A citation-based method for searching scientific literature

Kaate R J Vanmolkot, Esther E Kors, Jouke-Jan Hottenga, Gisela M Terwindt, Joost Haan, Wil A J Hoefnagels, David F Black, Lodewijk A Sandkuijl, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Ann Neurol 2003
Times Cited: 251







List of co-cited articles
1173 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
650
52

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
545
50

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
35


Epilepsy as part of the phenotype associated with ATP1A2 mutations.
Liesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, Tine Deconinck, Kristl G Claeys, Lieve R F Claes, Arvid Suls, Tine Van Dyck, André Palmini, Gert Matthijs,[...]. Epilepsia 2008
65
35

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
113
22

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
373
22

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
470
20

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
24

Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
193
19

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
796
18

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
224
17

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
A Escayg, B T MacDonald, M H Meisler, S Baulac, G Huberfeld, I An-Gourfinkel, A Brice, E LeGuern, B Moulard, D Chaigne,[...]. Nat Genet 2000
713
16

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
Kathryn J Swoboda, Emmanuel Kanavakis, Athina Xaidara, Justine E Johnson, Mark F Leppert, Mylynda B Schlesinger-Massart, Louis J Ptacek, Kenneth Silver, Sotiris Youroukos. Ann Neurol 2004
116
16

Suppression of cortical spreading depression in migraine prophylaxis.
Cenk Ayata, Hongwei Jin, Chiho Kudo, Turgay Dalkara, Michael A Moskowitz. Ann Neurol 2006
406
16

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
64
25

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe. Am J Hum Genet 2001
825
15

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs.
Maria Spadaro, Simona Ursu, Frank Lehmann-Horn, Liana Veneziano, Giovanni Antonini, Paola Giunti, Marina Frontali, Karin Jurkat-Rott. Neurogenetics 2004
89
16

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
960
15


Hypothesis on neurophysiopathological mechanisms linking epilepsy and headache.
Pasquale Parisi, Marta Piccioli, Maria Pia Villa, Carla Buttinelli, Dorothee G A Kasteleijn-Nolst Trenité. Med Hypotheses 2008
52
26

Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2.
Laura Segall, Alessandra Mezzetti, Rosemarie Scanzano, J Jay Gargus, Enrico Purisima, Rhoda Blostein. Proc Natl Acad Sci U S A 2005
57
24

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
14

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood.
M T Bassi, N Bresolin, A Tonelli, K Nazos, F Crippa, C Baschirotto, C Zucca, A Bersano, D Dolcetta, F M Boneschi,[...]. J Med Genet 2004
77
18

PRRT2 mutations cause hemiplegic migraine.
Florence Riant, Emmanuel Roze, Cecile Barbance, Aurélie Méneret, Lucie Guyant-Maréchal, Christian Lucas, Pascal Sabouraud, Agnes Trébuchon, Christel Depienne, Elisabeth Tournier-Lasserve. Neurology 2012
79
17

Sodium-channel defects in benign familial neonatal-infantile seizures.
Sarah E Heron, Kathryn M Crossland, Eva Andermann, Hilary A Phillips, Allison J Hall, Andrew Bleasel, Michael Shevell, Suha Mercho, Marie-Helene Seni, Marie-Christine Guiot,[...]. Lancet 2002
251
13

Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
A Ambrosini, M D'Onofrio, G S Grieco, A Di Mambro, G Montagna, D Fortini, F Nicoletti, G Nappi, G Sances, J Schoenen,[...]. Neurology 2005
69
18

Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.
Neslihan N Tavraz, Thomas Friedrich, Katharina L Dürr, Jan B Koenderink, Ernst Bamberg, Tobias Freilinger, Martin Dichgans. J Biol Chem 2008
60
21

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.
K R J Vanmolkot, H Stroink, J B Koenderink, E E Kors, J J M W van den Heuvel, E H van den Boogerd, A H Stam, J Haan, B B A De Vries, G M Terwindt,[...]. Ann Neurol 2006
60
21

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.
Unda Todt, Martin Dichgans, Karin Jurkat-Rott, Axel Heinze, Giovanni Zifarelli, Jan B Koenderink, Ingrid Goebel, Vera Zumbroich, Anne Stiller, Alfredo Ramirez,[...]. Hum Mutat 2005
55
23

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
13

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
134
13

Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
J C Jen, J Wan, T P Palos, B D Howard, R W Baloh. Neurology 2005
233
12

Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.
Kaate R J Vanmolkot, Esther E Kors, Ulku Turk, Dylsad Turkdogan, Antoine Keyser, Ludo A M Broos, Sima Kheradmand Kia, Jeroen J M W van den Heuvel, David F Black, Joost Haan,[...]. Eur J Hum Genet 2006
48
25

ATP1A2 mutations in 11 families with familial hemiplegic migraine.
Florence Riant, Maurizio De Fusco, Paolo Aridon, Anne Ducros, Claire Ploton, Florence Marchelli, Jacqueline Maciazek, Marie Germaine Bousser, Giorgio Casari, Elisabeth Tournier-Lasserve. Hum Mutat 2005
62
19

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes.
Michael A Moskowitz, Hayrunnisa Bolay, Turgay Dalkara. Ann Neurol 2004
154
12


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

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
61
19

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
12


A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
O K Steinlein, J C Mulley, P Propping, R H Wallace, H A Phillips, G R Sutherland, I E Scheffer, S F Berkovic. Nat Genet 1995
835
11

A novel ATP1A2 mutation in a family with FHM type II.
F Pierelli, G S Grieco, F Pauri, C Pirro, G Fiermonte, A Ambrosini, A Costa, M G Buzzi, M Valoppi, C Caltagirone,[...]. Cephalalgia 2006
35
31

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation.
Jan B Koenderink, Giovanni Zifarelli, Li Yan Qiu, Wolfgang Schwarz, Jan Joep H H M De Pont, Ernst Bamberg, Thomas Friedrich. Biochim Biophys Acta 2005
49
22



Spreading depression enhances human neocortical excitability in vitro.
M Berger, E-J Speckmann, H C Pape, A Gorji. Cephalalgia 2008
68
16

Familial hemiplegic migraine.
Daniela Pietrobon. Neurotherapeutics 2007
136
11

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
R H Wallace, D W Wang, R Singh, I E Scheffer, A L George, H A Phillips, K Saar, A Reis, E W Johnson, G R Sutherland,[...]. Nat Genet 1998
780
10

A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
Andrea Gallanti, Alessandra Tonelli, Veronica Cardin, Gennaro Bussone, Nereo Bresolin, Maria Teresa Bassi. J Neurol Sci 2008
28
35


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.