A citation-based method for searching scientific literature

D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
Times Cited: 579



O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
Times Cited: 1260




List of shared articles



Times cited

Paroxysmal Genetic Movement Disorders and Epilepsy.
Claudio M de Gusmão, Lucas Garcia, Mohamad A Mikati, Samantha Su, Laura Silveira-Moriyama. Front Neurol 2021
2

Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature.
Stephan Lauxmann, Lukas Sonnenberg, Nils A Koch, Christian Bosselmann, Natalie Winter, Niklas Schwarz, Thomas V Wuttke, Ulrike B S Hedrich, Yuanyuan Liu, Holger Lerche,[...]. Front Neurol 2021
0

Paroxysmal Movement Disorders: Recent Advances.
Zheyu Xu, Che-Kang Lim, Louis C S Tan, Eng-King Tan. Curr Neurol Neurosci Rep 2019
5

Paroxysmal movement disorders - practical update on diagnosis and management.
Claudio M De Gusmao, Laura Silveira-Moriyama. Expert Rev Neurother 2019
5

Episodic ataxias.
Joanna C Jen, Jijun Wan. Handb Clin Neurol 2018
4

Purkinje Cell Signaling Deficits in Animal Models of Ataxia.
Eriola Hoxha, Ilaria Balbo, Maria Concetta Miniaci, Filippo Tempia. Front Synaptic Neurosci 2018
36

Episodic ataxias.
Joanna C Jen, Jijun Wan. Handb Clin Neurol 2018
21

Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
Esther A R Nibbeling, Cathérine C S Delnooz, Tom J de Koning, Richard J Sinke, Hyder A Jinnah, Marina A J Tijssen, Dineke S Verbeek. Neurosci Biobehav Rev 2017
26

A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies.
Marie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, Juliette Konop, Claire-Sophie Davoine, Christelle Tesson, Rémi Valter, Mathieu Anheim, Anthony Behin, Giovanni Castelnovo,[...]. Brain 2017
57

Rare neurological channelopathies--networks to study patients, pathogenesis and treatment.
Joanna C Jen, Tetsuo Ashizawa, Robert C Griggs, Michael F Waters. Nat Rev Neurol 2016
6

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force.
Connie Marras, Anthony Lang, Bart P van de Warrenburg, Carolyn M Sue, Sarah J Tabrizi, Lars Bertram, Saadet Mercimek-Mahmutoglu, Darius Ebrahimi-Fakhari, Thomas T Warner, Alexandra Durr,[...]. Mov Disord 2016
126

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
30

Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
J Spillane, D M Kullmann, M G Hanna. J Neurol Neurosurg Psychiatry 2016
54