中国学者近期发表的论文
1.	Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvement Author: Lin Ge, Xiaona Fu, Wei Zhang, Dong Wang, Zhaoxia Wang, Yun Yuan, Ikuya Nonaka, Hui Xiong Journal: NEUROMUSCULAR DISORDERS, 2019, Vol., , DOI:10.1016/j.nmd.2019.03.007    DOI
2.	Congenital Disorder of Glycosylation Type 1T with a Novel Truncated Homozygous Mutation in PGM1 Gene and Literature Review Author: Wo-Tu Tian, Xing-Hua Luan, Hai-Yan Zhou, Chao Zhang, Xiao-Jun Huang, Xiao-Li Liu, Sheng-Di Chen, Hui-Dong Tang, Li Cao Journal: NEUROMUSCULAR DISORDERS, 2019, Vol., , DOI:10.1016/j.nmd.2019.01.001    DOI
3.	Idiopathic inflammatory myopathies with anti-mitochondrial antibodies: Clinical features and treatment outcomes in a Chinese cohort Author: Ying Hou, Meirong Liu, Yue-Bei Luo, Yuan Sun, Kai Shao, Tingjun Dai, Wei Li, Yuying Zhao, Chuanzhu Yan Journal: NEUROMUSCULAR DISORDERS, 2018, Vol., , DOI:10.1016/j.nmd.2018.11.004    DOI
4.	A novel homozygous nonsense mutation in NEFL causes autosomal recessive Charcot–Marie–Tooth disease Author: Jun Fu, Yun Yuan Journal: NEUROMUSCULAR DISORDERS, 2018, Vol.28, 44-47, DOI:10.1016/j.nmd.2017.09.018    DOI
5.	Three novel recessive mutations in LAMA2, SYNE1, and TTN are identified in a single case with congenital muscular dystrophy Author: Liang Wu, Bingwu Xiang, Huan Zhang, Xiaoxiao He, Celina Shih, Xiang Chen, Tao Cai Journal: NEUROMUSCULAR DISORDERS, 2017, Vol.27, 1018-1022, DOI:10.1016/j.nmd.2017.06.558    DOI
6.	Monoclonal gammopathy with both nemaline myopathy and amyloid myopathy Author: Min Wang, Lin Lei, Hai Chen, Li Di, Mi Pang, Yan Lu, Lu Lu, Xin-Ming Shen, Yuwei Da Journal: NEUROMUSCULAR DISORDERS, 2017, Vol.27, 942-946, DOI:10.1016/j.nmd.2017.05.007    DOI
7.	Similar clinical, pathological, and genetic features in Chinese patients with autosomal recessive and dominant Charcot–Marie–Tooth disease type 2K Author: Jun Fu, Shixu Dai, Yuanyuan Lu, Rui Wu, Zhaoxia Wang, Yun Yuan, He Lv Journal: NEUROMUSCULAR DISORDERS, 2017, Vol.27, 760-765, DOI:10.1016/j.nmd.2017.04.001    DOI
8.	Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndrome Author: Sushan Luo, Shuang Cai, Susan Maxwell, Dongyue Yue, Wenhua Zhu, Kai Qiao, Zhen Zhu, Lei Zhou, Jianying Xi, Jiahong Lu, David Beeson, Chongbo Zhao Journal: NEUROMUSCULAR DISORDERS, 2017, Vol.27, 557-564, DOI:10.1016/j.nmd.2017.03.004    DOI
9.	Clinical and mutational characteristics of Duchenne muscular dystrophy patients based on a comprehensive database in South China Author: Dan-Ni Wang, Zhi-Qiang Wang, Lei Yan, Jin He, Min-Ting Lin, Wan-Jin Chen, Ning Wang Journal: NEUROMUSCULAR DISORDERS, 2017, Vol.27, 715-722, DOI:10.1016/j.nmd.2017.02.010    DOI
10.	IGHMBP2-related clinical and genetic features in a cohort of Chinese Charcot–Marie–Tooth disease type 2 patients Author: Lei Liu, Xiaobo Li, Zhengmao Hu, Xiao Mao, Xiaohong Zi, Kun Xia, Beisha Tang, Ruxu Zhang Journal: NEUROMUSCULAR DISORDERS, 2017, Vol.27, 193-199, DOI:10.1016/j.nmd.2016.11.008    DOI

同类著名期刊名称 h-index CiteScore LANCET NEUROLOGY 259 44.60 Nature Reviews Neurology 124 23.70 Alzheimers & Dementia 94 21.10 BRAIN 308 17.40 NEURO-ONCOLOGY 105 16.10 SLEEP MEDICINE REVIEWS 122 17.70 ANNALS OF NEUROLOGY 273 16.00 NEUROLOGY 331 10.40 MOVEMENT DISORDERS 174 12.70 STROKE 292 10.00

中科院JCR同大类学科的热搜期刊 浏览次数 MEDICINE 302209 CANCER RESEARCH 166631 Molecular Medicine Reports 165554 International Journal of Nanomedicine 165169 CANCER LETTERS 160302 JOURNAL OF ETHNOPHARMACOLOGY 142590 BIOMEDICINE & PHARMACOTHERAPY 141912 Theranostics 136897 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 136696 International Journal of Environmental Research and Public Health 134374