A citation-based method for searching scientific literature

Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
Times Cited: 178







List of co-cited articles
1386 articles co-cited >1



Times Cited
  Times     Co-cited
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A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
455
60

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
59

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
Angelita Tottene, Rossella Conti, Alessandra Fabbro, Dania Vecchia, Maryna Shapovalova, Mirko Santello, Arn M J M van den Maagdenberg, Michel D Ferrari, Daniela Pietrobon. Neuron 2009
213
48

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma.
Angelita Tottene, Francesca Pivotto, Tommaso Fellin, Tiziana Cesetti, Arn M J M van den Maagdenberg, Daniela Pietrobon. J Biol Chem 2005
98
38

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
527
35

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.
Arn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, Nicole Terpolilli, Maryna Shapovalova, Freek E Hoebeek, Curtis F Barrett, Lisa Gherardini, Rob C G van de Ven, Boyan Todorov,[...]. Ann Neurol 2010
144
33

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
359
32

Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.
Katharina Eikermann-Haerter, Ergin Dileköz, Chiho Kudo, Sean I Savitz, Christian Waeber, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. J Clin Invest 2009
186
32

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine.
M Hans, S Luvisetto, M E Williams, M Spagnolo, A Urrutia, A Tottene, P F Brust, E C Johnson, M M Harpold, K A Stauderman,[...]. J Neurosci 1999
189
31

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
631
31

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model.
Hayrunnisa Bolay, Uwe Reuter, Andrew K Dunn, Zhihong Huang, David A Boas, Michael A Moskowitz. Nat Med 2002
769
31

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
E E Kors, G M Terwindt, F L Vermeulen, R B Fitzsimons, P E Jardine, P Heywood, S Love, A M van den Maagdenberg, J Haan, R R Frants,[...]. Ann Neurol 2001
232
30

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
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
29

Neurobiology of migraine.
Daniela Pietrobon, Jörg Striessnig. Nat Rev Neurosci 2003
383
24

Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels.
R E Westenbroek, T Sakurai, E M Elliott, J W Hell, T V Starr, T P Snutch, W A Catterall. J Neurosci 1995
448
22

Familial hemiplegic migraine.
Daniela Pietrobon. Neurotherapeutics 2007
135
22



CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
21

Mechanisms of migraine aura revealed by functional MRI in human visual cortex.
N Hadjikhani, M Sanchez Del Rio, O Wu, D Schwartz, D Bakker, B Fischl, K K Kwong, F M Cutrer, B R Rosen, R B Tootell,[...]. Proc Natl Acad Sci U S A 2001
924
20

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy.
Yu-Qing Cao, Erika S Piedras-Rentería, Geoffrey B Smith, Gong Chen, Nobutoshi C Harata, Richard W Tsien. Neuron 2004
124
20

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics.
R L Kraus, M J Sinnegger, H Glossmann, S Hering, J Striessnig. J Biol Chem 1998
155
20

The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation.
Norbert Weiss, Alejandro Sandoval, Ricardo Felix, Arn Van den Maagdenberg, Michel De Waard. Pflugers Arch 2008
39
48

Suppression of cortical spreading depression in migraine prophylaxis.
Cenk Ayata, Hongwei Jin, Chiho Kudo, Turgay Dalkara, Michael A Moskowitz. Ann Neurol 2006
388
18

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
Verneri Anttila, Hreinn Stefansson, Mikko Kallela, Unda Todt, Gisela M Terwindt, M Stella Calafato, Dale R Nyholt, Antigone S Dimas, Tobias Freilinger, Bertram Müller-Myhsok,[...]. Nat Genet 2010
242
18

Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
187
18

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.
Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari. PLoS Genet 2011
123
18

Migraine: new molecular mechanisms.
Daniela Pietrobon. Neuroscientist 2005
134
17



Gain of function in FHM-1 Cav2.1 knock-in mice is related to the shape of the action potential.
Carlota González Inchauspe, Francisco J Urbano, Mariano N Di Guilmi, Ian D Forsythe, Michel D Ferrari, Arn M J M van den Maagdenberg, Osvaldo D Uchitel. J Neurophysiol 2010
25
68

Trigeminal ganglion neuron subtype-specific alterations of Ca(V)2.1 calcium current and excitability in a Cacna1a mouse model of migraine.
B Fioretti, L Catacuzzeno, L Sforna, M B Gerke-Duncan, A M J M van den Maagdenberg, F Franciolini, M Connor, D Pietrobon. J Physiol 2011
40
42

A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria.
L L Thomsen, M K Eriksen, S F Roemer, I Andersen, J Olesen, M B Russell. Brain 2002
148
16


Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics.
R L Kraus, M J Sinnegger, A Koschak, H Glossmann, S Stenirri, P Carrera, J Striessnig. J Biol Chem 2000
104
16


Activation of central trigeminovascular neurons by cortical spreading depression.
Xichun Zhang, Dan Levy, Vanessa Kainz, Rodrigo Noseda, Moshe Jakubowski, Rami Burstein. Ann Neurol 2011
201
16

Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
Daniel I Chasman, Markus Schürks, Verneri Anttila, Boukje de Vries, Ulf Schminke, Lenore J Launer, Gisela M Terwindt, Arn M J M van den Maagdenberg, Konstanze Fendrich, Henry Völzke,[...]. Nat Genet 2011
234
16

The genetic spectrum of a population-based sample of familial hemiplegic migraine.
L L Thomsen, M Kirchmann, A Bjornsson, H Stefansson, R M Jensen, A C Fasquel, H Petursson, M Stefansson, M L Frigge, A Kong,[...]. Brain 2007
99
15

Ca(V)2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: implications for calcium channelopathies.
Paul J Adams, Esperanza Garcia, Laurence S David, Kirk J Mulatz, Sian D Spacey, Terrance P Snutch. Channels (Austin) 2009
49
30

Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice.
Katharina Eikermann-Haerter, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. Ann Neurol 2009
64
23

Activation of meningeal nociceptors by cortical spreading depression: implications for migraine with aura.
Xichun Zhang, Dan Levy, Rodrigo Noseda, Vanessa Kainz, Moshe Jakubowski, Rami Burstein. J Neurosci 2010
208
15

Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel.
Paul J Adams, Ravi L Rungta, Esperanza Garcia, Arn M J M van den Maagdenberg, Brian A MacVicar, Terrance P Snutch. Proc Natl Acad Sci U S A 2010
46
32



Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.
S Guida, F Trettel, S Pagnutti, E Mantuano, A Tottene, L Veneziano, T Fellin, M Spadaro, K Stauderman, M Williams,[...]. Am J Hum Genet 2001
107
13

The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition.
Selma A Serra, Noèlia Fernàndez-Castillo, Alfons Macaya, Bru Cormand, Miguel A Valverde, José M Fernández-Fernández. Pflugers Arch 2009
27
48

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.
Ronald G Lafrenière, M Zameel Cader, Jean-François Poulin, Isabelle Andres-Enguix, Maryse Simoneau, Namrata Gupta, Karine Boisvert, François Lafrenière, Shannon McLaughlan, Marie-Pierre Dubé,[...]. Nat Med 2010
220
13

Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraine.
Masashi Suzuki, Wim Van Paesschen, Ingeborg Stalmans, Shoko Horita, Hideomi Yamada, Bruno A Bergmans, Eric Legius, Florence Riant, Peter De Jonghe, Yuehong Li,[...]. Proc Natl Acad Sci U S A 2010
98
13

Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.
Katharina Eikermann-Haerter, Izumi Yuzawa, Tao Qin, Yumei Wang, Kwangyeol Baek, Young Ro Kim, Ulrike Hoffmann, Ergin Dilekoz, Christian Waeber, Michel D Ferrari,[...]. J Neurosci 2011
79
16


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.