A citation-based method for searching scientific literature

Laura Fedele, Joseph Newcombe, Maya Topf, Alasdair Gibb, Robert J Harvey, Trevor G Smart. Nat Commun 2018
Times Cited: 36







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



Times Cited
  Times     Co-cited
Similarity


Glutamate receptor ion channels: structure, regulation, and function.
Stephen F Traynelis, Lonnie P Wollmuth, Chris J McBain, Frank S Menniti, Katie M Vance, Kevin K Ogden, Kasper B Hansen, Hongjie Yuan, Scott J Myers, Ray Dingledine. Pharmacol Rev 2010
55

NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease.
Pierre Paoletti, Camilla Bellone, Qiang Zhou. Nat Rev Neurosci 2013
50

Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains.
Sharon A Swanger, Wenjuan Chen, Gordon Wells, Pieter B Burger, Anel Tankovic, Subhrajit Bhattacharya, Katie L Strong, Chun Hu, Hirofumi Kusumoto, Jing Zhang,[...]. Am J Hum Genet 2016
92
44

GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
Konrad Platzer, Hongjie Yuan, Hannah Schütz, Alexander Winschel, Wenjuan Chen, Chun Hu, Hirofumi Kusumoto, Henrike O Heyne, Katherine L Helbig, Sha Tang,[...]. J Med Genet 2017
112
41

De Novo Mutations and Rare Variants Occurring in NMDA Receptors.
Wenshu XiangWei, Yuwu Jiang, Hongjie Yuan. Curr Opin Physiol 2018
48
38

Surface Expression, Function, and Pharmacology of Disease-Associated Mutations in the Membrane Domain of the Human GluN2B Subunit.
Vojtech Vyklicky, Barbora Krausova, Jiri Cerny, Marek Ladislav, Tereza Smejkalova, Bohdan Kysilov, Miloslav Korinek, Sarka Danacikova, Martin Horak, Hana Chodounska,[...]. Front Mol Neurosci 2018
28
50

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
Sabine Endele, Georg Rosenberger, Kirsten Geider, Bernt Popp, Ceyhun Tamer, Irina Stefanova, Mathieu Milh, Fanny Kortüm, Angela Fritsch, Friederike K Pientka,[...]. Nat Genet 2010
321
36

A Rare Variant Identified Within the GluN2B C-Terminus in a Patient with Autism Affects NMDA Receptor Surface Expression and Spine Density.
Shuxi Liu, Liang Zhou, Hongjie Yuan, Marta Vieira, Antonio Sanz-Clemente, John D Badger, Wei Lu, Stephen F Traynelis, Katherine W Roche. J Neurosci 2017
39
33

Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology.
Kevin K Ogden, Wenjuan Chen, Sharon A Swanger, Miranda J McDaniel, Linlin Z Fan, Chun Hu, Anel Tankovic, Hirofumi Kusumoto, Gabrielle J Kosobucki, Anthony J Schulien,[...]. PLoS Genet 2017
77
33

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
99
33

Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases.
Hongjie Yuan, Chian-Ming Low, Olivia A Moody, Andrew Jenkins, Stephen F Traynelis. Mol Pharmacol 2015
118
30

NMDA receptor subunit mutations in neurodevelopmental disorders.
Nail Burnashev, Pierre Szepetowski. Curr Opin Pharmacol 2015
109
30

Human GRIN2B variants in neurodevelopmental disorders.
Chun Hu, Wenjuan Chen, Scott J Myers, Hongjie Yuan, Stephen F Traynelis. J Pharmacol Sci 2016
117
30


GRIN2A-related disorders: genotype and functional consequence predict phenotype.
Vincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, Katie F M Marwick, Gabrielle Rudolf, Julitta de Bellescize, Saskia Biskup, Eva H Brilstra, Oebele F Brouwer, Petra M C Callenbach,[...]. Brain 2019
58
27


Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.
Hongjie Yuan, Kasper B Hansen, Jing Zhang, Tyler Mark Pierson, Thomas C Markello, Karin V Fuentes Fajardo, Conisha M Holloman, Gretchen Golas, David R Adams, Cornelius F Boerkoel,[...]. Nat Commun 2014
86
25

Distinct functional and pharmacological properties of Triheteromeric GluN1/GluN2A/GluN2B NMDA receptors.
Kasper B Hansen, Kevin K Ogden, Hongjie Yuan, Stephen F Traynelis. Neuron 2014
175
25

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
151
25

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.
Wenshu XiangWei, Varun Kannan, Yuchen Xu, Gabrielle J Kosobucki, Anthony J Schulien, Hirofumi Kusumoto, Christelle Moufawad El Achkar, Subhrajit Bhattacharya, Gaetan Lesca, Sylvie Nguyen,[...]. Brain 2019
23
39

GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Dong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, Eric D Marsh, Lifeng Tian, Elizabeth M McCormick, Gabrielle J Kosobucki, Wenjuan Chen, Anthony J Schulien, Rosetta Chiavacci,[...]. Am J Hum Genet 2016
106
25

Structure, function, and allosteric modulation of NMDA receptors.
Kasper B Hansen, Feng Yi, Riley E Perszyk, Hiro Furukawa, Lonnie P Wollmuth, Alasdair J Gibb, Stephen F Traynelis. J Gen Physiol 2018
171
25

De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases.
Jia Li, Jin Zhang, Weiting Tang, Ruth K Mizu, Hirofumi Kusumoto, Wenshu XiangWei, Yuchen Xu, Wenjuan Chen, Johansen B Amin, Chun Hu,[...]. Hum Mutat 2019
23
39

X-ray structure, symmetry and mechanism of an AMPA-subtype glutamate receptor.
Alexander I Sobolevsky, Michael P Rosconi, Eric Gouaux. Nature 2009
712
22

NMDA receptor structures reveal subunit arrangement and pore architecture.
Chia-Hsueh Lee, Wei Lü, Jennifer Carlisle Michel, April Goehring, Juan Du, Xianqiang Song, Eric Gouaux. Nature 2014
304
22

Mechanism of NMDA receptor channel block by MK-801 and memantine.
Xianqiang Song, Morten Ø Jensen, Vishwanath Jogini, Richard A Stein, Chia-Hsueh Lee, Hassane S Mchaourab, David E Shaw, Eric Gouaux. Nature 2018
97
22

GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy.
Johannes R Lemke, Rik Hendrickx, Kirsten Geider, Bodo Laube, Michael Schwake, Robert J Harvey, Victoria M James, Alex Pepler, Isabelle Steiner, Konstanze Hörtnagel,[...]. Ann Neurol 2014
137
22

Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia.
J Tarabeux, O Kebir, J Gauthier, F F Hamdan, L Xiong, A Piton, D Spiegelman, É Henrion, B Millet, F Fathalli,[...]. Transl Psychiatry 2011
148
22


GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, Natalia Lozovaya, Audrey Labalme, Nadia Boutry-Kryza, Manal Salmi, Timur Tsintsadze, Laura Addis, Jacques Motte,[...]. Nat Genet 2013
262
22

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
Johannes R Lemke, Dennis Lal, Eva M Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin Finsterwalder,[...]. Nat Genet 2013
256
22

Functional Evaluation of a De Novo GRIN2A Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy.
Wenjuan Chen, Anel Tankovic, Pieter B Burger, Hirofumi Kusumoto, Stephen F Traynelis, Hongjie Yuan. Mol Pharmacol 2017
39
19

Activation of NMDA receptors and the mechanism of inhibition by ifenprodil.
Nami Tajima, Erkan Karakas, Timothy Grant, Noriko Simorowski, Ruben Diaz-Avalos, Nikolaus Grigorieff, Hiro Furukawa. Nature 2016
122
19

A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder.
Ana Fernández-Marmiesse, Hirofumi Kusumoto, Saray Rekarte, Iria Roca, Jin Zhang, Scott J Myers, Stephen F Traynelis, Mª Luz Couce, Luis Gutierrez-Solana, Hongjie Yuan. Mov Disord 2018
17
41


Influence of GluN2 subunit identity on NMDA receptor function.
D J A Wyllie, M R Livesey, G E Hardingham. Neuropharmacology 2013
142
19


Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation.
Joshua Traynelis, Michael Silk, Quanli Wang, Samuel F Berkovic, Liping Liu, David B Ascher, David J Balding, Slavé Petrovski. Genome Res 2017
83
19

Functional assessment of triheteromeric NMDA receptors containing a human variant associated with epilepsy.
Katie F M Marwick, Kasper B Hansen, Paul A Skehel, Giles E Hardingham, David J A Wyllie. J Physiol 2019
12
58

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
E M Kenny, P Cormican, S Furlong, E Heron, G Kenny, C Fahey, E Kelleher, S Ennis, D Tropea, R Anney,[...]. Mol Psychiatry 2014
116
19

De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.
Andrew E Fry, Katherine A Fawcett, Nathanel Zelnik, Hongjie Yuan, Belinda A N Thompson, Lilach Shemer-Meiri, Thomas D Cushion, Hood Mugalaasi, David Sims, Neil Stoodley,[...]. Brain 2018
46
19

A conserved glycine harboring disease-associated mutations permits NMDA receptor slow deactivation and high Ca2+ permeability.
Johansen B Amin, Xiaoling Leng, Aaron Gochman, Huan-Xiang Zhou, Lonnie P Wollmuth. Nat Commun 2018
22
31

Channel kinetics determine the time course of NMDA receptor-mediated synaptic currents.
R A Lester, J D Clements, G L Westbrook, C E Jahr. Nature 1990
430
16

Channel opening and gating mechanism in AMPA-subtype glutamate receptors.
Edward C Twomey, Maria V Yelshanskaya, Robert A Grassucci, Joachim Frank, Alexander I Sobolevsky. Nature 2017
119
16

Triheteromeric NMDA receptors at hippocampal synapses.
Kenneth R Tovar, Matthew J McGinley, Gary L Westbrook. J Neurosci 2013
129
16



Mutations of N-Methyl-D-Aspartate Receptor Subunits in Epilepsy.
Xing-Xing Xu, Jian-Hong Luo. Neurosci Bull 2018
24
25


GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function.
Wenjuan Chen, Christine Shieh, Sharon A Swanger, Anel Tankovic, Margaret Au, Marianne McGuire, Michele Tagliati, John M Graham, Suneeta Madan-Khetarpal, Stephen F Traynelis,[...]. J Hum Genet 2017
39
16


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.