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
331 - 340 of 400
- Distal limb deficiencies, micrognathia syndrome (OMIM 246560) and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements(2010)
Authors: Boyan Dimitrov, Thomy de Ravel de l'Argentière, J Van Driessche, C de Die-Smulders, A Toutain, Joris Vermeesch, Jean-Pierre Frijns, Koenraad Devriendt, Philippe Debeer
Pages: 103 - 111 - Distal limb deficiencies, micrognathia syndrome (OMIM 246560) and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements(2010)
Authors: Boyan Dimitrov, Thomy de Ravel de l'Argentière, Joris Vermeesch, Jean-Pierre Frijns, Koenraad Devriendt, Philippe Debeer
Pages: 103 - 111 - Hyperactive transposons for genetic modification of induced pluripotent and adult stem cells: a novel non-viral paradigm for coaxed differentiation(2010)
Authors: Marinee Chuah, Eyayu Belay, Janka Matrai, Abel Acosta Sanchez, L Ma, M Quattrocelli, L Mates, P Sancho-Bru, M Geraerts, B Yan, et al.
Pages: 1174 - 1174 - Somatic genomic variations in early human prenatal development(2010)
Authors: Caroline Robberecht, Evelyne Vanneste, Anne Pexsters, Thomas D'Hooghe, Thierry Voet, Joris Vermeesch
Pages: 397 - 401 - FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish(2010)
Authors: Irina Balikova, Koenraad Devriendt, Jean-Pierre Frijns, Joris Vermeesch
Pages: 255 - 261 - SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles(2010)
Authors: Karolien Volders, An Crepel, Liesbeth Backx, Rita De Vos, Kathleen Freson, Joris Vermeesch, Chris Van Geet, Wim Van de Ven, Jean Steyaert, Koenraad Devriendt, et al.
Pages: 1368 - 1378 - Preimplantation genetic screening for aneuploidy of embryos after in vitro fertilization in women aged at least 35 years: a prospective randomized trial(2010)
Authors: Sophie Debrock, Carl Spiessens, Karen Peeraer, Evelyne Vanneste, Christel Meuleman, Jean-Pierre Frijns, Joris Vermeesch, Thomas D'Hooghe
Pages: 364 - 373 - 'Mendelian CNV's' causing mental retardation and developmental disorders(2010)
Authors: Joris Vermeesch, Thomy de Ravel de l'Argentière
Pages: 114 - 125 - Analysis of array CGH data for the detection of single-cell chromosomal imbalances(2010)
Authors: Michèle Ampe, Geert Verbeke, Evelyne Vanneste, Joris Vermeesch
Pages: 224 - 244 - A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report(2009)
Authors: Joris Vermeesch
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)