中国学者近期发表的论文
1.	R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome Author: A. Catania, R. Battini, T. Pippucci, R. Pasquariello, M. L. Chiapparini, M. Seri, B. Garavaglia, G. Zorzi, N. Nardocci, D. Ghezzi, V. Tiranti Journal: NEUROGENETICS, 2018, Vol.19, 179-187, DOI:10.1007/s10048-018-0552-x    DOI
2.	An exome study of Parkinson’s disease in Sardinia, a Mediterranean genetic isolate Author: Marialuisa Quadri, Xu Yang, Giovanni Cossu, Simone Olgiati, Valeria M. Saddi, Guido J. Breedveld, Limei Ouyang, Jingchu Hu, Na Xu, Josja Graafland, Valeria Ricchi, Daniela Murgia, Leonor Correia Guedes, Claudio Mariani, Maria J. Marti, Patrizia Tarantino, Rosanna Asselta, Francesc Valldeoriola, Monica Gagliardi, Gianni Pezzoli, Mario Ezquerra, Aldo Quattrone, Joaquim Ferreira, Grazia Annesi, Stefano Goldwurm, Eduardo Tolosa, Ben A. Oostra, Maurizio Melis, Jun Wang, Vincenzo Bonifati Journal: NEUROGENETICS, 2014, Vol.16, 55-64, DOI:10.1007/s10048-014-0425-x    DOI
3.	The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation Author: Xinxiu Liu, Jiayu Chen, Wenchao liu, Xiaogang Li, Qi Chen, Tao Liu, Shaorong Gao, Min Deng Journal: NEUROGENETICS, 2015, Vol.16, 223-231, DOI:10.1007/s10048-015-0448-y    DOI
4.	A novel heat shock protein alpha 8 (<Emphasis Type="Italic">Hspa8</Emphasis>) molecular network mediating responses to stress- and ethanol-related behaviors Author: Kyle R. Urquhart, Yinghong Zhao, Jessica A. Baker, Ye Lu, Lei Yan, Melloni N. Cook, Byron C. Jones, Kristin M. Hamre, Lu Lu Journal: NEUROGENETICS, 2016, Vol.17, 91-105, DOI:10.1007/s10048-015-0470-0    DOI
5.	<Emphasis Type="Italic">ARHGEF9</Emphasis> mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation Author: Jing-Yang Wang, Peng Zhou, Jie Wang, Bin Tang, Tao Su, Xiao-Rong Liu, Bing-Mei Li, Heng Meng, Yi-Wu Shi, Yong-Hong Yi, Na He, Wei-Ping Liao Journal: NEUROGENETICS, 2017, Vol.19, 9-16, DOI:10.1007/s10048-017-0528-2    DOI
6.	Whole exome sequencing in Dandy-Walker variant with intellectual disability reveals an activating CIP2A mutation as novel genetic cause Author: Chin-An Yang, I-Ching Chou, Der-Yang Cho, Chien-Yu Lin, Hsi-Yuan Huang, Yu-Chen Ho, Ting-Yuan Liu, Ying-Hsuan Li, Jan-Gowth Chang Journal: NEUROGENETICS, 2018, Vol.19, 157-163, DOI:10.1007/s10048-018-0548-6    DOI
7.	A novel heat shock protein alpha 8 (Hspa8) molecular network mediating responses to stress-and ethanol-related behaviors Author: lulu521uthsc Journal: NEUROGENETICS, 2016.
8.	A novel heat shock protein alpha 8 (Hspa8) molecular network mediating responses to stress-and ethanol-related behaviors Author: lulu521uthsc Journal: NEUROGENETICS, 2016.
9.	Forkhead family transcription factor FoxO and neural differentiation. Author: Wen Q, Wang H, Little PJ, Quirion R, Zheng W. Journal: Neurogenetics. 2012 May;13(2):105-13. doi: 10.1007/s10048-012-0320-2. Epub 2012 Mar 28.    PubMed
10.	A novel binding protein of single-minded 2: the mitotic arrest-deficient protein MAD2B. Author: Meng X, Tian X, Wang X, Gao P, Zhang C. Journal: Neurogenetics. 2012 Aug;13(3):251-60. doi: 10.1007/s10048-012-0333-x. Epub 2012 Jun 2.    PubMed

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 302198 CANCER RESEARCH 166628 Molecular Medicine Reports 165551 International Journal of Nanomedicine 165168 CANCER LETTERS 160297 JOURNAL OF ETHNOPHARMACOLOGY 142587 BIOMEDICINE & PHARMACOTHERAPY 141910 Theranostics 136892 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 136687 International Journal of Environmental Research and Public Health 134370