Jianying Xi

Clinical features and <i>ETFDH</i> mutation spectrum in a cohort of 90 Chinese patients with late‐onset multiple acyl‐CoA dehydrogenase deficiency

Jianying Xi, Bing Wen, Jie Lin et al. · Journal of Inherited Metabolic Disease · 2013 · 106 citations

Life Sciences, Genetics, Molecular Genetics +10

Pediatric necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies

Wen‐Chen Liang, Akinori Uruha, Shigeaki Suzuki et al. · Lara D. Veeken · 2016 · 91 citations · Full text

Medicine, Pathology, Pediatrics +17

The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4

Jiaxi Yu, Jingli Shan, Meng Yu et al. · The American Journal of Human Genetics · 2022 · 82 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Decrease of CD4+CD25highFoxp3+ regulatory T cells and elevation of CD19+BAFF-R+ B cells and soluble ICAM-1 in myasthenia gravis

Xiang Li, Bao‐Guo Xiao, Jianying Xi et al. · Clinical Immunology · 2007 · 66 citations

Life Sciences, Cell Biology, Immunology +12

5′ UTR CGG repeat expansion in<i>GIPC1</i>is associated with oculopharyngodistal myopathy

Jianying Xi, Xilu Wang, Dongyue Yue et al. · Brain · 2020 · 65 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14