Associated Papers
FCRL3 genetic variants drive autoimmune pathogenesis in multiple sclerosis and neuromyelitis optica spectrum disorders.
Huang HF et al.
Frontiers in Neurology, 2025
A Comprehensive Review on the Role of Genetic Factors in Neuromyelitis Optica Spectrum Disorder.
Ghafouri-Fard S et al.
Frontiers in Immunology, 2021
The GTF2I rs117026326 polymorphism is associated with neuromyelitis optica spectrum disorder but not with multiple sclerosis in a Northern Han Chinese population.
Liang H et al.
Journal of Neuroimmunology, 2019
Association of TNFSF4 Polymorphisms with Neuromyelitis Optica Spectrum Disorders in a Chinese Population.
Lian Z et al.
Journal of Molecular Neuroscience : Mn, 2017
Significant Association Between Fc Receptor-Like 3 Polymorphisms (-1901A>G and -658C>T) and Neuromyelitis Optica (NMO) Susceptibility in the Chinese Population.
Wang X et al.
Molecular Neurobiology, 2016
The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma.
Wu G et al.
Nature Genetics, 2014
24705251 (PubMed )
Supplement: NIHMS573627-supplement-2.xlsx › ST4a
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