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J. Plomp · SciRah

Researcher profile · Semantic Scholar

J. Plomp

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J. Plomp — researcher profile on SciRah

h-index: 44
Works: 121
Citations: 8,215

Most-cited papers

Synaptic assembly of the brain in the absence of neurotransmitter secretion.
M. Verhage, A. Maia, J. Plomp, A. Brussaard +8 more
2000Science1,382 citations
Semantic Scholar
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
A. M. van den Maagdenberg, D. Pietrobon, T. Pizzorusso, S. Kaja +8 more
2004Neuron675 citations Open access
Semantic Scholar
MuSK IgG4 autoantibodies cause myasthenia gravis by inhibiting binding between MuSK and Lrp4
M. Huijbers, Wei Zhang, R. Klooster, E. Niks +10 more
2013Proceedings of the National Academy of Sciences of the United States of America262 citations Open access
Semantic Scholar
Eculizumab prevents anti-ganglioside antibody-mediated neuropathy in a murine model.
S. Halstead, F. M. Zitman, P. Humphreys, K. Greenshields +5 more
2008Brain : a journal of neurology238 citations Open access
Semantic Scholar
High cortical spreading depression susceptibility and migraine‐associated symptoms in Cav2.1 S218L mice
A. M. van den Maagdenberg, T. Pizzorusso, S. Kaja, N. Terpolilli +16 more
2010Annals of Neurology222 citations
Semantic Scholar
Muscle-specific kinase myasthenia gravis IgG4 autoantibodies cause severe neuromuscular junction dysfunction in mice.
R. Klooster, J. Plomp, M. Huijbers, E. Niks +10 more
2012Brain : a journal of neurology212 citations Open access
Semantic Scholar
Anti-GQ1b ganglioside antibodies mediate complement-dependent destruction of the motor nerve terminal.
G. O'Hanlon, J. Plomp, Mahua Chakrabarti, I. Morrison +9 more
2001Brain : a journal of neurology192 citations Open access
Semantic Scholar
Munc18-1 expression levels control synapse recovery by regulating readily releasable pool size
R. Toonen, Keimpe Wierda, M. S. Sons, H. de Wit +4 more
2006Proceedings of the National Academy of Sciences of the United States of America188 citations Open access
Semantic Scholar
Pathophysiology of myasthenia gravis with antibodies to the acetylcholine receptor, muscle-specific kinase and low-density lipoprotein receptor-related protein 4.
J. Verschuuren, M. Huijbers, J. Plomp, E. Niks +5 more
2013Autoimmunity Reviews179 citations
Semantic Scholar
The expanding field of IgG4‐mediated neurological autoimmune disorders
M. Huijbers, L. Querol, E. Niks, J. Plomp +5 more
2015European Journal of Neurology155 citations
Semantic Scholar
Anti-disialoside antibodies kill perisynaptic Schwann cells and damage motor nerve terminals via membrane attack complex in a murine model of neuropathy.
S. Halstead, G. O'Hanlon, P. Humphreys, Deborah Morrison +4 more
2004Brain : a journal of neurology144 citations
Semantic Scholar
Overexpression of GD1a Ganglioside Sensitizes Motor Nerve Terminals to Anti-GD1a Antibody-Mediated Injury in a Model of Acute Motor Axonal Neuropathy
J. Goodfellow, Tyrone Bowes, K. Sheikh, M. Odaka +8 more
2005Journal of Neuroscience130 citations Open access
Semantic Scholar
Natural disease history of the D2-mdx mouse model for Duchenne muscular dystrophy
M. van Putten, K. Putker, M. Overzier, W. Adamzek +3 more
2019The FASEB Journal128 citations Open access
Semantic Scholar
The neuropathic potential of anti-GM1 autoantibodies is regulated by the local glycolipid environment in mice.
K. Greenshields, S. Halstead, F. M. Zitman, S. Rinaldi +11 more
2009Journal of Clinical Investigation124 citations Open access
Semantic Scholar
Complex Gangliosides at the Neuromuscular Junction Are Membrane Receptors for Autoantibodies and Botulinum Neurotoxin But Redundant for Normal Synaptic Function
R. Bullens, G. O'Hanlon, E. Wagner, P. Molenaar +4 more
2002Journal of Neuroscience111 citations Open access
Semantic Scholar
Immunoglobulins inhibit pathophysiological effects of anti-GQ1b-positive sera at motor nerve terminals through inhibition of antibody binding.
B. Jacobs, G. O'Hanlon, R. Bullens, J. Veitch +2 more
2003Brain : a journal of neurology108 citations Open access
Semantic Scholar
Optogenetic termination of ventricular arrhythmias in the whole heart: towards biological cardiac rhythm management
E. Nyns, A. Kip, C. Bart, J. Plomp +4 more
2016European Heart Journal107 citations Open access
Semantic Scholar
Aberrant Morphology and Residual Transmitter Release at the Munc13-Deficient Mouse Neuromuscular Synapse
F. Varoqueaux, M. S. Sons, J. Plomp, N. Brose
2005Molecular and Cellular Biology104 citations Open access
Semantic Scholar
Calpain inhibitors protect against axonal degeneration in a model of anti-ganglioside antibody-mediated motor nerve terminal injury.
G. O'Hanlon, P. Humphreys, R. Goldman, S. Halstead +4 more
2003Brain : a journal of neurology97 citations
Semantic Scholar
Pathophysiological actions of neuropathy‐related anti‐ganglioside antibodies at the neuromuscular junction
J. Plomp, H. Willison
2009Journal of Physiology95 citations Open access
Semantic Scholar
Dystrophin Is Required for Appropriate Retrograde Control of Neurotransmitter Release at the Drosophila Neuromuscular Junction
Mariska van der Plas, G. Pilgram, J. Plomp, A. D. de Jong +2 more
2006Journal of Neuroscience86 citations Open access
Semantic Scholar
Loss of transforming growth factor-beta 2 leads to impairment of central synapse function
K. Heupel, V. Sargsyan, J. Plomp, M. Rickmann +3 more
2008Neural Development82 citations Open access
Semantic Scholar
Advances in the understanding of disease mechanisms of autoimmune neuromuscular junction disorders.
M. Huijbers, A. Marx, J. Plomp, R. Le Panse +1 more
2022Lancet Neurology80 citations Open access
Semantic Scholar
Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strains.
M. van Putten, Darshan Kumar, M. Hulsker, W. M. Hoogaars +7 more
2012Neuromuscular Disorders75 citations Open access
Semantic Scholar
Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models
E. M. van der Pijl, M. van Putten, E. Niks, J. Verschuuren +2 more
2016European Journal of Neuroscience68 citations
Semantic Scholar
The role of complement and complement regulators in mediating motor nerve terminal injury in murine models of Guillain-Barré syndrome.
H. Willison, S. Halstead, E. Beveridge, F. M. Zitman +3 more
2008Journal of Neuroimmunology68 citations
Semantic Scholar
An automated hybrid bioelectronic system for autogenous restoration of sinus rhythm in atrial fibrillation
E. Nyns, R. Poelma, L. Volkers, J. Plomp +8 more
2019Science Translational Medicine62 citations
Semantic Scholar
Anti‐disialosyl antibodies mediate selective neuronal or Schwann cell injury at mouse neuromuscular junctions
S. Halstead, I. Morrison, G. O'Hanlon, P. Humphreys +3 more
2005Glia62 citations
Semantic Scholar
Genetic models of migraine.
R. V. D. van de Ven, S. Kaja, J. Plomp, R. Frants +2 more
2007Archives of Neurology61 citations
Semantic Scholar
Pathogenic immune mechanisms at the neuromuscular synapse: the role of specific antibody‐binding epitopes in myasthenia gravis
M. Huijbers, A. F. Lipka, J. Plomp, E. Niks +2 more
2014Journal of Internal Medicine60 citations Open access
Semantic Scholar
Electrophysiological analysis of neuromuscular synaptic function in myasthenia gravis patients and animal models.
J. Plomp, M. Morsch, W. D. Phillips, J. Verschuuren
2015Experimental Neurology56 citations
Semantic Scholar
Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a‐mutant mouse rolling Nagoya
S. Kaja, R. V. D. van de Ven, J. V. van Dijk, J. Verschuuren +5 more
2007European Journal of Neuroscience56 citations
Semantic Scholar
Amendment history : Erratum ( December 1999 ) Monoclonal antibodies raised against Guillain-Barré syndrome – associated Campylobacter jejuni lipopolysaccharides react with neuronal gangliosides and paralyze muscle-nerve preparations
C. Goodyear, G. O'Hanlon, J. Plomp, E. Wagner +7 more
201854 citations
Semantic Scholar
Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness.
S. Kaja, R. V. D. van de Ven, L. Broos, H. Veldman +6 more
2005Neuroscience53 citations
Semantic Scholar
C5 inhibitor rEV576 protects against neural injury in an in vitro mouse model of Miller Fisher syndrome
S. Halstead, P. Humphreys, F. M. Zitman, J. Hamer +2 more
2008Journal of the peripheral nervous system49 citations
Semantic Scholar
Anti-ganglioside antibody internalization attenuates motor nerve terminal injury in a mouse model of acute motor axonal neuropathy.
S. N. Fewou, A. Rupp, Lauren E Nickolay, Kathryn Carrick +4 more
2012Journal of Clinical Investigation44 citations Open access
Semantic Scholar
Functional monovalency amplifies the pathogenicity of anti-MuSK IgG4 in myasthenia gravis
Dana L. E. Vergoossen, J. Plomp, Christoph Gstöttner, Yvonne E. Fillié-Grijpma +8 more
2020Proceedings of the National Academy of Sciences of the United States of America43 citations Open access
Semantic Scholar
Detection and prevalence of α‐latrotoxin–like effects of serum from patients with Guillain–Barré syndrome
B. Jacobs, Roland W. M. Bullens, G. O'Hanlon, C. W. Ang +2 more
2002Muscle and Nerve40 citations Open access
Semantic Scholar
Calcium channel mutations and migraine
E. Kors, A. M. van den Maagdenberg, J. Plomp, R. Frants +1 more
2002Current Opinion in Neurology40 citations
Semantic Scholar
Efgartigimod improves muscle weakness in a mouse model for muscle-specific kinase myasthenia gravis.
M. Huijbers, J. Plomp, I. V. van Es, Yvonne E. Fillié-Grijpma +6 more
2019Experimental Neurology39 citations Open access
Semantic Scholar
Conditional inactivation of the Cacna1a gene in transgenic mice
B. Todorov, R. V. D. van de Ven, S. Kaja, L. Broos +5 more
2006Genesis38 citations
Semantic Scholar
Complex Gangliosides as Autoantibody Targets at the Neuromuscular Junction in Miller Fisher Syndrome: A Current Perspective
G. O'Hanlon, R. Bullens, J. Plomp, H. Willison
2002Neurochemical Research36 citations
Semantic Scholar
The Ataxic Cacna1a-Mutant Mouse Rolling Nagoya: An Overview of Neuromorphological and Electrophysiological Findings
J. Plomp, A. M. van den Maagdenberg, S. Kaja
2009Cerebellum31 citations Open access
Semantic Scholar
Anti‐ganglioside Antibodies and the Presynaptic Motor Nerve Terminal
H. Willison, J. Plomp
2008Annals of the New York Academy of Sciences29 citations
Semantic Scholar
Neuromuscular synaptic function in mice lacking major subsets of gangliosides.
F. M. Zitman, B. Todorov, Bart C. Jacobs, J. Verschuuren +3 more
2008Neuroscience29 citations Open access
Semantic Scholar
Compensatory contribution of Cav2.3 channels to acetylcholine release at the neuromuscular junction of tottering mice.
S. Kaja, R. V. D. van de Ven, M. Ferrari, R. Frants +2 more
2006Journal of Neurophysiology29 citations
Semantic Scholar
Natural disease history of mouse models for limb girdle muscular dystrophy types 2D and 2F
S. Pasteuning-Vuhman, K. Putker, C. Tanganyika-de Winter, J. W. Boertje-van der Meulen +5 more
2017PLoS ONE27 citations Open access
Semantic Scholar
Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice.
S. Kaja, R. V. D. van de Ven, L. Broos, R. Frants +3 more
2010Journal of Neurophysiology26 citations
Semantic Scholar
Tomosyn-2 is required for normal motor performance in mice and sustains neurotransmission at motor endplates
C. J. Geerts, J. Plomp, B. Koopmans, M. Loos +4 more
2014Brain Structure and Function24 citations Open access
Semantic Scholar
Trans-synaptic homeostasis at the myasthenic neuromuscular junction.
J. Plomp
2017Frontiers in Bioscience23 citations
Semantic Scholar

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