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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
Neurological Institute
Houston Methodist Hospital
Houston Methodist
Weill Cornell Medical College
h-index
5976
Citations
40
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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Network
Projects
(4)
Research output
(111)
Similar Profiles
(6)
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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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Neuroscience
Action Potential
12%
Alzheimer's Disease
6%
Amyloid Protein
9%
Axon
9%
Axonal Degeneration
11%
Baclofen
5%
Cerebellum
9%
Charcot-Marie-Tooth Disease
62%
Copy Number Variation
6%
Gene Mutation
6%
Glia
6%
In Vitro
12%
In Vivo
10%
Leucine
5%
Longitudinal Study
7%
Magnetic Resonance Imaging
15%
Magnetic Resonance Imaging
10%
Microglia
13%
Missense Mutation
11%
Mitochondrion
5%
Myelin
50%
Myelin Protein
15%
Myelinated Nerve Fiber
16%
Myelinogenesis
9%
Nerve Block
9%
Nerve Cell Degeneration
12%
Nerve Conduction
7%
Nerve Conduction Study
11%
Nerve Fiber Degeneration
11%
Nerve Injury
6%
Nervous System
6%
Nervous System Regeneration
13%
Neural Stem Cell
9%
Neuropathy
100%
Neurotoxin
10%
Nitric Oxide
9%
P21 Activated Kinase 2
9%
Peripheral Myelin Protein 22
56%
Peripheral Nerve
27%
Peripheral Nervous System
10%
Phosphatase
8%
Phosphatidylinositol
12%
Polyneuropathy
19%
Receptor
5%
RING Finger Motif
5%
RNA-binding Protein
11%
Schwann Cell
27%
Sciatic Nerve
5%
Senile Plaque
9%
Tremor
6%
Medicine and Dentistry
Arm
5%
Axon
9%
Biological Marker
6%
Central Nervous System
5%
Clinical Trial
6%
Cross Sectional Study
9%
DeJerine-Sottas Disease
92%
Demyelination
10%
Disease Burden
6%
Disease Exacerbation
7%
Diseases
25%
Electrophysiology
6%
Foot Malformation
5%
Gene Mutation
6%
Hereditary Neuropathy with Liability to Pressure Palsy
26%
Injury
5%
Magnetic Resonance Imaging
18%
Magnetization Transfer
9%
Morphometric Analysis
5%
Motor Nerve
5%
Motor Unit Number Estimation
7%
Myelin
35%
Myelin Protein
20%
Myelinated Nerve Fiber
17%
Myelination
7%
Nerve Conduction
5%
Nerve Conduction Study
6%
Nerve Fiber Degeneration
10%
Neuropathy
85%
Paralysis
7%
Peripheral Myelin Protein 22
37%
Peripheral Nerve
19%
Polyneuropathy
8%
Schwann Cell
5%
Skin Biopsy
16%
Sural Nerve
5%
Tibial Nerve
5%
Ulnar Nerve
9%
Weakness
7%
Keyphrases
Alzheimer's Disease
6%
Amyotrophic Lateral Sclerosis
5%
Charcot-Marie-Tooth Disease
44%
Dermal Nerves
5%
Disease Pattern
6%
Hereditary Neuropathy with Liability to Pressure Palsies
9%
Inherited Neuropathy
9%
Inherited Peripheral Neuropathy
7%
Loss Function
5%
LRSAM1
7%
Microglia
12%
Motor Neuron
6%
Mouse Model
5%
MPZ Gene
5%
Myelin
6%
Myelination
6%
Neurodegeneration
5%
Neuropathy
11%
PAK2
9%
Peripheral Myelin Protein 22 (PMP22)
22%
Peripheral Nerve
5%
Peripheral Nervous System
6%
Plaque
7%
Sensory Loss
5%
Tremor
6%