Get started
Author

Bavo Heeman

The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
2015 · I Gijselinck, S Van Mossevelde, et al. · Molecular Psychiatry · 242
PDF
Depletion of PINK1 affects mitochondrial metabolism, calcium homeostasis and energy maintenance
2011 · Bavo Heeman, Chris Van den Haute, et al. · Journal of Cell Science · 199
PDF
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
2015 · Ilse Gijselinck, Sara Van Mossevelde, et al. · Neurology · 174
PDF
Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases
2022 · Andrew Chang, Xinyu Xiang, et al. · Cell · 150
PDF
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
2016 · Julie van der Zee, Ilse Gijselinck, et al. · Human Mutation · 104
PDF
Efficient and stable transduction of dopaminergic neurons in rat substantia nigra by rAAV 2/1, 2/2, 2/5, 2/6.2, 2/7, 2/8 and 2/9
2011 · A Van der Perren, J Toelen, et al. · Gene Therapy · 90
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease
2017 · Arne De Roeck, Tobi Van den Bossche, et al. · Acta Neuropathologica · 74
PDF
Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export
2020 · Shaun Martin, Stefanie Smolders, et al. · Acta Neuropathologica · 67
PDF
Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts
2012 · Federica Valsecchi, Claire Monge, et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 66
PDF
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and aging
2022 · Jolien Perneel, Manuela Neumann, et al. · Acta Neuropathologica · 65
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability
2019 · Rita Cacace, Bavo Heeman, et al. · Acta Neuropathologica · 58
PDF
Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations
2015 · Karolien Bettens, Steven Vermeulen, et al. · Molecular Neurodegeneration · 58
PDF
Loss-of-Function Rodent Models for Parkin and PINK1
2011 · Marusela Oliveras-Salv´, Anne-Sophie Van Rompuy, et al. · Journal of Parkinson s Disease · 43
PDF
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease
2021 · Stefanie Smolders, Stéphanie Philtjens, et al. · Acta Neuropathologica Communications · 42
PDF
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes
2023 · Cristina T. Vicente, Jolien Perneel, et al. · Brain · 38
PDF
Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathology
2023 · Manuela Neumann, Jolien Perneel, et al. · Acta Neuropathologica · 24
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
2017 · Jan Verheijen, Julie van der Zee, et al. · Neurobiology of Aging · 19
Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health
2025 · Jolien Perneel, Miranda Lastra Osua, et al. · Molecular Neurodegeneration · 13
PDF
Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder
2022 · Marije Meuwissen, Aline Verstraeten, et al. · Genetics in Medicine · 10
Analysis of the splicing landscape of the frontal cortex in FTLD-TDP reveals subtype specific patterns and cryptic splicing
2025 · Júlia Faura, Bavo Heeman, et al. · Acta Neuropathologica · 8
PDF
DT‐02‐01: Loss‐of‐function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort
2015 · Ilse Gijselinck, Sara Van Mossevelde, et al. · Alzheimer s & Dementia · 5
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes
2025 · Cristina T. Vicente, Tejasvi Niranjan, et al. · Molecular Neurodegeneration · 1
PDF
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and aging
2023 · Jolien Perneel, Manuela Neumann, et al. · Acta Neuropathologica
PDF
Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases
2020 · Stefanie Smolders, Stéphanie Philtjens, et al.
PDF
P1‐210: Investigating the Involvement of the Dpp6‐kv4.2 Protein Complex in Dementia
2019 · Rita Cacace, Kristof De Vos, et al. · Alzheimer s & Dementia
PDF
Works count: 59
Citation count: 1,548
H-index: 17
I10-index: 19
Year
Topic
Type