A citation-based method for searching scientific literature

Ágnes Till, Judith Zima, Anett Fekete, Judit Bene, Márta Czakó, András Szabó, Béla Melegh, Kinga Hadzsiev. Seizure 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Outcomes and comorbidities of SCN1A-related seizure disorders.
Iris M de Lange, Boudewijn Gunning, Anja C M Sonsma, Lisette van Gemert, Marjan van Kempen, Nienke E Verbeek, Claudia Sinoo, Joost Nicolai, Nine V A M Knoers, Bobby P C Koeleman,[...]. Epilepsy Behav 2019
16
100

Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome.
Jiaping Wang, Yongxin Wen, Qingping Zhang, Shujie Yu, Yan Chen, Xiru Wu, YueHua Zhang, Xinhua Bao. Seizure 2019
13
100

A screening test for the prediction of Dravet syndrome before one year of age.
Junri Hattori, Mamoru Ouchida, Junko Ono, Susumu Miyake, Satoshi Maniwa, Nobuyoshi Mimaki, Yoko Ohtsuka, Iori Ohmori. Epilepsia 2008
64
100

Carbamazepine and oxcarbazepine in adult patients with Dravet syndrome: Friend or foe?
F M Snoeijen-Schouwenaars, M J B M Veendrick, P van Mierlo, G van Erp, A J A de Louw, B U Kleine, H J Schelhaas, I Y Tan. Seizure 2015
9
100

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
96
100

Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes.
Iris M de Lange, Marco J Koudijs, Ruben van 't Slot, Boudewijn Gunning, Anja C M Sonsma, Lisette J J M van Gemert, Flip Mulder, Ellen C Carbo, Marjan J A van Kempen, Nienke E Verbeek,[...]. Epilepsia 2018
28
100

Diagnosis and long-term course of Dravet syndrome.
Ingrid E Scheffer. Eur J Paediatr Neurol 2012
37
100

PCDH19 mutation in Japanese females with epilepsy.
Norimichi Higurashi, Xiuyu Shi, Sawa Yasumoto, Hirokazu Oguni, Masako Sakauchi, Kazuya Itomi, Akie Miyamoto, Hideaki Shiraishi, Takeo Kato, Yoshio Makita,[...]. Epilepsy Res 2012
37
100

SCN1A Variants in vaccine-related febrile seizures: A prospective study.
John A Damiano, Lucy Deng, Wenhui Li, Rosemary Burgess, Amy L Schneider, Nigel W Crawford, Jim Buttery, Michael Gold, Peter Richmond, Kristine K Macartney,[...]. Ann Neurol 2020
6
100


Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.
Anna Ka-Yee Kwong, Cheuk-Wing Fung, Siu-Yuen Chan, Virginia Chun-Nei Wong. PLoS One 2012
37
100

Exomic variants of an elderly cohort of Brazilians in the ABraOM database.
Michel Satya Naslavsky, Guilherme Lopes Yamamoto, Tatiana Ferreira de Almeida, Suzana A M Ezquina, Daniele Yumi Sunaga, Nam Pho, Daniel Bozoklian, Tatiana Orli Milkewitz Sandberg, Luciano Abreu Brito, Monize Lazar,[...]. Hum Mutat 2017
116
100

When should clinicians order genetic testing for Dravet syndrome?
Jamie K Fountain-Capal, Katherine D Holland, Donald L Gilbert, Barbara E Hallinan. Pediatr Neurol 2011
14
100

PCDH19-related epilepsy and Dravet Syndrome: Face-off between two early-onset epilepsies with fever sensitivity.
Marina Trivisano, Nicola Pietrafusa, Vincenzo di Ciommo, Simona Cappelletti, Luca de Palma, Alessandra Terracciano, Enrico Bertini, Federico Vigevano, Nicola Specchio. Epilepsy Res 2016
13
100

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
100

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
42
100

Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutation.
Nicole Chemaly, Emma Losito, Jean Marc Pinard, Agnès Gautier, Nathalie Villeneuve, Anne Sophie Arbues, Isabelle An, Isabelle Desguerre, Olivier Dulac, Catherine Chiron,[...]. Epileptic Disord 2018
5
100

Efficacy of verapamil as an adjunctive treatment in children with drug-resistant epilepsy: a pilot study.
Francesco Nicita, Alberto Spalice, Laura Papetti, Marina Nikanorova, Paola Iannetti, Pasquale Parisi. Seizure 2014
35
100

Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
Claudio Zucca, Francesca Redaelli, Roberta Epifanio, Nicoletta Zanotta, Antonino Romeo, Monica Lodi, Pierangelo Veggiotti, Giovanni Airoldi, Chris Panzeri, Romina Romaniello,[...]. Arch Neurol 2008
28
100

Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy.
Karen L Skjei, Ephraim W Church, Brian N Harding, Mariarita Santi, Katherine D Holland-Bouley, Robert R Clancy, Brenda E Porter, Gregory G Heuer, Eric D Marsh. J Neurosurg Pediatr 2015
17
100

Common variants associated with general and MMR vaccine-related febrile seizures.
Bjarke Feenstra, Björn Pasternak, Frank Geller, Lisbeth Carstensen, Tongfei Wang, Fen Huang, Jennifer L Eitson, Mads V Hollegaard, Henrik Svanström, Mogens Vestergaard,[...]. Nat Genet 2014
86
100

Prevalence of SCN1A-related dravet syndrome among children reported with seizures following vaccination: a population-based ten-year cohort study.
Nienke E Verbeek, Nicoline A T van der Maas, Floor E Jansen, Marjan J A van Kempen, Dick Lindhout, Eva H Brilstra. PLoS One 2013
25
100

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.
Zaid Afawi, Karen L Oliver, Sara Kivity, Aziz Mazarib, Ilan Blatt, Miriam Y Neufeld, Katherine L Helbig, Hadassa Goldberg-Stern, Adel J Misk, Rachel Straussberg,[...]. Neurology 2016
19
100


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.