Researcher
Guy Froyen
- Disciplines:Medical imaging and therapy, Other paramedical sciences, Genetics, Systems biology, Molecular and cell biology
Affiliations
- Department of Human Genetics (Department)
Member
From1 Apr 2009 → 31 Dec 2015 - Human Genome Laboratory (Division)
Member
From4 Dec 2008 → 31 Dec 2013
Projects
1 - 10 of 10
- Molecular sequence-analysis to determine the variability and epigenetic signature of tandem repeats in the human genome.From1 Jan 2014 → 21 Dec 2018Funding: IWT personal funding - strategic basic research grants
- Characterization of tandem repeats in human genome and their role in diseaseFrom1 Oct 2012 → 22 Oct 2018Funding: Private funding of national origin - undefined
- A functional human genome project: integrated research of human congenital disorders.From1 Oct 2011 → 30 Sep 2016Funding: BOF - Concerted Research Project from 1994
- Gene identification in female patients with intellectual disability and skewed X-inactivation.From1 Sep 2011 → 31 Dec 2015Funding: IWT personal funding - strategic basic research grants
- Study of the role of the nuclear export factor 5 (NXF5) in neuronal mRNA transport and metabolism, and its involvement in mental retardation.From1 Jan 2011 → 31 Dec 2014Funding: FWO research project
- Tandem repeats as a source of genetic variability in the human genome.From1 Jan 2011 → 31 Dec 2014Funding: FWO research project (including WEAVE projects)
- Functional relevance of epigenetics in mental retardation.From1 Oct 2010 → 30 Sep 2013Funding: FWO fellowships
- A functional human genome project: integrated research of human congenital disorders.From1 Oct 2010 → 30 Sep 2012Funding: BOF - Concerted Research Project from 1994
- Functional relevance of epigenetic changes in mental retardation.From1 Jan 2010 → 31 Dec 2010Funding: BOF - Other initiatives
- Causal genomic duplications in patients with mental retardation: role of overexpression of genes on cognition.From1 Jan 2008 → 12 Jun 2012Funding: IWT personal funding - strategic basic research grants
Publications
1 - 10 of 54
- Characterization of tandem repeats in human genome and their role in disease(2018)
Authors: Alena Zablotskaya, Joris Vermeesch, Guy Froyen, Kevin Verstrepen
- Identification of Intellectual Disability Genes in Female Patients with A Skewed X Inactivation Pattern(2016)
Authors: Nathalie Fieremans, Hilde Van Esch, Koenraad Devriendt, Joris Vermeesch, Peter Marynen, Guy Froyen
Pages: 804 - 811 - X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2016)
Authors: Hilde Van Esch, Guy Froyen, Jean-Pierre Frijns, Koenraad Devriendt
Pages: 133 - 48 - X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2016)
Authors: H Hu, S A Haas, J Chelly, Hilde Van Esch, M Raynaud, A P M de Brouwer, S Weinert, Guy Froyen, S G M Frints, F Laumonnier, et al.
Pages: 133 - 48 - Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioural problems(2015)
Authors: Hilde Van Esch, Guy Froyen
Pages: 7171 - 81 - Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic features(2015)
Authors: Nathalie Fieremans, Hilde Van Esch, Thomy de Ravel de l'Argentière, Jozef Van Driessche, Stefanie Belet, Marijke Bauters, Guy Froyen
Pages: 324 - 7 - Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic features(2015)
Authors: Nathalie Fieremans, Hilde Van Esch, Thomy de Ravel de l'Argentière, Marijke Bauters, Guy Froyen
Pages: 324 - 7 - Novel microduplications at Xp11.22 including HUWE1: clinical and molecular insights into these genomic rearrangements associated with intellectual disability(2015)
Authors: Guy Froyen
Pages: 207 - 211 - A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function(2015)
Authors: Zeynep Okray, Hilde Van Esch, Koenraad Devriendt, Guy Froyen, Bassem Hassan
Pages: 423 - 37 - Expanding the phenotypic spectrum of PORCN variants in two males with syndromic microphthalmia(2015)
Authors: Paul Brady, Hilde Van Esch, Nathalie Fieremans, Guy Froyen, Jan Deprest, Koenraad Devriendt, Joris Vermeesch
Pages: 551 - 4