A citation-based method for searching scientific literature

Yasuto Tanabe, Takumi Taira, Akihiro Shimotake, Takeshi Inoue, Tomonari Awaya, Takeo Kato, Akira Kuzuya, Akio Ikeda, Ryosuke Takahashi. Rinsho Shinkeigaku 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Lacosamide for SCN2A-related intractable neonatal and infantile seizures.
Hadar Flor-Hirsch, Eli Heyman, Ayelet Livneh, Orit Reish, Nathan Watemberg, Ita Litmanovits, Anat Ben Sason Lilli, Dorit Lev, Tally Lerman Sagie, Haim Bassan. Epileptic Disord 2018
13
33

Malformations of cortical development: clinical features and genetic causes.
Renzo Guerrini, William B Dobyns. Lancet Neurol 2014
231
33

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.
Heather C Mefford, Hiltrud Muhle, Philipp Ostertag, Sarah von Spiczak, Karen Buysse, Carl Baker, Andre Franke, Alain Malafosse, Pierre Genton, Pierre Thomas,[...]. PLoS Genet 2010
345
33

Brain malformations and mutations in α- and β-tubulin genes: a review of the literature and description of two new cases.
Romina Romaniello, Filippo Arrigoni, Anna Cavallini, Erika Tenderini, Cinzia Baschirotto, Fabio Triulzi, Maria-Teresa Bassi, Renato Borgatti. Dev Med Child Neurol 2014
30
33

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.
Todor Arsov, Saul A Mullen, John A Damiano, Kate M Lawrence, Linda L Huh, Melinda Nolan, Helen Young, Anaïs Thouin, Hans-Henrik M Dahl, Samuel F Berkovic,[...]. Epilepsia 2012
67
33

Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
Federico Zara, Nicola Specchio, Pasquale Striano, Angela Robbiano, Elena Gennaro, Roberta Paravidino, Nicola Vanni, Francesca Beccaria, Giuseppe Capovilla, Amedeo Bianchi,[...]. Epilepsia 2013
78
33

Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.
Saul A Mullen, Gemma L Carvill, Susannah Bellows, Marta A Bayly, Holger Trucks, Dennis Lal, Thoman Sander, Samuel F Berkovic, Leanne M Dibbens, Ingrid E Scheffer,[...]. Neurology 2013
104
33

GRIN2A-related disorders: genotype and functional consequence predict phenotype.
Vincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, Katie F M Marwick, Gabrielle Rudolf, Julitta de Bellescize, Saskia Biskup, Eva H Brilstra, Oebele F Brouwer, Petra M C Callenbach,[...]. Brain 2019
68
33

Advancing epilepsy genetics in the genomic era.
Candace T Myers, Heather C Mefford. Genome Med 2015
109
33

Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel.
Elaine C Wirrell, Linda Laux, Elizabeth Donner, Nathalie Jette, Kelly Knupp, Mary Anne Meskis, Ian Miller, Joseph Sullivan, Michelle Welborn, Anne T Berg. Pediatr Neurol 2017
130
33


Recent advances in epilepsy genetics.
Alessandro Orsini, Federico Zara, Pasquale Striano. Neurosci Lett 2018
47
33

Whole-genome CNV analysis: advances in computational approaches.
Mehdi Pirooznia, Fernando S Goes, Peter P Zandi. Front Genet 2015
91
33

GRIN2A mutation and early-onset epileptic encephalopathy: personalized therapy with memantine.
Tyler Mark Pierson, Hongjie Yuan, Eric D Marsh, Karin Fuentes-Fajardo, David R Adams, Thomas Markello, Gretchen Golas, Dimitre R Simeonov, Conisha Holloman, Anel Tankovic,[...]. Ann Clin Transl Neurol 2014
154
33

Clinical and genetic findings in 26 Italian patients with Lafora disease.
Silvana Franceschetti, Antonio Gambardella, Laura Canafoglia, Pasquale Striano, Hannes Lohi, Elena Gennaro, Leonarda Ianzano, Pierangelo Veggiotti, Vito Sofia, Roberto Biondi,[...]. Epilepsia 2006
47
33

Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
Elena Gardella, Felicitas Becker, Rikke S Møller, Julian Schubert, Johannes R Lemke, Line H G Larsen, Hans Eiberg, Michael Nothnagel, Holger Thiele, Janine Altmüller,[...]. Ann Neurol 2016
112
33

Identifying mutations in epilepsy genes: Impact on treatment selection.
Piero Perucca, Emilio Perucca. Epilepsy Res 2019
43
33

Benign childhood focal epilepsies.
Renzo Guerrini, Simona Pellacani. Epilepsia 2012
59
33

Management of genetic epilepsies: From empirical treatment to precision medicine.
Pasquale Striano, Maria Stella Vari, Chiara Mazzocchetti, Alberto Verrotti, Federico Zara. Pharmacol Res 2016
35
33

ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies.
Caitlin A Bennett, Slavé Petrovski, Karen L Oliver, Samuel F Berkovic. Neurol Genet 2017
24
33

A developmental and genetic classification for malformations of cortical development: update 2012.
A James Barkovich, Renzo Guerrini, Ruben I Kuzniecky, Graeme D Jackson, William B Dobyns. Brain 2012
552
33

Treatable newborn and infant seizures due to inborn errors of metabolism.
Jaume Campistol, Barbara Plecko. Epileptic Disord 2015
29
33

Definition of refractory epilepsy: defining the indefinable?
Patrick Kwan, Martin J Brodie. Lancet Neurol 2010
92
33


Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
Paolo Bonanni, Michela Malcarne, Francesca Moro, Pierangelo Veggiotti, Daniela Buti, Anna Rita Ferrari, Elena Parrini, Davide Mei, Anna Volzone, Federico Zara,[...]. Epilepsia 2004
48
33

Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy.
Marina Trivisano, Alessandra Terracciano, Teresa Milano, Simona Cappelletti, Nicola Pietrafusa, Enrico Silvio Bertini, Federico Vigevano, Nicola Specchio. Epilepsia 2015
14
33

Mechanistic Target of Rapamycin Pathway in Epileptic Disorders.
Jang Keun Kim, Jeong Ho Lee. J Korean Neurosurg Soc 2019
14
33

Epileptic encephalopathies: new genes and new pathways.
Sahar Esmaeeli Nieh, Elliott H Sherr. Neurotherapeutics 2014
49
33

Mutations in EFHC1 cause juvenile myoclonic epilepsy.
Toshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, Maria E Alonso, Jun Shi, Yuji Hara, Motohiro Nishida, Tomohiro Numata, Marco T Medina, Tamaki Takeuchi,[...]. Nat Genet 2004
228
33

Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy.
Nicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, Pasquale Striano, Angela Robbiano, Monica Traverso, Thomas Sander, Antonio Falace, Elisabetta Gazzerro, Placido Bramanti,[...]. Ann Neurol 2014
50
33

Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation.
I-Ching Chou, Sheng-Shing Lin, Wei-De Lin, Chung-Hsing Wang, Yu-Tzu Chang, Fuu-Jen Tsai, Chang-Hai Tsai. Biomedicine (Taipei) 2014
6
33


Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
Emanuela Dazzo, Manuela Fanciulli, Elena Serioli, Giovanni Minervini, Patrizia Pulitano, Simona Binelli, Carlo Di Bonaventura, Concetta Luisi, Elena Pasini, Salvatore Striano,[...]. Am J Hum Genet 2015
65
33

GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
Konrad Platzer, Hongjie Yuan, Hannah Schütz, Alexander Winschel, Wenjuan Chen, Chun Hu, Hirofumi Kusumoto, Henrike O Heyne, Katherine L Helbig, Sha Tang,[...]. J Med Genet 2017
119
33

Medical genetics: a marker for Stevens-Johnson syndrome.
Wen-Hung Chung, Shuen-Iu Hung, Hong-Shang Hong, Mo-Song Hsih, Li-Cheng Yang, Hsin-Chun Ho, Jer-Yuarn Wu, Yuan-Tsong Chen. Nature 2004
33

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Wan-Jin Chen, Yu Lin, Zhi-Qi Xiong, Wei Wei, Wang Ni, Guo-He Tan, Shun-Ling Guo, Jin He, Ya-Fang Chen, Qi-Jie Zhang,[...]. Nat Genet 2011
312
33

The genetic landscape of the epileptic encephalopathies of infancy and childhood.
Amy McTague, Katherine B Howell, J Helen Cross, Manju A Kurian, Ingrid E Scheffer. Lancet Neurol 2016
288
33

The role of mTOR inhibitors in preventing epileptogenesis in patients with TSC: Current evidence and future perspectives.
Susanne Schubert-Bast, Felix Rosenow, Karl Martin Klein, Philipp S Reif, Matthias Kieslich, Adam Strzelczyk. Epilepsy Behav 2019
20
33

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.
E Parrini, A Ramazzotti, W B Dobyns, D Mei, F Moro, P Veggiotti, C Marini, E H Brilstra, B Dalla Bernardina, L Goodwin,[...]. Brain 2006
230
33


Precision medicine in genetic epilepsies: break of dawn?
Philipp Sebastian Reif, Meng-Han Tsai, Ingo Helbig, Felix Rosenow, Karl Martin Klein. Expert Rev Neurother 2017
41
33

GLUT1 deficiency syndrome in clinical practice.
Joerg Klepper. Epilepsy Res 2012
92
33

Clinical Genetic Testing in Epilepsy.
Heather C Mefford. Epilepsy Curr 2015
15
33


Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag,[...]. Brain 2010
326
33

Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear.
Paolo Aridon, Carla Marini, Chiara Di Resta, Elisa Brilli, Maurizio De Fusco, Fausta Politi, Elena Parrini, Irene Manfredi, Tiziana Pisano, Dario Pruna,[...]. Am J Hum Genet 2006
151
33

SCN1A clinical spectrum includes the self-limited focal epilepsies of childhood.
Sara Kivity, Karen L Oliver, Zaid Afawi, John A Damiano, Todor Arsov, Melanie Bahlo, Samuel F Berkovic. Epilepsy Res 2017
6
33

Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects.
Amre Shahwan, Michael Farrell, Norman Delanty. Lancet Neurol 2005
135
33

Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
Laura Canafoglia, Elena Gennaro, Giuseppe Capovilla, Giuseppe Gobbi, Antonella Boni, Francesca Beccaria, Maurizio Viri, Roberto Michelucci, Pamela Agazzi, Stefania Assereto,[...]. Epilepsia 2012
21
33

Progressive Myoclonus Epilepsies.
Reetta Kälviäinen. Semin Neurol 2015
36
33


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.