Bing Wen

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

Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations

Bing Wen, Tingjun Dai, Wei Li et al. · Journal of Neurology Neurosurgery & Psychiatry · 2009 · 104 citations

Life Sciences, Biochemistry, Molecular Genetics +15

Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation

Wei Wang, Qianqian Zhuang, Kunqian Ji et al. · Scientific Reports · 2017 · 52 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Comparison of Whole-Body DWI and ¹⁸F-FDG PET/CT for Detecting Intramedullary and Extramedullary Lesions in Multiple Myeloma

Jianpu Chen, Chongjiao Li, Yueli Tian et al. · American Journal of Roentgenology · 2019 · 51 citations

Medicine, Nuclear Medicine, Radiology +13

<scp><i>ETFDH</i></scp> Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin‐Responsive Multiple Acyl–Coenzyme <scp>A</scp> Dehydrogenation Deficiency

Jingwen Xu, Duoling Li, Jingwei Lv et al. · Annals of Neurology · 2018 · 47 citations

Life Sciences, Genetics, Molecular Genetics +17