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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
Projects
1 - 10 of 71
- Validation of cell-free multi-omics-based cancer detection.From1 Oct 2024 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Multi-omics liquid biopsy platform to advance precision cancer medicine.From16 Sep 2024 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Genome-wide genetic screening of equine embryos and fetuses: the start of a new era in breeding top horsesFrom1 Aug 2024 → TodayFunding: IWT / VLAIO personal funding - innovation mandates
- Making de novo haplotype and epigenome aware reference-free genome assemblies accessibleFrom1 Jul 2024 → TodayFunding: BOF - research organisations
- T2T-Biology: Comprehensive Genomics via Accurate Single-Molecule SequencingFrom1 May 2024 → TodayFunding: FWO Medium Size Research Infrastructure
- Impact of ccfDNA on clinical decision making in NEN patientsFrom8 Jan 2024 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Functional analysis of non-coding variation in human craniofacial-related disorders.From1 Oct 2023 → TodayFunding: BOF - projects
- Towards a better understanding of incidental cancer detection upon non-invasive prenatal testingFrom17 Sep 2023 → 1 Apr 2024Funding: 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
Publications
1 - 10 of 374
- Comprehensive Recommendations for the Clinical Management of Pregnant Women With Noninvasive Prenatal Test Results Suspicious of a Maternal Malignancy(2024)
Authors: Liesbeth Lenaerts, Frédéric Amant, Miel Theunis, Joris Vermeesch
- Rare Autosomal Trisomies and Adverse Perinatal Outcomes.(2024)
Authors: Lore Lannoo, Joris Vermeesch, Kristel Van Calsteren
Pages: 184 - 185 - Polygenic embryo screening: quo vadis?(2024)
Authors: Maria Siermann, Joris Vermeesch, Pascal Borry
- Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening.(2024)
Authors: Maria Siermann, Joris Vermeesch, Karen Peeraer, Pascal Borry
Pages: 104294 - Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology(2024)
Authors: Tatjana Jatsenko, Stefania Tuveri, Lore Lannoo, Kristel Van Calsteren, Marie De Borre, Liesbeth Lenaerts, Sabine Tejpar, Bernard Thienpont, Joris Vermeesch
- A novel method for the isolation of single cells mimicking circulating tumour cells adhered on Smart Bio Surface slides by Laser Capture Microdissection(2024)
Authors: Joris Vermeesch
- 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
- 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 - "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
Patents
1 - 8 of 8
- 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)
- 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)