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Researcher
Elke Bogaert
- Keywords:Neuroscience, Neurodegeneration
- Disciplines:Neurological and neuromuscular diseases
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Feb 2019 → Today
Projects
1 - 2 of 2
- RNF216 dysfunction: unraveling its nuclear role in biomolecular condensates and splicing regulationFrom1 Nov 2025 → TodayFunding: FWO fellowships
- Expanding the TDP-43 proteinopathy spectrum from the neuron to the muscle: a cellular, biophysical and multi-omics study.From1 Jan 2024 → TodayFunding: FWO research project (including WEAVE projects)
Publications
1 - 10 of 13
- Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder(2025)Published in: AMERICAN JOURNAL OF HUMAN GENETICSISSN: 1537-6605Issue: 6Volume: 112Pages: 1388 - 1414
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder(2024)Number of pages: 1
- Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability(2024)Published in: AMERICAN JOURNAL OF HUMAN GENETICSISSN: 1537-6605Issue: 3Volume: 111Pages: 509 - 528
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder(2024)Number of pages: 1
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder(2024)Number of pages: 1
- Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism : possible implication for Alzheimer's disease(2023)Published in: PROGRESS IN NEUROBIOLOGYISSN: 1873-5118Volume: 223
- C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD(2023)Published in: ACTA NEUROPATHOLOGICAISSN: 1432-0533Volume: 145Pages: 793 - 814
- Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders(2023)Published in: NEUROLOGY-GENETICSISSN: 2376-7839Issue: 3Volume: 9
- SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability(2023)Published in: AMERICAN JOURNAL OF HUMAN GENETICSISSN: 1537-6605Issue: 5Volume: 110Pages: 790 - 808
- Lipodystrophy due to genetic deficiency of picornavirus host factor and obesity regulator PLAAT3(2022)Volume: 30Pages: 80 - 80