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Researcher
Eric Legius
- Disciplines:Neurosciences, Biological and physiological psychology, Cognitive science and intelligent systems, Developmental psychology and ageing
Affiliations
- Laboratory for Neurofibromatosis Research (Division)
Member
From15 Jul 2022 → Today - Department of Human Genetics (Department)
Member
From1 Oct 1999 → 14 Jul 2022
Projects
11 - 19 of 19
- SUZ12 as a new modifier gene in NF1-related MPNST development.From16 Dec 2011 → 15 Dec 2012Funding: Foundations, funds and other with scientific goal
- NF1-like syndromes: identification of new genes and further characterization of Legius syndrome using the mouse model.From1 Oct 2011 → 30 Sep 2017Funding: FWO fellowships
- Deregulated signaling pathways in cancer: from genetic insights towards targeted therapy.From1 Oct 2010 → 30 Nov 2016Funding: BOF - Concerted Research Project from 1994
- Characterization and treatment of the cognitive defects in Spred1 knockout mice, and in patients with Legius syndrome and neurofibromatosis type 1.From1 Jan 2010 → 31 Dec 2015Funding: FWO research project
- Genomic aberrations in children with malignancy and associated abnormalities.From1 Jan 2010 → 31 Dec 2013Funding: FWO research project
- Cognition and Behavior in Neurofibromatosis Type 1 and Legius SyndromeFrom1 Dec 2009 → 9 Feb 2015Funding: Private funding of national origin - undefined
- Loss of function of Spred in the Drosophila model for Legius syndromeFrom1 Oct 2009 → 23 Apr 2010Funding: Own budget, for example: patrimony, inscription fees, gifts
- A genomic approach for the identification of genes involved in mental retardation and brain anomalies.From1 Oct 2008 → 30 Sep 2023Funding: FWO fellowships
- Investigation of a new tumor supressor gene causing an autosomal dominant condition resembling neurofibromatosis type 1.From1 Jan 2008 → 31 Dec 2013Funding: FWO research project
Publications
1 - 10 of 214
- Gonadal and gonadosomatic mosaicism in NF1: report of two families(2024)
Authors: Eric Legius, Hilde Brems
- Capillary malformations in a child caused by a novel HRAS mutation(2024)
Authors: Eric Legius, Hilde Brems
Pages: 289 - 291 - Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization(2024)
Authors: Sarah Borrie, Eric Legius
Pages: 161 - 174 - Detection of constitutional mismatch repair deficiency in two suspected Lynch syndrome cases with first cancer diagnoses in their late 30s and early 40s(2024)
Authors: Eric Legius, Hilde Brems
Pages: 255 - 255 - Germline heterozygous deletion containing CDKN2A/CDKN2B as genetic substrate for rare familial neural and skin tumor syndrome(2024)
Authors: Hilde Brems, Paul Clement, Steven De Vleeschouwer, Frank Van Calenbergh, Eric Legius
Pages: 583 - 583 - Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families(2023)
Authors: Hilde Brems, Anne Uyttebroeck, Eric Legius, Brigitte Decallonne
Pages: 402 - 408 - YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse(2023)
Authors: Eric Legius
- Establishing the neurodevelopmental phenotype and genotype-phenotype correlations in individuals with a TRIP12 mutation(2023)
Authors: Mio Aerden, Eric Legius, Hilde Van Esch
Pages: 446 - 446 - TET2-Driver and NLRC4-Passenger Variants in Adult-Onset Autoinflammation(2023)
Authors: Ellen De Langhe, Frederik Staels, Raf Sciot, Olga Tsuiko, Mieke Gouwy, Patrick Verschueren, Carine Wouters, Paul Proost, Patrick Matthys, Eric Legius, et al.
Pages: 1626 - 1629 - The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant(2023)
Authors: Mio Aerden, Eric Legius, Miel Theunis, Hilde Van Esch
Pages: 461 - 468