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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
1 - 10 of 19
- Monogenic immune disorders in adults: from Mendelian inheritance to somatic mosaicismFrom3 Oct 2022 → TodayFunding: FWO fellowships
- Importance of SPRED1 in melanomaFrom9 Dec 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- EU Patient- cEntric clinicAl tRial pLatformFrom1 Nov 2019 → 30 Apr 2023Funding: H2020 - European Institute of Innovation and Technology
- The effect of genetic factors on the severity of the ASD phenotypeFrom1 Sep 2018 → 1 Sep 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
- Importance of SPRED1 in melanomaFrom1 Jan 2017 → 30 Jun 2021Funding: Other federal scientific institutions
- Unraveling the genetics of familial SchwannomatosisFrom1 Oct 2016 → 30 Sep 2017Funding: Nonprofit institution or equivalents
- Importance of SPRED1 in melanomaFrom1 Oct 2015 → 27 Mar 2020Funding: Own budget, for example: patrimony, inscription fees, gifts
- Periosteal cell therapy as a new treatment of pseudarthrosis in children with NF1.From21 Oct 2013 → 10 Dec 2019Funding: IWT personal funding - strategic basic research grants, BOF - Doctoral projects
- A molecular approach to understand breast cancer cell dormancy.From1 Oct 2012 → 4 Jul 2019Funding: FWO fellowships
- Pathogenesis of congenital tibial bowing and pseudarthrosis in neurofibromatosis type 1.From1 Jan 2012 → 31 Dec 2015Funding: FWO research project
Publications
1 - 10 of 210
- Encephalocraniocutaneous lipomatosis phenotype associated with mosaic biallelic pathogenic variants in the NF1 gene(2024)
Authors: Steven Smeijers, Hilde Brems, Wim Van Paesschen, Johan van Loon, Seppe Van der Auweraer, Raf Sciot, Dietmar Thal, Lieven Lagae, Eric Legius, Tom Theys
- Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants(2024)
Authors: Jeroen Dekervel, Gert De Hertogh, Hilde Brems, Eric Legius
- Gonadal and gonadosomatic mosaicism in NF1: report of two families(2024)
Authors: Eric Legius, Hilde Brems
Pages: 429 - 429 - Gonadal and gonadosomatic mosaicism in NF1: report of two families(2024)
Authors: Eric Legius, Hilde Brems
Pages: 426 - 429 - Capillary malformations in a child caused by a novel HRAS mutation(2024)
Authors: Eric Legius, Hilde Brems
Pages: 289 - 291 - Platform trial design for neurofibromatosis type 1, NF2-related schwannomatosis and non-NF2-related schwannomatosis: A potential model for rare diseases(2024)
Authors: Charlotte Carton, Eric Legius
Pages: 395 - 403 - Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization(2024)
Authors: Sarah Borrie, Eric Legius
Pages: 161 - 174 - SREBP modulates the NADP+/NADPH cycle to control night sleep in Drosophila(2023)
Authors: Eric Legius
- 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