Researcher
Joris Vermeesch
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Laboratory for Cytogenetics and Genome Research (Division)
Responsible
From1 Jan 2008 → Today - Department of Human Genetics (Department)
Member
From27 Sep 2004 → Today
Infrastructure
1 - 3 of 3
- PACBIO; third -generation sequencing platform with Single Molecule Real Time technology (SMRT) (Consortium coordinator)
- EU-Genomics: EU Infrastructure for genomic analysis. (Consortium coordinator)
- Belgian Genome Biobank (Consortium coordinator)
Projects
1 - 10 of 63
- Impact of ccfDNA on clinical decision making in NEN patientsFrom8 Jan 2024 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Towards a better understanding of incidental cancer detection upon non-invasive prenatal testingFrom17 Sep 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Mapping the functional role of the low copy repeats in the phenotypic variability of the 22q11.2 Deletion SyndromeFrom27 Jan 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Impact of ccfDNA on clinical decision making in NEN patientsFrom1 Jan 2023 → TodayFunding: Foundations, funds and other with scientific goal
- Sabbatical Joris Vermeesch: Computational analyses of large sequencing data setsFrom1 Oct 2022 → 30 Apr 2023Funding: BOF - mobility
- SymBioSys: Computationally mapping genomic heterogeneity from long read sequencing dataFrom1 Oct 2022 → TodayFunding: BOF - projects
- Implementation and validation of liquid biopsies as a diagnostic tool for early breast cancer detection in South African black womenFrom1 Sep 2022 → TodayFunding: VLIR-UOS South Initiatives
- Belgian Genome BiobankFrom1 May 2022 → TodayFunding: FWO Large scale research infrastructure
- 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
- Mapping the role of the low copy repeats in the phenotypic variability of the 22q11 Deletion SyndromeFrom1 Jan 2022 → TodayFunding: FWO research project (including WEAVE projects)
Publications
41 - 50 of 399
- Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing(2022)
Authors: Eftychia Dimitriadou, Sophie Debrock, Olga Tsuiko, Karen Peeraer, Yves Moreau, Thierry Voet, Masoud Zamani Esteki, Joris Vermeesch
- Pushing the boundaries. Concurrent Hodgkin lymphoma and breast cancer treatment with preservation of pregnancy: A case report(2022)
Authors: Charlotte Lejeune, Daan Dierickx, Hans Wildiers, Lore Lannoo, Kristel Van Calsteren, Joris Vermeesch, Frédéric Amant
- A benchmark of structural variation detection by long reads through a realistic simulated model(2021)
Authors: Nicolas Dierckxsens, Joris Vermeesch
- Genome-wide abnormalities resulting from heterogoneic cell division persist in the blastocyst-stage bovine embryo(2021)
Authors: Tine De Coster, Olga Tsuiko, Joris Vermeesch
Pages: 260 - 261 - Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples(2021)
Authors: Joris Vermeesch
- Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation(2021)
Authors: Olga Tsuiko, Michiel Vanneste, Sophie Debrock, Heleen Masset, Karen Peeraer, Ellen Denayer, Joris Vermeesch, Eftychia Dimitriadou
- International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies(2021)
Authors: Joris Vermeesch
Pages: 1222 - 1232 - Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?(2021)
Authors: Lore Lannoo, Liesbeth Lenaerts, Kris Van Den Bogaert, Huiwen Che, Nathalie Brison, Koenraad Devriendt, Frédéric Amant, Joris Vermeesch, Kristel Van Calsteren
Pages: 1 - 9 - 22q11.2 Low Copy Repeats Expanded in the Human Lineage(2021)
Authors: Lisanne Vervoort, Nicolas Dierckxsens, Joris Vermeesch
- Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations(2021)
Authors: Margot van Riel, Nathalie Brison, Koenraad Devriendt, Lore Lannoo, Kris Van Den Bogaert, Joris Vermeesch
Pages: 1102 - 1108
Patents
1 - 8 of 8
- Method for analysing cell-free nucleic acids (Inventor)
- Method for analysing cell-free nucleic acids (Inventor)
- High-throughput genotyping by sequencing low amounts of genetic material (Inventor)
- Method for analysing cell-free nucleic acids (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)