Citation Impact
Citing Papers
Activation and Function of the MAPKs and Their Substrates, the MAPK-Activated Protein Kinases
2011 Standout
Protein Misfolding, Amyloid Formation, and Human Disease: A Summary of Progress Over the Last Decade
2017 Standout
Ferroptosis regulation by the NGLY1/NFE2L1 pathway
2022 StandoutNobel
Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis
2016
Human genetic disorders of sphingolipid biosynthesis
2014
Parkinson's disease
2021 Standout
Local unfolding of the HSP27 monomer regulates chaperone activity
2019
AMPK: guardian of metabolism and mitochondrial homeostasis
2017 Standout
Role of ROS and RNS Sources in Physiological and Pathological Conditions
2016 Standout
Sphingolipids and their metabolism in physiology and disease
2017 Standout
Functional and morphological impact of ER stress on mitochondria
2013
Non-canonical Glutamate-Cysteine Ligase Activity Protects against Ferroptosis
2020
Guillain-Barré syndrome
2016 Standout
Ferroptosis turns 10: Emerging mechanisms, physiological functions, and therapeutic applications
2022 Standout
The Role of Lipid Bodies in the Microglial Aging Process and Related Diseases
2017
Ankle dorsi- and plantar-flexion torques measured by dynamometry in healthy subjects from 5 to 80 years
2013
Many Ceramides
2011
The Human Plasma Lipidome
2011
Macrolides sensitize EGFR-TKI-induced non-apoptotic cell death via blocking autophagy flux in pancreatic cancer cell lines
2015 StandoutNobel
Myelination and the trophic support of long axons
2010
Increased Plasma Levels of Select Deoxy-ceramide and Ceramide Species are Associated with Increased Odds of Diabetic Neuropathy in Type 1 Diabetes: A Pilot Study
2016
A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease
2014
Heat shock protein 27 phosphorylation: kinases, phosphatases, functions and pathology
2009
Lipid-droplet-accumulating microglia represent a dysfunctional and proinflammatory state in the aging brain
2020 StandoutNobel
Small fiber neuropathy in Fabry disease
2012
Oxidative stress and mitochondrial dysfunction in Alzheimer's disease
2013 Standout
The yeast sphingolipid signaling landscape
2013
Biochemistry of Mitochondrial Coenzyme Q Biosynthesis
2017
Targeting ferroptosis as a vulnerability in cancer
2022 Standout
Mitochondria as multifaceted regulators of cell death
2019 Standout
A systematic review of muscle morphology and function in intermittent claudication
2017 StandoutNobel
The Pathobiology of Vascular Dementia
2013 Standout
HSAN1 mutations in serine palmitoyltransferase reveal a close structure–function–phenotype relationship
2015
O-GlcNAc modification of small heat shock proteins enhances their anti-amyloid chaperone activity
2021 StandoutNobel
Sphingolipids and lysosomal pathologies
2013
Topological and Functional Characterization of the ssSPTs, Small Activating Subunits of Serine Palmitoyltransferase
2013
Tackling the biophysical properties of sphingolipids to decipher their biological roles
2015
Ectopic expression of ceramide synthase 2 in neurons suppresses neurodegeneration induced by ceramide synthase 1 deficiency
2016
Neuropathic Pain: From Mechanisms to Treatment
2020 Standout
Quantitative Serum Nuclear Magnetic Resonance Metabolomics in Cardiovascular Epidemiology and Genetics
2015 Standout
How neuroinflammation contributes to neurodegeneration
2016 StandoutScience
Fusion and Fission: Interlinked Processes Critical for Mitochondrial Health
2011
Blood NfL
2019
Mito-Morphosis: Mitochondrial Fusion, Fission, and Cristae Remodeling as Key Mediators of Cellular Function
2015
Plasma 1-deoxysphingolipids are predictive biomarkers for type 2 diabetes mellitus
2015
Elevation of 20-carbon long chain bases due to a mutation in serine palmitoyltransferase small subunit b results in neurodegeneration
2015
“Inverse Drug Discovery” Strategy To Identify Proteins That Are Targeted by Latent Electrophiles As Exemplified by Aryl Fluorosulfates
2017 StandoutNobel
Animal Models of Autoimmune Neuropathy
2014
Works of Matilde Laurá being referenced
Plasma neurofilament light chain concentration in the inherited peripheral neuropathies
2018
Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing
2012
Novel HSAN1 Mutation in Serine Palmitoyltransferase Resides at a Putative Phosphorylation Site That Is Involved in Regulating Substrate Specificity
2015
Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease
2006
Reliability of clinical outcome measures in Charcot-Marie-Tooth disease
2007
Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids
2010
Rapid progression of late onset axonal Charcot Marie Tooth disease associated with a novel MPZ mutation in the extracellular domain
2007
Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation
2013
Charcot‐Marie‐Tooth disease
2011
A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK
2015
Mutations in the HSP27 ( HSPB1 ) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2
2008
Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2
2013
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations
2011