Guo-Hong Chen. Exp Ther Med 2015
Times Cited: 6
Times Cited: 6
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
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
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
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
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
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
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
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
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Treatment of paroxysmal dyskinesias.
Adam Strzelczyk, Katrin Bürk, Wolfgang H Oertel. Expert Opin Pharmacother 2011
Adam Strzelczyk, Katrin Bürk, Wolfgang H Oertel. Expert Opin Pharmacother 2011
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
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
33
Fast and accurate short read alignment with Burrows-Wheeler transform.
Heng Li, Richard Durbin. Bioinformatics 2009
Heng Li, Richard Durbin. Bioinformatics 2009
33
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets.
Sudhir Kumar, Glen Stecher, Koichiro Tamura. Mol Biol Evol 2016
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
Pia Rossi, Bruno Sterlini, Enrico Castroflorio, Antonella Marte, Franco Onofri, Flavia Valtorta, Luca Maragliano, Anna Corradi, Fabio Benfenati. J Biol Chem 2016
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
Atsushi Ishii, Sawa Yasumoto, Yukiko Ihara, Takahito Inoue, Takako Fujita, Noriko Nakamura, Masaharu Ohfu, Yushiro Yamashita, Hideo Takatsuka, Toshiaki Taga,[...]. Brain Dev 2013
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
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
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
Carla Marini, Valerio Conti, Davide Mei, Domenica Battaglia, Donatella Lettori, Emma Losito, Grazia Bruccini, Gaetano Tortorella, Renzo Guerrini. Neurology 2012
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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
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
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
Akihisa Okumura, Keiko Shimojima, Tetsuo Kubota, Shinpei Abe, Shintaro Yamashita, Katsumi Imai, Tohru Okanishi, Hideo Enoki, Tatsuya Fukasawa, Takuya Tanabe,[...]. Brain Dev 2013
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
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
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
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
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
Li Cao, Xiao-Jun Huang, Lan Zheng, Qin Xiao, Xi-Jin Wang, Sheng-Di Chen. Parkinsonism Relat Disord 2012
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
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
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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
S B Bressman, D de Leon, M F Brin, N Risch, H Shale, R E Burke, P E Greene, S Fahn. Adv Neurol 1988
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
Tamsin Owen, Hortensia Gimeno, Richard Selway, Jean-Pierre Lin. Eur J Paediatr Neurol 2015
16
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
Steven J Frucht, Yvette Bordelon, William H Houghton, Dayton Reardan. Mov Disord 2005
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
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
16
Levodopa does not improve function in individuals with dystonic cerebral palsy.
Inna Pozin, Tali Bdolah-Abram, Hilla Ben-Pazi. J Child Neurol 2014
Inna Pozin, Tali Bdolah-Abram, Hilla Ben-Pazi. J Child Neurol 2014
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
P David Charles, Charles H Adler, Mark Stacy, Cynthia Comella, Joseph Jankovic, Aubrey Manack Adams, Marc Schwartz, Mitchell F Brin. J Neurol 2014
16
Treatment of Tardive Dystonia Induced by Antipsychotics, Old and New.
Philippos Gourzis, Maria Skokou, Evanthia Soubasi, Aggeliki Katrivanou, Panagiotis Polychronopoulos. Clin Neuropharmacol 2015
Philippos Gourzis, Maria Skokou, Evanthia Soubasi, Aggeliki Katrivanou, Panagiotis Polychronopoulos. Clin Neuropharmacol 2015
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
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
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Dopa-responsive dystonia--clinical and genetic heterogeneity.
Subhashie Wijemanne, Joseph Jankovic. Nat Rev Neurol 2015
Subhashie Wijemanne, Joseph Jankovic. Nat Rev Neurol 2015
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
Chun-Chi Liang, Lauren M Tanabe, Stephanie Jou, Frank Chi, William T Dauer. J Clin Invest 2014
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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
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
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Isolated and combined dystonia syndromes - an update on new genes and their phenotypes.
B Balint, K P Bhatia. Eur J Neurol 2015
B Balint, K P Bhatia. Eur J Neurol 2015
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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
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
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Isolated head tremor: part of the clinical spectrum of essential tremor? Data from population-based and clinic-based case samples.
Elan D Louis, Okan Dogu. Mov Disord 2009
Elan D Louis, Okan Dogu. Mov Disord 2009
16
Assessment: Botulinum neurotoxin for the treatment of movement disorders (an evidence-based review): report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology.
D M Simpson, A Blitzer, A Brashear, C Comella, R Dubinsky, M Hallett, J Jankovic, B Karp, C L Ludlow, J M Miyasaki,[...]. Neurology 2008
D M Simpson, A Blitzer, A Brashear, C Comella, R Dubinsky, M Hallett, J Jankovic, B Karp, C L Ludlow, J M Miyasaki,[...]. Neurology 2008
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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
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
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
Mark Hallett, Alberto Albanese, Dirk Dressler, Karen R Segal, David M Simpson, Daniel Truong, Joseph Jankovic. Toxicon 2013
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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
Sara Meoni, Mateusz Zurowski, Andres M Lozano, Mojgan Hodaie, Yu-Yan Poon, Melanie Fallis, Valerie Voon, Elena Moro. Neurology 2015
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
Kunal S Patel, Jacob Kazam, Apostolos J Tsiouris, Vijay K Anand, Theodore H Schwartz. World Neurosurg 2014
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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
Angelo Y Luciano, H A Jinnah, Ronald F Pfeiffer, Daniel D Truong, Martha A Nance, Mark S LeDoux. Parkinsonism Relat Disord 2014
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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
Arvid Suls, Peter Dedeken, Karolien Goffin, Hilde Van Esch, Patrick Dupont, David Cassiman, Judith Kempfle, Thomas V Wuttke, Yvonne Weber, Holger Lerche,[...]. Brain 2008
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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
Joo Pyung Kim, Won Seok Chang, Young Seok Park, Jin Woo Chang. Stereotact Funct Neurosurg 2012
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The genetics of dystonia: new twists in an old tale.
Gavin Charlesworth, Kailash P Bhatia, Nicholas W Wood. Brain 2013
Gavin Charlesworth, Kailash P Bhatia, Nicholas W Wood. Brain 2013
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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
Susannah Payne, Stephen Tisch, Ian Cole, Helen Brake, Judy Rough, Paul Darveniza. Mov Disord 2014
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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
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
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
Norbert Brüggemann, Andrea Kühn, Susanne A Schneider, Christoph Kamm, Alexander Wolters, Patricia Krause, Elena Moro, Frank Steigerwald, Matthias Wittstock, Volker Tronnier,[...]. Neurology 2015
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.