A citation-based method for searching scientific literature

Genetic updates on paroxysmal dyskinesias.
James Y Liao, Philippe A Salles, Umar A Shuaib, Hubert H Fernandez. J Neural Transm (Vienna) 2021
Times Cited: 3






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



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  Times     Co-cited
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CHRNA4 variant causes paroxysmal kinesigenic dyskinesia and genetic epilepsy with febrile seizures plus?
Yong-Li Jiang, Fang Yuan, Ying Yang, Xiao-Long Sun, Lu Song, Wen Jiang. Seizure 2018
16
2
66

Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.
Giacomo Garone, Alessandro Capuano, Lorena Travaglini, Federica Graziola, Fabrizia Stregapede, Ginevra Zanni, Federico Vigevano, Enrico Bertini, Francesco Nicita. Int J Mol Sci 2020
18
2
66

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Xiao-Meng Yin, Jing-Han Lin, Li Cao, Tong-Mei Zhang, Sheng Zeng, Kai-Lin Zhang, Wo-Tu Tian, Zheng-Mao Hu, Nan Li, Jun-Ling Wang,[...]. Hum Mol Genet 2018
29
2
66

TMEM151A variants cause paroxysmal kinesigenic dyskinesia.
Hong-Fu Li, Yu-Lan Chen, Ling Zhuang, Dian-Fu Chen, Hua-Zhen Ke, Wen-Jiao Luo, Gong-Lu Liu, Sheng-Nan Wu, Wen-Hao Zhou, Zhi-Qi Xiong,[...]. Cell Discov 2021
8
2
66

Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.
M K Bruno, M Hallett, K Gwinn-Hardy, B Sorensen, E Considine, S Tucker, D R Lynch, K D Mathews, K J Swoboda, J Harris,[...]. Neurology 2004
252
2
66

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
204
2
66

The prevalence of primary dystonia: a systematic review and meta-analysis.
Thomas D Steeves, Lundy Day, Jonathan Dykeman, Nathalie Jette, Tamara Pringsheim. Mov Disord 2012
165
1
33

Contemporary functional neuroanatomy and pathophysiology of dystonia.
Norbert Brüggemann. J Neural Transm (Vienna) 2021
11
1
33

Translation of Oppenheim's 1911 paper on dystonia.
Christine Klein, Stanley Fahn. Mov Disord 2013
26
1
33

X-linked dystonia Parkinsonism: crossing a new threshold.
Arlene R Ng, Roland Dominic G Jamora, Raymond L Rosales. J Neural Transm (Vienna) 2021
2
1
50

Contemporary clinical neurophysiology applications in dystonia.
Petr Kaňovský, Raymond Rosales, Pavel Otruba, Martin Nevrlý, Lenka Hvizdošová, Robert Opavský, Michaela Kaiserová, Pavel Hok, Kateřina Menšíková, Petr Hluštík,[...]. J Neural Transm (Vienna) 2021
2
1
50

The prevalence of primary dystonia in the general community.
J Müller, S Kiechl, G K Wenning, K Seppi, J Willeit, A Gasperi, J Wissel, T Gasser, W Poewe. Neurology 2002
79
1
33

Neurorehabilitation in dystonia: a holistic perspective.
Lynley V Bradnam, Rebecca M Meiring, Melani Boyce, Alana McCambridge. J Neural Transm (Vienna) 2021
6
1
33

Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticity.
Dirk Dressler, Maria Concetta Altavista, Eckart Altenmueller, Roongroj Bhidayasiri, Saeed Bohlega, Pedro Chana, Tae Mo Chung, Carlo Colosimo, Klemens Fheodoroff, Pedro J Garcia-Ruiz,[...]. J Neural Transm (Vienna) 2021
12
1
33

New modalities and directions for dystonia care.
Genko Oyama, Nobutaka Hattori. J Neural Transm (Vienna) 2021
3
1
33

Arching deep brain stimulation in dystonia types.
Han-Joon Kim, Beomseok Jeon. J Neural Transm (Vienna) 2021
2
1
50

The importance of genetic testing for dystonia patients and translational research.
Jelena Pozojevic, Christian Beetz, Ana Westenberger. J Neural Transm (Vienna) 2021
3
1
33

Botulinum toxin therapy of dystonia.
Dirk Dressler, Fereshte Adib Saberi, Raymond L Rosales. J Neural Transm (Vienna) 2021
5
1
33

Dystonia updates: definition, nomenclature, clinical classification, and etiology.
Karen Grütz, Christine Klein. J Neural Transm (Vienna) 2021
9
1
33

Emerging and converging molecular mechanisms in dystonia.
Paulina Gonzalez-Latapi, Nicolas Marotta, Niccolò E Mencacci. J Neural Transm (Vienna) 2021
12
1
33

Isolated dystonia: clinical and genetic updates.
Aloysius Domingo, Rachita Yadav, Laurie J Ozelius. J Neural Transm (Vienna) 2021
10
1
33

Combined dystonias: clinical and genetic updates.
Anne Weissbach, Gerard Saranza, Aloysius Domingo. J Neural Transm (Vienna) 2021
4
1
33

Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms.
Lucia Abela, Manju A Kurian. J Inherit Metab Dis 2018
13
1
33

Promise and challenges of dystonia brain banking: establishing a human tissue repository for studies of X-Linked Dystonia-Parkinsonism.
Cara Fernandez-Cerado, G Paul Legarda, M Salvie Velasco-Andrada, Abegail Aguil, Niecy G Ganza-Bautista, J Benedict B Lagarde, Jasmin Soria, Roland Dominic G Jamora, Patrick J Acuña, Charles Vanderburg,[...]. J Neural Transm (Vienna) 2021
3
1
33

Dystonia and leveraging oral pharmacotherapy.
Michelle Ann C Sy, Hubert H Fernandez. J Neural Transm (Vienna) 2021
2
1
50

Complex dystonias: an update on diagnosis and care.
Rebecca Herzog, Anne Weissbach, Tobias Bäumer, Alexander Münchau. J Neural Transm (Vienna) 2021
6
1
33

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
1
33

Increased interhemispheric resting-state functional connectivity in paroxysmal kinesigenic dyskinesia: a resting-state fMRI study.
Jiechuan Ren, Du Lei, Tianhua Yang, Dongmei An, Fenglai Xiao, Lei Li, Xiaoqi Huang, Qiyong Gong, Dong Zhou. J Neurol Sci 2015
17
1
33

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
17
1
33

Aberrant Sensory Gating of the Primary Somatosensory Cortex Contributes to the Motor Circuit Dysfunction in Paroxysmal Kinesigenic Dyskinesia.
Yo-Tsen Liu, Yi-Chieh Chen, Shang-Yeong Kwan, Chien-Chen Chou, Hsiang-Yu Yu, Der-Jen Yen, Kwong-Kum Liao, Wei-Ta Chen, Yung-Yang Lin, Rou-Shayn Chen,[...]. Front Neurol 2018
6
1
33

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, Sumit Middha, Shannon K McDonnell, Saurabh Baheti, Anthony Musolf, Qing Li, Emily Holzinger, Danielle Karyadi,[...]. Am J Hum Genet 2016
692
1
33

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
36
1
33

Synaptic or ion channel modifier? PRRT2 is a chameleon-like regulator of neuronal excitability.
Holger Lerche. Brain 2018
5
1
33

Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
Elena Gardella, Felicitas Becker, Rikke S Møller, Julian Schubert, Johannes R Lemke, Line H G Larsen, Hans Eiberg, Michael Nothnagel, Holger Thiele, Janine Altmüller,[...]. Ann Neurol 2016
112
1
33

Abnormal Somatosensory Synchronization in Patients With Paroxysmal Kinesigenic Dyskinesia: A Magnetoencephalographic Study.
Fu-Jung Hsiao, Wan-Yu Hsu, Wei-Ta Chen, Rou-Shayn Chen, Yung-Yang Lin. Clin EEG Neurosci 2017
9
1
33

Altered intrinsic brain activity in patients with paroxysmal kinesigenic dyskinesia by PRRT2 mutation: altered brain activity by PRRT2 mutation.
ChunYan Luo, Yongping Chen, Wei Song, Qin Chen, QiYong Gong, Hui-Fang Shang. Neurol Sci 2013
18
1
33

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
149
1
33

Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.
Wo-Tu Tian, Xiao-Jun Huang, Xiao Mao, Qing Liu, Xiao-Li Liu, Sheng Zeng, Xia-Nan Guo, Jun-Yi Shen, Yang-Qi Xu, Hui-Dong Tang,[...]. Mov Disord 2018
25
1
33

GRIPT: a novel case-control analysis method for Mendelian disease gene discovery.
Jun Wang, Li Zhao, Xia Wang, Yong Chen, Mingchu Xu, Zachry T Soens, Zhongqi Ge, Peter Ronghan Wang, Fei Wang, Rui Chen. Genome Biol 2018
1
1
100

The endoplasmic reticulum: structure, function and response to cellular signaling.
Dianne S Schwarz, Michael D Blower. Cell Mol Life Sci 2016
475
1
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
1
33

Episodic neurological channelopathies.
Devon P Ryan, Louis J Ptácek. Neuron 2010
48
1
33

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
5
1
33

Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients.
Xiao-Jun Huang, Tian Wang, Jun-Ling Wang, Xiao-Li Liu, Xiang-Qian Che, Jin Li, Xiao Mao, Mei Zhang, Guang-Hui Bi, Li Wu,[...]. Neurology 2015
44
1
33

An interaction between PRRT2 and Na+/K+ ATPase contributes to the control of neuronal excitability.
Bruno Sterlini, Alessandra Romei, Chiara Parodi, Davide Aprile, Michele Oneto, Anita Aperia, Pierluigi Valente, Flavia Valtorta, Anna Fassio, Pietro Baldelli,[...]. Cell Death Dis 2021
2
1
50

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
46
1
33

Paroxysmal movement disorders - practical update on diagnosis and management.
Claudio M De Gusmao, Laura Silveira-Moriyama. Expert Rev Neurother 2019
10
1
33

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.
Kelsey Paulhus, Lauren Ammerman, Edward Glasscock. Int J Mol Sci 2020
28
1
33

When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.
Kymberleigh A Pagel, Vikas Pejaver, Guan Ning Lin, Hyun-Jun Nam, Matthew Mort, David N Cooper, Jonathan Sebat, Lilia M Iakoucheva, Sean D Mooney, Predrag Radivojac. Bioinformatics 2017
24
1
33

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
2456
1
33


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.

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