A citation-based method for searching scientific literature

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, M D Ferrari. Ann Neurol 2001
Times Cited: 236







List of co-cited articles
1300 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
37

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
467
34

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
152
30

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.
A H Stam, G-J Luijckx, B T Poll-Thé, I B Ginjaar, R R Frants, J Haan, M D Ferrari, G M Terwindt, A M J M van den Maagdenberg. J Neurol Neurosurg Psychiatry 2009
67
43

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
371
26

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
102
24

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
223
22

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
192
21


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
19

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.
Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
183
18

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
88
19

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
540
16

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.
F Riant, A Ducros, C Ploton, C Barbance, C Depienne, E Tournier-Lasserve. Neurology 2010
82
19

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
647
15

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
139
15

Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
193
15

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
133
14

Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation.
Lubov Blumkin, Marina Michelson, Esther Leshinsky-Silver, Sara Kivity, Dorit Lev, Tally Lerman-Sagie. J Child Neurol 2010
37
37

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
788
13

Cerebellar ataxia by enhanced Ca(V)2.1 currents is alleviated by Ca2+-dependent K+-channel activators in Cacna1a(S218L) mutant mice.
Zhenyu Gao, Boyan Todorov, Curtis F Barrett, Stijn van Dorp, Michel D Ferrari, Arn M J M van den Maagdenberg, Chris I De Zeeuw, Freek E Hoebeek. J Neurosci 2012
64
20

The Neurometabolic Cascade of Concussion.
Christopher C. Giza, David A. Hovda. J Athl Train 2001
716
12

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
101
12

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
47
25

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
152
12

Minor head trauma-induced sporadic hemiplegic migraine coma.
Robert P Curtain, Robert L Smith, Mick Ovcaric, Lyn R Griffiths. Pediatr Neurol 2006
42
28

The new neurometabolic cascade of concussion.
Christopher C Giza, David A Hovda. Neurosurgery 2014
571
12

Familial hemiplegic migraine.
Daniela Pietrobon. Neurotherapeutics 2007
136
11

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.
K Vahedi, C Denier, A Ducros, V Bousson, C Levy, H Chabriat, M Haguenau, E Tournier-Lasserve, M G Bousser. Neurology 2000
109
11

The spectrum of disease in chronic traumatic encephalopathy.
Ann C McKee, Robert A Stern, Christopher J Nowinski, Thor D Stein, Victor E Alvarez, Daniel H Daneshvar, Hyo-Soon Lee, Sydney M Wojtowicz, Garth Hall, Christine M Baugh,[...]. Brain 2013
11

Familial and sporadic hemiplegic migraine: diagnosis and treatment.
Nadine Pelzer, Anine H Stam, Joost Haan, Michel D Ferrari, Gisela M Terwindt. Curr Treat Options Neurol 2013
55
20

Chronic traumatic encephalopathy in athletes: progressive tauopathy after repetitive head injury.
Ann C McKee, Robert C Cantu, Christopher J Nowinski, E Tessa Hedley-Whyte, Brandon E Gavett, Andrew E Budson, Veronica E Santini, Hyo-Soon Lee, Caroline A Kubilus, Robert A Stern. J Neuropathol Exp Neurol 2009
10


Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation.
Yee-Cheun Chan, Jean-Marc Burgunder, Einar Wilder-Smith, Soh-Eng Chew, Karen M J Lam-Mok-Sing, Vijay Sharma, Benjamin K C Ong. J Clin Neurosci 2008
40
25

A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline.
T Freilinger, N Ackl, A Ebert, C Schmidt, B Rautenstrauss, M Dichgans, A Danek. J Neurol Sci 2011
20
50

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
41
24

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
28
35


Activation of central trigeminovascular neurons by cortical spreading depression.
Xichun Zhang, Dan Levy, Vanessa Kainz, Rodrigo Noseda, Moshe Jakubowski, Rami Burstein. Ann Neurol 2011
220
10

Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
151
10

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.
E E Kors, J Haan, N J Giffin, L Pazdera, C Schnittger, G G Lennox, G M Terwindt, F L M J Vermeulen, A M J M Van den Maagdenberg, R R Frants,[...]. Arch Neurol 2003
68
14

Assessment of metabolic brain damage and recovery following mild traumatic brain injury: a multicentre, proton magnetic resonance spectroscopic study in concussed patients.
Roberto Vagnozzi, Stefano Signoretti, Luciano Cristofori, Franco Alessandrini, Roberto Floris, Eugenio Isgrò, Antonio Ria, Simone Marziali, Giada Zoccatelli, Barbara Tavazzi,[...]. Brain 2010
262
10

The epidemiology and impact of traumatic brain injury: a brief overview.
Jean A Langlois, Wesley Rutland-Brown, Marlena M Wald. J Head Trauma Rehabil 2006
10


Summary of evidence-based guideline update: evaluation and management of concussion in sports: report of the Guideline Development Subcommittee of the American Academy of Neurology.
Christopher C Giza, Jeffrey S Kutcher, Stephen Ashwal, Jeffrey Barth, Thomas S D Getchius, Gerard A Gioia, Gary S Gronseth, Kevin Guskiewicz, Steven Mandel, Geoffrey Manley,[...]. Neurology 2013
573
10

Cumulative effects associated with recurrent concussion in collegiate football players: the NCAA Concussion Study.
Kevin M Guskiewicz, Michael McCrea, Stephen W Marshall, Robert C Cantu, Christopher Randolph, William Barr, James A Onate, James P Kelly. JAMA 2003
9

Chronic traumatic encephalopathy in a National Football League player.
Bennet I Omalu, Steven T DeKosky, Ryan L Minster, M Ilyas Kamboh, Ronald L Hamilton, Cyril H Wecht. Neurosurgery 2005
564
9

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
A Ducros, C Denier, A Joutel, K Vahedi, A Michel, F Darcel, M Madigand, D Guerouaou, F Tison, J Julien,[...]. Am J Hum Genet 1999
118
9

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia.
S Battistini, S Stenirri, M Piatti, C Gelfi, P G Righetti, R Rocchi, F Giannini, N Battistini, G C Guazzi, M Ferrari,[...]. Neurology 1999
140
9

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
108
9


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.