Bernadett Kalmár

Medicine · Health Sciences

31h-index3.5kcitations78works1.02yr avg
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Research Topics

Amyotrophic Lateral Sclerosis Research(31), Endoplasmic Reticulum Stress and Disease(18), Heat shock proteins research(12), Hereditary Neurological Disorders(12), Neurogenetic and Muscular Disorders Research(11)

Publications78 total

Innervation and cargo-specific axonal transport impairments in FUS-ALS mice with gain and loss of function
2025· 1 cited
Microglial Expression of the Wnt Signaling Modulator<i>DKK2</i>Differs between Human Alzheimer’s Disease Brains and Mouse Neurodegeneration Models
eNeuro·2023· 11 citedOpen Access
Microglial expression of the Wnt signalling modulator <i>DKK2</i> differs between human Alzheimer’s disease brains and mouse neurodegeneration models
2022· 1 citedOpen Access
Sectioning and Counting of Motor Neurons in the L3 to L6 Region of the Adult Mouse Spinal Cord
Current Protocols·2022· 9 citedOpen Access
Enhanced Expression of TRAP1 Protects Mitochondrial Function in Motor Neurons under Conditions of Oxidative Stress
International Journal of Molecular Sciences·2022· 8 citedOpen Access
Astrocytes display cell autonomous and diverse early reactive states in familial amyotrophic lateral sclerosis
Brain·2021· 48 citedOpen Access
Diversity of early astrocyte reactive profiles in familial amyotrophic lateral sclerosis
Brain·2021
An iPSC model of hereditary sensory neuropathy-1 reveals L-serine-responsive deficits in neuronal ganglioside composition and axoglial interactions
Cell Reports Medicine·2021· 33 citedOpen Access
Regional Differences in Heat Shock Protein 25 Expression in Brain and Spinal Cord Astrocytes of Wild-Type and SOD1 G93A Mice
Cells·2021· 4 citedOpen Access
Regional differences in the inflammatory and heat shock response in glia: implications for ALS
Cell Stress and Chaperones·2019· 9 citedOpen Access
Protective Role of Glial Heat Shock Proteins in Amyotrophic Lateral Sclerosis
Heat shock proteins·2019
Tournaments
European Journal of Neurology·2018Open Access
Inhibiting p38 MAPK alpha rescues axonal retrograde transport defects in a mouse model of ALS
Cell Death and Disease·2018· 100 citedOpen Access
Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitro
Neurobiology of Disease·2018· 48 citedOpen Access
Mice with endogenous <scp>TDP</scp> ‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis
The EMBO Journal·2018· 180 citedOpen Access
Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration
PLoS Genetics·2018· 45 citedOpen Access
Region specific glial stress responses: implications for ALS
Neuromuscular Disorders·2018
Do diverse Charcot-Marie-Tooth disease-causing mutations show convergent disease pathomechanisms? Investigation of mitochondrial dysfunction in CMT
Neuromuscular Disorders·2018
Dissecting TDP-43 gain- and loss-of-function in neurodegeneration
Neuromuscular Disorders·2018
Assessment of metal concentrations in the SOD1G93A mouse model of amyotrophic lateral sclerosis and its potential role in muscular denervation, with particular focus on muscle tissue
Molecular and Cellular Neuroscience·2018· 9 citedOpen Access
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Frequent Co-authors

Linda Greensmith(46), Mary M. Reilly(7), Elizabeth Fisher(6), Giampietro Schiavo(6), Geoffrey Burnstock(4), Alexander M. Rossor(4), Abraham Acevedo‐Arozena(4), Benjamin Clarke(4), Sergey S. Novoselov(3), Anna L. Gray(3), Michael E. Cheetham(3), Mhoriam Ahmed(3), Ching‐Hua Lu(3), Majid Hafezparast(3), Paul J. Whiting(3), Henry Houlden(3), David Bennett(3), Dairín Kieran(2), James R. Dick(2), Prasanth Sivakumar(2)