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
361 - 370 of 400
- Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome(2009)
Authors: Thomy de Ravel de l'Argentière, Joris Vermeesch, Koenraad Devriendt
Pages: 145 - 147 - Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome(2009)
Authors: Thomy de Ravel de l'Argentière, Liliane Ameye, Katleen Ballon, Martine Borghgraef, Joris Vermeesch, Koenraad Devriendt
Pages: 145 - 147 - Array CGH: Opening new horizons(2009)
Authors: Joris Vermeesch
Pages: 421 - 437 - Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1(2009)
Authors: Bernard Thienpont, Eftychia Dimitriadou, Jeroen Breckpot, Joris Vermeesch, Koenraad Devriendt
Pages: 393 - 7 - Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation(2009)
Authors: Liesbeth Backx, Joris Vermeesch
Pages: 109 - 114 - Pathogenesis of vestibular schwannoma in ring chromosome 22(2009)
Authors: Ellen Denayer, Hilde Brems, Paul De Cock, Frank Van Calenbergh, Raf Sciot, Maria Debiec-Rychter, Joris Vermeesch, Jean-Pierre Frijns, Eric Legius
- An experimental loop design improves the detection of congenital chromosomal aberrati(2009)
Authors: Joke Allemeersch, Steven Van Vooren, Femke Hannes, Bart De Moor, Joris Vermeesch, Yves Moreau
- Identification of underlying mechanisms in x-chromosome disorders(2009)
Authors: Christodoulos Christodoulou, Elena Panayiotou, George Koumbaris, Diana Rajan, Tomas Fitzgerald, Susan Gribble, Stephen Clayton, Chariklia Hatzisevastou, Aunts Kurg, Kitsiou Sophia Tzeli, et al.
Pages: 114 - 115 - The C20orf133 gene is disrupted in a patient with Kabuki syndrome.(2009)
Authors: Koenraad Devriendt, Jean-Pierre Frijns, Joris Vermeesch
Pages: bcr06.2009 - Hyperactive transposons for gene delivery into iPS and adult stem cells: a novel paradigm for coaxed differentiation(2009)
Authors: Eyayu Belay, Janka Matrai, M Quatrocelli, L Mates, Abel Acosta Sanchez, P Sancho Bru, Martine Geraerts, Kim Vanuytsel, Bing Yan, L Ma, et al.
Pages: 1410 - 1410
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)