A citation-based method for searching scientific literature

Renée A Shellhaas, Courtney J Wusthoff, Tammy N Tsuchida, Hannah C Glass, Catherine J Chu, Shavonne L Massey, Janet S Soul, Natrujee Wiwattanadittakun, Nicholas S Abend, Maria Roberta Cilio. Neurology 2017
Times Cited: 82







List of co-cited articles
755 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
31

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
240
26

Early and effective treatment of KCNQ2 encephalopathy.
Tiziana Pisano, Adam L Numis, Sinéad B Heavin, Sarah Weckhuysen, Marco Angriman, Arvid Suls, Barbara Podesta, Ronald L Thibert, Kevin A Shapiro, Renzo Guerrini,[...]. Epilepsia 2015
120
26

Contemporary Profile of Seizures in Neonates: A Prospective Cohort Study.
Hannah C Glass, Renée A Shellhaas, Courtney J Wusthoff, Taeun Chang, Nicholas S Abend, Catherine J Chu, M Roberta Cilio, David V Glidden, Sonia L Bonifacio, Shavonne Massey,[...]. J Pediatr 2016
118
25

The American Clinical Neurophysiology Society's Guideline on Continuous Electroencephalography Monitoring in Neonates.
Renée A Shellhaas, Taeun Chang, Tammy Tsuchida, Mark S Scher, James J Riviello, Nicholas S Abend, Sylvie Nguyen, Courtney J Wusthoff, Robert R Clancy. J Clin Neurophysiol 2011
244
24

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Dominique Audenaert, Tine Deconinck, Lieve R F Claes, Liesbet Deprez, Katrien Smets, Dimitrina Hristova, Iglika Yordanova,[...]. Ann Neurol 2012
301
21

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 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
280
19

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
959
18

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
142
18

Rapid and safe response to low-dose carbamazepine in neonatal epilepsy.
Tristan T Sands, Martina Balestri, Giulia Bellini, Sarah B Mulkey, Olivier Danhaive, Eliza Hayes Bakken, Maurizio Taglialatela, Michael S Oldham, Federico Vigevano, Gregory L Holmes,[...]. Epilepsia 2016
50
30

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
18

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
76
18

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
15

Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.
Heather E Olson, McKenna Kelly, Christopher M LaCoursiere, Rebecca Pinsky, Dimira Tambunan, Catherine Shain, Sriram Ramgopal, Masanori Takeoka, Mark H Libenson, Kristina Julich,[...]. Ann Neurol 2017
69
18

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.
Sarah Weckhuysen, Vanja Ivanovic, Rik Hendrickx, Rudy Van Coster, Helle Hjalgrim, Rikke S Møller, Sabine Grønborg, An-Sofie Schoonjans, Berten Ceulemans, Sinead B Heavin,[...]. Neurology 2013
132
14

Treatment Duration After Acute Symptomatic Seizures in Neonates: A Multicenter Cohort Study.
Renée A Shellhaas, Taeun Chang, Courtney J Wusthoff, Janet S Soul, Shavonne L Massey, Catherine J Chu, M Roberta Cilio, Sonia L Bonifacio, Nicholas S Abend, Tammy N Tsuchida,[...]. J Pediatr 2017
38
31

Seizures in Preterm Neonates: A Multicenter Observational Cohort Study.
Hannah C Glass, Renée A Shellhaas, Tammy N Tsuchida, Taeun Chang, Courtney J Wusthoff, Catherine J Chu, M Roberta Cilio, Sonia L Bonifacio, Shavonne L Massey, Nicholas S Abend,[...]. Pediatr Neurol 2017
49
24

Neonatal epilepsies: Clinical management.
Marie-Coralie Cornet, Tristan T Sands, Maria Roberta Cilio. Semin Fetal Neonatal Med 2018
19
63

KCNQ2 encephalopathy: delineation of the electroclinical phenotype and treatment response.
Adam L Numis, Marco Angriman, Joseph E Sullivan, Ann J Lewis, Pasquale Striano, Rima Nabbout, Maria R Cilio. Neurology 2014
72
15

KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients.
John J Millichap, Kristen L Park, Tammy Tsuchida, Bruria Ben-Zeev, Lionel Carmant, Robert Flamini, Nishtha Joshi, Paul M Levisohn, Eric Marsh, Srishti Nangia,[...]. Neurol Genet 2016
108
13

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
279
12

Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.
Gökce Orhan, Merle Bock, Dorien Schepers, Elena I Ilina, Stephanie Nadine Reichel, Heidi Löffler, Nicole Jezutkovic, Sarah Weckhuysen, Simone Mandelstam, Arvid Suls,[...]. Ann Neurol 2014
136
12

Phenobarbital compared with phenytoin for the treatment of neonatal seizures.
M J Painter, M S Scher, A D Stein, S Armatti, Z Wang, J C Gardiner, N Paneth, B Minnigh, J Alvin. N Engl J Med 1999
355
12

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
12

Quinidine in the treatment of KCNT1-positive epilepsies.
Mohamad A Mikati, Yong-Hui Jiang, Michael Carboni, Vandana Shashi, Slave Petrovski, Rebecca Spillmann, Carol J Milligan, Melody Li, Annette Grefe, Allyn McConkie,[...]. Ann Neurol 2015
108
9

Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H.
Sarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, John L Carroll, Sabine Grønborg, Yong-Hui Jiang, Nishtha Joshi, Megan Kelly, David A Koolen, Mohamad A Mikati,[...]. Epilepsia 2017
37
21

Targeted treatment of migrating partial seizures of infancy with quinidine.
David Bearden, Alanna Strong, Jessica Ehnot, Marissa DiGiovine, Dennis Dlugos, Ethan M Goldberg. Ann Neurol 2014
133
9

Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.
Bronwyn E Grinton, Sarah E Heron, James T Pelekanos, Sameer M Zuberi, Sara Kivity, Zaid Afawi, Tristiana C Williams, Dan M Casalaz, Simone Yendle, Ilan Linder,[...]. Epilepsia 2015
55
14

SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
Katherine B Howell, Jacinta M McMahon, Gemma L Carvill, Dimira Tambunan, Mark T Mackay, Victoria Rodriguez-Casero, Richard Webster, Damian Clark, Jeremy L Freeman, Sophie Calvert,[...]. Neurology 2015
138
9

Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.
Mitsuhiro Kato, Takanori Yamagata, Masaya Kubota, Hiroshi Arai, Sumimasa Yamashita, Taku Nakagawa, Takanari Fujii, Kenji Sugai, Kaoru Imai, Tami Uster,[...]. Epilepsia 2013
138
9

Interobserver agreement in neonatal seizure identification.
Aileen Malone, C Anthony Ryan, Anthony Fitzgerald, Louise Burgoyne, Sean Connolly, Geraldine B Boylan. Epilepsia 2009
99
9

Uncoupling of EEG-clinical neonatal seizures after antiepileptic drug use.
Mark S Scher, John Alvin, Lisa Gaus, Beth Minnigh, Michael J Painter. Pediatr Neurol 2003
135
9


Neonatal epilepsy genetics.
Erika J T Axeen, Heather E Olson. Semin Fetal Neonatal Med 2018
19
42

American clinical neurophysiology society standardized EEG terminology and categorization for the description of continuous EEG monitoring in neonates: report of the American Clinical Neurophysiology Society critical care monitoring committee.
Tammy N Tsuchida, Courtney J Wusthoff, Renée A Shellhaas, Nicholas S Abend, Cecil D Hahn, Joseph E Sullivan, Sylvie Nguyen, Steven Weinstein, Mark S Scher, James J Riviello,[...]. J Clin Neurophysiol 2013
163
9

A population-based cost-effectiveness study of early genetic testing in severe epilepsies of infancy.
Katherine B Howell, Stefanie Eggers, Kim Dalziel, Jessica Riseley, Simone Mandelstam, Candace T Myers, Jacinta M McMahon, Amy Schneider, Gemma L Carvill, Heather C Mefford,[...]. Epilepsia 2018
41
19

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
110
9

Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases.
Chloé Di Meglio, Gaetan Lesca, Nathalie Villeneuve, Caroline Lacoste, Affef Abidi, Pierre Cacciagli, Cécilia Altuzarra, Agathe Roubertie, Alexandra Afenjar, Florence Renaldo-Robin,[...]. Epilepsia 2015
27
25

A Distinctive Ictal Amplitude-Integrated Electroencephalography Pattern in Newborns with Neonatal Epilepsy Associated with KCNQ2 Mutations.
Ana Vilan, José Mendes Ribeiro, Pasquale Striano, Sarah Weckhuysen, Lauren C Weeke, Eva Brilstra, Linda S de Vries, Maria Roberta Cilio. Neonatology 2017
23
30

Video-EEG monitoring in newborns with hypoxic-ischemic encephalopathy treated with hypothermia.
K B Nash, S L Bonifacio, H C Glass, J E Sullivan, A J Barkovich, D M Ferriero, M R Cilio. Neurology 2011
103
8

The current etiologic profile and neurodevelopmental outcome of seizures in term newborn infants.
Hasan Tekgul, Kimberlee Gauvreau, Janet Soul, Lauren Murphy, Richard Robertson, Jane Stewart, Joseph Volpe, Blaise Bourgeois, Adré J du Plessis. Pediatrics 2006
215
8

Instruction manual for the ILAE 2017 operational classification of seizure types.
Robert S Fisher, J Helen Cross, Carol D'Souza, Jacqueline A French, Sheryl R Haut, Norimichi Higurashi, Edouard Hirsch, Floor E Jansen, Lieven Lagae, Solomon L Moshé,[...]. Epilepsia 2017
335
8

Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.
Natalie Trump, Amy McTague, Helen Brittain, Apostolos Papandreou, Esther Meyer, Adeline Ngoh, Rodger Palmer, Deborah Morrogh, Christopher Boustred, Jane A Hurst,[...]. J Med Genet 2016
128
8

Diagnostic Yield From 339 Epilepsy Patients Screened on a Clinical Gene Panel.
Kameryn M Butler, Cristina da Silva, John J Alexander, Madhuri Hegde, Andrew Escayg. Pediatr Neurol 2017
40
17

Incidence of neonatal seizures in Harris County, Texas, 1992-1994.
R M Saliba, J F Annegers, D K Waller, J E Tyson, E M Mizrahi. Am J Epidemiol 1999
96
8

Amplitude-integrated EEG for detection of neonatal seizures: a systematic review.
Abhijeet Rakshasbhuvankar, Saritha Paul, Lakshmi Nagarajan, Soumya Ghosh, Shripada Rao. Seizure 2015
56
12

Outcomes after acute symptomatic seizures in neonates.
Hannah C Glass, Zachary M Grinspan, Renée A Shellhaas. Semin Fetal Neonatal Med 2018
26
26

Clinical and genetic spectrum of a large cohort of children with epilepsy in China.
Lin Yang, Yanting Kong, Xinran Dong, Liyuan Hu, Yifeng Lin, Xiang Chen, Qi Ni, Yulan Lu, Bingbing Wu, Huijun Wang,[...]. Genet Med 2019
57
12

Epileptic encephalopathy: Use and misuse of a clinically and conceptually important concept.
Katherine B Howell, A Simon Harvey, John S Archer. Epilepsia 2016
35
17


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.