A citation-based method for searching scientific literature

Yongcheng Pan, Qiong Liu, Jennifer Zhang, Yang Yang, Yun Tian, Junsheng Zeng, Peng Yin, Lin Mei, Wen-Cheng Xiong, Xiao-Jiang Li, Shihua Li, Beisha Tang. Biochem Biophys Res Commun 2020
Times Cited: 5







List of co-cited articles
15 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery.
Pierluigi Valente, Enrico Castroflorio, Pia Rossi, Manuela Fadda, Bruno Sterlini, Romina Ines Cervigni, Cosimo Prestigio, Silvia Giovedì, Franco Onofri, Elisa Mura,[...]. Cell Rep 2016
84
80

PRRT2 mutations and paroxysmal disorders.
A Méneret, C Gaudebout, F Riant, M Vidailhet, C Depienne, E Roze. Eur J Neurol 2013
72
60

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
42
60

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
60
60

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
149
60

PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum.
Guo-He Tan, Yuan-Yuan Liu, Lu Wang, Kui Li, Ze-Qiang Zhang, Hong-Fu Li, Zhong-Fei Yang, Yang Li, Dan Li, Ming-Yue Wu,[...]. Cell Res 2018
46
60

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
20
40

A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE.
Pia Rossi, Bruno Sterlini, Enrico Castroflorio, Antonella Marte, Franco Onofri, Flavia Valtorta, Luca Maragliano, Anna Corradi, Fabio Benfenati. J Biol Chem 2016
39
40

Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.
Marion Delcourt, Florence Riant, Josette Mancini, Mathieu Milh, Vincent Navarro, Emmanuel Roze, Véronique Humbertclaude, Christian Korff, Vincent Des Portes, Pierre Szepetowski,[...]. J Neurol Neurosurg Psychiatry 2015
50
40

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
39
40

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Wan-Jin Chen, Yu Lin, Zhi-Qi Xiong, Wei Wei, Wang Ni, Guo-He Tan, Shun-Ling Guo, Jin He, Ya-Fang Chen, Qi-Jie Zhang,[...]. Nat Genet 2011
312
40

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
48
40

High-resolution proteomics unravel architecture and molecular diversity of native AMPA receptor complexes.
Jochen Schwenk, Nadine Harmel, Aline Brechet, Gerd Zolles, Henrike Berkefeld, Catrin Swantje Müller, Wolfgang Bildl, David Baehrens, Björn Hüber, Akos Kulik,[...]. Neuron 2012
276
40

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
8
40

PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia.
Akihisa Okumura, Keiko Shimojima, Hirokazu Kurahashi, Shingo Numoto, Shino Shimada, Atsushi Ishii, Iori Ohmori, Satoru Takahashi, Tomonari Awaya, Tetsuo Kubota,[...]. Seizure 2019
13
40



Neural expression of the transcription factor THAP1 during development in rat.
Y Zhao, J Xiao, S Gong, J A Clara, M S Ledoux. Neuroscience 2013
17
20

Paroxysmal dyskinesias: clinical features and classification.
M Demirkiran, J Jankovic. Ann Neurol 1995
356
20

Paroxysmal dyskinesias.
Kailash P Bhatia. Mov Disord 2011
109
20

Synaptogenesis in the developing mouse visual cortex.
Mingshan Li, Zhanjun Cui, Yanli Niu, Bin Liu, Wenjuan Fan, Dongming Yu, Jinbo Deng. Brain Res Bull 2010
48
20


A human protein-protein interaction network: a resource for annotating the proteome.
Ulrich Stelzl, Uwe Worm, Maciej Lalowski, Christian Haenig, Felix H Brembeck, Heike Goehler, Martin Stroedicke, Martina Zenkner, Anke Schoenherr, Susanne Koeppen,[...]. Cell 2005
20

Mild paroxysmal kinesigenic dyskinesia caused by PRRT2 missense mutation with reduced penetrance.
Jennifer Friedman, Jesus Olvera, Jennifer L Silhavy, Stacey B Gabriel, Joseph G Gleeson. Neurology 2012
20
20

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
36
20

Developmental expression of rat torsinA transcript and protein.
Jianfeng Xiao, Suzhen Gong, Yu Zhao, Mark S LeDoux. Brain Res Dev Brain Res 2004
50
20

Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia.
Peter Hedera, Jianfeng Xiao, Andreas Puschmann, Dragana Momčilović, Steve W Wu, Mark S LeDoux. BMC Neurol 2012
21
20

Channelopathy: hypothesis of a common pathophysiologic mechanism in different forms of paroxysmal dyskinesia.
Lucia Margari, Anna Presicci, Patrizia Ventura, Francesco Margari, Tommaso Perniola. Pediatr Neurol 2005
29
20


Topiramate therapy for paroxysmal kinesigenic choreoathetosis.
Yuan-Gui Huang, Yun-Chun Chen, Fang Du, Rui Li, Ge-Lin Xu, Wen Jiang, Jing Huang. Mov Disord 2005
25
20

Excitatory synaptic currents in Purkinje cells.
D J Perkel, S Hestrin, P Sah, R A Nicoll. Proc Biol Sci 1990
205
20

Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation.
I-Ching Chou, Sheng-Shing Lin, Wei-De Lin, Chung-Hsing Wang, Yu-Tzu Chang, Fuu-Jen Tsai, Chang-Hai Tsai. Biomedicine (Taipei) 2014
6
20



Levetiracetam in the treatment of paroxysmal kinesiogenic choreoathetosis.
Anjan Chatterjee, Elan D Louis, Steven Frucht. Mov Disord 2002
26
20

The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, Maria Stamelou, Matthew Walker, Dimitri Kullmann,[...]. Brain 2015
81
20

Treatment of paroxysmal dyskinesias in children.
Jonathan W Mink. Curr Treat Options Neurol 2015
13
20




Cloning, developmental regulation and neural localization of rat epsilon-sarcoglycan.
Jianfeng Xiao, Mark S LeDoux. Brain Res Mol Brain Res 2003
27
20

PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population.
Aurélie Méneret, David Grabli, Christel Depienne, Cécile Gaudebout, Fabienne Picard, Alexandra Dürr, Isabelle Lagroua, Delphine Bouteiller, Cyril Mignot, Diane Doummar,[...]. Neurology 2012
69
20


Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism.
Rachel Fremont, D Paola Calderon, Sara Maleki, Kamran Khodakhah. J Neurosci 2014
70
20


PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, Zaid Afawi, Sameer M Zuberi, James N Hughes, Clair Pridmore, Bree L Hodgson, Xenia Iona, Lynette G Sadleir,[...]. Am J Hum Genet 2012
181
20

Gabapentin for familial paroxysmal dystonic choreoathetosis.
R S Chudnow, R A Mimbela, D B Owen, E S Roach. Neurology 1997
40
20

Adaptation of granule cell to Purkinje cell synapses to high-frequency transmission.
Antoine M Valera, Frédéric Doussau, Bernard Poulain, Boris Barbour, Philippe Isope. J Neurosci 2012
52
20

Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.
Yvonne G Weber, Andrea Berger, Nerses Bebek, Sabine Maier, Skevos Karafyllakes, Nancy Meyer, Yukio Fukuyama, Anne Halbach, Christiane Hikel, Gerhard Kurlemann,[...]. Epilepsia 2004
34
20

High-fidelity transmission of sensory information by single cerebellar mossy fibre boutons.
Ede A Rancz, Taro Ishikawa, Ian Duguid, Paul Chadderton, Séverine Mahon, Michael Häusser. Nature 2007
203
20


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.