A citation-based method for searching scientific literature

Neslihan N Tavraz, Thomas Friedrich, Katharina L Dürr, Jan B Koenderink, Ernst Bamberg, Tobias Freilinger, Martin Dichgans. J Biol Chem 2008
Times Cited: 60







List of co-cited articles
765 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
653
65

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
546
45

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
41

Crystal structure of the sodium-potassium pump.
J Preben Morth, Bjørn P Pedersen, Mads S Toustrup-Jensen, Thomas L-M Sørensen, Janne Petersen, Jens Peter Andersen, Bente Vilsen, Poul Nissen. Nature 2007
591
36

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
36

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
33

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
135
31

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
30

Familial hemiplegic migraine.
Daniela Pietrobon. Neurotherapeutics 2007
136
28

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
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,[...]. Ann Neurol 2003
252
26

Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.
Neslihan N Tavraz, Katharina L Dürr, Jan B Koenderink, Tobias Freilinger, Ernst Bamberg, Martin Dichgans, Thomas Friedrich. Channels (Austin) 2009
25
64

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
798
26

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
193
26

Crystal structure of the sodium-potassium pump at 2.4 A resolution.
Takehiro Shinoda, Haruo Ogawa, Flemming Cornelius, Chikashi Toyoshima. Nature 2009
417
26

Altered Na+ transport after an intracellular alpha-subunit deletion reveals strict external sequential release of Na+ from the Na/K pump.
Siddhartha Yaragatupalli, J Fernando Olivera, Craig Gatto, Pablo Artigas. Proc Natl Acad Sci U S A 2009
34
44

Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
193
25

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
75
23

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
23

The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations.
J Preben Morth, Hanne Poulsen, Mads S Toustrup-Jensen, Vivien Rodacker Schack, Jan Egebjerg, Jens Peter Andersen, Bente Vilsen, Poul Nissen. Philos Trans R Soc Lond B Biol Sci 2009
61
23

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
154
23


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
58
22

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
26

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
75
21

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
253
21

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
20

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
21

Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.
Sandrine Cestèle, Paolo Scalmani, Raffaella Rusconi, Benedetta Terragni, Silvana Franceschetti, Massimo Mantegazza. J Neurosci 2008
83
20




Neurological disease mutations compromise a C-terminal ion pathway in the Na(+)/K(+)-ATPase.
Hanne Poulsen, Himanshu Khandelia, J Preben Morth, Maike Bublitz, Ole G Mouritsen, Jan Egebjerg, Poul Nissen. Nature 2010
90
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
83
20

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
Patricia de Carvalho Aguiar, Kathleen J Sweadner, John T Penniston, Jacek Zaremba, Liu Liu, Marsha Caton, Gurutz Linazasoro, Michel Borg, Marina A J Tijssen, Susan B Bressman,[...]. Neuron 2004
328
18

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
68
18


Suppression of cortical spreading depression in migraine prophylaxis.
Cenk Ayata, Hongwei Jin, Chiho Kudo, Turgay Dalkara, Michael A Moskowitz. Ann Neurol 2006
407
18

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
62
18

Glutamate transporter coupling to Na,K-ATPase.
Erin M Rose, Joseph C P Koo, Jordan E Antflick, Syed M Ahmed, Stephane Angers, David R Hampson. J Neurosci 2009
228
18



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
234
18

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
49
20

Transport and pharmacological properties of nine different human Na, K-ATPase isozymes.
G Crambert, U Hasler, A T Beggah, C Yu, N N Modyanov, J D Horisberger, L Lelièvre, K Geering. J Biol Chem 2000
330
16


Neurobiology of migraine.
Daniela Pietrobon, Jörg Striessnig. Nat Rev Neurosci 2003
390
16

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
103
16

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
185
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
964
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
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.