Researcher
Marijke Bauters
- Keywords:Biomedical sciences (incl. biochemistry)
Affiliations
- Human Genome Laboratory (Division)
Member
From1 Mar 2009 → 31 Dec 2013
Projects
1 - 2 of 2
- Functional relevance of epigenetics in mental retardation.From1 Oct 2010 → 30 Sep 2013Funding: FWO fellowships
- Functional relevance of epigenetic changes in mental retardation.From1 Jan 2010 → 31 Dec 2010Funding: BOF - Other initiatives
Publications
1 - 10 of 17
- A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency(2018)
Authors: Hilde Van Esch, Marijke Bauters
Pages: 54 - 63 - 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 - Evidence for increased SOX3 dosage as a risk factor for X-linked hypopituitarism and neural tube defects(2014)
Authors: Marijke Bauters, Hilde Van Esch, Marcella Baldewijns, Jean-Pierre Frijns, Peter Marynen, Guy Froyen
Pages: 1947 - 52 - Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/beta-Catenin Pathway in a Drosophila Model for Intellectual Disability(2013)
Authors: Joke Vandewalle, Hilde Brems, Marijke Bauters, Elsa Lauwers, Peter Marynen, Patrik Verstreken, Bassem Hassan, Guy Froyen
- The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability(2013)
Authors: Marijke Bauters, Hilde Van Esch, Nathalie Fieremans, Koenraad Devriendt, Jean-Pierre Frijns, Peter Marynen, Guy Froyen
Pages: 1177 - 85 - Promoting role of cholecystokinin 2 receptor (CCK2R) in gastrointestinal stromal tumours pathogenesis(2012)
Authors: Anna Quattrone, Barbara Dewaele, Agnieszka Wozniak, Marijke Bauters, Beppe Floris, Patrick Schöffski, Raf Sciot, Maria Debiec-Rychter
Pages: 565 - 574 - Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1(2012)
Authors: Jeroen Breckpot, Bernard Thienpont, Marijke Bauters, Léon-Charles Tranchevent, Marc Gewillig, Karel Allegaert, Joris Vermeesch, Yves Moreau, Koenraad Devriendt
Pages: 574 - 580 - BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome(2012)
Authors: Jeroen Breckpot, Léon-Charles Tranchevent, Bernard Thienpont, Marijke Bauters, Marc Gewillig, Joris Vermeesch, Yves Moreau, Koenraad Devriendt, Hilde Van Esch
Pages: 12 - 16 - MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression(2008)
Authors: Marijke Bauters, Hilde Van Esch, Peter Marynen, Jean-Pierre Frijns, Guy Froyen
Pages: 1029 - 1037