A citation-based method for searching scientific literature

Garret R Anderson, Timothy Galfin, Wei Xu, Jason Aoto, Robert C Malenka, Thomas C Südhof. Proc Natl Acad Sci U S A 2012
Times Cited: 142







List of co-cited articles
1361 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
619
63

Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons.
Olga Varea, Maria Dolores Martin-de-Saavedra, Katherine J Kopeikina, Britta Schürmann, Hunter J Fleming, Jessica M Fawcett-Patel, Anthony Bach, Seil Jang, Elior Peles, Eunjoon Kim,[...]. Proc Natl Acad Sci U S A 2015
75
60

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1.
Sebastian Poliak, Daniela Salomon, Hadas Elhanany, Helena Sabanay, Brent Kiernan, Larysa Pevny, Colin L Stewart, Xiaorong Xu, Shing-Yan Chiu, Peter Shrager,[...]. J Cell Biol 2003
374
37

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.
Kevin A Strauss, Erik G Puffenberger, Matthew J Huentelman, Steven Gottlieb, Seth E Dobrin, Jennifer M Parod, Dietrich A Stephan, D Holmes Morton. N Engl J Med 2006
432
32

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
Betul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, Abha R Gupta, Jesse F Abelson, Thomas M Morgan, Katarzyna Chawarska, Ami Klin, A Gulhan Ercan-Sencicek, Althea A Stillman,[...]. Am J Hum Genet 2008
386
30

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.
Maricela Alarcón, Brett S Abrahams, Jennifer L Stone, Jacqueline A Duvall, Julia V Perederiy, Jamee M Bomar, Jonathan Sebat, Michael Wigler, Christa L Martin, David H Ledbetter,[...]. Am J Hum Genet 2008
554
29

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels.
S Poliak, L Gollan, R Martinez, A Custer, S Einheber, J L Salzer, J S Trimmer, P Shrager, E Peles. Neuron 1999
371
26

Shining a light on CNTNAP2: complex functions to complex disorders.
Pedro Rodenas-Cuadrado, Joses Ho, Sonja C Vernes. Eur J Hum Genet 2014
150
26

The Autism Related Protein Contactin-Associated Protein-Like 2 (CNTNAP2) Stabilizes New Spines: An In Vivo Mouse Study.
Amos Gdalyahu, Maria Lazaro, Olga Penagarikano, Peyman Golshani, Joshua T Trachtenberg, Daniel H Geschwind. PLoS One 2015
46
47

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
868
21

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Dan E Arking, David J Cutler, Camille W Brune, Tanya M Teslovich, Kristen West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H Cook,[...]. Am J Hum Genet 2008
413
19


CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.
J I Friedman, T Vrijenhoek, S Markx, I M Janssen, W A van der Vliet, B H W Faas, N V Knoers, W Cahn, R S Kahn, L Edelmann,[...]. Mol Psychiatry 2008
218
16

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
15

Characterisation of CASPR2 deficiency disorder--a syndrome involving autism, epilepsy and language impairment.
Pedro Rodenas-Cuadrado, Nicola Pietrafusa, Teresa Francavilla, Angela La Neve, Pasquale Striano, Sonja C Vernes. BMC Med Genet 2016
40
37


A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.
Katsuhiko Tabuchi, Jacqueline Blundell, Mark R Etherton, Robert E Hammer, Xinran Liu, Craig M Powell, Thomas C Südhof. Science 2007
651
14

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.
Christiane Zweier, Eiko K de Jong, Markus Zweier, Alfredo Orrico, Lilian B Ousager, Amanda L Collins, Emilia K Bijlsma, Merel A W Oortveld, Arif B Ekici, André Reis,[...]. Am J Hum Genet 2009
240
14

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
376
14

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.
Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, Lisa I Sonnenblick, Jeffrey D Rudie, Dara Ghahremani, Jeanette A Mumford, Russell A Poldrack, Mirella Dapretto, Daniel H Geschwind,[...]. Sci Transl Med 2010
176
14

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission.
T Karayannis, E Au, J C Patel, I Kruglikov, S Markx, R Delorme, D Héron, D Salomon, J Glessner, S Restituito,[...]. Nature 2014
104
13

Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotonia.
Sarosh R Irani, Sian Alexander, Patrick Waters, Kleopas A Kleopa, Philippa Pettingill, Luigi Zuliani, Elior Peles, Camilla Buckley, Bethan Lang, Angela Vincent. Brain 2010
827
13

Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers.
Maria Traka, Laurence Goutebroze, Natalia Denisenko, Maria Bessa, Artemisia Nifli, Sophia Havaki, Yoichiro Iwakura, Fumihiko Fukamauchi, Kazutada Watanabe, Betty Soliven,[...]. J Cell Biol 2003
175
13

A functional genetic link between distinct developmental language disorders.
Sonja C Vernes, Dianne F Newbury, Brett S Abrahams, Laura Winchester, Jérôme Nicod, Matthias Groszer, Maricela Alarcón, Peter L Oliver, Kay E Davies, Daniel H Geschwind,[...]. N Engl J Med 2008
402
13

Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum.
Mateja Smogavec, Alison Cleall, Juliane Hoyer, Damien Lederer, Marie-Cécile Nassogne, Elizabeth E Palmer, Marie Deprez, Valérie Benoit, Isabelle Maystadt, Charlotte Noakes,[...]. J Med Genet 2016
29
44


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
12

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
12

Expression of Cntnap2 (Caspr2) in multiple levels of sensory systems.
Aaron Gordon, Daniela Salomon, Noy Barak, Yefim Pen, Michael Tsoory, Tali Kimchi, Elior Peles. Mol Cell Neurosci 2016
30
40

Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV+ Cortical Interneurons.
Daniel Vogt, Kathleen K A Cho, Samantha M Shelton, Anirban Paul, Z Josh Huang, Vikaas S Sohal, John L R Rubenstein. Cereb Cortex 2018
37
32

Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors.
Patrick E Rothwell, Marc V Fuccillo, Stephan Maxeiner, Scott J Hayton, Ozgun Gokce, Byung Kook Lim, Stephen C Fowler, Robert C Malenka, Thomas C Südhof. Cell 2014
265
11

Genome-wide analyses of human perisylvian cerebral cortical patterning.
B S Abrahams, D Tentler, J V Perederiy, M C Oldham, G Coppola, D H Geschwind. Proc Natl Acad Sci U S A 2007
130
11

Organization of myelinated axons by Caspr and Caspr2 requires the cytoskeletal adapter protein 4.1B.
Ido Horresh, Vered Bar, Joseph L Kissil, Elior Peles. J Neurosci 2010
80
13

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.
Annemieke J M H Verkerk, Carol A Mathews, Marijke Joosse, Bert H J Eussen, Peter Heutink, Ben A Oostra. Genomics 2003
167
11

Model of autism: increased ratio of excitation/inhibition in key neural systems.
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
11

Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2).
Zhuoyang Lu, M V V V Sekhar Reddy, Jianfang Liu, Ana Kalichava, Jiankang Liu, Lei Zhang, Fang Chen, Yun Wang, Luis Marcelo F Holthauzen, Mark A White,[...]. J Biol Chem 2016
33
33

Modulation of prefrontal cortex excitation/inhibition balance rescues social behavior in CNTNAP2-deficient mice.
Aslihan Selimbeyoglu, Christina K Kim, Masatoshi Inoue, Soo Yeun Lee, Alice S O Hong, Isaac Kauvar, Charu Ramakrishnan, Lief E Fenno, Thomas J Davidson, Matthew Wright,[...]. Sci Transl Med 2017
144
11

Multiple molecular interactions determine the clustering of Caspr2 and Kv1 channels in myelinated axons.
Ido Horresh, Sebastian Poliak, Seth Grant, David Bredt, Matthew N Rasband, Elior Peles. J Neurosci 2008
85
11

Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2.
Michael J Schmeisser, Elodie Ey, Stephanie Wegener, Juergen Bockmann, A Vanessa Stempel, Angelika Kuebler, Anna-Lena Janssen, Patrick T Udvardi, Ehab Shiban, Christina Spilker,[...]. Nature 2012
407
10

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function.
Hyejung Won, Hye-Ryeon Lee, Heon Yung Gee, Won Mah, Jae-Ick Kim, Jiseok Lee, Seungmin Ha, Changuk Chung, Eun Suk Jung, Yi Sul Cho,[...]. Nature 2012
443
10

Inhibitory axons are targeted in hippocampal cell culture by anti-Caspr2 autoantibodies associated with limbic encephalitis.
Delphine Pinatel, Bruno Hivert, José Boucraut, Margaux Saint-Martin, Véronique Rogemond, Lida Zoupi, Domna Karagogeos, Jérôme Honnorat, Catherine Faivre-Sarrailh. Front Cell Neurosci 2015
40
25

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3.
Xiaoming Wang, Portia A McCoy, Ramona M Rodriguiz, Yanzhen Pan, H Shawn Je, Adam C Roberts, Caroline J Kim, Janet Berrios, Jennifer S Colvin, Danielle Bousquet-Moore,[...]. Hum Mol Genet 2011
354
10


Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism.
Olga Peñagarikano, María T Lázaro, Xiao-Hong Lu, Aaron Gordon, Hongmei Dong, Hoa A Lam, Elior Peles, Nigel T Maidment, Niall P Murphy, X William Yang,[...]. Sci Transl Med 2015
206
9

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
9

Morvan syndrome: clinical and serological observations in 29 cases.
Sarosh R Irani, Philippa Pettingill, Kleopas A Kleopa, Natasa Schiza, Patrick Waters, Claudio Mazia, Luigi Zuliani, Osamu Watanabe, Bethan Lang, Camilla Buckley,[...]. Ann Neurol 2012
289
9

Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia.
Eric Lancaster, Maartje G M Huijbers, Vered Bar, Anna Boronat, Andrew Wong, Eugenia Martinez-Hernandez, Christina Wilson, Dina Jacobs, Meizan Lai, Russell W Walker,[...]. Ann Neurol 2011
286
9

CNTNAP2 variants affect early language development in the general population.
A J O Whitehouse, D V M Bishop, Q W Ang, C E Pennell, S E Fisher. Genes Brain Behav 2011
114
9

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Hsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, Mingshan Xue, Maria Chahrour, Jong Yoo, Jeffrey L Neul, Shiaoching Gong, Hui-Chen Lu, Nathaniel Heintz,[...]. Nature 2010
777
9

Caspr2-reactive antibody cloned from a mother of an ASD child mediates an ASD-like phenotype in mice.
L Brimberg, S Mader, V Jeganathan, R Berlin, T R Coleman, P K Gregersen, P T Huerta, B T Volpe, B Diamond. Mol Psychiatry 2016
56
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.