A citation-based method for searching scientific literature

Jenna C Carpenter, Roope Männikkö, Catherine Heffner, Jana Heneine, Marisol Sampedro-Castañeda, Gabriele Lignani, Stephanie Schorge. Epilepsia 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.
Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, Karen L Oliver, Snezana Maljevic, Marta A Bayly, Tarja Joensuu, Laura Canafoglia, Silvana Franceschetti, Roberto Michelucci,[...]. Nat Genet 2015
157
100

CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model mice.
Tetsushi Yamagata, Matthieu Raveau, Kenta Kobayashi, Hiroyuki Miyamoto, Tetsuya Tatsukawa, Ikuo Ogiwara, Shigeyoshi Itohara, Takao K Hensch, Kazuhiro Yamakawa. Neurobiol Dis 2020
25
50

Neurobiology: Setting the Set Point for Neural Homeostasis.
Torrey L S Truszkowski, Carlos D Aizenman. Curr Biol 2015
4
50

Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 Epilepsy.
Daniel T Pederick, Kay L Richards, Sandra G Piltz, Raman Kumar, Stefka Mincheva-Tasheva, Simone A Mandelstam, Russell C Dale, Ingrid E Scheffer, Jozef Gecz, Steven Petrou,[...]. Neuron 2018
50
50


Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.
Karen L Oliver, Silvana Franceschetti, Carol J Milligan, Mikko Muona, Simone A Mandelstam, Laura Canafoglia, Anna M Boguszewska-Chachulska, Amos D Korczyn, Francesca Bisulli, Carlo Di Bonaventura,[...]. Ann Neurol 2017
31
50

Modulating gene regulation to treat genetic disorders.
Navneet Matharu, Nadav Ahituv. Nat Rev Drug Discov 2020
10
50

Advancing epilepsy genetics in the genomic era.
Candace T Myers, Heather C Mefford. Genome Med 2015
106
50

Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies.
Gemma L Carvill, Krysta L Engel, Aishwarya Ramamurthy, J Nicholas Cochran, Jolien Roovers, Hannah Stamberger, Nicholas Lim, Amy L Schneider, Georgie Hollingsworth, Dylan H Holder,[...]. Am J Hum Genet 2018
40
50

Dissecting the genetic basis of focal cortical dysplasia: a large cohort study.
Sara Baldassari, Théo Ribierre, Elise Marsan, Homa Adle-Biassette, Sarah Ferrand-Sorbets, Christine Bulteau, Nathalie Dorison, Martine Fohlen, Marc Polivka, Sarah Weckhuysen,[...]. Acta Neuropathol 2019
86
50

Further delineation of the MECP2 duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features.
Marguerite Miguet, Laurence Faivre, Jeanne Amiel, Mathilde Nizon, Renaud Touraine, Fabienne Prieur, Laurent Pasquier, Mathilde Lefebvre, Julien Thevenon, Christèle Dubourg,[...]. J Med Genet 2018
25
50

Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors.
Andrew V Anzalone, Luke W Koblan, David R Liu. Nat Biotechnol 2020
385
50


Genetics update: Monogenetics, polygene disorders and the quest for modifying genes.
Joseph D Symonds, Sameer M Zuberi. Neuropharmacology 2018
9
50

Gene Editing and Genotoxicity: Targeting the Off-Targets.
Georges Blattner, Alessia Cavazza, Adrian J Thrasher, Giandomenico Turchiano. Front Genome Ed 2020
6
50

High frequency of mosaic pathogenic variants in genes causing epilepsy-related neurodevelopmental disorders.
Mary Beth Stosser, Amanda S Lindy, Elizabeth Butler, Kyle Retterer, Caitlin M Piccirillo-Stosser, Gabriele Richard, Dianalee A McKnight. Genet Med 2018
76
50



The Epidemiology of Epilepsy.
Ettore Beghi. Neuroepidemiology 2020
113
50

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
Amy McTague, Umesh Nair, Sony Malhotra, Esther Meyer, Natalie Trump, Elena V Gazina, Apostolos Papandreou, Adeline Ngoh, Sally Ackermann, Gautam Ambegaonkar,[...]. Neurology 2018
46
50


Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disorders.
Kathleen A Christie, David G Courtney, Larry A DeDionisio, Connie Chao Shern, Shyamasree De Majumdar, Laura C Mairs, M Andrew Nesbit, C B Tara Moore. Sci Rep 2017
42
50

Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery.
Andree Delahaye-Duriez, Prashant Srivastava, Kirill Shkura, Sarah R Langley, Liisi Laaniste, Aida Moreno-Moral, Bénédicte Danis, Manuela Mazzuferi, Patrik Foerch, Elena V Gazina,[...]. Genome Biol 2016
44
50

Genetically Engineering the Nervous System with CRISPR-Cas.
Alfredo Sandoval, Hajira Elahi, Jonathan E Ploski. eNeuro 2020
9
50

Comparative characterization of PCDH19 missense and truncating variants in PCDH19-related epilepsy.
Mami Shibata, Atsushi Ishii, Ayako Goto, Shinichi Hirose. J Hum Genet 2021
3
50

Viral manipulation of functionally distinct interneurons in mice, non-human primates and humans.
Douglas Vormstein-Schneider, Jessica D Lin, Kenneth A Pelkey, Ramesh Chittajallu, Baolin Guo, Mario A Arias-Garcia, Kathryn Allaway, Sofia Sakopoulos, Gates Schneider, Olivia Stevenson,[...]. Nat Neurosci 2020
34
50

mTORopathies: A Road Well-Traveled.
Peter B Crino. Epilepsy Curr 2020
5
50

Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.
Rikke S Møller, Yvonne G Weber, Laura L Klitten, Holger Trucks, Hiltrud Muhle, Wolfram S Kunz, Heather C Mefford, Andre Franke, Monika Kautza, Peter Wolf,[...]. Epilepsia 2013
47
50

Advances in genome editing through control of DNA repair pathways.
Charles D Yeh, Christopher D Richardson, Jacob E Corn. Nat Cell Biol 2019
116
50

dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice.
Gaia Colasante, Gabriele Lignani, Simone Brusco, Claudia Di Berardino, Jenna Carpenter, Serena Giannelli, Nicholas Valassina, Simone Bido, Raffaele Ricci, Valerio Castoldi,[...]. Mol Ther 2020
65
50

Malformations of cortical development and epilepsy.
A James Barkovich, William B Dobyns, Renzo Guerrini. Cold Spring Harb Perspect Med 2015
59
50


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
90
50

Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.
Jennifer A Kearney, Anna K Wiste, Ulrich Stephani, Michelle M Trudeau, Anne Siegel, Rajesh RamachandranNair, Roy D Elterman, Hiltrud Muhle, Juliane Reinsdorf, W Donald Shields,[...]. Pediatr Neurol 2006
41
50

An Activity-Mediated Transition in Transcription in Early Postnatal Neurons.
Hume Stroud, Marty G Yang, Yael N Tsitohay, Christopher P Davis, Maxwell A Sherman, Sinisa Hrvatin, Emi Ling, Michael E Greenberg. Neuron 2020
13
50

Balanced Activity between Kv3 and Nav Channels Determines Fast-Spiking in Mammalian Central Neurons.
Yuanzheng Gu, Dustin Servello, Zhi Han, Rupa R Lalchandani, Jun B Ding, Kun Huang, Chen Gu. iScience 2018
9
50

Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome.
Zhou Han, Chunling Chen, Anne Christiansen, Sophina Ji, Qian Lin, Charles Anumonwo, Chante Liu, Steven C Leiser, Meena, Isabel Aznarez,[...]. Sci Transl Med 2020
66
50


Homeostatic Plasticity in Epilepsy.
Gabriele Lignani, Pietro Baldelli, Vincenzo Marra. Front Cell Neurosci 2020
9
50

CRISPR technologies for precise epigenome editing.
Muneaki Nakamura, Yuchen Gao, Antonia A Dominguez, Lei S Qi. Nat Cell Biol 2021
39
50


Recent advances in the CRISPR genome editing tool set.
Su Bin Moon, Do Yon Kim, Jeong-Heon Ko, Yong-Sam Kim. Exp Mol Med 2019
55
50

Re-expression of SynGAP protein in adulthood improves translatable measures of brain function and behavior.
Thomas K Creson, Camilo Rojas, Ernie Hwaun, Thomas Vaissiere, Murat Kilinc, Andres Jimenez-Gomez, Jimmy Lloyd Holder, Jianrong Tang, Laura L Colgin, Courtney A Miller,[...]. Elife 2019
24
50

Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study.
Jacqueline A French, John A Lawson, Zuhal Yapici, Hiroko Ikeda, Tilman Polster, Rima Nabbout, Paolo Curatolo, Petrus J de Vries, Dennis J Dlugos, Noah Berkowitz,[...]. Lancet 2016
325
50

Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy.
Yuliya Voskobiynyk, Gopal Battu, Stephanie A Felker, J Nicholas Cochran, Megan P Newton, Laura J Lambert, Robert A Kesterson, Richard M Myers, Gregory M Cooper, Erik D Roberson,[...]. PLoS Genet 2021
3
50

Expanded encyclopaedias of DNA elements in the human and mouse genomes.
Jill E Moore, Michael J Purcaro, Henry E Pratt, Charles B Epstein, Noam Shoresh, Jessika Adrian, Trupti Kawli, Carrie A Davis, Alexander Dobin, Rajinder Kaul,[...]. Nature 2020
299
50

Treatment during a vulnerable developmental period rescues a genetic epilepsy.
Stephan Lawrence Marguet, Vu Thao Quyen Le-Schulte, Andrea Merseburg, Axel Neu, Ronny Eichler, Igor Jakovcevski, Anton Ivanov, Ileana Livia Hanganu-Opatz, Christophe Bernard, Fabio Morellini,[...]. Nat Med 2015
66
50

Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses.
James P Clement, Massimiliano Aceti, Thomas K Creson, Emin D Ozkan, Yulin Shi, Nicholas J Reish, Antoine G Almonte, Brooke H Miller, Brian J Wiltgen, Courtney A Miller,[...]. Cell 2012
198
50

The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration.
Jing-Qiong Kang, Wangzhen Shen, Chengwen Zhou, Dong Xu, Robert L Macdonald. Nat Neurosci 2015
59
50

Dravet Syndrome: A Sodium Channel Interneuronopathy.
William A Catterall. Curr Opin Physiol 2018
49
50


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.