A citation-based method for searching scientific literature

S M Zuberi, A Brunklaus, R Birch, E Reavey, J Duncan, G H Forbes. Neurology 2011
Times Cited: 142







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



Times Cited
  Times     Co-cited
Similarity


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
41

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
31

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
30

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
28

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
29

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
26

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
23

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
19

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
262
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
17

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
925
17

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
201
16

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
238
15

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.
Gemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, Corinna Hartmann, Rikke S Møller, Helle Hjalgrim, Joseph Cook, Eileen Geraghty, Brian J O'Roak, Steve Petrou,[...]. Neurology 2014
147
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

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
14

A long-term follow-up study of Dravet syndrome up to adulthood.
Mari Akiyama, Katsuhiro Kobayashi, Harumi Yoshinaga, Yoko Ohtsuka. Epilepsia 2010
111
13

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
13

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
152
13

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome.
Christel Depienne, Oriane Trouillard, Isabelle Gourfinkel-An, Cécile Saint-Martin, Delphine Bouteiller, Denis Graber, Marie-Anne Barthez-Carpentier, Agnès Gautier, Nathalie Villeneuve, Charlotte Dravet,[...]. J Med Genet 2010
95
13

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert,[...]. Nat Genet 2013
405
13

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
12

Lamotrigine and seizure aggravation in severe myoclonic epilepsy.
R Guerrini, C Dravet, P Genton, A Belmonte, A Kaminska, O Dulac. Epilepsia 1998
311
12

The phenotypic spectrum of SCN8A encephalopathy.
Jan Larsen, Gemma L Carvill, Elena Gardella, Gerhard Kluger, Gudrun Schmiedel, Nina Barisic, Christel Depienne, Eva Brilstra, Yuan Mang, Jens Erik Klint Nielsen,[...]. Neurology 2015
162
12

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
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
30

Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype.
Lynette G Sadleir, Emily I Mountier, Deepak Gill, Suzanne Davis, Charuta Joshi, Catherine DeVile, Manju A Kurian, Simone Mandelstam, Elaine Wirrell, Katherine C Nickels,[...]. Neurology 2017
43
27


Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
Markus Wolff, Catherine Cassé-Perrot, Charlotte Dravet. Epilepsia 2006
174
11

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
14

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.
Yu Liu, Luis F Lopez-Santiago, Yukun Yuan, Julie M Jones, Helen Zhang, Heather A O'Malley, Gustavo A Patino, Janelle E O'Brien, Raffaella Rusconi, Ajay Gupta,[...]. Ann Neurol 2013
148
11

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Krishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, Xiaoyang Cheng, Sulayman D Dib-Hajj, Stephen G Waxman, Dinesh Talwar, Santhosh Girirajan, Evan E Eichler, Linda L Restifo,[...]. Am J Hum Genet 2012
254
11

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
208
11

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.
R H Wallace, I E Scheffer, S Barnett, M Richards, L Dibbens, R R Desai, T Lerman-Sagie, D Lev, A Mazarib, N Brand,[...]. Am J Hum Genet 2001
255
11

Genetic epilepsy with febrile seizures plus: Refining the spectrum.
Yue-Hua Zhang, Rosemary Burgess, Jodie P Malone, Georgie C Glubb, Katherine L Helbig, Lata Vadlamudi, Sara Kivity, Zaid Afawi, Andrew Bleasel, Padraic Grattan-Smith,[...]. Neurology 2017
46
23

De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies.
I Ogiwara, K Ito, Y Sawaishi, H Osaka, E Mazaki, I Inoue, M Montal, T Hashikawa, T Shike, T Fujiwara,[...]. Neurology 2009
137
10

Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene.
Renzo Guerrini, Elena Cellini, Davide Mei, Tiziana Metitieri, Cristina Petrelli, Daniela Pucatti, Carla Marini, Nelia Zamponi. Epilepsia 2010
39
25


Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome.
Kazuyuki Nakamura, Mitsuhiro Kato, Hitoshi Osaka, Sumimasa Yamashita, Eiji Nakagawa, Kazuhiro Haginoya, Jun Tohyama, Mitsuko Okuda, Takahito Wada, Shuichi Shimakawa,[...]. Neurology 2013
129
10

Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome.
Atsushi Ishii, Joseph C Watkins, Debbie Chen, Shinichi Hirose, Michael F Hammer. Epilepsia 2017
28
35

Dravet syndrome: the long-term outcome.
Pierre Genton, Reana Velizarova, Charlotte Dravet. Epilepsia 2011
139
9


A catalog of SCN1A variants.
Christoph Lossin. Brain Dev 2009
142
9

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
9

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.
Tateki Fujiwara, Takashi Sugawara, Emi Mazaki-Miyazaki, Yukitoshi Takahashi, Katsuyuki Fukushima, Masako Watanabe, Keita Hara, Tateki Morikawa, Kazuichi Yagi, Kazuhiro Yamakawa,[...]. Brain 2003
228
9

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
773
9

Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.
Linda Volkers, Kristopher M Kahlig, Nienke E Verbeek, Joost H G Das, Marjan J A van Kempen, Hans Stroink, Paul Augustijn, Onno van Nieuwenhuizen, Dick Lindhout, Alfred L George,[...]. Eur J Neurosci 2011
42
21

SCN1A mutations and epilepsy.
John C Mulley, Ingrid E Scheffer, Steven Petrou, Leanne M Dibbens, Samuel F Berkovic, Louise A Harkin. Hum Mutat 2005
242
9

Dravet syndrome--from epileptic encephalopathy to channelopathy.
Andreas Brunklaus, Sameer M Zuberi. Epilepsia 2014
68
13

The clinical utility of an SCN1A genetic diagnosis in infantile-onset epilepsy.
Andreas Brunklaus, Liam Dorris, Rachael Ellis, Eleanor Reavey, Elizabeth Lee, Gordon Forbes, Richard Appleton, J Helen Cross, Colin Ferrie, Imelda Hughes,[...]. Dev Med Child Neurol 2013
45
20


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.