A citation-based method for searching scientific literature

Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
Times Cited: 128



Yo-Tsen Liu, Fang-Shin Nian, Wan-Ju Chou, Chin-Yin Tai, Shang-Yeong Kwan, Chien Chen, Pei-Wen Kuo, Po-Hsi Lin, Chin-Yi Chen, Chia-Wei Huang, Yi-Chung Lee, Bing-Wen Soong, Jin-Wu Tsai. Oncotarget 2016
Times Cited: 38




List of shared articles



Times cited

Recent advances in gene therapy for neurodevelopmental disorders with epilepsy.
Thomas J Turner, Clara Zourray, Stephanie Schorge, Gabriele Lignani. J Neurochem 2021
6

Increased responsiveness at the cerebellar input stage in the PRRT2 knockout model of paroxysmal kinesigenic dyskinesia.
Francesca Binda, Pierluigi Valente, Antonella Marte, Pietro Baldelli, Fabio Benfenati. Neurobiol Dis 2021
3

Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China.
Li Cao, Xiaojun Huang, Ning Wang, Zhiying Wu, Cheng Zhang, Weihong Gu, Shuyan Cong, Jianhua Ma, Ling Wei, Yanchun Deng,[...]. Transl Neurodegener 2021
0

The Spectrum of PRRT2-Associated Disorders: Update on Clinical Features and Pathophysiology.
Annamaria Landolfi, Paolo Barone, Roberto Erro. Front Neurol 2021
0

Age-dependent neurological phenotypes in a mouse model of PRRT2-related diseases.
Fay Aj, McMahon T, Im C, Bair-Marshall C, Niesner Kj, Li H, Nelson A, Voglmaier Sm, Fu Y-H, Ptáček Lj. Neurogenetics 2021
0

PRRT2 modulates presynaptic Ca2+ influx by interacting with P/Q-type channels.
Daniele Ferrante, Bruno Sterlini, Cosimo Prestigio, Antonella Marte, Anna Corradi, Franco Onofri, Giorgio Tortarolo, Giuseppe Vicidomini, Andrea Petretto, Jessica Muià,[...]. Cell Rep 2021
0

An Emerging Role of PRRT2 in Regulating Growth Cone Morphology.
Elisa Savino, Fabrizia Claudia Guarnieri, Jin-Wu Tsai, Anna Corradi, Fabio Benfenati, Flavia Valtorta. Cells 2021
0

Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disorders.
Shao-Yun Zhao, Li-Xi Li, Yu-Lan Chen, Yi-Jun Chen, Gong-Lu Liu, Hai-Lin Dong, Dian-Fu Chen, Hong-Fu Li, Zhi-Ying Wu. CNS Neurosci Ther 2020
4


The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.
Xiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, Wo-Tu Tian, Fei-Xia Zhan, Ze-Yu Zhu, Xiao-Meng Yin, Qing Liu, Kai-Li Yin, Xiao-Rong Liu,[...]. Mov Disord 2020
6

Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic Dyskinesia.
Dylan J Calame, Jianfeng Xiao, Mohammad Moshahid Khan, T J Hollingsworth, Yi Xue, Abigail L Person, Mark S LeDoux. Neuroscience 2020
3

Proline-rich transmembrane protein 2 (PRRT2) regulates the actin cytoskeleton during synaptogenesis.
Elisa Savino, Romina Inès Cervigni, Miriana Povolo, Alessandra Stefanetti, Daniele Ferrante, Pierluigi Valente, Anna Corradi, Fabio Benfenati, Fabrizia Claudia Guarnieri, Flavia Valtorta. Cell Death Dis 2020
4

Constitutive Inactivation of the PRRT2 Gene Alters Short-Term Synaptic Plasticity and Promotes Network Hyperexcitability in Hippocampal Neurons.
Pierluigi Valente, Alessandra Romei, Manuela Fadda, Bruno Sterlini, Davide Lonardoni, Nicola Forte, Floriana Fruscione, Enrico Castroflorio, Caterina Michetti, Giorgia Giansante,[...]. Cereb Cortex 2019
16


Paroxysmal and cognitive phenotypes in Prrt2 mutant mice.
Louise Robertson, Travis Featherby, Stuart Howell, James Hughes, Paul Thomas. Genes Brain Behav 2019
2

PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalization.
Meng-Han Tsai, Fang-Shin Nian, Mei-Hsin Hsu, Wei-Szu Liu, Yo-Tsen Liu, Chen Liu, Po-Hsi Lin, Daw-Yang Hwang, Yao-Chung Chuang, Jin-Wu Tsai. Epilepsia 2019
6

PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?
Piero Pavone, Giovanni Corsello, Sung Yoon Cho, Xena Giada Pappalardo, Martino Ruggieri, Simona Domenica Marino, Dong Kyu Jin, Silvia Marino, Raffaele Falsaperla. Ital J Pediatr 2019
6

Neurodevelopmental synaptopathies: Insights from behaviour in rodent models of synapse gene mutations.
J Luo, R H Norris, S L Gordon, J Nithianantharajah. Prog Neuropsychopharmacol Biol Psychiatry 2018
14

PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity.
Floriana Fruscione, Pierluigi Valente, Bruno Sterlini, Alessandra Romei, Simona Baldassari, Manuela Fadda, Cosimo Prestigio, Giorgia Giansante, Jacopo Sartorelli, Pia Rossi,[...]. Brain 2018
48

A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B.
Hongying Ma, Shenglei Feng, Xuejun Deng, Li Wang, Sheng Zeng, Cheng Wang, Xixiang Ma, Hao Sun, Rui Chen, Shiyue Du,[...]. Epilepsia 2018
6