A citation-based method for searching scientific literature

Miriam H Meisler, Sophie F Hill, Wenxi Yu. Nat Rev Neurosci 2021
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Distinct contributions of Na(v)1.6 and Na(v)1.2 in action potential initiation and backpropagation.
Wenqin Hu, Cuiping Tian, Tun Li, Mingpo Yang, Han Hou, Yousheng Shu. Nat Neurosci 2009
394
44

The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex.
Perry W E Spratt, Roy Ben-Shalom, Caroline M Keeshen, Kenneth J Burke, Rebecca L Clarkson, Stephan J Sanders, Kevin J Bender. Neuron 2019
56
44

Progress in Understanding and Treating SCN2A-Mediated Disorders.
Stephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, Rikke S Moller, Florence F Wagner, Angie L Auldridge, Raphael A Bernier, William A Catterall, Wendy K Chung, James R Empfield,[...]. Trends Neurosci 2018
104
44

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
167
33

Action potential initiation in neocortical inhibitory interneurons.
Tun Li, Cuiping Tian, Paolo Scalmani, Carolina Frassoni, Massimo Mantegazza, Yonghong Wang, Mingpo Yang, Si Wu, Yousheng Shu. PLoS Biol 2014
52
33

Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures.
Roy Ben-Shalom, Caroline M Keeshen, Kiara N Berrios, Joon Y An, Stephan J Sanders, Kevin J Bender. Biol Psychiatry 2017
104
33

A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome.
Morgana Favero, Nathaniel P Sotuyo, Emily Lopez, Jennifer A Kearney, Ethan M Goldberg. J Neurosci 2018
59
33

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
511
33

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
212
33

Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability.
Yuanyuan Liu, Julian Schubert, Lukas Sonnenberg, Katherine L Helbig, Christina E Hoei-Hansen, Mahmoud Koko, Maert Rannap, Stephan Lauxmann, Mahbubul Huq, Michael C Schneider,[...]. Brain 2019
38
33

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
677
33

'Neonatal' Nav1.2 reduces neuronal excitability and affects seizure susceptibility and behaviour.
Elena V Gazina, Bryan T W Leaw, Kay L Richards, Verena C Wimmer, Tae H Kim, Timothy D Aumann, Travis J Featherby, Leonid Churilov, Vicki E Hammond, Christopher A Reid,[...]. Hum Mol Genet 2015
33
33

Molecular identity of axonal sodium channels in human cortical pyramidal cells.
Cuiping Tian, Kaiyan Wang, Wei Ke, Hui Guo, Yousheng Shu. Front Cell Neurosci 2014
47
33

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
33

Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic Encephalopathy.
Jacy L Wagnon, Miriam H Meisler. Front Neurol 2015
79
33

Alternative splicing potentiates dysfunction of early-onset epileptic encephalopathy SCN2A variants.
Christopher H Thompson, Roy Ben-Shalom, Kevin J Bender, Alfred L George. J Gen Physiol 2020
11
33

Severe deficiency of the voltage-gated sodium channel NaV1.2 elevates neuronal excitability in adult mice.
Jingliang Zhang, Xiaoling Chen, Muriel Eaton, Jiaxiang Wu, Zhixiong Ma, Shirong Lai, Anthony Park, Talha S Ahmad, Zhefu Que, Ji Hea Lee,[...]. Cell Rep 2021
6
50

Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach.
Ragna S Boerma, Kees P Braun, Marcel P H van den Broek, Frederique M C van Berkestijn, Marielle E Swinkels, Eveline O Hagebeuk, Dick Lindhout, Marjan van Kempen, Maartje Boon, Joost Nicolai,[...]. Neurotherapeutics 2016
81
33

The phenotype of SCN8A developmental and epileptic encephalopathy.
Elena Gardella, Carla Marini, Marina Trivisano, Mark P Fitzgerald, Michael Alber, Katherine B Howell, Francesca Darra, Sabrina Siliquini, Bigna K Bölsterli, Silva Masnada,[...]. Neurology 2018
64
33

Pathogenic mechanism of recurrent mutations of SCN8A in epileptic encephalopathy.
Jacy L Wagnon, Bryan S Barker, James A Hounshell, Charlotte A Haaxma, Amy Shealy, Timothy Moss, Sumit Parikh, Ricka D Messer, Manoj K Patel, Miriam H Meisler. Ann Clin Transl Neurol 2015
65
22

SCN8A encephalopathy: Research progress and prospects.
Miriam H Meisler, Guy Helman, Michael F Hammer, Brandy E Fureman, William D Gaillard, Alan L Goldin, Shinichi Hirose, Atsushi Ishii, Barbara L Kroner, Christoph Lossin,[...]. Epilepsia 2016
76
22

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
22

Prominent role of forebrain excitatory neurons in SCN8A encephalopathy.
Rosie K A Bunton-Stasyshyn, Jacy L Wagnon, Eric R Wengert, Bryan S Barker, Alexa Faulkner, Pravin K Wagley, Kritika Bhatia, Julie M Jones, Marissa R Maniaci, Jack M Parent,[...]. Brain 2019
41
22

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013
353
22

Localization of voltage-gated ion channels in mammalian brain.
James S Trimmer, Kenneth J Rhodes. Annu Rev Physiol 2004
320
22

SynGAP isoforms differentially regulate synaptic plasticity and dendritic development.
Yoichi Araki, Ingie Hong, Timothy R Gamache, Shaowen Ju, Leonardo Collado-Torres, Joo Heon Shin, Richard L Huganir. Elife 2020
11
22

SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy.
Danique R M Vlaskamp, Benjamin J Shaw, Rosemary Burgess, Davide Mei, Martino Montomoli, Han Xie, Candace T Myers, Mark F Bennett, Wenshu XiangWei, Danielle Williams,[...]. Neurology 2019
45
22

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
638
22

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
22

De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability.
Michael J Parker, Alan E Fryer, Deborah J Shears, Katherine L Lachlan, Shane A McKee, Alex C Magee, Shehla Mohammed, Pradeep C Vasudevan, Soo-Mi Park, Valérie Benoit,[...]. Am J Med Genet A 2015
53
22

Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.
Richard S Smith, Connor J Kenny, Vijay Ganesh, Ahram Jang, Rebeca Borges-Monroy, Jennifer N Partlow, R Sean Hill, Taehwan Shin, Allen Y Chen, Ryan N Doan,[...]. Neuron 2018
55
22

Integrative functional genomic analysis of human brain development and neuropsychiatric risks.
Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, Oleg V Evgrafov, Forrest O Gulden, Sirisha Pochareddy, Susan M Sunkin, Zhen Li, Yurae Shin, Ying Zhu,[...]. Science 2018
216
22

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
195
22

Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons.
Fei Yi, Tamas Danko, Salome Calado Botelho, Christopher Patzke, ChangHui Pak, Marius Wernig, Thomas C Südhof. Science 2016
157
22

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
989
22

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.
Fadi F Hamdan, Julie Gauthier, Dan Spiegelman, Anne Noreau, Yan Yang, Stéphanie Pellerin, Sylvia Dobrzeniecka, Mélanie Côté, Elizabeth Perreau-Linck, Lionel Carmant,[...]. N Engl J Med 2009
197
22

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
131
22

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
22

Early hyperactivity and precocious maturation of corticostriatal circuits in Shank3B(-/-) mice.
Rui T Peixoto, Wengang Wang, Donyell M Croney, Yevgenia Kozorovitskiy, Bernardo L Sabatini. Nat Neurosci 2016
107
22

A catalog of SCN1A variants.
Christoph Lossin. Brain Dev 2009
143
22

Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2.
Tetsushi Yamagata, Ikuo Ogiwara, Emi Mazaki, Yuchio Yanagawa, Kazuhiro Yamakawa. Biochem Biophys Res Commun 2017
23
22

De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy.
Maxime G Blanchard, Marjolein H Willemsen, Jaclyn B Walker, Sulayman D Dib-Hajj, Stephen G Waxman, Marjolijn C J Jongmans, Tjitske Kleefstra, Bart P van de Warrenburg, Peter Praamstra, Joost Nicolai,[...]. J Med Genet 2015
81
22

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
775
22

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
215
22

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
419
22

Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance.
Christopher D Makinson, Brian S Tanaka, Tyra Lamar, Alan L Goldin, Andrew Escayg. Neurobiol Dis 2014
30
22

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
653
22

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication.
Ozlem Bozdagi, Takeshi Sakurai, Danae Papapetrou, Xiaobin Wang, Dara L Dickstein, Nagahide Takahashi, Yuji Kajiwara, Mu Yang, Adam M Katz, Maria Luisa Scattoni,[...]. Mol Autism 2010
358
22

Loss-of-function variants of SCN8A in intellectual disability without seizures.
Jacy L Wagnon, Bryan S Barker, Matteo Ottolini, Young Park, Alicia Volkheimer, Purnima Valdez, Marielle E M Swinkels, Manoj K Patel, Miriam H Meisler. Neurol Genet 2017
37
22



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.