Q. Fei

发表

Two novel mutations in the Spastin gene of Chinese patients with hereditary spastic paraplegia

Y. Fu, Tian-Yi Rong, L. Cao, 2011, European journal of neurology.

Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia

S. Chen, Li Cao, Q. Xiao, 2011, Movement disorders : official journal of the Movement Disorder Society.

Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China

Ying Wang, Gang Wang, S. Chen, 2010, Neuroscience Letters.

The association between two single nucleotide polymorphisms within the insulin-degrading enzyme gene and Alzheimer’s disease in a Chinese Han population

Ying Wang, Yulei Deng, Gang Wang, 2012, Journal of Clinical Neuroscience.

Population Polymorphism rs 11136000 With Late Onset Alzheimer ' s Disease in Clusterin Association Study

Ying Wang, Huidong Tang, Yulei Deng, 2012 .

Analysis of Lingo1 variant in sporadic and familial essential tremor among Asians

E. Tan, Tian-Yi Rong, Q. Fei, 2011, Acta neurologica Scandinavica.

Association Study of Clusterin Polymorphism rs11136000 With Late Onset Alzheimer’s Disease in Chinese Han Population

W. Xu, Ying Wang, Huidong Tang, 2011, American journal of Alzheimer's disease and other dementias.

Association of thromboxane A2 receptor gene polymorphisms with cerebral infarction in a Chinese population

Hui Wu, J. Zhao, Yuming Xu, 2013, Neurological Sciences.

GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients

Ying Wang, S. Chen, Li Cao, 2009, Neuroscience Letters.

The GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese population.

T. Zhang, Q. Xiao, J. Zhang, 2010, Parkinsonism & related disorders.