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
301 - 310 of 399
- Determining the accuracy of (single cell) molecular karyotyping by inernal and external quality assessment schemes(2011)
Authors: Joris Vermeesch
Pages: S21 - S22 - A balanced translocation t(6;14)(q25.3;q13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum(2011)
Authors: Liesbeth Backx, Eve Seuntjens, Koenraad Devriendt, Joris Vermeesch, Hilde Van Esch
Pages: S59 - S59 - Pre-implantation genetic selection against balanced translocations(2011)
Authors: C Melotte, Sophie Debrock, Thomas D'Hooghe, Eric Legius, Jean-Pierre Fryns, Joris Vermeesch
Pages: S220 - S220 - Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech(2011)
Authors: Joris Vermeesch
Pages: 2148 - 54 - Recent Developments in the Genetic Factors Underlying Congenital Diaphragmatic Hernia(2011)
Authors: Paul Brady, Koenraad Devriendt, Jean-Pierre Frijns, Jan Deprest, Joris Vermeesch
Pages: 25 - 39 - A Balanced Translocation t(6;14)(q25.3;q13.2) Leading to Reciprocal Fusion Transcripts in a Patient with Intellectual Disability and Agenesis of Corpus Callosum(2011)
Authors: Liesbeth Backx, Eve Seuntjens, Koenraad Devriendt, Joris Vermeesch, Hilde Van Esch
Pages: 135 - 143 - Array technology in prenatal diagnosis(2011)
Authors: Paul Brady, Joris Vermeesch
Pages: 94 - 98 - The Human Cleavage Stage Embryo Is a Cradle of Chromosomal Rearrangements(2011)
Authors: Thierry Voet, Evelyne Vanneste, Joris Vermeesch
Pages: 160 - 168 - Comparative genomic hybridisation and next-generation sequencing: powerful tools to investigate chromosome number and structure in human embryos(2011)
Authors: Thierry Voet, Evelyne Vanneste, M Zamani Esteki, Niels Van der Aa, C Melotte, S Jackmaert, Peter Konings, Sophie Debrock, Jean-Pierre Fryns, Yves Moreau, et al.
Pages: I60 - I60 - 'Mendelian CNVs' causing mental retardation and developmental disorders(2010)
Authors: Joris Vermeesch, Thomy de Ravel de l'Argentière
Pages: 114 - 125
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)