A citation-based method for searching scientific literature

Romina Romaniello, Claudio Zucca, Alessandra Tonelli, Sara Bonato, Cinzia Baschirotto, Nicoletta Zanotta, Roberta Epifanio, Andrea Righini, Nereo Bresolin, Maria T Bassi, Renato Borgatti. J Neurol Neurosurg Psychiatry 2010
Times Cited: 34



J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
Times Cited: 199




List of shared articles



Times cited

Genetic Variants Associated with Episodic Ataxia in Korea.
Kwang-Dong Choi, Ji-Soo Kim, Hyo-Jung Kim, Ileok Jung, Seong-Hae Jeong, Seung-Han Lee, Dong Uk Kim, Sang-Ho Kim, Seo Young Choi, Jin-Hong Shin,[...]. Sci Rep 2017
31

Novel CACNA1A mutation(s) associated with slow saccade velocities.
Stefan Kipfer, Simon Jung, Johannes R Lemke, Anna Kipfer-Kauer, Jeremy P Howell, Alain Kaelin-Lang, Thomas Nyffeler, Klemens Gutbrod, Angela Abicht, René M Müri. J Neurol 2013
10

Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna. Nat Rev Neurol 2012
86

Zebrafish as a Model System for the Study of Severe CaV2.1 (α1A) Channelopathies.
Sidharth Tyagi, Angeles B Ribera, Roger A Bannister. Front Mol Neurosci 2020
6

A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
Katrin Bürk, Frank J Kaiser, Stephanie Tennstedt, Ludger Schöls, Friedmar R Kreuz, Thomas Wieland, Tim M Strom, Thomas Büttner, Ronja Hollstein, Diana Braunholz,[...]. Eur J Med Genet 2014
13

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
13

A Novel Frameshift CACNA1A Mutation Causing Episodic Ataxia Type 2.
Alexander Balck, Sinem Tunc, Johanna Schmitz, Ronja Hollstein, Frank J Kaiser, Norbert Brüggemann. Cerebellum 2018
2

Episodic ataxia type 2: phenotype characteristics of a novel CACNA1A mutation and review of the literature.
Wolfgang Nachbauer, Michael Nocker, Elfriede Karner, Iva Stankovic, Iris Unterberger, Andreas Eigentler, Rainer Schneider, Werner Poewe, Margarete Delazer, Sylvia Boesch. J Neurol 2014
33