A citation-based method for searching scientific literature

Jennifer K Forsyth, Robert F Asarnow. Child Adolesc Psychiatr Clin N Am 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies.
Patrick F Sullivan, Kenneth S Kendler, Michael C Neale. Arch Gen Psychiatry 2003
33



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
49
33

P-type ATPases.
Michael G Palmgren, Poul Nissen. Annu Rev Biophys 2011
326
33

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
80
33

Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3.
August A Allocco, Sheng Chih Jin, Phan Q Duy, Charuta G Furey, Xue Zeng, Weilai Dong, Carol Nelson-Williams, Jason K Karimy, Tyrone DeSpenza, Le T Hao,[...]. Front Cell Neurosci 2019
6
33

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
66
33

ATP1A3-related epileptic encephalopathy responding to ketogenic diet.
Tommaso Schirinzi, Federica Graziola, Raffaella Cusmai, Lucia Fusco, Francesco Nicita, Mirella Elia, Lorena Travaglini, Enrico Bertini, Paolo Curatolo, Federico Vigevano,[...]. Brain Dev 2018
13
33

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
67
33

Relapsing encephalopathy with cerebellar ataxia are caused by variants involving p.Arg756 in ATP1A3.
Pascal Sabouraud, Audrey Riquet, Marie-Aude Spitz, Kumaran Deiva, Sona Nevsimalova, Cyril Mignot, Gaëtan Lesca, Nathalie Bednarek, Diane Doummar, Christine Pietrement,[...]. Eur J Paediatr Neurol 2019
11
33

Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing.
Ihtsham U Haq, Beverly M Snively, Kathleen J Sweadner, Cynthia K Suerken, Jared F Cook, Laurie J Ozelius, Charlotte Miller, William V McCall, Christopher T Whitlow, Allison Brashear. Mov Disord 2019
10
33

Neuronal function and alpha3 isoform of the Na/K-ATPase.
Maxim Dobretsov, Joseph R Stimers. Front Biosci 2005
107
33

A case of rapid-onset dystonia-parkinsonism accompanied by pyramidal tract impairment.
Yanqiu Liu, Yan Lu, Xinqing Zhang, Shuping Xie, Tingting Wang, Tianwen Wu, Chaoyan Wang. BMC Neurol 2016
6
33

Generalized Dystonia and Paroxysmal Dystonic Attacks due to a Novel ATP1A3 Variant.
Carlos Zúñiga-Ramírez, Mirelle Kramis-Hollands, Rodrigo Mercado-Pimentel, Héctor Alberto González-Usigli, Michel Sáenz-Farret, Alberto Soto-Escageda, Alfonso Fasano. Tremor Other Hyperkinet Mov (N Y) 2019
8
33

A novel de novo mutation in ATP1A3 and childhood-onset schizophrenia.
Niklas Smedemark-Margulies, Catherine A Brownstein, Sigella Vargas, Sahil K Tembulkar, Meghan C Towne, Jiahai Shi, Elisa Gonzalez-Cuevas, Kevin X Liu, Kaya Bilguvar, Robin J Kleiman,[...]. Cold Spring Harb Mol Case Stud 2016
27
33

Functional consequences of the CAPOS mutation E818K of Na+,K+-ATPase.
Christian P Roenn, Melody Li, Vivien R Schack, Ian C Forster, Rikke Holm, Mads S Toustrup-Jensen, Jens P Andersen, Steven Petrou, Bente Vilsen. J Biol Chem 2019
6
33

Beyond Dystonia-Parkinsonism: Chorea and Ataxia with ATP1A3 Mutations.
Claudio M de Gusmao, Marisela Dy, Nutan Sharma. Mov Disord Clin Pract 2016
6
33

Epileptic encephalopathy with features of rapid-onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation.
Linh Tran, Jason Richards, Marie McDonald, Allyn McConkie-Rosell, Nicholas Stong, Joan Jasien, Vandana Shashi, Mohamad A Mikati. Epileptic Disord 2020
4
50

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
50
33

Mosaicism in ATP1A3-related disorders: not just a theoretical risk.
Marie Hully, Juliette Ropars, Laurence Hubert, Nathalie Boddaert, Marlene Rio, Mathieu Bernardelli, Isabelle Desguerre, Valerie Cormier-Daire, Arnold Munnich, Pascale de Lonlay,[...]. Neurogenetics 2017
15
33

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
23
33

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia.
Boris Chaumette, Vladimir Ferrafiat, Amirthagowri Ambalavanan, Alice Goldenberg, Alexandre Dionne-Laporte, Dan Spiegelman, Patrick A Dion, Priscille Gerardin, Claudine Laurent, David Cohen,[...]. Mol Psychiatry 2020
17
33

Phenotypic overlap of alternating hemiplegia of childhood and CAPOS syndrome.
Hendrik Rosewich, Dagmar Weise, Andreas Ohlenbusch, Jutta Gärtner, Knut Brockmann. Neurology 2014
35
33

ATP1A3-related disorders: An update.
Miryam Carecchio, Giovanna Zorzi, Francesca Ragona, Federica Zibordi, Nardo Nardocci. Eur J Paediatr Neurol 2018
31
33

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
21
33

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
111
33

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
109
33

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
73
33

Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations.
Tommaso Schirinzi, Federica Graziola, Francesco Nicita, Lorena Travaglini, Fabrizia Stregapede, Massimiliano Valeriani, Paolo Curatolo, Enrico Bertini, Federico Vigevano, Alessandro Capuano. Cerebellum 2018
13
33

Childhood-Onset Schizophrenia and Early-onset Schizophrenia Spectrum Disorders: An Update.
David I Driver, Shari Thomas, Nitin Gogtay, Judith L Rapoport. Child Adolesc Psychiatr Clin N Am 2020
14
33

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited.
Judith Rapoport, Alex Chavez, Deanna Greenstein, Anjene Addington, Nitin Gogtay. J Am Acad Child Adolesc Psychiatry 2009
214
33

Genome-wide association studies of bipolar disorder: A systematic review of recent findings and their clinical implications.
Masashi Ikeda, Takeo Saito, Kenji Kondo, Nakao Iwata. Psychiatry Clin Neurosci 2018
28
16



Common polygenic variation and risk for childhood-onset schizophrenia.
K Ahn, S S An, Y Y Shugart, J L Rapoport. Mol Psychiatry 2016
33
16

Smoking Rates and Number of Cigarettes Smoked per Day in Schizophrenia: A Large Cohort Meta-Analysis in a Japanese Population.
Kazutaka Ohi, Takamitsu Shimada, Aki Kuwata, Yuzuru Kataoka, Hiroaki Okubo, Kohei Kimura, Toshiki Yasuyama, Takashi Uehara, Yasuhiro Kawasaki. Int J Neuropsychopharmacol 2019
14
16

Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
Masashi Ikeda, Atsushi Takahashi, Yoichiro Kamatani, Yukihide Momozawa, Takeo Saito, Kenji Kondo, Ayu Shimasaki, Kohei Kawase, Takaya Sakusabe, Yoshimi Iwayama,[...]. Schizophr Bull 2019
34
16

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Naomi R Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M Byrne, Abdel Abdellaoui, Mark J Adams, Esben Agerbo, Tracy M Air, Till M F Andlauer,[...]. Nat Genet 2018
847
16

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
16

Genome-wide association study identifies a potent locus associated with human opioid sensitivity.
D Nishizawa, K Fukuda, S Kasai, J Hasegawa, Y Aoki, A Nishi, N Saita, Y Koukita, M Nagashima, R Katoh,[...]. Mol Psychiatry 2014
58
16

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
Daniel Moreno-De-Luca, Jennifer G Mulle, Erin B Kaminsky, Stephan J Sanders, Scott M Myers, Margaret P Adam, Amy T Pakula, Nancy J Eisenhauer, Kim Uhas, LuAnn Weik,[...]. Am J Hum Genet 2010
198
16

Impaired intellect and memory: a missing link between genetic risk and schizophrenia?
Timothea Toulopoulou, Terry E Goldberg, Irene Rebollo Mesa, Marco Picchioni, Fruhling Rijsdijk, Daniel Stahl, Stacey S Cherny, Pak Sham, Stephen V Faraone, Ming Tsuang,[...]. Arch Gen Psychiatry 2010
86
16

A general approach for haplotype phasing across the full spectrum of relatedness.
Jared O'Connell, Deepti Gurdasani, Olivier Delaneau, Nicola Pirastu, Sheila Ulivi, Massimiliano Cocca, Michela Traglia, Jie Huang, Jennifer E Huffman, Igor Rudan,[...]. PLoS Genet 2014
280
16



Neuropsychological impairments in schizophrenia and psychotic bipolar disorder: findings from the Bipolar-Schizophrenia Network on Intermediate Phenotypes (B-SNIP) study.
S Kristian Hill, James L Reilly, Richard S E Keefe, James M Gold, Jeffrey R Bishop, Elliot S Gershon, Carol A Tamminga, Godfrey D Pearlson, Matcheri S Keshavan, John A Sweeney. Am J Psychiatry 2013
207
16

Meta-analysis of physical activity and effects of social function and quality of life on the physical activity in patients with schizophrenia.
Kazutaka Ohi, Yuzuru Kataoka, Takamitsu Shimada, Aki Kuwata, Hiroaki Okubo, Kohei Kimura, Toshiki Yasuyama, Takashi Uehara, Yasuhiro Kawasaki. Eur Arch Psychiatry Clin Neurosci 2019
14
16

Polygenetic components for schizophrenia, bipolar disorder and rheumatoid arthritis predict risk of schizophrenia.
Kazutaka Ohi, Masataka Kikuchi, Masashi Ikeda, Hidenaga Yamamori, Yuka Yasuda, Michiko Fujimoto, Haruo Fujino, Kenichiro Miura, Masaki Fukunaga, Akihiro Nakaya,[...]. Schizophr Res 2016
15
16

eQTLs Weighted Genetic Correlation Analysis Detected Brain Region Differences in Genetic Correlations for Complex Psychiatric Disorders.
Yan Wen, Feng Zhang, Xiancang Ma, Qianrui Fan, Wenyu Wang, Jiawen Xu, Feng Zhu, Jingcan Hao, Awen He, Li Liu,[...]. Schizophr Bull 2019
2
50


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.