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



Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
Times Cited: 148




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
5

Rare CACNA1A mutations leading to congenital ataxia.
Mercè Izquierdo-Serra, José M Fernández-Fernández, Mercedes Serrano. Pflugers Arch 2020
5

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia.
Claudia Stendel, Maria Cristina D'Adamo, Manuela Wiessner, Marina Dusl, Marta Cenciarini, Silvia Belia, Ehsan Nematian-Ardestani, Peter Bauer, Jan Senderek, Thomas Klopstock,[...]. Int J Mol Sci 2020
6

Targeting Alternative Splicing as a Potential Therapy for Episodic Ataxia Type 2.
Fanny Jaudon, Simona Baldassari, Ilaria Musante, Agnes Thalhammer, Federico Zara, Lorenzo A Cingolani. Biomedicines 2020
3

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

The Role of Calcium Channels in Epilepsy.
Sanjeev Rajakulendran, Michael G Hanna. Cold Spring Harb Perspect Med 2016
29

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

[Hereditary episodic ataxia].
F Riant, K Vahedi, E Tournier-Lasserve. Rev Neurol (Paris) 2011
9

Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
Sanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, Dimitrios Kotzadimitriou, Louise Eunson, Mary B Davis, Rosalyn Davies, Nicholas W Wood, Dimitri M Kullmann, Michael G Hanna,[...]. J Physiol 2010
52

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134

Neurological channelopathies.
Dimitri M Kullmann. Annu Rev Neurosci 2010
79

Genetics of headaches.
Arn M J M Van Den Maagdenberg, Gisela M Terwindt, Joost Haan, Rune R Frants, Michel D Ferrari. Handb Clin Neurol 2010
11

Dysfunction of the Ca(V)2.1 calcium channel in cerebellar ataxias.
Sanjeev Rajakulendran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hanna. F1000 Biol Rep 2010
7

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


Reduced ACh release at neuromuscular synapses of heterozygous leaner Ca(v)2.1-mutant mice.
Simon Kaja, Rob C G Van De Ven, Rune R Frants, Michel D Ferrari, Arn M J M Van Den Maagdenberg, Jaap J Plomp. Synapse 2008
10

Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2.
Tracey D Graves, Paola Imbrici, Esther E Kors, Gisela M Terwindt, Louise H Eunson, Rune R Frants, Joost Haan, Michel D Ferrari, Peter J Goadsby, Michael G Hanna,[...]. Neurobiol Dis 2008
19

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

Familial hemiplegic migraine.
Curtis F Barrett, Arn M J M van den Maagdenberg, Rune R Frants, Michel D Ferrari. Adv Genet 2008
25

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

Episodic ataxia type 2.
Michael Strupp, Andreas Zwergal, Thomas Brandt. Neurotherapeutics 2007
96

Essential, completely conserved glycine residue in the domain III S2-S3 linker of voltage-gated calcium channel alpha1 subunits in yeast and mammals.
Kazuko Iida, Jinfeng Teng, Tomoko Tada, Ayaka Saka, Masumi Tamai, Hiroko Izumi-Nakaseko, Satomi Adachi-Akahane, Hidetoshi Iida. J Biol Chem 2007
15

Calcium channelopathies: voltage-gated calcium channels.
P J Adams, T P Snutch. Subcell Biochem 2007
30

Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2.
Chung-Jiuan Jeng, Yu-Ting Chen, Yi-Wen Chen, Chih-Yung Tang. Am J Physiol Cell Physiol 2006
38

CACNA1A mutation in a EA-2 patient responsive to acetazolamide and valproic acid.
Kylie A Scoggan, Joseph H Friedman, Dennis E Bulman. Can J Neurol Sci 2006
21


Voltage-gated calcium channels and idiopathic generalized epilepsies.
Houman Khosravani, Gerald W Zamponi. Physiol Rev 2006
126

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