A citation-based method for searching scientific literature

S Guida, F Trettel, S Pagnutti, E Mantuano, A Tottene, L Veneziano, T Fellin, M Spadaro, K Stauderman, M Williams, S Volsen, R Ophoff, R Frants, C Jodice, M Frontali, D Pietrobon. Am J Hum Genet 2001
Times Cited: 108



S Battistini, S Stenirri, M Piatti, C Gelfi, P G Righetti, R Rocchi, F Giannini, N Battistini, G C Guazzi, M Ferrari, P Carrera. Neurology 1999
Times Cited: 138




List of shared articles



Times cited

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

Meta-Analysis of Public Microarray Datasets Reveals Voltage-Gated Calcium Gene Signatures in Clinical Cancer Patients.
Chih-Yang Wang, Ming-Derg Lai, Nam Nhut Phan, Zhengda Sun, Yen-Chang Lin. PLoS One 2015
47

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

Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivo.
Susan E Tomlinson, Michael G Hanna, Dimitri M Kullmann, S Veronica Tan, David Burke. Clin Neurophysiol 2009
27

Disease causing mutations of calcium channels.
Nancy M Lorenzon, Kurt G Beam. Channels (Austin) 2008
21

Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits.
Robert S Raike, Holly B Kordasiewicz, Randall M Thompson, Christopher M Gomez. Mol Cell Neurosci 2007
21

The cerebellum and migraine.
Maurice Vincent, Nouchine Hadjikhani. Headache 2007
59

Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
Alessandra Tonelli, Maria Grazia D'Angelo, Roberto Salati, Laura Villa, Chiara Germinasi, Tiziano Frattini, Giovanni Meola, Anna Carla Turconi, Nereo Bresolin, Maria Teresa Bassi. J Neurol Sci 2006
34

Channeling studies in yeast: yeast as a model for channelopathies?
Devin M Wolfe, David A Pearce. Neuromolecular Med 2006
12

Potassium channel blockers inhibit the triggers of attacks in the calcium channel mouse mutant tottering.
Catherine J C Weisz, Robert S Raike, Luis E Soria-Jasso, Ellen J Hess. J Neurosci 2005
48

Migraine genetics: an update.
J Haan, E E Kors, Kaate R J Vanmolkot, Arn M J M van den Maagdenberg, Rune R Frants, M D Ferrari. Curr Pain Headache Rep 2005
30

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
178

Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.
E Mantuano, L Veneziano, M Spadaro, P Giunti, S Guida, M G Leggio, L Verriello, N Wood, C Jodice, M Frontali. J Med Genet 2004
33

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
Isabel Alonso, José Barros, Assunção Tuna, João Coelho, Jorge Sequeiros, Isabel Silveira, Paula Coutinho. Arch Neurol 2003
58

In vivo analysis of voltage-dependent calcium channels.
Ling Liu, Theresa A Zwingman, Colin F Fletcher. J Bioenerg Biomembr 2003
16


Genetics of episodic ataxia.
Joanna C Jen, Robert W Baloh. Adv Neurol 2002
16

The neuronal channelopathies.
Dimitri M Kullmann. Brain 2002
100

Genetics of migraine: possible links to neurophysiological abnormalities.
Peter S Sándor, Anna Ambrosini, Reto M Agosti, Jean Schoenen. Headache 2002
19