A citation-based method for searching scientific literature

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, Peter Penzes. Proc Natl Acad Sci U S A 2015
Times Cited: 66







List of co-cited articles
979 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
566
75

Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development.
Garret R Anderson, Timothy Galfin, Wei Xu, Jason Aoto, Robert C Malenka, Thomas C Südhof. Proc Natl Acad Sci U S A 2012
127
68

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
414
42

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
358
39

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
540
39

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
38
57

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
376
31

Shining a light on CNTNAP2: complex functions to complex disorders.
Pedro Rodenas-Cuadrado, Joses Ho, Sonja C Vernes. Eur J Hum Genet 2014
137
31

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
356
27



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
22

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
402
21


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
792
18

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
24
50

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
34
35

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
212
18

Inherited genetic variants in autism-related CNTNAP2 show perturbed trafficking and ATF6 activation.
Giulia Falivelli, Antonella De Jaco, Flores Lietta Favaloro, Hyuck Kim, Jennifer Wilson, Noga Dubi, Mark H Ellisman, Brett S Abrahams, Palmer Taylor, Davide Comoletti. Hum Mol Genet 2012
32
34

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
16

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
623
16

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
165
16

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
168
15

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
15

Model of autism: increased ratio of excitation/inhibition in key neural systems.
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
15

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
230
15

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
37
24

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
98
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
770
13

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
167
13

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
54
16

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
34
26

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
121
13

Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.
Ricardo Scott, Alberto Sánchez-Aguilera, Kim van Elst, Lynette Lim, Nathalie Dehorter, Sung Eun Bae, Giorgia Bartolini, Elior Peles, Martien J H Kas, Hilgo Bruining,[...]. Cereb Cortex 2019
28
32

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
766
12

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
81
12

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
244
12

Structural Characterization of the Extracellular Domain of CASPR2 and Insights into Its Association with the Novel Ligand Contactin1.
Eva N Rubio-Marrero, Gabriele Vincelli, Cy M Jeffries, Tanvir R Shaikh, Irene S Pakos, Fanomezana M Ranaivoson, Sventja von Daake, Borries Demeler, Antonella De Jaco, Guy Perkins,[...]. J Biol Chem 2016
21
38

Interaction proteomics of canonical Caspr2 (CNTNAP2) reveals the presence of two Caspr2 isoforms with overlapping interactomes.
Ning Chen, Frank Koopmans, Aaron Gordon, Iryna Paliukhovich, Remco V Klaassen, Roel C van der Schors, Elior Peles, Matthijs Verhage, August B Smit, Ka Wan Li. Biochim Biophys Acta 2015
22
36


Adult restoration of Shank3 expression rescues selective autistic-like phenotypes.
Yuan Mei, Patricia Monteiro, Yang Zhou, Jin-Ah Kim, Xian Gao, Zhanyan Fu, Guoping Feng. Nature 2016
178
12


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
29
27

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
186
10

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
10

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
77
10

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.
Peter T Tsai, Court Hull, YunXiang Chu, Emily Greene-Colozzi, Abbey R Sadowski, Jarrett M Leech, Jason Steinberg, Jacqueline N Crawley, Wade G Regehr, Mustafa Sahin. Nature 2012
474
10

Identifying autism loci and genes by tracing recent shared ancestry.
Eric M Morrow, Seung-Yun Yoo, Steven W Flavell, Tae-Kyung Kim, Yingxi Lin, Robert Sean Hill, Nahit M Mukaddes, Soher Balkhy, Generoso Gascon, Asif Hashmi,[...]. Science 2008
496
10

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
10

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
525
10


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.