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Researcher
Hilde Brems
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Laboratory for Neurofibromatosis Research (Division)
Responsible
From15 Jul 2022 → Today - Laboratory for Neurofibromatosis Research (Division)
Member
From19 Oct 2009 → 30 Sep 2017 - Department of Human Genetics (Department)
Member
From1 Oct 1999 → Today
Projects
1 - 7 of 7
- Molecular and functional characterization of Legius syndrome and related disorders: Improved diagnosis and understanding of the underlying mechanisms.From1 Aug 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Development of new analytic tools and pathways to accelerate diagnosis and facilitate diagnostic monitoring of rare diseases”From1 Aug 2023 → TodayFunding: FWO research project (including WEAVE projects)
- Importance of SPRED1 in melanomaFrom9 Dec 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- 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
- Pathogenesis of congenital tibial bowing and pseudarthrosis in neurofibromatosis type 1.From1 Jan 2012 → 31 Dec 2015Funding: FWO research project
- 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
Publications
1 - 10 of 84
- Gonadales und gonadosomatisches Neurofibromatose-Typ-1-Mosaik: ein Bericht über zwei Familien: Gonadal and gonadosomatic mosaicism in NF1: report of two families.(2024)
Authors: Hilde Brems
Pages: 426 - 429 - 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 - Mosaic RASopathies concept: different skin lesions, same systemic manifestations?(2024)
Authors: Hilde Brems
- 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 - Cancer prognosis in PTEN Hamartoma Tumor Syndrome - a European cohort study(2024)
Authors: Hilde Brems
Pages: 563 - 564 - 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 - Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes(2024)
Authors: Hilde Brems
Pages: 689 - 691 - Lifestyle factors and breast cancer risk in females with PTEN Hamartoma Tumor Syndrome(2024)
Authors: Hilde Brems
Pages: 568 - 568 - 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