A citation-based method for searching scientific literature

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, Tim M Strom. Lancet 2005
Times Cited: 529







List of co-cited articles
1499 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
51

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
635
51

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
192
26

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
457
25


Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Padhraig Gormley, Verneri Anttila, Bendik S Winsvold, Priit Palta, Tonu Esko, Tune H Pers, Kai-How Farh, Ester Cuenca-Leon, Mikko Muona, Nicholas A Furlotte,[...]. Nat Genet 2016
261
24

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata,[...]. J Neurosci 2007
499
22


Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
Frank H Yu, Massimo Mantegazza, Ruth E Westenbroek, Carol A Robbins, Franck Kalume, Kimberly A Burton, William J Spain, G Stanley McKnight, Todd Scheuer, William A Catterall. Nat Neurosci 2006
643
19

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
226
18

Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects.
Sandrine Cestèle, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza. Proc Natl Acad Sci U S A 2013
55
32

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
125
17

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
237
17

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
785
17

Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
Chunxiang Fan, Stefan Wolking, Frank Lehmann-Horn, Ulrike Bs Hedrich, Tobias Freilinger, Holger Lerche, Guntram Borck, Christian Kubisch, Karin Jurkat-Rott. Cephalalgia 2016
23
69

Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.
Sandrine Cestèle, Angelo Labate, Raffaella Rusconi, Patrizia Tarantino, Laura Mumoli, Silvana Franceschetti, Grazia Annesi, Massimo Mantegazza, Antonio Gambardella. Epilepsia 2013
42
38

Pathophysiology of Migraine: A Disorder of Sensory Processing.
Peter J Goadsby, Philip R Holland, Margarida Martins-Oliveira, Jan Hoffmann, Christoph Schankin, Simon Akerman. Physiol Rev 2017
537
16

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
360
15

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
24

Genome-wide association analysis identifies susceptibility loci for migraine without aura.
Tobias Freilinger, Verneri Anttila, Boukje de Vries, Rainer Malik, Mikko Kallela, Gisela M Terwindt, Patricia Pozo-Rosich, Bendik Winsvold, Dale R Nyholt, Willebrordus P J van Oosterhout,[...]. Nat Genet 2012
200
15

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
929
15

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
260
15

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
244
15

Pathophysiology of migraine.
Daniela Pietrobon, Michael A Moskowitz. Annu Rev Physiol 2013
344
15

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
71
21

Defective glutamate and K+ clearance by cortical astrocytes in familial hemiplegic migraine type 2.
Clizia Capuani, Marcello Melone, Angelita Tottene, Luca Bragina, Giovanna Crivellaro, Mirko Santello, Giorgio Casari, Fiorenzo Conti, Daniela Pietrobon. EMBO Mol Med 2016
61
22

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
214
14

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
693
14

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
145
13

Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Verneri Anttila, Bendik S Winsvold, Padhraig Gormley, Tobias Kurth, Francesco Bettella, George McMahon, Mikko Kallela, Rainer Malik, Boukje de Vries, Gisela Terwindt,[...]. Nat Genet 2013
235
13

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
775
13

Activation of central trigeminovascular neurons by cortical spreading depression.
Xichun Zhang, Dan Levy, Vanessa Kainz, Rodrigo Noseda, Moshe Jakubowski, Rami Burstein. Ann Neurol 2011
205
13

Genetic and environmental influences on migraine: a twin study across six countries.
Elles J Mulder, Caroline Van Baal, David Gaist, Mikko Kallela, Jaakko Kaprio, Dan A Svensson, Dale R Nyholt, Nicholas G Martin, Alex J MacGregor, Lynn F Cherkas,[...]. Twin Res 2003
210
13

Casein kinase iδ mutations in familial migraine and advanced sleep phase.
K C Brennan, Emily A Bates, Robert E Shapiro, Jekaterina Zyuzin, William C Hallows, Yong Huang, Hsien-Yang Lee, Christopher R Jones, Ying-Hui Fu, Andrew C Charles,[...]. Sci Transl Med 2013
120
12

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
179
12

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
76
15

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
79
15

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
11

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
18

Two novel SCN1A mutations identified in families with familial hemiplegic migraine.
Claudia M Weller, Nadine Pelzer, Boukje de Vries, Mercè Artigas López, Oriol De Fàbregues, Julio Pascual, María A Ramos Arroyo, Stephany C Koelewijn, Anine H Stam, Joost Haan,[...]. Cephalalgia 2014
20
55

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
13

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
187
11

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
212
11




Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
188
10

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
245
10

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
238
10

Functional analysis of missense variants in the TRESK (KCNK18) K channel.
Isabelle Andres-Enguix, Lijun Shang, Phillip J Stansfeld, Julia M Morahan, Mark S P Sansom, Ronald G Lafrenière, Bishakha Roy, Lyn R Griffiths, Guy A Rouleau, George C Ebers,[...]. Sci Rep 2012
60
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.