A citation-based method for searching scientific literature

Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, Natalia Lozovaya, Audrey Labalme, Nadia Boutry-Kryza, Manal Salmi, Timur Tsintsadze, Laura Addis, Jacques Motte, Sukhvir Wright, Vera Tsintsadze, Anne Michel, Diane Doummar, Karine Lascelles, Lisa Strug, Patrick Waters, Julitta de Bellescize, Pascal Vrielynck, Anne de Saint Martin, Dorothee Ville, Philippe Ryvlin, Alexis Arzimanoglou, Edouard Hirsch, Angela Vincent, Deb Pal, Nail Burnashev, Damien Sanlaville, Pierre Szepetowski. Nat Genet 2013
Times Cited: 249







List of co-cited articles
1212 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
242
60

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
214
54

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
304
35

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
28

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
138
25

NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease.
Pierre Paoletti, Camilla Bellone, Qiang Zhou. Nat Rev Neurosci 2013
25

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
94
24

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
82
26

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
97
21

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
81
24


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
90
22

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
925
19

A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2.
Sarra Dimassi, Audrey Labalme, Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, Edouard Hirsch, Alexis Arzimanoglou, Jacques Motte, Anne de Saint Martin, Nadia Boutry-Kryza,[...]. Epilepsia 2014
45
42

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
72
25

NMDA receptor subunit mutations in neurodevelopmental disorders.
Nail Burnashev, Pierre Szepetowski. Curr Opin Pharmacol 2015
104
18

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
129
17

Human GRIN2B variants in neurodevelopmental disorders.
Chun Hu, Wenjuan Chen, Scott J Myers, Hongjie Yuan, Stephen F Traynelis. J Pharmacol Sci 2016
110
15

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
970
14

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
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
27
48

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
34
38

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
61
21

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
139
13


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
13

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.
Fadi F Hamdan, Julie Gauthier, Yoichi Araki, Da-Ting Lin, Yuhki Yoshizawa, Kyohei Higashi, A-Reum Park, Dan Spiegelman, Sylvia Dobrzeniecka, Amélie Piton,[...]. Am J Hum Genet 2011
231
12

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
112
12

Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism.
Gaetan Lesca, Gabrielle Rudolf, Audrey Labalme, Edouard Hirsch, Alexis Arzimanoglou, Pierre Genton, Jacques Motte, Anne de Saint Martin, Maria-Paola Valenti, Clotilde Boulay,[...]. Epilepsia 2012
105
12

Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.
C von Stülpnagel, M Ensslen, R S Møller, D K Pal, S Masnada, P Veggiotti, E Piazza, M Dreesmann, T Hartlieb, T Herberhold,[...]. Eur J Paediatr Neurol 2017
20
55


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
19
57


Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
11

De Novo Mutations and Rare Variants Occurring in NMDA Receptors.
Wenshu XiangWei, Yuwu Jiang, Hongjie Yuan. Curr Opin Physiol 2018
43
25

Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.
Sunita Venkateswaran, Ken A Myers, Amanda C Smith, Chandree L Beaulieu, Jeremy A Schwartzentruber, Jacek Majewski, Dennis Bulman, Kym M Boycott, David A Dyment. Epilepsia 2014
25
40

Encephalopathy with electrical status epilepticus during slow sleep or ESES syndrome including the acquired aphasia.
C A Tassinari, G Rubboli, L Volpi, S Meletti, G d'Orsi, M Franca, A R Sabetta, P Riguzzi, E Gardella, A Zaniboni,[...]. Clin Neurophysiol 2000
187
10

Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.
Katherine L Helbig, Kelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, Zöe Powis, Shuwei Li, Sha Tang, Ingo Helbig. Genet Med 2016
172
10

SRPX2 mutations in disorders of language cortex and cognition.
Patrice Roll, Gabrielle Rudolf, Sandrine Pereira, Barbara Royer, Ingrid E Scheffer, Annick Massacrier, Maria-Paola Valenti, Nathalie Roeckel-Trevisiol, Sarah Jamali, Christophe Beclin,[...]. Hum Mol Genet 2006
181
9



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
38
23

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Ingo Helbig, Heather C Mefford, Andrew J Sharp, Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak,[...]. Nat Genet 2009
396
9

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Xiaowei Sylvia Chen, Rose H Reader, Alexander Hoischen, Joris A Veltman, Nuala H Simpson, Clyde Francks, Dianne F Newbury, Simon E Fisher. Sci Rep 2017
43
20

EEG criteria predictive of complicated evolution in idiopathic rolandic epilepsy.
R Massa, A de Saint-Martin, R Carcangiu, G Rudolf, C Seegmuller, C Kleitz, M N Metz-Lutz, E Hirsch, C Marescaux. Neurology 2001
191
9

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
42
21

GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders.
Chihiro Ohba, Masaaki Shiina, Jun Tohyama, Kazuhiro Haginoya, Tally Lerman-Sagie, Nobuhiko Okamoto, Lubov Blumkin, Dorit Lev, Souichi Mukaida, Fumihito Nozaki,[...]. Epilepsia 2015
47
17

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, Tania Djémié, Stephan Müller, Rikke S Møller, Bridget Maher, Laura Hernandez-Hernandez, Matthis Synofzik, Hande S Caglayan,[...]. Nat Genet 2015
142
8

Functional and pharmacological differences between recombinant N-methyl-D-aspartate receptors.
S Vicini, J F Wang, J H Li, W J Zhu, Y H Wang, J H Luo, B B Wolfe, D R Grayson. J Neurophysiol 1998
505
8

Investigation of GRIN2A in common epilepsy phenotypes.
Dennis Lal, Sandra Steinbrücker, Julian Schubert, Thomas Sander, Felicitas Becker, Yvonne Weber, Holger Lerche, Holger Thiele, Roland Krause, Anna-Elina Lehesjoki,[...]. Epilepsy Res 2015
14
57


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.