A citation-based method for searching scientific literature

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
Times Cited: 62







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



Times Cited
  Times     Co-cited
Similarity


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
59

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
50

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
46

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
41

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
37

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
32

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
25

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
22

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
80
22

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
20

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
20

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
20

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
20

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
178
19

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
106
19

Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
187
19

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
M-J Castro, A H Stam, C Lemos, B de Vries, K R J Vanmolkot, J Barros, G M Terwindt, R R Frants, J Sequeiros, M D Ferrari,[...]. Cephalalgia 2009
61
18

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
17


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
17



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
16

Minor head trauma-induced sporadic hemiplegic migraine coma.
Robert P Curtain, Robert L Smith, Mick Ovcaric, Lyn R Griffiths. Pediatr Neurol 2006
42
21

Calcium channels and migraine.
Daniela Pietrobon. Biochim Biophys Acta 2013
42
21

Migraine pathophysiology: lessons from mouse models and human genetics.
Michel D Ferrari, Roselin R Klever, Gisela M Terwindt, Cenk Ayata, Arn M J M van den Maagdenberg. Lancet Neurol 2015
190
14

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
A Jouvenceau, L H Eunson, A Spauschus, V Ramesh, S M Zuberi, D M Kullmann, M G Hanna. Lancet 2001
259
12

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
12

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
12

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.
K Jurkat-Rott, T Freilinger, J P Dreier, J Herzog, H Göbel, G C Petzold, P Montagna, T Gasser, F Lehmann-Horn, M Dichgans. Neurology 2004
110
12

Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
K Vahedi, C Depienne, D Le Fort, F Riant, P Chaine, O Trouillard, A Gaudric, M A Morris, E Leguern, E Tournier-Lasserve,[...]. Neurology 2009
60
13

The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literature.
S Debiais, C Hommet, I Bonnaud, M A Barthez, S Rimbaux, F Riant, A Autret. Cephalalgia 2009
17
47

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine.
B de Vries, T Freilinger, K R J Vanmolkot, J B Koenderink, A H Stam, G M Terwindt, E Babini, E H van den Boogerd, J J M W van den Heuvel, R R Frants,[...]. Neurology 2007
73
12

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
38
21

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
12

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
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
46
17

Divergent sodium channel defects in familial hemiplegic migraine.
Kristopher M Kahlig, Thomas H Rhodes, Michael Pusch, Tobias Freilinger, José M Pereira-Monteiro, Michel D Ferrari, Arn M J M van den Maagdenberg, Martin Dichgans, Alfred L George. Proc Natl Acad Sci U S A 2008
70
11

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
147
11

CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.
B de Vries, A H Stam, F Beker, A M J M van den Maagdenberg, K R J Vanmolkot, Laem Laan, I B Ginjaar, R R Frants, H Lauffer, J Haan,[...]. Cephalalgia 2008
42
16

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
67
11

Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine.
Lise L Thomsen, Elsebet Ostergaard, Jes Olesen, Michael B Russell. Neurology 2003
93
11

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
11

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
11

Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation.
Timothy J Malpas, Florence Riant, Elisabeth Tournier-Lasserve, Katayoun Vahedi, Brian G R Neville. Dev Med Child Neurol 2010
19
36

Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutation.
Sawako Yamazaki, Kanju Ikeno, Tokinari Abe, Jun Tohyama, Yoshiki Adachi. Pediatr Neurol 2011
32
21


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
60
11


Spreading depression triggers headache by activating neuronal Panx1 channels.
Hulya Karatas, Sefik Evren Erdener, Yasemin Gursoy-Ozdemir, Sevda Lule, Emine Eren-Koçak, Zümrüt Duygu Sen, Turgay Dalkara. Science 2013
255
11


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.