastoma: towards tumour-immune interactions driven precision medicine using spatially resolved radio-multiomics.From15 Jan 2023 → TodayFunding: BOF - various
- High-throughput multiplex quantitative PCRFrom1 Jan 2023 → TodayFunding: BOF - scientific equipment program
- SymBioSys: Computationally mapping genomic heterogeneity from long read sequencing dataFrom1 Oct 2022 → TodayFunding: BOF - projects
- Single-cell and spatial multi-omics for biomedicineFrom1 Oct 2022 → TodayFunding: IOF - mandates
- Single-cell and spatial genome-plus-transcriptome analyses to understand cellular heterogeneity and cell competition in embryogenesisFrom26 Sep 2022 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Survival of the fittest on a chip: A microfluidic toolbox to study cell-cell competition.From31 Aug 2022 → TodayFunding: FWO Strategic Basic Research Grant
- Single-objective light sheet instrument for fast and highthroughput imaging of 3D tissueFrom1 May 2022 → TodayFunding: FWO Medium Size Research Infrastructure
- COLUMBO: Engineered CRISPR toolbox for revolutionizing single-cell genome imaging in embryogenesis and oncologyFrom1 Oct 2021 → TodayFunding: BOF - projects
Publications
1 - 10 of 130
- Adipose tissue macrophage dysfunction is associated with a breach of vascular integrity in NASH.(2024)
Authors: Matthias Lannoo, Ellen Deleus, Baki Topal, Tessa Ostyn, Lena Smets, Lukas Van Melkebeke, Tania Roskams, Jef Verbeek, Olivier Govaere, Alejandro Sifrim, et al.
Pages: 397 - 408 - A TCF4-dependent gene regulatory network confers resistance to immunotherapy in melanoma(2024)
Authors: Dennis Pedri, Ewout Landeloos, Yannick Van Herck, Katy Vandereyken, Thierry Voet, Wim Annaert, Diether Lambrechts, Veerle Boecxstaens, Joost van den Oord, Francesca Bosisio, et al.
- A multi-omics genome-plus-transcriptome single-cell atlas of human preimplantation development(2023)
Authors: Elia Fernandez Gallardo, Thierry Voet, Sophie Debrock, Joris Vermeesch
- SINGLE-NUCLEUS GENOME-PLUS-TRANSCRIPTOME SEQUENCING TO UNDERSTAND THE EXTENT AND CONSEQUENCES OF SOMATIC GENOME INSTABILITY IN NEUROTYPICAL AND TAUOPATHY BRAIN(2023)
Authors: Sarah Geurs, Thierry Voet, Bart Dermaut
- Development of novel methods for single-cell whole-genome amplification to study cancer heterogeneity.(2023)
Authors: Koen Theunis, Thierry Voet, Chris Marine
- Pharmacological targeting of netrin-1 inhibits EMT in cancer(2023)
Authors: Alejandro Sifrim, Thierry Voet
Pages: 402 - + - Methods and applications for single-cell and spatial multi-omics(2023)
Authors: Katy Vandereyken, Alejandro Sifrim, Bernard Thienpont, Thierry Voet
Pages: 494 - 515 - Dedicated macrophages organize and maintain the enteric nervous system(2023)
Authors: Elodie Modave, Marcello Delfini, Nathalie Stakenborg, Tobie Martens, Katy Vandereyken, Alejandro Sifrim, Gianluca Matteoli, Pieter Vanden Berghe, Thierry Voet, Guy Boeckxstaens
Pages: 818 - 826 - Exploring the possibility of non-invasive prenatal diagnosis using cervical cells(2023)
Authors: Margot van Riel, Joris Vermeesch, Thierry Voet, Dirk Timmerman
- Imaging the unimaginable: leveraging signal generation of CRISPR-Cas for sensitive genome imaging.(2023)
Authors: Charlotte Van Tricht, Thierry Voet, Jeroen Lammertyn, Dragana Spasic
Pages: 769 - 784
Patents
1 - 5 of 5
- High-throughput genotyping by sequencing low amounts of genetic material (Inventor)
- Haplotyping and copy number typing using polymorphic variant allelic frequencies (Inventor)
- Methods for haplotyping single cells (Inventor)
- HAPLOTYPING AND COPY NUMBER TYPING USING POLYMORPHIC VARIANT ALLELIC FREQUENCIES (Inventor)
- HIGH-THROUGHPUT GENOTYPING BY SEQUENCING LOW AMOUNTS OF GENETIC MATERIAL (Inventor)