A citation-based method for searching scientific literature

Jennifer J Rilstone, Fernando M Coelho, Berge A Minassian, Danielle M Andrade. Epilepsia 2012
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity


Progressive gait deterioration in adolescents with Dravet syndrome.
Jill M Rodda, Ingrid E Scheffer, Jacinta M McMahon, Samuel F Berkovic, H Kerr Graham. Arch Neurol 2012
54
48

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.
A Brunklaus, R Ellis, E Reavey, G H Forbes, S M Zuberi. Brain 2012
173
38

Lamotrigine and seizure aggravation in severe myoclonic epilepsy.
R Guerrini, C Dravet, P Genton, A Belmonte, A Kaminska, O Dulac. Epilepsia 1998
311
35

Dravet syndrome: the long-term outcome.
Pierre Genton, Reana Velizarova, Charlotte Dravet. Epilepsia 2011
139
35

Antecollis and levodopa-responsive parkinsonism are late features of Dravet syndrome.
Alfonso Fasano, Felippe Borlot, Anthony E Lang, Danielle M Andrade. Neurology 2014
33
42

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe. Am J Hum Genet 2001
785
30

Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
Markus Wolff, Catherine Cassé-Perrot, Charlotte Dravet. Epilepsia 2006
174
30

A long-term follow-up study of Dravet syndrome up to adulthood.
Mari Akiyama, Katsuhiro Kobayashi, Harumi Yoshinaga, Yoko Ohtsuka. Epilepsia 2010
111
30

Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults.
F E Jansen, L G Sadleir, L A Harkin, L Vadlamudi, J M McMahon, J C Mulley, I E Scheffer, S F Berkovic. Neurology 2006
87
28

Incidence of Dravet Syndrome in a US Population.
Yvonne W Wu, Joseph Sullivan, Sharon S McDaniel, Miriam H Meisler, Eileen M Walsh, Sherian Xu Li, Michael W Kuzniewicz. Pediatrics 2015
92
28

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
C Depienne, O Trouillard, C Saint-Martin, I Gourfinkel-An, D Bouteiller, W Carpentier, B Keren, B Abert, A Gautier, S Baulac,[...]. J Med Genet 2009
225
25

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
643
25

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
103
25

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
238
23

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Claudia B Catarino, Joan Y W Liu, Ioannis Liagkouras, Vaneesha S Gibbons, Robyn W Labrum, Rachael Ellis, Cathy Woodward, Mary B Davis, Shelagh J Smith, J Helen Cross,[...]. Brain 2011
119
23

The spectrum of SCN1A-related infantile epileptic encephalopathies.
Louise A Harkin, Jacinta M McMahon, Xenia Iona, Leanne Dibbens, James T Pelekanos, Sameer M Zuberi, Lynette G Sadleir, Eva Andermann, Deepak Gill, Kevin Farrell,[...]. Brain 2007
345
23

Overall management of patients with Dravet syndrome.
Berten Ceulemans. Dev Med Child Neurol 2011
30
30

Stiripentol in Dravet syndrome: results of a retrospective U.S. study.
Elaine C Wirrell, Linda Laux, David N Franz, Joseph Sullivan, Russell P Saneto, Richard P Morse, Orrin Devinsky, Harry Chugani, Angel Hernandez, Lorie Hamiwka,[...]. Epilepsia 2013
56
20

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
262
20

Long-term course of Dravet syndrome: a study from an epilepsy center in Japan.
Rumiko Takayama, Tateki Fujiwara, Hideo Shigematsu, Katsumi Imai, Yukitoshi Takahashi, Kazuhiro Yamakawa, Yushi Inoue. Epilepsia 2014
45
20

Motor neuropathy contributes to crouching in patients with Dravet syndrome.
Cyril Gitiaux, Nicole Chemaly, Susana Quijano-Roy, Christine Barnerias, Isabelle Desguerre, Marie Hully, Catherine Chiron, Olivier Dulac, Rima Nabbout. Neurology 2016
25
32

Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in SCN1A-related seizure phenotypes.
Iris M de Lange, Boudewijn Gunning, Anja C M Sonsma, Lisette van Gemert, Marjan van Kempen, Nienke E Verbeek, Joost Nicolai, Nine V A M Knoers, Bobby P C Koeleman, Eva H Brilstra. Epilepsia 2018
39
20

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy.
Franck Kalume, Frank H Yu, Ruth E Westenbroek, Todd Scheuer, William A Catterall. J Neurosci 2007
170
17

Genotype-phenotype associations in SCN1A-related epilepsies.
S M Zuberi, A Brunklaus, R Birch, E Reavey, J Duncan, G H Forbes. Neurology 2011
142
17

Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy.
Rima Nabbout, Nicole Chemaly, Mathilde Chipaux, Giulia Barcia, Charles Bouis, Celia Dubouch, Dorothee Leunen, Isabelle Jambaqué, Olivier Dulac, Georges Dellatolas,[...]. Orphanet J Rare Dis 2013
88
17

Stiripentol in severe myoclonic epilepsy in infancy: a randomised placebo-controlled syndrome-dedicated trial. STICLO study group.
C Chiron, M C Marchand, A Tran, E Rey, P d'Athis, J Vincent, O Dulac, G Pons. Lancet 2000
327
17

Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndrome.
Nathalie Villeneuve, Virginie Laguitton, Marine Viellard, Anne Lépine, Brigitte Chabrol, Charlotte Dravet, Mathieu Milh. Epilepsy Behav 2014
43
17

The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype.
Heng Meng, Hai-Qing Xu, Lu Yu, Guo-Wang Lin, Na He, Tao Su, Yi-Wu Shi, Bin Li, Jie Wang, Xiao-Rong Liu,[...]. Hum Mutat 2015
93
17

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
A Escayg, B T MacDonald, M H Meisler, S Baulac, G Huberfeld, I An-Gourfinkel, A Brice, E LeGuern, B Moulard, D Chaigne,[...]. Nat Genet 2000
693
15

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata,[...]. J Neurosci 2007
499
15


Mortality in Dravet syndrome.
Monica S Cooper, Anne Mcintosh, Douglas E Crompton, Jacinta M McMahon, Amy Schneider, Kevin Farrell, Vijeya Ganesan, Deepak Gill, Sara Kivity, Tally Lerman-Sagie,[...]. Epilepsy Res 2016
105
15

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
Nanda A Singh, Chris Pappas, E Jill Dahle, Lieve R F Claes, Timothy H Pruess, Peter De Jonghe, Joel Thompson, Missy Dixon, Christina Gurnett, Andy Peiffer,[...]. PLoS Genet 2009
164
15

Quality of life and comorbidities associated with Dravet syndrome severity: a multinational cohort survey.
Lieven Lagae, Isabella Brambilla, Ana Mingorance, Eddie Gibson, Alysia Battersby. Dev Med Child Neurol 2018
53
15

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
15

Dravet syndrome: Characteristics, comorbidities, and caregiver concerns.
Nicole Villas, Mary Anne Meskis, Sue Goodliffe. Epilepsy Behav 2017
57
15

Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features.
Danah Aljaafari, Alfonso Fasano, Fábio A Nascimento, Anthony E Lang, Danielle M Andrade. Epilepsia 2017
17
35

Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
Francesca Ragona, Tiziana Granata, Bernardo Dalla Bernardina, Francesca Offredi, Francesca Darra, Domenica Battaglia, Monica Morbi, Daniela Brazzo, Simona Cappelletti, Daniela Chieffo,[...]. Epilepsia 2011
74
12

Stiripentol open study in Japanese patients with Dravet syndrome.
Yushi Inoue, Yoko Ohtsuka, Hirokazu Oguni, Jun Tohyama, Hiroshi Baba, Katsuyuki Fukushima, Hideyuki Ohtani, Yukitoshi Takahashi, Shunya Ikeda. Epilepsia 2009
58
12

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations.
Xiaojing Xu, Yuehua Zhang, Huihui Sun, Xiaoyan Liu, Xiaoling Yang, Hui Xiong, Yuwu Jiang, Xinhua Bao, Shuang Wang, Zhixian Yang,[...]. Brain Dev 2014
24
20

Efficacy and tolerability of the ketogenic diet in Dravet syndrome - Comparison with various standard antiepileptic drug regimen.
Anastasia Dressler, Petra Trimmel-Schwahofer, Eva Reithofer, Angelika Mühlebner, Gudrun Gröppel, Edith Reiter-Fink, Franz Benninger, Roland Grassl, Martha Feucht. Epilepsy Res 2015
57
12

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
R Nabbout, E Gennaro, B Dalla Bernardina, O Dulac, F Madia, E Bertini, G Capovilla, C Chiron, G Cristofori, M Elia,[...]. Neurology 2003
186
12

Ketogenic diet also benefits Dravet syndrome patients receiving stiripentol: a prospective pilot study.
Rima Nabbout, Cristiana Copioli, Mathilde Chipaux, Nicole Chemaly, Isabelle Desguerre, Olivier Dulac, Catherine Chiron. Epilepsia 2011
55
12

Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.
Eija Gaily, Anna-Kaisa Anttonen, Leena Valanne, Elina Liukkonen, Ann-Liz Träskelin, Anne Polvi, Markus Lommi, Mikko Muona, Kai Eriksson, Anna-Elina Lehesjoki. Epilepsia 2013
29
17


Topiramate in the treatment of severe myoclonic epilepsy in infancy.
M Nieto-Barrera, R Candau, M Nieto-Jimenez, A Correa, L R del Portal. Seizure 2000
73
12

Sleep abnormalities in children with Dravet syndrome.
Radhika Dhamija, Maia K Erickson, Erik K St Louis, Elaine Wirrell, Suresh Kotagal. Pediatr Neurol 2014
16
31

Dravet syndrome--from epileptic encephalopathy to channelopathy.
Andreas Brunklaus, Sameer M Zuberi. Epilepsia 2014
68
12

Pitfalls in genetic testing: the story of missed SCN1A mutations.
Tania Djémié, Sarah Weckhuysen, Sarah von Spiczak, Gemma L Carvill, Johanna Jaehn, Anna-Kaisa Anttonen, Eva Brilstra, Hande S Caglayan, Carolien G de Kovel, Christel Depienne,[...]. Mol Genet Genomic Med 2016
38
13

Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations.
Valentina Cetica, Sara Chiari, Davide Mei, Elena Parrini, Laura Grisotto, Carla Marini, Daniela Pucatti, Annarita Ferrari, Federico Sicca, Nicola Specchio,[...]. Neurology 2017
40
12


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.