A citation-based method for searching scientific literature

Guo-Hong Chen. Exp Ther Med 2015
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
158
66

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
322
50

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.
Hsien-Yang Lee, Yong Huang, Nadine Bruneau, Patrice Roll, Elisha D O Roberson, Mark Hermann, Emily Quinn, James Maas, Robert Edwards, Tetsuo Ashizawa,[...]. Cell Rep 2012
183
50

Phenomenology and classification of dystonia: a consensus update.
Alberto Albanese, Kailash Bhatia, Susan B Bressman, Mahlon R Delong, Stanley Fahn, Victor S C Fung, Mark Hallett, Joseph Jankovic, Hyder A Jinnah, Christine Klein,[...]. Mov Disord 2013
33

Treatment of paroxysmal dyskinesias.
Adam Strzelczyk, Katrin Bürk, Wolfgang H Oertel. Expert Opin Pharmacother 2011
20
33

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.
Jun-Ling Wang, Li Cao, Xun-Hua Li, Zheng-Mao Hu, Jia-Da Li, Jian-Guo Zhang, Yu Liang, San-A, Nan Li, Su-Qin Chen,[...]. Brain 2011
207
33


MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets.
Sudhir Kumar, Glen Stecher, Koichiro Tamura. Mol Biol Evol 2016
33

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
41
33

Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis.
Atsushi Ishii, Sawa Yasumoto, Yukiko Ihara, Takahito Inoue, Takako Fujita, Noriko Nakamura, Masaharu Ohfu, Yushiro Yamashita, Hideo Takatsuka, Toshiaki Taga,[...]. Brain Dev 2013
23
33

PRRT2 mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response.
Hong-Fu Li, Wan-Jin Chen, Wang Ni, Kai-Yan Wang, Gong-Lu Liu, Ning Wang, Zhi-Qi Xiong, Jianfeng Xu, Zhi-Ying Wu. Neurology 2013
43
33

PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.
Carla Marini, Valerio Conti, Davide Mei, Domenica Battaglia, Donatella Lettori, Emma Losito, Grazia Bruccini, Gaetano Tortorella, Renzo Guerrini. Neurology 2012
81
33

Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.
Natalie Trump, Amy McTague, Helen Brittain, Apostolos Papandreou, Esther Meyer, Adeline Ngoh, Rodger Palmer, Deborah Morrogh, Christopher Boustred, Jane A Hurst,[...]. J Med Genet 2016
139
33

PRRT2 mutation in Japanese children with benign infantile epilepsy.
Akihisa Okumura, Keiko Shimojima, Tetsuo Kubota, Shinpei Abe, Shintaro Yamashita, Katsumi Imai, Tohru Okanishi, Hideo Enoki, Tatsuya Fukasawa, Takuya Tanabe,[...]. Brain Dev 2013
25
33

PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions.
Rianne van Vliet, Guido Breedveld, Johanneke de Rijk-van Andel, Eva Brilstra, Nienke Verbeek, Corien Verschuuren-Bemelmans, Maartje Boon, Johnny Samijn, Karin Diderich, Ingrid van de Laar,[...]. Neurology 2012
63
33

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
186
33

Identification of a novel PRRT2 mutation in patients with paroxysmal kinesigenic dyskinesias and c.649dupC as a mutation hot-spot.
Li Cao, Xiao-Jun Huang, Lan Zheng, Qin Xiao, Xi-Jin Wang, Sheng-Di Chen. Parkinsonism Relat Disord 2012
47
33

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
33

Inheritance of idiopathic torsion dystonia among Ashkenazi Jews.
S B Bressman, D de Leon, M F Brin, N Risch, H Shale, R E Burke, P E Greene, S Fahn. Adv Neurol 1988
13
16

Wilson Disease.
Ronald F Pfeiffer. Continuum (Minneap Minn) 2016
28
16

Cognitive function in children with primary dystonia before and after deep brain stimulation.
Tamsin Owen, Hortensia Gimeno, Richard Selway, Jean-Pierre Lin. Eur J Paediatr Neurol 2015
19
16

Exteroceptive and interoceptive stimuli in dystonia.
P E Greene, S Bressman. Mov Disord 1998
59
16

A pilot tolerability and efficacy trial of sodium oxybate in ethanol-responsive movement disorders.
Steven J Frucht, Yvette Bordelon, William H Houghton, Dayton Reardan. Mov Disord 2005
54
16

Diagnosis and treatment of dystonia.
H A Jinnah, Stewart A Factor. Neurol Clin 2015
70
16

Mutations in GNAL cause primary torsion dystonia.
Tania Fuchs, Rachel Saunders-Pullman, Ikuo Masuho, Marta San Luciano, Deborah Raymond, Stewart Factor, Anthony E Lang, Tsao-Wei Liang, Richard M Trosch, Sierra White,[...]. Nat Genet 2013
202
16

Levodopa does not improve function in individuals with dystonic cerebral palsy.
Inna Pozin, Tali Bdolah-Abram, Hilla Ben-Pazi. J Child Neurol 2014
16
16

Cervical dystonia and pain: characteristics and treatment patterns from CD PROBE (Cervical Dystonia Patient Registry for Observation of OnabotulinumtoxinA Efficacy).
P David Charles, Charles H Adler, Mark Stacy, Cynthia Comella, Joseph Jankovic, Aubrey Manack Adams, Marc Schwartz, Mitchell F Brin. J Neurol 2014
42
16

Treatment of Tardive Dystonia Induced by Antipsychotics, Old and New.
Philippos Gourzis, Maria Skokou, Evanthia Soubasi, Aggeliki Katrivanou, Panagiotis Polychronopoulos. Clin Neuropharmacol 2015
7
16

Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.
Gavin Charlesworth, Vincent Plagnol, Kira M Holmström, Jose Bras, Una-Marie Sheerin, Elisavet Preza, Ignacio Rubio-Agusti, Mina Ryten, Susanne A Schneider, Maria Stamelou,[...]. Am J Hum Genet 2012
163
16

Dopa-responsive dystonia--clinical and genetic heterogeneity.
Subhashie Wijemanne, Joseph Jankovic. Nat Rev Neurol 2015
134
16

TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration.
Chun-Chi Liang, Lauren M Tanabe, Stephanie Jou, Frank Chi, William T Dauer. J Clin Invest 2014
100
16

Practice guideline update summary: Botulinum neurotoxin for the treatment of blepharospasm, cervical dystonia, adult spasticity, and headache: Report of the Guideline Development Subcommittee of the American Academy of Neurology.
David M Simpson, Mark Hallett, Eric J Ashman, Cynthia L Comella, Mark W Green, Gary S Gronseth, Melissa J Armstrong, David Gloss, Sonja Potrebic, Joseph Jankovic,[...]. Neurology 2016
284
16


Pallidal neurostimulation in patients with medication-refractory cervical dystonia: a randomised, sham-controlled trial.
Jens Volkmann, Joerg Mueller, Günther Deuschl, Andrea A Kühn, Joachim K Krauss, Werner Poewe, Lars Timmermann, Daniela Falk, Andreas Kupsch, Anatol Kivi,[...]. Lancet Neurol 2014
199
16



Psychiatric disorders, myoclonus dystonia and SGCE: an international study.
Kathryn J Peall, Joke M Dijk, Rachel Saunders-Pullman, Yasmine E M Dreissen, Ilke van Loon, Danielle Cath, Manju A Kurian, Michael J Owen, Elisabeth M J Foncke, Huw R Morris,[...]. Ann Clin Transl Neurol 2015
33
16

Dystonic tremor.
G Deuschl. Rev Neurol (Paris) 2003
40
16

Evidence-based review and assessment of botulinum neurotoxin for the treatment of movement disorders.
Mark Hallett, Alberto Albanese, Dirk Dressler, Karen R Segal, David M Simpson, Daniel Truong, Joseph Jankovic. Toxicon 2013
141
16

Long-term neuropsychiatric outcomes after pallidal stimulation in primary and secondary dystonia.
Sara Meoni, Mateusz Zurowski, Andres M Lozano, Mojgan Hodaie, Yu-Yan Poon, Melanie Fallis, Valerie Voon, Elena Moro. Neurology 2015
15
16

Utility of early postoperative high-resolution volumetric magnetic resonance imaging after transsphenoidal pituitary tumor surgery.
Kunal S Patel, Jacob Kazam, Apostolos J Tsiouris, Vijay K Anand, Theodore H Schwartz. World Neurosurg 2014
15
16

Treatment of myoclonus-dystonia syndrome with tetrabenazine.
Angelo Y Luciano, H A Jinnah, Ronald F Pfeiffer, Daniel D Truong, Martha A Nance, Mark S LeDoux. Parkinsonism Relat Disord 2014
23
16

Brain Stimulation for Torsion Dystonia.
Michael D Fox, Ron L Alterman. JAMA Neurol 2015
53
16

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Arvid Suls, Peter Dedeken, Karolien Goffin, Hilde Van Esch, Patrick Dupont, David Cassiman, Judith Kempfle, Thomas V Wuttke, Yvonne Weber, Holger Lerche,[...]. Brain 2008
210
16

Effects of relative low-frequency bilateral globus pallidus internus stimulation for treatment of cervical dystonia.
Joo Pyung Kim, Won Seok Chang, Young Seok Park, Jin Woo Chang. Stereotact Funct Neurosurg 2012
17
16

The genetics of dystonia: new twists in an old tale.
Gavin Charlesworth, Kailash P Bhatia, Nicholas W Wood. Brain 2013
69
16

Drug-induced movement disorders.
Shyamal H Mehta, John C Morgan, Kapil D Sethi. Neurol Clin 2015
35
16

The clinical spectrum of laryngeal dystonia includes dystonic cough: observations of a large series.
Susannah Payne, Stephen Tisch, Ian Cole, Helen Brake, Judy Rough, Paul Darveniza. Mov Disord 2014
16
16

CACNA1B mutation is linked to unique myoclonus-dystonia syndrome.
Justus L Groen, Arturo Andrade, Katja Ritz, Hamid Jalalzadeh, Martin Haagmans, Ted E J Bradley, Aldo Jongejan, Dineke S Verbeek, Peter Nürnberg, Sylvia Denome,[...]. Hum Mol Genet 2015
48
16

Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia.
Norbert Brüggemann, Andrea Kühn, Susanne A Schneider, Christoph Kamm, Alexander Wolters, Patricia Krause, Elena Moro, Frank Steigerwald, Matthias Wittstock, Volker Tronnier,[...]. Neurology 2015
92
16


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.