A citation-based method for searching scientific literature

Shinichi Hirose, Yasuyoshi Tanaka, Mami Shibata, Yuichi Kimura, Mitsuru Ishikawa, Norimichi Higurashi, Toshiyuki Yamamoto, Eisuke Ichise, Tomohiro Chiyonobu, Atsushi Ishii. Mol Cell Neurosci 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening.
Aliesha Griffin, Kyla R Hamling, SoonGweon Hong, Mana Anvar, Luke P Lee, Scott C Baraban. Front Pharmacol 2018
46
50


De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy.
Hirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi, Keisuke Hamada, Hitoshi Osaka, Jun Tohyama, Katsuhisa Uruno, Satoko Kumada, Kiyomi Nishiyama, Akira Nishimura,[...]. Nat Genet 2008
353
50

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, Silvia Masnada, Guido Rubboli, Elena Gardella, Gaetan Lesca, Dorothée Ville, Mathieu Milh, Laurent Villard,[...]. Brain 2017
212
50

Mislocalization of syntaxin-1 and impaired neurite growth observed in a human iPSC model for STXBP1-related epileptic encephalopathy.
Satoshi Yamashita, Tomohiro Chiyonobu, Michiko Yoshida, Hiroshi Maeda, Masashi Zuiki, Satoshi Kidowaki, Kenichi Isoda, Masafumi Morimoto, Mitsuhiro Kato, Hirotomo Saitsu,[...]. Epilepsia 2016
28
50

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
653
50

SCN1A-related phenotypes: Epilepsy and beyond.
Ingrid E Scheffer, Rima Nabbout. Epilepsia 2019
37
50

STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.
Hannah Stamberger, Marina Nikanorova, Marjolein H Willemsen, Patrizia Accorsi, Marco Angriman, Hartmut Baier, Ira Benkel-Herrenbrueck, Valérie Benoit, Mauro Budetta, Almuth Caliebe,[...]. Neurology 2016
132
50

Goliath family E3 ligases regulate the recycling endosome pathway via VAMP3 ubiquitylation.
Yasuo Yamazaki, Christina Schönherr, Gaurav K Varshney, Murat Dogru, Bengt Hallberg, Ruth H Palmer. EMBO J 2013
26
25

A Genetic Screen for Genes That Impact Peroxisomes in Drosophila Identifies Candidate Genes for Human Disease.
Hillary K Graves, Sharayu Jangam, Kai Li Tan, Antonella Pignata, Elaine S Seto, Shinya Yamamoto, Michael F Wangler. G3 (Bethesda) 2020
2
50

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Kathleen M Gorman, Esther Meyer, Detelina Grozeva, Egidio Spinelli, Amy McTague, Alba Sanchis-Juan, Keren J Carss, Emily Bryant, Adi Reich, Amy L Schneider,[...]. Am J Hum Genet 2019
14
25


Critical roles of αII spectrin in brain development and epileptic encephalopathy.
Yu Wang, Tuo Ji, Andrew D Nelson, Katarzyna Glanowska, Geoffrey G Murphy, Paul M Jenkins, Jack M Parent. J Clin Invest 2018
34
25

Detection of copy number variations in epilepsy using exome data.
N Tsuchida, M Nakashima, M Kato, E Heyman, T Inui, K Haginoya, S Watanabe, T Chiyonobu, M Morimoto, M Ohta,[...]. Clin Genet 2018
26
25

Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases.
Joana Branco, Ismael Al-Ramahi, Lubna Ukani, Alma M Pérez, Pedro Fernandez-Funez, Diego Rincón-Limas, Juan Botas. Hum Mol Genet 2008
55
25

A Drosophila model for Angelman syndrome.
Yaning Wu, Francois V Bolduc, Kimberly Bell, Tim Tully, Yanshan Fang, Amita Sehgal, Janice A Fischer. Proc Natl Acad Sci U S A 2008
70
25

Mushroom body memoir: from maps to models.
Martin Heisenberg. Nat Rev Neurosci 2003
804
25

The RhoGEF Zizimin-related acts in the Drosophila cellular immune response via the Rho GTPases Rac2 and Cdc42.
Christopher J Sampson, Susanna Valanne, Marie-Odile Fauvarque, Dan Hultmark, Mika Rämet, Michael J Williams. Dev Comp Immunol 2012
12
25

Treatment with the antiepileptic drugs phenytoin and gabapentin ameliorates seizure and paralysis of Drosophila bang-sensitive mutants.
Elaine R Reynolds, Eric A Stauffer, Laura Feeney, Elizabeth Rojahn, Benjamin Jacobs, Carol McKeever. J Neurobiol 2004
46
25

West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1.
Ali Abdullah Alfaiz, Verena Müller, Nadia Boutry-Kryza, Dorothée Ville, Nicolas Guex, Julitta de Bellescize, Clotilde Rivier, Audrey Labalme, Vincent des Portes, Patrick Edery,[...]. Eur J Hum Genet 2016
10
25

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
Amy McTague, Umesh Nair, Sony Malhotra, Esther Meyer, Natalie Trump, Elena V Gazina, Apostolos Papandreou, Adeline Ngoh, Sally Ackermann, Gautam Ambegaonkar,[...]. Neurology 2018
42
25

prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies.
Salleh N Ehaideb, Atulya Iyengar, Atsushi Ueda, Gary J Iacobucci, Cathryn Cranston, Alexander G Bassuk, David Gubb, Jeffrey D Axelrod, Shermali Gunawardena, Chun-Fang Wu,[...]. Proc Natl Acad Sci U S A 2014
39
25

Glia and epilepsy: excitability and inflammation.
Orrin Devinsky, Annamaria Vezzani, Souhel Najjar, Nihal C De Lanerolle, Michael A Rogawski. Trends Neurosci 2013
397
25

Disruption of Endocytosis with the Dynamin Mutant shibirets1 Suppresses Seizures in Drosophila.
Jason R Kroll, Karen G Wong, Faria M Siddiqui, Mark A Tanouye. Genetics 2015
10
25

Knock-in model of Dravet syndrome reveals a constitutive and conditional reduction in sodium current.
Ryan J Schutte, Soleil S Schutte, Jacqueline Algara, Eden V Barragan, Jeff Gilligan, Cynthia Staber, Yiannis A Savva, Martin A Smith, Robert Reenan, Diane K O'Dowd. J Neurophysiol 2014
32
25

Axonal transport of mitochondria to synapses depends on milton, a novel Drosophila protein.
R Steven Stowers, Laura J Megeath, Jolanta Górska-Andrzejak, Ian A Meinertzhagen, Thomas L Schwarz. Neuron 2002
442
25


CDKL5 Deficiency Disorder-A Complex Epileptic Encephalopathy.
Martyna Jakimiec, Justyna Paprocka, Robert Śmigiel. Brain Sci 2020
14
25




A low-cost method for analyzing seizure-like activity and movement in Drosophila.
Bryan Stone, Brian Burke, Joseph Pathakamuri, John Coleman, Daniel Kuebler. J Vis Exp 2014
10
25

Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine.
Yifan Zhang, Angéla Kecskés, Daniëlle Copmans, Mélanie Langlois, Alexander D Crawford, Berten Ceulemans, Lieven Lagae, Peter A M de Witte, Camila V Esguerra. PLoS One 2015
51
25

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
25

Drosophila as a model for intractable epilepsy: gilgamesh suppresses seizures in para(bss1) heterozygote flies.
Iris C Howlett, Zeid M Rusan, Louise Parker, Mark A Tanouye. G3 (Bethesda) 2013
17
25



Seizure suppression by top1 mutations in Drosophila.
Juan Song, Joyce Hu, Mark Tanouye. J Neurosci 2007
21
25

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Xiao-Meng Yin, Jing-Han Lin, Li Cao, Tong-Mei Zhang, Sheng Zeng, Kai-Lin Zhang, Wo-Tu Tian, Zheng-Mao Hu, Nan Li, Jun-Ling Wang,[...]. Hum Mol Genet 2018
26
25

Mutations in the K+/Cl- cotransporter gene kazachoc (kcc) increase seizure susceptibility in Drosophila.
Daria S Hekmat-Scafe, Miriam Y Lundy, Rakhee Ranga, Mark A Tanouye. J Neurosci 2006
59
25

Skywalker-TBC1D24 has a lipid-binding pocket mutated in epilepsy and required for synaptic function.
Baptiste Fischer, Kevin Lüthy, Jone Paesmans, Charlotte De Koninck, Ine Maes, Jef Swerts, Sabine Kuenen, Valerie Uytterhoeven, Patrik Verstreken, Wim Versées. Nat Struct Mol Biol 2016
36
25


Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation.
B Abou-Khalil, Q Ge, R Desai, R Ryther, A Bazyk, R Bailey, J L Haines, J S Sutcliffe, A L George. Neurology 2001
150
25

High-throughput behavioral assay to investigate seizure sensitivity in zebrafish implicates ZFHX3 in epilepsy.
Tyson D Fuller, Trudi A Westfall, Tirthasree Das, Deborah V Dawson, Diane C Slusarski. J Neurogenet 2018
7
25

Drosophila canopy b is a cochaperone of glycoprotein 93.
Crystal Morales, Zihai Li. J Biol Chem 2017
4
25


Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy.
Sali M K Farhan, Kevin C J Nixon, Michelle Everest, Tara N Edwards, Shirley Long, Dmitri Segal, Maria J Knip, Heleen H Arts, Rana Chakrabarti, Jian Wang,[...]. Hum Mol Genet 2017
20
25

North Sea Progressive Myoclonus Epilepsy is Exacerbated by Heat, A Phenotype Primarily Associated with Affected Glia.
Roald A Lambrechts, Sjoukje S Polet, Alejandra Hernandez-Pichardo, Lisa van Ninhuys, Jenke A Gorter, Nicola A Grzeschik, Marina A J de Koning-Tijssen, Tom J de Koning, Ody C M Sibon. Neuroscience 2019
4
25

Mouse strain differences in kainic acid sensitivity, seizure behavior, mortality, and hippocampal pathology.
G M McKhann, H J Wenzel, C A Robbins, A A Sosunov, P A Schwartzkroin. Neuroscience 2003
143
25



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.