A citation-based method for searching scientific literature

Hsien-Yang Lee, Yong Huang, Nadine Bruneau, Patrice Roll, Elisha D O Roberson, Mark Hermann, Emily Quinn, James Maas, Robert Edwards, Tetsuo Ashizawa, Betul Baykan, Kailash Bhatia, Susan Bressman, Michiko K Bruno, Ewout R Brunt, Roberto Caraballo, Bernard Echenne, Natalio Fejerman, Steve Frucht, Christina A Gurnett, Edouard Hirsch, Henry Houlden, Joseph Jankovic, Wei-Ling Lee, David R Lynch, Shehla Mohammed, Ulrich Müller, Mark P Nespeca, David Renner, Jacques Rochette, Gabrielle Rudolf, Shinji Saiki, Bing-Wen Soong, Kathryn J Swoboda, Sam Tucker, Nicholas Wood, Michael Hanna, Anne M Bowcock, Pierre Szepetowski, Ying-Hui Fu, Louis J Ptáček. Cell Rep 2012
Times Cited: 181



Marion Delcourt, Florence Riant, Josette Mancini, Mathieu Milh, Vincent Navarro, Emmanuel Roze, Véronique Humbertclaude, Christian Korff, Vincent Des Portes, Pierre Szepetowski, Diane Doummar, Bernard Echenne, Samuel Quintin, Nicolas Leboucq, Rabbind Singh Amrathlal, Jacques Rochette, Agathe Roubertie. J Neurol Neurosurg Psychiatry 2015
Times Cited: 51




List of shared articles



Times cited

Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study.
Florence Riant, Caroline Roos, Agathe Roubertie, Cécile Barbance, Jessica Hadjadj, Stéphane Auvin, Guillaume Baille, Marion Beltramone, Cécile Boulanger, Alice Cahn,[...]. Neurology 2022
3


The Spectrum of PRRT2-Associated Disorders: Update on Clinical Features and Pathophysiology.
Annamaria Landolfi, Paolo Barone, Roberto Erro. Front Neurol 2021
4

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
1

Paroxysmal Movement Disorders.
Susan Harvey, Mary D King, Kathleen M Gorman. Front Neurol 2021
3

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
5

Novel and de novo point and large microdeletion mutation in PRRT2-related epilepsy.
Li Yang, Cuiping You, Shiyan Qiu, Xiaofan Yang, Yufen Li, Feng Liu, Dongqing Zhang, Yue Niu, Liyun Xu, Na Xu,[...]. Brain Behav 2020
9

Treatment of Paroxysmal Dyskinesia.
Anna Latorre, Kailash P Bhatia. Neurol Clin 2020
11

The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood.
Jan Henje Döring, Afshin Saffari, Thomas Bast, Knut Brockmann, Laura Ehrhardt, Walid Fazeli, Wibke G Janzarik, Gerhard Kluger, Hiltrud Muhle, Rikke S Møller,[...]. Biomedicines 2020
11

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
22

Paroxysmal and cognitive phenotypes in Prrt2 mutant mice.
Louise Robertson, Travis Featherby, Stuart Howell, James Hughes, Paul Thomas. Genes Brain Behav 2019
3

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.
Qi Zeng, Xiaoling Yang, Jing Zhang, Aijie Liu, Zhixian Yang, Xiaoyan Liu, Ye Wu, Xiru Wu, Liping Wei, Yuehua Zhang. J Hum Genet 2018
9


PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex Assembly.
Jeff Coleman, Ouardane Jouannot, Sathish K Ramakrishnan, Maria N Zanetti, Jing Wang, Vincenzo Salpietro, Henry Houlden, James E Rothman, Shyam S Krishnakumar. Cell Rep 2018
40

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
67

The expanding spectrum of paroxysmal movement disorders: update from clinical features to therapeutics.
Eavan M McGovern, Emmanuel Roze, Timothy J Counihan. Curr Opin Neurol 2018
13

The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations.
Caterina Michetti, Enrico Castroflorio, Ivan Marchionni, Nicola Forte, Bruno Sterlini, Francesca Binda, Floriana Fruscione, Pietro Baldelli, Flavia Valtorta, Federico Zara,[...]. Neurobiol Dis 2017
44

The epileptic and nonepileptic spectrum of paroxysmal dyskinesias: Channelopathies, synaptopathies, and transportopathies.
Roberto Erro, Kailash P Bhatia, Alberto J Espay, Pasquale Striano. Mov Disord 2017
43

PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects.
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,[...]. Oncotarget 2016
41

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
36

PRRT2: from Paroxysmal Disorders to Regulation of Synaptic Function.
Flavia Valtorta, Fabio Benfenati, Federico Zara, Jacopo Meldolesi. Trends Neurosci 2016
50

PRRT2 Mutant Leads to Dysfunction of Glutamate Signaling.
Ming Li, Fenghe Niu, Xilin Zhu, Xiaopan Wu, Ning Shen, Xiaozhong Peng, Ying Liu. Int J Mol Sci 2015
49

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
155