Area of research
Molecular Biology · Epidemiology
Research interest
Research interests include Muscle Physiology and Disorders, RNA modifications and cancer, Autoimmune Neurological Disorders and Treatments, and Virology and Viral Diseases.
<scp>m6A</scp> Methylation‐Induced Autophagy Impairment by <scp>TFEB</scp> Regulation in <scp>SOD1</scp> ‐ <scp>G93A ALS</scp> Cell Model
Exploration of molecular diagnosis for HHV-6 encephalitis in immunocompetent individuals: A study combining mNGS and PCR
A case report of Kikuchi-Fujimoto disease initially presented as aseptic meningitis
A case report of Kikuchi-Fujimoto disease initially presented as aseptic meningitis
Evidence for the potential role of m6A modification in regulating autophagy in models of amyotrophic lateral sclerosis
Exploring the appropriate situation of performing CSF mNGS in patients with proposed intracranial infections
Research hotspots and trends for Duchenne muscular dystrophy: a machine learning bibliometric analysis from 2004 to 2023
Interventional closure in the treatment of cardiac cavity perforation caused by pericardial puncture: a case report
Comprehensive analysis of m6A regulators characterized by the immune microenvironment in Duchenne muscular dystrophy
Additional file 7 of Comprehensive analysis of m6A regulators characterized by the immune microenvironment in Duchenne muscular dystrophy
Identification of Auxiliary Biomarkers and Description of the Immune Microenvironmental Characteristics in Duchenne Muscular Dystrophy by Bioinformatical Analysis and Experiment
The clinical, myopathological, and molecular characteristics of 26 Chinese patients with dysferlinopathy: a high proportion of misdiagnosis and novel variants
Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency
MORC2 p.R252W Mutant Axonal Charcot–Marie–Tooth Disease Causes Peripheral Neuropathies and Pathological Myofiber Destruction
Clinical heterogeneity and molecular characteristics in a group of Chinese patients with dysferlinopathy
Embolectomy of acute embolic stroke associated with ipsilateral carotid web: a case report and literature review
Mutation at a new allele of the dysferlin gene causes Miyoshi myopathy: A case report.
PubMed 2021cited by 3position: middle
A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation
Four patients with infarction in key areas of the Papez circuit, with anterograde amnesia as the main manifestation
A case of hypokalemia-induced bidirectional ventricular tachycardia
A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene
Neutral lipid storage disease with myopathy presenting asymmetrical muscle weakness: a case report.
PubMed 2020cited by 2position: middle
A Case of Hypokalemia-induced Bidirectional Ventricular Tachycardia
Adolescent Hyperuricemia with Lipid Storage Myopathy: A Clinical Study
Acute diffuse edematous-hemorrhagic Epstein–Barr virus meningoencephalitis
Birt-Hogg-Dubé syndrome caused by a mutation of FLCN gene in a CVST patient: a case report
A case of surgically-associated anti GQ1b antibody syndrome accompanied by saccadic ping pong gaze
Clinical and magnetic resonance analysis of varicella-zoster virus (VZV) transcranial nerve into brain-induced brainstem encephalitis
Successive occurrence of vertebrobasilar dolichectasia induced trigeminal neuralgia, vestibular paroxysmia and hemifacial spasm