Lingchao Meng
Wuhan University(CN)Renmin Hospital of Wuhan University(CN)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Peripheral Neuropathies and Disorders, RNA Research and Splicing
Most-Cited Works
- → Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy(2020)152 cited
- → The GGC repeat expansion inNOTCH2NLCis associated with oculopharyngodistal myopathy type 3(2021)134 cited
- → The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4(2022)80 cited
- → Variation inICE1Methylation Primarily Determines Phenotypic Variation in Freezing Tolerance inArabidopsis thaliana(2018)51 cited
- → CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model(2022)48 cited
- → Long‐read whole‐genome sequencing for the genetic diagnosis of dystrophinopathies(2020)47 cited
- → Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study(2021)39 cited
- → Circulating cell-free mtDNA release is associated with the activation of cGAS-STING pathway and inflammation in mitochondrial diseases(2022)36 cited
- → Heterogeneous characteristics of MRI changes of thigh muscles in patients with dysferlinopathy(2016)35 cited
- → Immobilization and Characterization of Pectinase onto the Cationic Polystyrene Resin(2021)30 cited