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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
31 - 40 of 63
- Genomic and epigenomic profiling of circulating tumor DNA for non-invasive breast cancer detectionFrom1 Jan 2019 → 31 Dec 2021Funding: Other federal scientific institutions
- Genomics structural variations analysis in family with Gollop-Wolfgang SyndromeFrom15 Oct 2018 → 15 Oct 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
- SymBioSys: Computationally disentangling cellular heterogeneityFrom1 Oct 2018 → 30 Sep 2022Funding: Fund Recuperation Fiscal Exemption
- Single-cell omics in high throughput and at spatial resolutionFrom1 May 2018 → 30 Apr 2022Funding: FWO Medium Size Research Infrastructure
- Genomic Medicine: Translation of Whole Genome Analyses to Health GenomicsFrom1 May 2018 → TodayFunding: IOF - mandates, IOF - Industrial Research Fund
- Genetically conditions diseases - education and diagnosis (EDUGEN).From1 Apr 2018 → 31 Jan 2021Funding: Private funding of national origin - undefined
- Genomic profiling of cell-free DNAFrom12 Oct 2017 → 4 May 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
- Prenatal diagnosis via cervical cellsFrom1 Sep 2017 → 16 Jun 2023Funding: FWO Strategic Basic Research Grant
- Genomic structure as a contributing factor for the psychopathology of the 22q11 deletion syndromeFrom1 Aug 2017 → 31 Jul 2018Funding: Foreign Nonprofit organisations and equivalents
- Segmental duplication structural variation as the cause for the 22q11DS phenotypic variabilityFrom1 Jan 2017 → 31 Dec 2020Funding: FWO research project (including WEAVE projects)
Publications
1 - 10 of 399
- Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology.(2024)
Authors: Stefania Tuveri, Lore Lannoo, Kristel Van Calsteren, Liesbeth Lenaerts, Sabine Tejpar, Bernard Thienpont, Joris Vermeesch
Pages: 2220 - Should non-invasive prenatal testing (NIPT) be used for fetal sex determination? Perspectives and experiences of healthcare professionals(2024)
Authors: Joris Vermeesch, Pascal Borry
Pages: 309 - 316 - Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.(2024)
Authors: Ann Swillen, Jeroen Breckpot, Joris Vermeesch, Koenraad Devriendt
Pages: 368.e1 - 368.e12 - "Are we not going too far?": Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals(2024)
Authors: Maria Siermann, Joris Vermeesch, Olga Tsuiko, Pascal Borry
- Genome-wide equine preimplantation genetic testing enabled by simultaneous haplotyping and copy number detection(2024)
Authors: Olga Tsuiko, Joris Vermeesch
- WiNGS SV: A platform for analysis and federated sharing of structural variants(2024)
Authors: Joris Vermeesch
Pages: 659 - 660 - Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11(2024)
Authors: Philippe Debeer, Joris Vermeesch, Przemko Tylzanowski
- Should non-invasive prenatal testing be used for fetal sex determination? Perspectives and experiences from healthcare professionals(2024)
Authors: Joris Vermeesch
Pages: 766 - 766 - Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles(2024)
Authors: Koenraad Devriendt, Kris Van Den Bogaert, Joris Vermeesch
Pages: 31 - 36 - Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation(2024)
Authors: Joris Vermeesch
Pages: 278 - 278
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)