Publications

Wang J#, Hou Y, Qi L, Zhai S, Zheng L, Han L, Guo Y, Zhang B, Miao P, Lou Y, Xu X, Wang Y, Ren Y, Cao Z, Feng JH*. Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1. Neurogenetics, 2020Jul;21(3):169-177.

Miao P#, Tang S#, Ye J#, Wang J, Lou Y, Zhang B, Xu X, Chen X, Li Y, Feng JH*. Electrophysiological features: the next precise step for SCN2A developmental epileptic encephalopathy. Mol Genet Genomic Med, 2020 Jul;8.

Miao P#, Feng JH*, Guo Y, Wang J, Xu X, Wang Y, Li Y, Gao L, Zheng C, Cheng H. Genotype and phenotype analysis using an epilepsy-associated gene panel in Chinese pediatric epilepsy patients,Clin genet, 2018 ,94(6):512-520.

Zhu YK#, Feng JH#, Hou HF#, Chen L, Wu S, Liu Q, Yao Q, Du P, Zhang K, Chen Q, Chen Z, Zhang H, Tian M*. Alteration of Monoamine Receptor Activity and Glucose Metabolism in Pediatric Patients with Anticonvulsant-Induced Cognitive Impairment. Journal of Nuclear Medicine, 2017,58(9):1490-1497. doi: 10.2967/jnumed.116.189290.

Zhu YK#, Feng JH#, Hou HF#, Ji JF, Zhang K, Chen Q, Chen L,Chen HY, Gao LY, Chen ZX, Zhang H, Tian M*. Glucose Metabolic Profile by Visual Assessment Combined with SPM Analysis in Pediatric Patients with Epilepsy. Journal of Nuclear Medicine, 2017 ,58(8):1293-1299. doi: 10.2967/jnumed.116.187492.

Ji GJ#, Liao W#, Yu Y, Miao HH, Feng YX, Wang K*, Feng JH*, Zang YF. Globus Pallidus Interna in Tourette Syndrome: Decreased Local Activity and Disrupted Functional Connectivity. Frontiers in Neuroanatomy, 2016, 10:93. eCollection 2016. doi: 10.3389/fnana.2016.00093

Liao W, Yu Y, Miao HH, Feng YX, Ji GJ*, Feng JH*. Inter-hemispheric Intrinsic Connectivity as a Neuromarker for the Diagnosis of Boys with Tourette Syndrome. Mol Neurobiol, 2016, 54(4):2781-2789. DOI 10.1007/s12035-016-9863-9.