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Jun Li, MD, PhD, FANA, FAAN
John M. O’Quinn Foundation Presidential Distinguished Chair in Neurology
,
Stanley H. Appel Department of Neurology
Professor of Neurology
,
Academic Institute
Member, Research Institute
,
Academic Institute
Chair
,
Stanley H. Appel Department of Neurology
Co-Director
,
Neurological Institute
Houston Methodist Hospital
Houston Methodist
Weill Cornell Medical College
h-index
6486
Citations
43
h-index
Calculated based on number of publications stored in Pure and citations from Scopus
1991 …
2024
Research activity per year
Overview
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Research output
(112)
Similar Profiles
(1)
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Dive into the research topics where Jun Li is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Keyphrases
Charcot-Marie-Tooth Disease
100%
Peripheral Myelin Protein 22 (PMP22)
54%
Neuropathy
38%
Myelin
35%
Disease Pattern
30%
Hereditary Neuropathy with Liability to Pressure Palsies
24%
Nerve
23%
Schwann Cells
22%
Peripheral Nerve
19%
Microglia
18%
Inherited Neuropathy
18%
Demyelination
16%
Lysosomal Storage Disease
16%
Myelin Protein Zero
16%
Myelinated Nerve Fibers
15%
Myelination
15%
Skin Biopsy
15%
Peripheral Nervous System
14%
Natural History
14%
Neurodegeneration
13%
Peripheral Neuropathy
13%
Examination Scores
13%
Mouse Model
12%
Nerve Conduction Studies
12%
Axonal Loss
11%
Disability
11%
Axon
10%
Charcot-Marie-Tooth
9%
Tremor
9%
PAK2
9%
Plaque
9%
Hereditary Neuropathy
9%
Axonal Degeneration
8%
Nervous System
8%
Loss Function
8%
Lysosome
8%
Segmental Demyelination
8%
Charcot-Marie-Tooth Neuropathy
8%
Knock-in Mouse Model
8%
Myelin Basic Protein
8%
Biallelic mutations
8%
Conduction Velocity
8%
Magnetization Transfer Ratio
7%
Peripheral Nerve Defect
7%
Rodents
7%
Sensory Loss
7%
Internodal Length
7%
CMTX1
7%
Charcot-Marie-Tooth Type 1A
7%
Sciatic Nerve
7%
Neuroscience
Neuropathy
95%
Charcot-Marie-Tooth Disease
58%
Myelin
49%
Peripheral Myelin Protein 22
47%
Peripheral Nerve
33%
Schwann Cell
28%
Microglia
20%
Polyneuropathy
18%
Myelinated Nerve Fiber
15%
Myelinogenesis
14%
Axon
14%
Nerve Cell Degeneration
14%
Conduction Velocity
12%
In Vitro
11%
Myelin Protein
11%
Action Potential
11%
Magnetic Resonance Imaging
10%
Peripheral Nervous System
10%
Nerve Conduction Study
10%
Nervous System
9%
Nervous System Regeneration
9%
P21 Activated Kinase 2
9%
Amyloid Protein
9%
Sensory Neuron
9%
Magnetic Resonance Imaging
9%
Missense Mutation
9%
In Vivo
9%
Phosphatidylinositol
9%
Tremor
9%
Plaque
9%
Glia
8%
Nerve Conduction
8%
Lysosome
8%
Phosphatidylinositide
8%
Axonal Degeneration
8%
Nerve Fiber Degeneration
8%
Alzheimer's Disease
7%
RNA-binding Protein
7%
Cerebellum
7%
Phosphatase
7%
Cytokine
7%
Neurotoxin
7%
Nerve Block
7%
Neurodegeneration
6%
Neural Stem Cell
6%
Senile Plaque
6%
Nitric Oxide
6%
Mononuclear Phagocyte
6%
West Nile Virus
6%
Sciatic Nerve
6%
Medicine and Dentistry
DeJerine-Sottas Disease
93%
Neuropathy
81%
Peripheral Myelin Protein 22
40%
Myelin
37%
Diseases
32%
Hereditary Neuropathy with Liability to Pressure Palsy
21%
Peripheral Nerve
20%
Myelin Protein
15%
Magnetic Resonance Imaging
14%
Skin Biopsy
13%
Axon
12%
Myelinated Nerve Fiber
12%
Demyelination
11%
Polyneuropathy
10%
Clinical Trial
10%
Nerve Regeneration
9%
Nerve Conduction Study
9%
Magnetization Transfer
8%
Schwann Cell
8%
Vacuolization
7%
Biological Marker
7%
Nerve Fiber Degeneration
7%
Ulnar Nerve
7%
Genome Wide Association Study
6%
Nerve Block
6%
Cross Sectional Study
6%
West Nile Virus
6%
Virus Infection
6%
Phosphatidylinositide
6%
Nerve Cell Degeneration
6%
Paralysis
6%
Fibroblast
6%
Weakness
6%
Gene Mutation
5%
Sciatic Nerve
5%
Genotype Phenotype Correlation
5%
Myelination
5%
Compound Muscle Action Potential
5%
Motor Unit Number Estimation
5%
Lysosome
5%
Morphometric Analysis
5%
Sensory Neuropathy
5%
Action Potential
5%
Central Nervous System
5%
Electrophysiology
5%
Disease Exacerbation
5%
