A citation-based method for searching scientific literature

Gali Heimer, Yair Sadaka, Lori Israelian, Ariel Feiglin, Alessandra Ruggieri, Christian R Marshall, Stephen W Scherer, Esther Ganelin-Cohen, Dina Marek-Yagel, Michal Tzadok, Andreea Nissenkorn, Yair Anikster, Berge A Minassian, Bruria Ben Zeev. J Child Neurol 2015
Times Cited: 29







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



Times Cited
  Times     Co-cited
Similarity


A novel recurrent mutation in ATP1A3 causes CAPOS syndrome.
Michelle K Demos, Clara Dm van Karnebeek, Colin Jd Ross, Shelin Adam, Yaoqing Shen, Shing Hei Zhan, Casper Shyr, Gabriella Horvath, Mohnish Suri, Alan Fryer,[...]. Orphanet J Rare Dis 2014
100
86

Phenotypic overlap of alternating hemiplegia of childhood and CAPOS syndrome.
Hendrik Rosewich, Dagmar Weise, Andreas Ohlenbusch, Jutta Gärtner, Knut Brockmann. Neurology 2014
33
62


Distinct neurological disorders with ATP1A3 mutations.
Erin L Heinzen, Alexis Arzimanoglou, Allison Brashear, Steven J Clapcote, Fiorella Gurrieri, David B Goldstein, Sigurður H Jóhannesson, Mohamad A Mikati, Brian Neville, Sophie Nicole,[...]. Lancet Neurol 2014
130
48


Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutation.
Rodolphe Dard, Cyril Mignot, Alexandra Durr, Gaetan Lesca, Damien Sanlaville, Emmanuel Roze, Fanny Mochel. Dev Med Child Neurol 2015
45
44


Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly.
Alex R Paciorkowski, Sharon S McDaniel, Laura A Jansen, Hannah Tully, Emily Tuttle, Dalia H Ghoneim, Srinivasan Tupal, Sonya A Gunter, Valeria Vasta, Qing Zhang,[...]. Epilepsia 2015
56
41

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.
Hendrik Rosewich, Holger Thiele, Andreas Ohlenbusch, Ulrike Maschke, Janine Altmüller, Peter Frommolt, Birgit Zirn, Friedrich Ebinger, Hartmut Siemes, Peter Nürnberg,[...]. Lancet Neurol 2012
144
41

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
287
41

The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene.
Roderick P P W M Maas, Jolanda H Schieving, Meyke Schouten, Erik-Jan Kamsteeg, Bart P C van de Warrenburg. Pediatr Neurol 2016
20
60

The expanding clinical and genetic spectrum of ATP1A3-related disorders.
Hendrik Rosewich, Andreas Ohlenbusch, Peter Huppke, Lars Schlotawa, Martina Baethmann, Inês Carrilho, Simona Fiori, Charles Marques Lourenço, Sarah Sawyer, Robert Steinfeld,[...]. Neurology 2014
67
34

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L Heinzen, Carmen Fons, Sanjay Sisodiya, Boukje de Vries, Christophe Goubau, Sarah Weckhuysen, David Kemlink,[...]. Orphanet J Rare Dis 2015
71
34

ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients.
Xiaoling Yang, Hua Gao, Jie Zhang, Xiaojing Xu, Xiaoyan Liu, Xiru Wu, Liping Wei, Yuehua Zhang. PLoS One 2014
37
31

Distribution of Na/K-ATPase alpha 3 isoform, a sodium-potassium P-type pump associated with rapid-onset of dystonia parkinsonism (RDP) in the adult mouse brain.
Pernille Bøttger, Zuzanna Tracz, Anders Heuck, Poul Nissen, Marina Romero-Ramos, Karin Lykke-Hartmann. J Comp Neurol 2011
106
31

Genotype-phenotype correlations in alternating hemiplegia of childhood.
Masayuki Sasaki, Atsushi Ishii, Yoshiaki Saito, Naoya Morisada, Kazumoto Iijima, Satoshi Takada, Atsushi Araki, Yuko Tanabe, Hidee Arai, Sumimasa Yamashita,[...]. Neurology 2014
67
31

Distribution of the Na,K-ATPase alpha subunit in the rat spiral ganglion and organ of corti.
Will J McLean, K Anne Smith, Elisabeth Glowatzki, Sonja J Pyott. J Assoc Res Otolaryngol 2009
74
31

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Erin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries, F Danilo Tiziano, Bertrand Fontaine, Nicole M Walley, Sinéad Heavin,[...]. Nat Genet 2012
223
31

Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults.
Eleni Panagiotakaki, Giuseppe Gobbi, Brian Neville, Friedrich Ebinger, Jaume Campistol, Sona Nevsímalová, Laura Laan, Paul Casaer, Georg Spiel, Melania Giannotta,[...]. Brain 2010
83
24

Deficiency in Na,K-ATPase alpha isoform genes alters spatial learning, motor activity, and anxiety in mice.
Amy E Moseley, Michael T Williams, Tori L Schaefer, Cynthia S Bohanan, Jon C Neumann, Michael M Behbehani, Charles V Vorhees, Jerry B Lingrel. J Neurosci 2007
190
24


Early Diagnosis of CAPOS Syndrome Before Acute-Onset Ataxia-Review of the Literature and a New Family.
Anna Duat Rodriguez, Michaela Prochazkova, Saturnino Santos Santos, Oscar Rubio Cabezas, Veronica Cantarin Extremera, Luis Gonzalez-Gutierrez-Solana. Pediatr Neurol 2017
12
58

Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase α3 sodium pump.
Greer S Kirshenbaum, Steven J Clapcote, Steven Duffy, Christian R Burgess, Janne Petersen, Karolina J Jarowek, Yeni H Yücel, Miguel A Cortez, O Carter Snead, Bente Vilsen,[...]. Proc Natl Acad Sci U S A 2011
86
20

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
Louis Viollet, Gustavo Glusman, Kelley J Murphy, Tara M Newcomb, Sandra P Reyna, Matthew Sweney, Benjamin Nelson, Frederick Andermann, Eva Andermann, Gyula Acsadi,[...]. PLoS One 2015
34
20

Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS.
Steven J Clapcote, Steven Duffy, Gang Xie, Greer Kirshenbaum, Allison R Bechard, Vivien Rodacker Schack, Janne Petersen, Laleh Sinai, Bechara J Saab, Jason P Lerch,[...]. Proc Natl Acad Sci U S A 2009
95
20

Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization.
Arsen S Hunanyan, Nina A Fainberg, Molly Linabarger, Eric Arehart, A Soren Leonard, Syed M Adil, Ashley R Helseth, Amanda K Swearingen, Stacy L Forbes, Ramona M Rodriguiz,[...]. Epilepsia 2015
42
20

The multiple faces of the ATP1A3-related dystonic movement disorder.
Anne Roubergue, Emmanuel Roze, Sandrine Vuillaumier-Barrot, Marie-Joséphine Fontenille, Aurélie Méneret, Marie Vidailhet, Bertrand Fontaine, Diane Doummar, Bertrand Philibert, Florence Riant,[...]. Mov Disord 2013
42
20

Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3-deficient heterozygous mice.
Keiko Ikeda, Shin'Ichiro Satake, Tatsushi Onaka, Hiroki Sugimoto, Naoki Takeda, Keiji Imoto, Kiyoshi Kawakami. J Physiol 2013
43
20

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.
Mark P DeAndrade, Fumiaki Yokoi, Thomas van Groen, Jerry B Lingrel, Yuqing Li. Behav Brain Res 2011
51
20

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Fatima Jaffer, Andreja Avbersek, Rosaria Vavassori, Carmen Fons, Jaume Campistol, Michela Stagnaro, Elisa De Grandis, Edvige Veneselli, Hendrik Rosewich, Melania Gianotta,[...]. Brain 2015
19
31

Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.
I A Anselm, K J Sweadner, S Gollamudi, L J Ozelius, B T Darras. Neurology 2009
41
20

The treatment and management of alternating hemiplegia of childhood.
B G R Neville, M Ninan. Dev Med Child Neurol 2007
51
17

Alternating hemiplegia of childhood: early characteristics and evolution of a neurodevelopmental syndrome.
Matthew T Sweney, Kenneth Silver, Marion Gerard-Blanluet, Jean-Michel Pedespan, Francis Renault, Alexis Arzimanoglou, Mylynda Schlesinger-Massart, Aga J Lewelt, Sandra P Reyna, Kathryn J Swoboda. Pediatrics 2009
87
17


ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.
Allison Brashear, Jonathan W Mink, Deborah F Hill, Niki Boggs, W Vaughn McCall, Mark A Stacy, Beverly Snively, Laney S Light, Kathleen J Sweadner, Laurie J Ozelius,[...]. Dev Med Child Neurol 2012
53
17

Intermediate Phenotypes of ATP1A3 Mutations: Phenotype-Genotype Correlations.
Pichet Termsarasab, Amy C Yang, Steven J Frucht. Tremor Other Hyperkinet Mov (N Y) 2015
14
35

ATP1A3 Mutation in Adult Rapid-Onset Ataxia.
Kathleen J Sweadner, Camilo Toro, Christopher T Whitlow, Beverly M Snively, Jared F Cook, Laurie J Ozelius, Thomas C Markello, Allison Brashear. PLoS One 2016
21
23


A functional correlate of severity in alternating hemiplegia of childhood.
Melody Li, Dana Jazayeri, Ben Corry, K Melodi McSweeney, Erin L Heinzen, David B Goldstein, Steven Petrou. Neurobiol Dis 2015
26
19

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
552
17

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
534
17


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
96
13


A specific and essential role for Na,K-ATPase α3 in neurons co-expressing α1 and α3.
Guillaume Azarias, Markus Kruusmägi, Siobhan Connor, Evgeny E Akkuratov, Xiao-Li Liu, David Lyons, Hjalmar Brismar, Christian Broberger, Anita Aperia. J Biol Chem 2013
64
13

Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.
Greer S Kirshenbaum, Neil Dawson, Jonathan G L Mullins, Tom H Johnston, Mark J Drinkhill, Ian J Edwards, Susan H Fox, Judith A Pratt, Jonathan M Brotchie, John C Roder,[...]. PLoS One 2013
30
13

Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism.
Masayuki Sasaki, Atsushi Ishii, Yoshiaki Saito, Shinichi Hirose. Mov Disord 2014
14
28

Alternating Hemiplegia of Childhood mutations have a differential effect on Na(+),K(+)-ATPase activity and ouabain binding.
Karl M Weigand, Muriël Messchaert, Herman G P Swarts, Frans G M Russel, Jan B Koenderink. Biochim Biophys Acta 2014
22
18

Alternating hemiplegia of childhood.
M Bourgeois, J Aicardi, F Goutières. J Pediatr 1993
100
13

Alternating hemiplegia of childhood: clinical manifestations and long-term outcome.
M A Mikati, U Kramer, M L Zupanc, R J Shanahan. Pediatr Neurol 2000
101
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.