Publications

Fang J, Jirsch J, Wang S, Zhou D, Mu J, An D, Si Y, Zhao G*. Neurologists' attitudes toward driving among people with epilepsy in China: A pilot electronic survey. Epilepsia and Behavior, 2019, 94:47-51. 

Xu H, Zhang C, Cao L, Zhang B, Chen B*, Zhao G*. ATL3 mutation in a Chinese family with hereditary sensory neuropathy type 1F. Journal of the Peripheral Nervous System, 2019, 24(1): 50-55. 

Wang K, Wu D, Zhang B, Zhao G*. Novel CCM1 and CCM2 gene variants in two Chinese families with cerebral cavemous malformation. Frontiers in Neurology, 2018, 9:1128.

Zhao G, Liu X, Zhang Q, Wang K*. PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures. International Journal of Neuroscience, 2018, 128(8): 751-760. 

Zhao G, Song J, Yang M, Song X, Liu X*. A novel mutation of LRSAM1 in a Chinese family with Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System, 2018, 23(1):55-59. 

Zhao G, Chen F, Zhang Q*, Shen M*, Gao Z. Feature-based information filtering in visual working memory is impaired in Parkinson's disease. Neuropsychologia, 2018, 111:317-323. 

Zhao GH, Liu XM*. Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: a literature reanalysis. Translational Neurodegeneration, 2017, 6: 9.

Zhao G, Liu X*, Jiang P*. Identification of a novel SPG4 tandem base substitution in a Chinese hereditary spastic paraplegia family. Neurological Sciences, 2017, 38(5):903-905.

Zhao G, Zhu PP, Renvoisé B, Maldonado-Báez L, Park SH, Blackstone C*. Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology. Experimental Cell Research, 2016, 349(1): 32-44.

Wang K, Zhao G*. Exon 8-17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: A case report and literature review. Journal of the Neurological Science, 2015, 357(1-2): 282-4.

Zhao G, Blackstone C*. ER Morphology: Sculpting with XendoU. Current Biology, 2014, 24(24): R1170-1172. 

Wu JY, Zhang BR, Zhao GH*. Cerebral infarction and cranial venous sinus thrombosis caused by paragonimiasis. CNS Neuroscience Therapeutics, 2013, 19(9): 734-736. 

Zhao GH, Yin XZ, Wu DW, Mao SY, Yin H, Zhang BR*. Clinical features and Cu/Zn superoxide dismutase gene mutations in two Mainland Chinese families with amyotrophic lateral sclerosis. International Journal of Neuroscience, 2011, 121(4): 191-195.

Yin XZ, Liu JR, Zhang BR, Zhang L, Wang PZ, Zhou FY, Ding MP, Zhao GH*. Report of two Chinese families and a review of Chinese CADASIL patients. Journal of the Neurological Sciences, 2009, 279(1-2): 88-92. 

Zhao G, Ding M, Zhang B, Lv W, Yin H, Zhang L, Ying Z, Zhang Q*. Clinical manifestations and management of acute thallium poisoning. European Neurology, 2008, 60(6): 292-297.

Zhao G, Hu Z, Shen L, Jiang H, Ren ZJ, Liu XM, Xia K, Guo P, Pan Q, Tang BS*. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia. Chinese Medical Journal, 2008, 121(5): 430-434. 

Tang B*, Zhao G, Luo W, et al. Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L. Human Genetics, 2005, 116(3): 222-224.

Tang B*, Zhao G, Xia K, et al. Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia. Archives of Neurology, 2004, 61(1): 49-55.