A citation-based method for searching scientific literature

Oliver Crawley, María J Conde-Dusman, Isabel Pérez-Otaño. J Physiol 2022
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels.
Kasper B Hansen, Lonnie P Wollmuth, Derek Bowie, Hiro Furukawa, Frank S Menniti, Alexander I Sobolevsky, Geoffrey T Swanson, Sharon A Swanger, Ingo H Greger, Terunaga Nakagawa,[...]. Pharmacol Rev 2021
71
71

NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease.
Pierre Paoletti, Camilla Bellone, Qiang Zhou. Nat Rev Neurosci 2013
71

Increased NMDA current and spine density in mice lacking the NMDA receptor subunit NR3A.
S Das, Y F Sasaki, T Rothe, L S Premkumar, M Takasu, J E Crandall, P Dikkes, D A Conner, P V Rayudu, W Cheung,[...]. Nature 1998
463
57

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
84
57

Control of aversion by glycine-gated GluN1/GluN3A NMDA receptors in the adult medial habenula.
Y Otsu, E Darcq, K Pietrajtis, F Mátyás, E Schwartz, T Bessaih, S Abi Gerges, C V Rousseau, T Grand, S Dieudonné,[...]. Science 2019
37
57

Unmasking GluN1/GluN3A excitatory glycine NMDA receptors.
Teddy Grand, Sarah Abi Gerges, Mélissa David, Marco A Diana, Pierre Paoletti. Nat Commun 2018
43
57


Excitatory glycine receptors containing the NR3 family of NMDA receptor subunits.
Jon E Chatterton, Marc Awobuluyi, Louis S Premkumar, Hiroto Takahashi, Maria Talantova, Yeonsook Shin, Jiankun Cui, Shichun Tu, Kevin A Sevarino, Nobuki Nakanishi,[...]. Nature 2002
476
57

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
34
42

De Novo Mutations and Rare Variants Occurring in NMDA Receptors.
Wenshu XiangWei, Yuwu Jiang, Hongjie Yuan. Curr Opin Physiol 2018
59
42


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
102
42

Reduced hippocampal LTP and spatial learning in mice lacking NMDA receptor epsilon 1 subunit.
K Sakimura, T Kutsuwada, I Ito, T Manabe, C Takayama, E Kushiya, T Yagi, S Aizawa, Y Inoue, H Sugiyama. Nature 1995
636
42


Characterization and comparison of the NR3A subunit of the NMDA receptor in recombinant systems and primary cortical neurons.
Yasnory F Sasaki, Thomas Rothe, Louis S Premkumar, Saumya Das, Jiankun Cui, Maria V Talantova, Hon-Kit Wong, Xiandi Gong, Shing Fai Chan, Dongxian Zhang,[...]. J Neurophysiol 2002
145
42

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
42

Emerging roles of GluN3-containing NMDA receptors in the CNS.
Isabel Pérez-Otaño, Rylan S Larsen, John F Wesseling. Nat Rev Neurosci 2016
97
42

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
228
42

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
77
28

A de novo GRIN1 Variant Associated With Myoclonus and Developmental Delay: From Molecular Mechanism to Rescue Pharmacology.
Jin Zhang, Weiting Tang, Nidhi K Bhatia, Yuchen Xu, Nabina Paudyal, Ding Liu, Sukhan Kim, Rui Song, Wenshu XiangWei, Gil Shaulsky,[...]. Front Genet 2021
4
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
111
28

Transient microstructural brain anomalies and epileptiform discharges in mice defective for epilepsy and language-related NMDA receptor subunit gene Grin2a.
Manal Salmi, Radu Bolbos, Sylvian Bauer, Marat Minlebaev, Nail Burnashev, Pierre Szepetowski. Epilepsia 2018
20
28

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
131
28

Targeted disruption of NMDA receptor 1 gene abolishes NMDA response and results in neonatal death.
D Forrest, M Yuzaki, H D Soares, L Ng, D C Luk, M Sheng, C L Stewart, J I Morgan, J A Connor, T Curran. Neuron 1994
385
28

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
43
28

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
49
28

Impaired vocal communication, sleep-related discharges, and transient alteration of slow-wave sleep in developing mice lacking the GluN2A subunit of N-methyl-d-aspartate receptors.
Manal Salmi, Federico Del Gallo, Marat Minlebaev, Andrey Zakharov, Vanessa Pauly, Pauline Perron, Alexandre Pons-Bennaceur, Séverine Corby-Pellegrino, Laurent Aniksztejn, Pierre-Pascal Lenck-Santini,[...]. Epilepsia 2019
12
28

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
31
28

Consequences of NMDA receptor deficiency can be rescued in the adult brain.
Catharine A Mielnik, Mary A Binko, Yuxiao Chen, Adam J Funk, Emily M Johansson, Katheron Intson, Nirun Sivananthan, Rehnuma Islam, Marija Milenkovic, Wendy Horsfall,[...]. Mol Psychiatry 2021
17
28

Impairment of suckling response, trigeminal neuronal pattern formation, and hippocampal LTD in NMDA receptor epsilon 2 subunit mutant mice.
T Kutsuwada, K Sakimura, T Manabe, C Takayama, N Katakura, E Kushiya, R Natsume, M Watanabe, Y Inoue, T Yagi,[...]. Neuron 1996
405
28

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
160
28

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
53
28


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
30
28

GRIN2B gain of function mutations are sensitive to radiprodil, a negative allosteric modulator of GluN2B-containing NMDA receptors.
Brice Mullier, Christian Wolff, Zara Amanda Sands, Philippe Ghisdal, Pierandrea Muglia, Rafal Marian Kaminski, Véronique Marie André. Neuropharmacology 2017
32
28

Distinct roles of GRIN2A and GRIN2B variants in neurological conditions.
Scott J Myers, Hongjie Yuan, Jing-Qiong Kang, Francis Chee Kuan Tan, Stephen F Traynelis, Chian-Ming Low. F1000Res 2019
50
28

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
37
28

Subunit-specific NMDA receptor trafficking to synapses.
Andres Barria, Roberto Malinow. Neuron 2002
392
28

Rapid bidirectional switching of synaptic NMDA receptors.
Camilla Bellone, Roger A Nicoll. Neuron 2007
249
28

ER to synapse trafficking of NMDA receptors.
Martin Horak, Ronald S Petralia, Martina Kaniakova, Nathalie Sans. Front Cell Neurosci 2014
51
28

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
277
28

Rapid, experience-dependent expression of synaptic NMDA receptors in visual cortex in vivo.
E M Quinlan, B D Philpot, R L Huganir, M F Bear. Nat Neurosci 1999
429
28


GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
Gemma L Carvill, Brigid M Regan, Simone C Yendle, Brian J O'Roak, Natalia Lozovaya, Nadine Bruneau, Nail Burnashev, Adiba Khan, Joseph Cook, Eileen Geraghty,[...]. Nat Genet 2013
241
28


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
271
28

NMDA receptor subunits: diversity, development and disease.
S Cull-Candy, S Brickley, M Farrant. Curr Opin Neurobiol 2001
28

Functional Properties of Human NMDA Receptors Associated with Epilepsy-Related Mutations of GluN2A Subunit.
Dmitry A Sibarov, Nadine Bruneau, Sergei M Antonov, Pierre Szepetowski, Nail Burnashev, Rashid Giniatullin. Front Cell Neurosci 2017
22
28




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.