A citation-based method for searching scientific literature

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
Times Cited: 113







List of co-cited articles
898 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
78

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
68

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
65

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
251
53

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
47

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
50

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
59


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
33

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
55

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
27

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
51

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
M A Kaunisto, H Harno, K R J Vanmolkot, J J Gargus, G Sun, E Hämäläinen, E Liukkonen, M Kallela, A M J M van den Maagdenberg, R R Frants,[...]. Neurogenetics 2004
48
52

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
34

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
36

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
237
23

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
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
57
38

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
40

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
62

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
21

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
21

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
28

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
110
20


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
33

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
24

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.
A Ducros, A Joutel, K Vahedi, M Cecillon, A Ferreira, E Bernard, A Verier, B Echenne, A Lopez de Munain, M G Bousser,[...]. Ann Neurol 1997
160
19

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
39

The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
Kaate R J Vanmolkot, Elena Babini, Boukje de Vries, Anine H Stam, Tobias Freilinger, Gisela M Terwindt, Lisa Norris, Joost Haan, Rune R Frants, Nabih M Ramadan,[...]. Hum Mutat 2007
70
27

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.
Katell Beauvais, Florence Cavé-Riant, Claire De Barace, Marc Tardieu, Elisabeth Tournier-Lasserve, Alain Furby. Eur Neurol 2004
36
50

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation.
E E Kors, A Melberg, K R J Vanmolkot, E Kumlien, J Haan, R Raininko, R Flink, H B Ginjaar, R R Frants, M D Ferrari,[...]. Neurology 2004
80
22

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
25

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.
Roberto Marconi, Maurizio De Fusco, Paolo Aridon, Katrin Plewnia, Maja Rossi, Sadia Carapelli, Andrea Ballabio, Letterio Morgante, Rosa Musolino, Antonio Epifanio,[...]. Ann Neurol 2003
64
26

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
18

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.
Gisela Terwindt, Esther Kors, Joost Haan, Frans Vermeulen, Arn Van den Maagdenberg, Rune Frants, Michel Ferrari. Arch Neurol 2002
67
25

Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.
Laura Segall, Rosemarie Scanzano, Mari A Kaunisto, Maija Wessman, Aarno Palotie, J Jay Gargus, Rhoda Blostein. J Biol Chem 2004
45
37

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
26

Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
193
16

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
15

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
14

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes.
Michael A Moskowitz, Hayrunnisa Bolay, Turgay Dalkara. Ann Neurol 2004
154
14

The Na,K-ATPase alpha 2 isoform is expressed in neurons, and its absence disrupts neuronal activity in newborn mice.
Amy E Moseley, Steve P Lieske, Randall K Wetzel, Paul F James, Suiwen He, Daniel A Shelly, Richard J Paul, Gregory P Boivin, David P Witte, Jan Marino Ramirez,[...]. J Biol Chem 2003
116
14

A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
Desiree M Fernandez, Collette K Hand, Brian J Sweeney, Nollaig A Parfrey. Headache 2008
25
56

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
586
14

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
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
152
14

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.
S Cevoli, G Pierangeli, L Monari, M L Valentino, P Bernardoni, M Mochi, P Cortelli, P Montagna. Neurol Sci 2002
27
48

A gene for familial hemiplegic migraine maps to chromosome 19.
A Joutel, M G Bousser, V Biousse, P Labauge, H Chabriat, A Nibbio, J Maciazek, B Meyer, M A Bach, J Weissenbach. Nat Genet 1993
304
13

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
184
13


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.