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
11 - 20 of 399
- MetDecode: a novel methylation-based method for cell-free DNA tissue-of-origin assignment(2024)
Authors: Antoine Passemiers, Liesbeth Lenaerts, Joris Vermeesch
Pages: 611 - 611 - A multi-omics genome-plus-transcriptome single-cell atlas of human preimplantation development(2023)
Authors: Elia Fernandez Gallardo, Thierry Voet, Sophie Debrock, Joris Vermeesch
- Non-invasive prenatal testing: when results suggests maternal cancer(2023)
Authors: Liesbeth Lenaerts, Miel Theunis, Frédéric Amant, Joris Vermeesch
Pages: 285 - 295 - Single closed-tube quantitative real-time PCR assay with dual-labelled probes for improved sex determination of equine embryos(2023)
Authors: Joris Vermeesch
- Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores(2023)
Authors: Maria Siermann, Joris Vermeesch, Olga Tsuiko, Pascal Borry
Pages: 1133 - 1138 - What helps define outcomes in persistent uninterpretable non-invasive prenatal testing: Maternal factors, fetal fraction or quality scores?(2023)
Authors: Lore Lannoo, Nathalie Brison, Kris Van Den Bogaert, Joris Vermeesch, Koenraad Devriendt, Kristel Van Calsteren
Pages: 1333 - 1343 - Ultrasensitive Microhaplotype-Based Detection of Minor Alleles in Cervical Samples of Pregnant Women Identifies Sperm Rather Than Fetal DNA(2023)
Authors: Lore Lannoo, Dirk Timmerman, Joris Vermeesch
Pages: 1089 - 1091 - Cell-free DNA methylome analysis for early preeclampsia prediction(2023)
Authors: Marie De Borre, Lore Lannoo, Kobe De Ridder, Mio Aerden, Jeroen Breckpot, Koenraad Devriendt, Joris Vermeesch, Kristel Van Calsteren, Bernard Thienpont
Pages: 2206 - + - Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS(2023)
Authors: Ann Swillen, Jeroen Breckpot, Joris Vermeesch
- Exploring the possibility of non-invasive prenatal diagnosis using cervical cells(2023)
Authors: Margot van Riel, Joris Vermeesch, Thierry Voet, Dirk Timmerman
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)