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



E Mantuano, L Veneziano, C Jodice, M Frontali. Cytogenet Genome Res 2003
Times Cited: 35




List of shared articles



Times cited

Next-generation sequencing identifies novel CACNA1A gene mutations in episodic ataxia type 2.
Neven Maksemous, Bishakha Roy, Robert A Smith, Lyn R Griffiths. Mol Genet Genomic Med 2016
21


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

New CACNA1A deletions are associated to migraine phenotypes.
G S Grieco, S Gagliardi, I Ricca, O Pansarasa, M Neri, F Gualandi, G Nappi, A Ferlini, C Cereda. J Headache Pain 2018
9

Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1A.
Alexander Balck, Henrike Hanssen, Yorck Hellenbroich, Katja Lohmann, Alexander Münchau. J Neurol 2017
7

Keeping Our Calcium in Balance to Maintain Our Balance.
Melanie D Mark, Jan Claudius Schwitalla, Michelle Groemmke, Stefan Herlitze. Biochem Biophys Res Commun 2017
17

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