A citation-based method for searching scientific literature

Saul A Mullen, Samuel F Berkovic. Epilepsia 2018
Times Cited: 26







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



Times Cited
  Times     Co-cited
Similarity


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
57

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou, Christopher A Reid. Pharmacol Rev 2018
69
19


The prognosis of idiopathic generalized epilepsy.
Udaya Seneviratne, Mark Cook, Wendyl D'Souza. Epilepsia 2012
35
15


Epilepsy genetics: Current knowledge, applications, and future directions.
K A Myers, D L Johnstone, D A Dyment. Clin Genet 2019
39
15

The hidden genetics of epilepsy-a clinically important new paradigm.
Rhys H Thomas, Samuel F Berkovic. Nat Rev Neurol 2014
136
15

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Erin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, Elizabeth K Ruzzo, Nicole M Walley, Anna C Need, Dongliang Ge, Min He, Elizabeth T Cirulli, Qian Zhao,[...]. Am J Hum Genet 2012
81
15


Epidemiology of idiopathic generalized epilepsies.
Pierre Jallon, Patrick Latour. Epilepsia 2005
179
15


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
311
15

Juvenile myoclonic epilepsy: A system disorder of the brain.
Peter Wolf, Elza Márcia Targas Yacubian, Giuliano Avanzini, Thomas Sander, Bettina Schmitz, Britta Wandschneider, Matthias Koepp. Epilepsy Res 2015
52
11

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Michael Steffens, Costin Leu, Ann-Kathrin Ruppert, Federico Zara, Pasquale Striano, Angela Robbiano, Giuseppe Capovilla, Paolo Tinuper, Antonio Gambardella, Amedeo Bianchi,[...]. Hum Mol Genet 2012
105
11

Epidemiology of juvenile myoclonic epilepsy.
Carol S Camfield, Pasquale Striano, Peter R Camfield. Epilepsy Behav 2013
64
11

Genetic Causes of Generalized Epilepsies.
Ingo Helbig. Semin Neurol 2015
19
15

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
11

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
R H Wallace, D W Wang, R Singh, I E Scheffer, A L George, H A Phillips, K Saar, A Reis, E W Johnson, G R Sutherland,[...]. Nat Genet 1998
772
11

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
127
11

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures.
R H Wallace, C Marini, S Petrou, L A Harkin, D N Bowser, R G Panchal, D A Williams, G R Sutherland, J C Mulley, I E Scheffer,[...]. Nat Genet 2001
567
11

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
92
11

Early-Life Epilepsies and the Emerging Role of Genetic Testing.
Anne T Berg, Jason Coryell, Russell P Saneto, Zachary M Grinspan, John J Alexander, Mariana Kekis, Joseph E Sullivan, Elaine C Wirrell, Renée A Shellhaas, John R Mytinger,[...]. JAMA Pediatr 2017
71
11

Epilepsy genetics--past, present, and future.
Annapurna Poduri, Daniel Lowenstein. Curr Opin Genet Dev 2011
81
11

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
11

Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy.
Betsy E P Ostrander, Russell J Butterfield, Brent S Pedersen, Andrew J Farrell, Ryan M Layer, Alistair Ward, Chase Miller, Tonya DiSera, Francis M Filloux, Meghan S Candee,[...]. NPJ Genom Med 2018
30
11

Is the underlying cause of epilepsy a major prognostic factor for recurrence?
F Semah, M C Picot, C Adam, D Broglin, A Arzimanoglou, B Bazin, D Cavalcanti, M Baulac. Neurology 1998
625
11

Polygenic burden in focal and generalized epilepsies.
Costin Leu, Remi Stevelink, Alexander W Smith, Slavina B Goleva, Masahiro Kanai, Lisa Ferguson, Ciaran Campbell, Yoichiro Kamatani, Yukinori Okada, Sanjay M Sisodiya,[...]. Brain 2019
17
17

The landscape of epilepsy-related GATOR1 variants.
Sara Baldassari, Fabienne Picard, Nienke E Verbeek, Marjan van Kempen, Eva H Brilstra, Gaetan Lesca, Valerio Conti, Renzo Guerrini, Francesca Bisulli, Laura Licchetta,[...]. Genet Med 2019
50
11

Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology.
Robert S Fisher, J Helen Cross, Jacqueline A French, Norimichi Higurashi, Edouard Hirsch, Floor E Jansen, Lieven Lagae, Solomon L Moshé, Jukka Peltola, Eliane Roulet Perez,[...]. Epilepsia 2017
893
11

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.
Patrick May, Simon Girard, Merle Harrer, Dheeraj R Bobbili, Julian Schubert, Stefan Wolking, Felicitas Becker, Pamela Lachance-Touchette, Caroline Meloche, Micheline Gravel,[...]. Lancet Neurol 2018
33
11

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Ingo Helbig, Heather C Mefford, Andrew J Sharp, Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak,[...]. Nat Genet 2009
394
11

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Hiroyuki Ishiura, Koichiro Doi, Jun Mitsui, Jun Yoshimura, Miho Kawabe Matsukawa, Asao Fujiyama, Yasuko Toyoshima, Akiyoshi Kakita, Hitoshi Takahashi, Yutaka Suzuki,[...]. Nat Genet 2018
108
11

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
915
11

Advancing epilepsy genetics in the genomic era.
Candace T Myers, Heather C Mefford. Genome Med 2015
95
11

Evidence-based guideline: Management of an unprovoked first seizure in adults: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the American Epilepsy Society.
Allan Krumholz, Samuel Wiebe, Gary S Gronseth, David S Gloss, Ana M Sanchez, Arif A Kabir, Aisha T Liferidge, Justin P Martello, Andres M Kanner, Shlomo Shinnar,[...]. Neurology 2015
108
7

Genetic generalized epilepsies.
William B Gallentine, Mohamad A Mikati. J Clin Neurophysiol 2012
15
13

Eyelid myoclonia with typical absences: an epilepsy syndrome.
R E Appleton, C P Panayiotopoulos, B A Acomb, M Beirne. J Neurol Neurosurg Psychiatry 1993
69
7

The role of cognitive-motor function in precipitation and inhibition of epileptic seizures.
Hiroo Matsuoka, Masaki Nakamura, Takashi Ohno, Jin Shimabukuro, Takeshi Suzuki, Yohtaro Numachi, Shuichi Awata. Epilepsia 2005
26
7

BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.
Deb K Pal, Oleg V Evgrafov, Paula Tabares, Fengli Zhang, Martina Durner, David A Greenberg. Am J Hum Genet 2003
126
7

DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians.
Shilpa Pathak, James Miller, Emily C Morris, William C L Stewart, David A Greenberg. Epilepsia 2018
11
18

ILAE official report: a practical clinical definition of epilepsy.
Robert S Fisher, Carlos Acevedo, Alexis Arzimanoglou, Alicia Bogacz, J Helen Cross, Christian E Elger, Jerome Engel, Lars Forsgren, Jacqueline A French, Mike Glynn,[...]. Epilepsia 2014
7

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.
Giulia Barcia, Matthew R Fleming, Aline Deligniere, Valeswara-Rao Gazula, Maile R Brown, Maeva Langouet, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio,[...]. Nat Genet 2012
261
7

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
193
7


Recent advances in epilepsy genetics.
Alessandro Orsini, Federico Zara, Pasquale Striano. Neurosci Lett 2018
36
7


Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders.
Amanda S Lindy, Mary Beth Stosser, Elizabeth Butler, Courtney Downtain-Pickersgill, Anita Shanmugham, Kyle Retterer, Tracy Brandt, Gabriele Richard, Dianalee A McKnight. Epilepsia 2018
84
7

Mechanisms of human inherited epilepsies.
Christopher A Reid, Samuel F Berkovic, Steven Petrou. Prog Neurobiol 2009
128
7

The genetic variant "C588T" of GABARG2 is linked to childhood idiopathic generalized epilepsy and resistance to antiepileptic drugs.
Soheir S Abou El Ella, Maha Atef Tawfik, Wafaa Moustafa M Abo El Fotoh, Omar Ahmed M Soliman. Seizure 2018
12
16

The genetic basis of DOORS syndrome: an exome-sequencing study.
Philippe M Campeau, Dalia Kasperaviciute, James T Lu, Lindsay C Burrage, Choel Kim, Mutsuki Hori, Berkley R Powell, Fiona Stewart, Têmis Maria Félix, Jenneke van den Ende,[...]. Lancet Neurol 2014
86
7


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.