A citation-based method for searching scientific literature

Samuel W Cramer, Laurentiu S Popa, Russell E Carter, Gang Chen, Timothy J Ebner. J Neurosci 2015
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


The K+/Cl- co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation.
C Rivera, J Voipio, J A Payne, E Ruusuvuori, H Lahtinen, K Lamsa, U Pirvola, M Saarma, K Kaila. Nature 1999
50

A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia.
Kai Gao, Anel Tankovic, Yujia Zhang, Hirofumi Kusumoto, Jin Zhang, Wenjuan Chen, Wenshu XiangWei, Gil H Shaulsky, Chun Hu, Stephen F Traynelis,[...]. PLoS One 2017
31
50

A small molecule activator of Nav 1.1 channels increases fast-spiking interneuron excitability and GABAergic transmission in vitro and has anti-convulsive effects in vivo.
Kristen Frederiksen, Dunguo Lu, Jinhui Yang, Henrik Sindal Jensen, Jesper Frank Bastlund, Peter Hjørringgaard Larsen, Henry Liu, François Crestey, Kim Dekermendjian, Lassina Badolo,[...]. Eur J Neurosci 2017
13
50

Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome.
Dezhi Cao, Hideyuki Ohtani, Ikuo Ogiwara, Sanae Ohtani, Yukitoshi Takahashi, Kazuhiro Yamakawa, Yushi Inoue. Epilepsia 2012
29
50


Neuronal hyperexcitability in a mouse model of SCN8A epileptic encephalopathy.
Luis F Lopez-Santiago, Yukun Yuan, Jacy L Wagnon, Jacob M Hull, Chad R Frasier, Heather A O'Malley, Miriam H Meisler, Lori L Isom. Proc Natl Acad Sci U S A 2017
44
50


Activity of NaV1.2 promotes neurodegeneration in an animal model of multiple sclerosis.
Benjamin Schattling, Walid Fazeli, Birgit Engeland, Yuanyuan Liu, Holger Lerche, Dirk Isbrandt, Manuel A Friese. JCI Insight 2016
13
50

GRIN2A mutation and early-onset epileptic encephalopathy: personalized therapy with memantine.
Tyler Mark Pierson, Hongjie Yuan, Eric D Marsh, Karin Fuentes-Fajardo, David R Adams, Thomas Markello, Gretchen Golas, Dimitre R Simeonov, Conisha Holloman, Anel Tankovic,[...]. Ann Clin Transl Neurol 2014
143
50

Epileptic encephalopathy de novo GABRB mutations impair γ-aminobutyric acid type A receptor function.
Vaishali S Janve, Ciria C Hernandez, Kelienne M Verdier, Ningning Hu, Robert L Macdonald. Ann Neurol 2016
41
50


Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.
Johannes R Lemke, Kirsten Geider, Katherine L Helbig, Henrike O Heyne, Hannah Schütz, Julia Hentschel, Carolina Courage, Christel Depienne, Caroline Nava, Delphine Heron,[...]. Neurology 2016
96
50

Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy.
Carolien G F de Kovel, Miriam H Meisler, Eva H Brilstra, Frederique M C van Berkestijn, Ruben van 't Slot, Stef van Lieshout, Isaac J Nijman, Janelle E O'Brien, Michael F Hammer, Mark Estacion,[...]. Epilepsy Res 2014
66
50

Models for discovery of targeted therapy in genetic epileptic encephalopathies.
Snezana Maljevic, Christopher A Reid, Steven Petrou. J Neurochem 2017
23
50


Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy.
Marina Trivisano, Alessandra Terracciano, Teresa Milano, Simona Cappelletti, Nicola Pietrafusa, Enrico Silvio Bertini, Federico Vigevano, Nicola Specchio. Epilepsia 2015
14
50


How mutations in the nAChRs can cause ADNFLE epilepsy.
D Bertrand, F Picard, S Le Hellard, S Weiland, I Favre, H Phillips, S Bertrand, S F Berkovic, A Malafosse, J Mulley. Epilepsia 2002
116
50

Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu Rev Cell Dev Biol 2000
50


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
344
50

Reduced spontaneous activity of mice defective in the epsilon 4 subunit of the NMDA receptor channel.
K Ikeda, K Araki, C Takayama, Y Inoue, T Yagi, S Aizawa, M Mishina. Brain Res Mol Brain Res 1995
119
50

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
50

Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.
Constanze Reutlinger, Ingo Helbig, Barbara Gawelczyk, Jose Ignacio Martin Subero, Holger Tönnies, Hiltrud Muhle, Katrin Finsterwalder, Sascha Vermeer, Rolph Pfundt, Jürgen Sperner,[...]. Epilepsia 2010
62
50


Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities.
Melinda S Martin, Karoni Dutt, Ligia A Papale, Céline M Dubé, Stacey B Dutton, Georgius de Haan, Anupama Shankar, Sergio Tufik, Miriam H Meisler, Tallie Z Baram,[...]. J Biol Chem 2010
147
50

A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.
John F Staropoli, Amel Karaa, Elaine T Lim, Andrew Kirby, Naser Elbalalesy, Stephen G Romansky, Karen B Leydiker, Scott H Coppel, Rosemary Barone, Winnie Xin,[...]. Am J Hum Genet 2012
65
50

The sodium-activated potassium channel Slack is required for optimal cognitive flexibility in mice.
Anne E Bausch, Rebekka Dieter, Yvette Nann, Mario Hausmann, Nora Meyerdierks, Leonard K Kaczmarek, Peter Ruth, Robert Lukowski. Learn Mem 2015
17
50

Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
Sarah E Heron, Houman Khosravani, Diego Varela, Chris Bladen, Tristiana C Williams, Michelle R Newman, Ingrid E Scheffer, Samuel F Berkovic, John C Mulley, Gerald W Zamponi. Ann Neurol 2007
127
50


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
124
50

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
50

GRIN2A: an aptly named gene for speech dysfunction.
Samantha J Turner, Angela K Mayes, Andrea Verhoeven, Simone A Mandelstam, Angela T Morgan, Ingrid E Scheffer. Neurology 2015
41
50


Multiple molecular mechanisms for a single GABAA mutation in epilepsy.
Christopher A Reid, Taehwan Kim, A Marie Phillips, Jun Low, Samuel F Berkovic, Bernhard Luscher, Steven Petrou. Neurology 2013
51
50

Novel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent manner.
Yuki Nakamura, Xiuyu Shi, Tomohiro Numata, Yasuo Mori, Ryuji Inoue, Christoph Lossin, Tallie Z Baram, Shinichi Hirose. PLoS One 2013
33
50

A potassium channel mutation in neonatal human epilepsy.
C Biervert, B C Schroeder, C Kubisch, S F Berkovic, P Propping, T J Jentsch, O K Steinlein. Science 1998
795
50

Role of the alpha1G T-type calcium channel in spontaneous absence seizures in mutant mice.
Inseon Song, Daesoo Kim, Soonwook Choi, Minjeong Sun, Yeongin Kim, Hee-Sup Shin. J Neurosci 2004
100
50


Autosomal dominant SCN8A mutation with an unusually mild phenotype.
G Anand, F Collett-White, A Orsini, S Thomas, S Jayapal, N Trump, Z Zaiwalla, S Jayawant. Eur J Paediatr Neurol 2016
26
50

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.
T M DeLorey, A Handforth, S G Anagnostaras, G E Homanics, B A Minassian, A Asatourian, M S Fanselow, A Delgado-Escueta, G D Ellison, R W Olsen. J Neurosci 1998
327
50


An impaired neocortical Ih is associated with enhanced excitability and absence epilepsy.
Ulf Strauss, Maarten H P Kole, Anja U Bräuer, Jens Pahnke, Rika Bajorat, Arndt Rolfs, Robert Nitsch, Rudolf A Deisz. Eur J Neurosci 2004
136
50

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag,[...]. Brain 2010
320
50


A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions.
H Lerche, C Biervert, A K Alekov, L Schleithoff, M Lindner, W Klinger, F Bretschneider, N Mitrovic, K Jurkat-Rott, H Bode,[...]. Ann Neurol 1999
100
50

A novel epileptic encephalopathy mutation in KCNB1 disrupts Kv2.1 ion selectivity, expression, and localization.
Isabelle Thiffault, David J Speca, Daniel C Austin, Melanie M Cobb, Kenneth S Eum, Nicole P Safina, Lauren Grote, Emily G Farrow, Neil Miller, Sarah Soden,[...]. J Gen Physiol 2015
48
50

Differential molecular and behavioural alterations in mouse models of GABRG2 haploinsufficiency versus dominant negative mutations associated with human epilepsy.
Timothy A Warner, Wangzhen Shen, Xuan Huang, Zhong Liu, Robert L Macdonald, Jing-Qiong Kang. Hum Mol Genet 2016
24
50

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
50

NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease.
Pierre Paoletti, Camilla Bellone, Qiang Zhou. Nat Rev Neurosci 2013
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.