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B. Asselbergh · SciRah

Researcher profile · Semantic Scholar

B. Asselbergh

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B. Asselbergh — researcher profile on SciRah

h-index: 34
Works: 69
Citations: 4,613

Most-cited papers

Neutrophil extracellular trap cell death requires both autophagy and superoxide generation
Q. Remijsen, T. V. Berghe, E. Wirawan, B. Asselbergh +6 more
2011Cell Research814 citations Open access
Semantic Scholar
Global switches and fine-tuning-ABA modulates plant pathogen defense.
B. Asselbergh, D. De Vleesschauwer, M. Höfte
2008Molecular Plant-Microbe Interactions442 citations Open access
Semantic Scholar
Resistance to Botrytis cinerea in sitiens, an Abscisic Acid-Deficient Tomato Mutant, Involves Timely Production of Hydrogen Peroxide and Cell Wall Modifications in the Epidermis1[C][W][OA]
B. Asselbergh, K. Curvers, S. França, K. Audenaert +3 more
2007Plant Physiology376 citations Open access
Semantic Scholar
Profiling peripheral nerve macrophages reveals two macrophage subsets with distinct localization, transcriptome and response to injury
E. Ydens, Lukas Amann, B. Asselbergh, Charlotte L. Scott +14 more
2020Nature Neuroscience218 citations Open access
Semantic Scholar
Mitochondria-associated membranes as hubs for neurodegeneration
M. Krols, G. Van Isterdael, B. Asselbergh, A. Kremer +3 more
2016Acta Neuropathologica208 citations Open access
Semantic Scholar
Acute injury in the peripheral nervous system triggers an alternative macrophage response
E. Ydens, A. Cauwels, B. Asselbergh, Sofie Goethals +6 more
2012Journal of Neuroinflammation168 citations Open access
Semantic Scholar
Abscisic Acid Deficiency Causes Changes in Cuticle Permeability and Pectin Composition That Influence Tomato Resistance to Botrytis cinerea1[C][W][OA]
K. Curvers, H. Seifi, G. Mouille, R. De Rycke +7 more
2010Plant Physiology158 citations Open access
Semantic Scholar
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)
Alejandro Estrada-Cuzcano, Shaun Martin, T. Chamova, M. Synofzik +18 more
2017Brain : a journal of neurology149 citations Open access
Semantic Scholar
Abscisic acid deficiency leads to rapid activation of tomato defence responses upon infection with Erwinia chrysanthemi.
B. Asselbergh, A. E. Achuo, M. Höfte, F. Van Gijsegem
2007Molecular plant pathology148 citations Open access
Semantic Scholar
Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance.
K. Peeters, I. Litvinenko, B. Asselbergh, L. Almeida-Souza +11 more
2013American Journal of Human Genetics129 citations Open access
Semantic Scholar
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
K. Hardies, C. de Kovel, S. Weckhuysen, B. Asselbergh +23 more
2015Brain : a journal of neurology116 citations Open access
Semantic Scholar
Small Heat-Shock Protein HSPB1 Mutants Stabilize Microtubules in Charcot-Marie-Tooth Neuropathy
L. Almeida-Souza, B. Asselbergh, C. d’Ydewalle, K. Moonens +10 more
2011Journal of Neuroscience105 citations Open access
Semantic Scholar
Developing 3D SEM in a broad biological context
A. Kremer, S. Lippens, S. Bartunkova, B. Asselbergh +18 more
2015Journal of Microscopy101 citations Open access
Semantic Scholar
Mutant HSPB8 causes motor neuron-specific neurite degeneration
J. Irobi, L. Almeida-Souza, B. Asselbergh, V. de Winter +9 more
2010Human Molecular Genetics93 citations Open access
Semantic Scholar
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8
D. Bouhy, M. Juneja, I. Katona, A. Holmgren +10 more
2017Acta Neuropathologica74 citations Open access
Semantic Scholar
Small heat shock proteins operate as molecular chaperones in the mitochondrial intermembrane space
Elias Adriaenssens, B. Asselbergh, Pablo Rivera-Mejías, S. Bervoets +8 more
2023Nature Cell Biology72 citations Open access
Semantic Scholar
Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies
Mansour Haidar, B. Asselbergh, Elias Adriaenssens, V. de Winter +4 more
2019Autophagy69 citations Open access
Semantic Scholar
Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy
D. Atkinson, Jelena Nikodinovic Glumac, B. Asselbergh, Biljana Ermanoska +10 more
2017Neurology63 citations Open access
Semantic Scholar
Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction
J. Van Lent, P. Verstraelen, B. Asselbergh, Elias Adriaenssens +7 more
2021Brain : a journal of neurology53 citations Open access
Semantic Scholar
Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations
K. Bettens, Steven Vermeulen, C. Van Cauwenberghe, B. Heeman +9 more
2015Molecular Neurodegeneration51 citations Open access
Semantic Scholar
Charcot–Marie–Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments
A. Holmgren, D. Bouhy, V. de Winter, B. Asselbergh +3 more
2013Acta Neuropathologica50 citations Open access
Semantic Scholar
Diffusion kurtosis imaging to detect amyloidosis in an APP/PS1 mouse model for Alzheimer's disease
G. Vanhoutte, S. Pereson, R. D. Y. Palacios, P. Guns +6 more
2013Magnetic Resonance in Medicine49 citations
Semantic Scholar
Disruption of the SapM locus in Mycobacterium bovis BCG improves its protective efficacy as a vaccine against M. tuberculosis
N. Festjens, P. Bogaert, A. Batni, E. Houthuys +13 more
2011EMBO Molecular Medicine47 citations Open access
Semantic Scholar
Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I
A. Rotthier, Anke Penno, B. Rautenstrauss, M. Auer-Grumbach +8 more
2011Human Mutation46 citations Open access
Semantic Scholar
Caspase-14-deficient mice are more prone to the development of parakeratosis.
E. Hoste, G. Denecker, B. Gilbert, F. van Nieuwerburgh +8 more
2013Journal of Investigative Dermatology44 citations Open access
Semantic Scholar
Loss-of-function mutations in the ATP 13 A 2 / PARK 9 gene cause complicated hereditary spastic paraplegia ( SPG 78 )
Alejandro Estrada-Cuzcano, Shaun Martin, T. Chamova, M. Synofzik +19 more
201742 citations
Semantic Scholar
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease
S. Smolders, S. Philtjens, D. Crosiers, A. Sieben +15 more
2021Acta Neuropathologica Communications40 citations Open access
Semantic Scholar
Sensory neuropathy-causing mutations in ATL3 affect ER–mitochondria contact sites and impair axonal mitochondrial distribution
M. Krols, B. Asselbergh, R. De Rycke, V. de Winter +6 more
2018Human Molecular Genetics40 citations Open access
Semantic Scholar
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes
Elias Adriaenssens, B. Tedesco, Laura Mediani, B. Asselbergh +5 more
2020Scientific Reports39 citations Open access
Semantic Scholar
CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila
Biljana Ermanoska, W. Motley, R. Leitão-Gonçalves, B. Asselbergh +8 more
2014Neurobiology of Disease39 citations Open access
Semantic Scholar
Systematic Quantification of Synapses in Primary Neuronal Culture
P. Verstraelen, G. Garcia-Diaz Barriga, M. Verschuuren, B. Asselbergh +4 more
2020bioRxiv37 citations Open access
Semantic Scholar
Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients.
J. Irobi, A. Holmgren, V. de Winter, B. Asselbergh +6 more
2012Neuromuscular Disorders36 citations
Semantic Scholar
Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy.
D. Beijer, T. Deconinck, J. De Bleecker, M. Dotti +7 more
2019Brain : a journal of neurology34 citations Open access
Semantic Scholar
Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy
S. Bervoets, Na Wei, Maria-Luise Erfurth, Shazie Yusein-Myashkova +12 more
2019Nature Communications34 citations Open access
Semantic Scholar
Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in Drosophila.
K. Janssens, Sofie Goethals, D. Atkinson, Biljana Ermanoska +5 more
2014Neurobiology of Disease34 citations Open access
Semantic Scholar
Basal tomato defences to Botrytis cinerea include abscisic acid-dependent callose formation
B. Asselbergh, M. Höfte
200733 citations Open access
Semantic Scholar
Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1A
J. Van Lent, Leen Vendredy, Elias Adriaenssens, Tatiana Da Silva Authier +6 more
2022Brain : a journal of neurology32 citations Open access
Semantic Scholar
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease
T. Geuens, V. de Winter, N. Rajan, T. Achsel +7 more
2017Acta Neuropathologica Communications31 citations Open access
Semantic Scholar
Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer’s disease
Elena S. Gusareva, J. Twizere, K. Sleegers, P. Dourlen +27 more
2018Neurobiology of Aging30 citations Open access
Semantic Scholar
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
W. De Ridder, I. Nelson, B. Asselbergh, B. De Paepe +17 more
2019Neurology: Genetics28 citations Open access
Semantic Scholar
HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies
B. Tedesco, Leen Vendredy, Elias Adriaenssens, M. Cozzi +23 more
2023Autophagy27 citations Open access
Semantic Scholar
Inhibition of spontaneous neutrophil apoptosis by parabutoporin acts independently of NADPH oxidase inhibition but by lipid raft‐dependent stimulation of Akt
Q. Remijsen, T. V. Berghe, E. Parthoens, B. Asselbergh +2 more
2009Journal of Leukocyte Biology26 citations Open access
Semantic Scholar
Protein CoAlation and antioxidant function of coenzyme A in prokaryotic cells
M. Krols, S. Detry, B. Asselbergh, L. Almeida-Souza +10 more
2017bioRxiv25 citations Open access
Semantic Scholar
C9orf72 hexanucleotide repeat expansions impair microglial response in ALS
Pegah Masrori, Baukje Bijnens, Laura Fumagalli, K. Davie +18 more
2025Nature Neuroscience24 citations Open access
Semantic Scholar
A weakened interface in the P182L variant of HSP27 associated with severe Charcot‐Marie‐Tooth neuropathy causes aberrant binding to interacting proteins
T. Alderson, Elias Adriaenssens, B. Asselbergh, I. Pritišanac +7 more
2021EMBO Journal22 citations Open access
Semantic Scholar
Rare missense mutations in ABCA7 might increase Alzheimer’s disease risk by plasma membrane exclusion
Liene Bossaerts, Elisabeth Hendrickx Van de Craen, Rita Cacace, B. Asselbergh +1 more
2022Acta Neuropathologica Communications21 citations Open access
Semantic Scholar
Tyrosyl-tRNA synthetase has a noncanonical function in actin bundling
Biljana Ermanoska, B. Asselbergh, Laura Morant, Maria-Luise Petrovic-Erfurth +18 more
2023Nature Communications16 citations Open access
Semantic Scholar
HSPB1 Facilitates the Formation of Non-Centrosomal Microtubules
L. Almeida-Souza, B. Asselbergh, V. de Winter, Sofie Goethals +2 more
2013PLoS ONE16 citations Open access
Semantic Scholar
Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health
Jolien Perneel, Miranda Lastra Osua, Sara Alidadiani, Nele Peeters +15 more
2025Molecular Neurodegeneration12 citations Open access
Semantic Scholar
Regulation of human microglial gene expression and function via RNAase-H active antisense oligonucleotides in vivo in Alzheimer’s disease
Lina Vandermeulen, Ivana Geric, Laura Fumagalli, Mohamed Kreir +13 more
2024Molecular Neurodegeneration12 citations Open access
Semantic Scholar

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