A citation-based method for searching scientific literature

Alexia M Thomas, Michael D Schwartz, Michael D Saxe, Thomas S Kilduff. Sleep 2017
Times Cited: 32







List of co-cited articles
377 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
635
59

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
439
43

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
564
31

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
386
28

Shining a light on CNTNAP2: complex functions to complex disorders.
Pedro Rodenas-Cuadrado, Joses Ho, Sonja C Vernes. Eur J Hum Genet 2014
155
28

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
378
25

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
145
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
415
21


Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder.
Daniela Brunner, Patricia Kabitzke, Dansha He, Kimberly Cox, Lucinda Thiede, Taleen Hanania, Emily Sabath, Vadim Alexandrov, Michael Saxe, Elior Peles,[...]. PLoS One 2015
51
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
906
21

Fmr1 and Nlgn3 knockout rats: novel tools for investigating autism spectrum disorders.
Shannon M Hamilton, Jennie R Green, Surabi Veeraragavan, Lisa Yuva, Aaron McCoy, Yumei Wu, Joe Warren, Lara Little, Diana Ji, Xiaoxia Cui,[...]. Behav Neurosci 2014
91
18

Hyperactivity and male-specific sleep deficits in the 16p11.2 deletion mouse model of autism.
Christopher C Angelakos, Adam J Watson, W Timothy O'Brien, Kyle S Krainock, Thomas Nickl-Jockschat, Ted Abel. Autism Res 2017
36
18

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
78
18

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
158
18

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
32
15

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
389
15


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

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
33
15

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
50
15


Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons.
Fei Yi, Tamas Danko, Salome Calado Botelho, Christopher Patzke, ChangHui Pak, Marius Wernig, Thomas C Südhof. Science 2016
179
15

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
809
15

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
37
15

Rodent models in neuroscience research: is it a rat race?
Bart Ellenbroek, Jiun Youn. Dis Model Mech 2016
298
15

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
179
12

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.
Heather C Whalley, Garret O'Connell, Jessika E Sussmann, Anna Peel, Andrew C Stanfield, Marianna E Hayiou-Thomas, Eve C Johnstone, Stephen M Lawrie, Andrew M McIntosh, Jeremy Hall. Am J Med Genet B Neuropsychiatr Genet 2011
71
12

Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2.
Emily L Dennis, Neda Jahanshad, Jeffrey D Rudie, Jesse A Brown, Kori Johnson, Katie L McMahon, Greig I de Zubicaray, Grant Montgomery, Nicholas G Martin, Margaret J Wright,[...]. Brain Connect 2011
72
12

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
12

Neuroligin-1 links neuronal activity to sleep-wake regulation.
Janine El Helou, Erika Bélanger-Nelson, Marlène Freyburger, Stéphane Dorsaz, Thomas Curie, Francesco La Spada, Pierre-Olivier Gaudreault, Éric Beaumont, Philippe Pouliot, Frédéric Lesage,[...]. Proc Natl Acad Sci U S A 2013
58
12

Neuroligin 3 R451C mutation alters electroencephalography spectral activity in an animal model of autism spectrum disorders.
Jackie J Liu, Kevin P Grace, Richard L Horner, Miguel A Cortez, Yiwen Shao, Zhengping Jia. Mol Brain 2017
20
20

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
666
12

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
949
12

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice.
S S Moy, J J Nadler, A Perez, R P Barbaro, J M Johns, T R Magnuson, J Piven, J N Crawley. Genes Brain Behav 2004
913
12



Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2.
Ellen J Hoffman, Katherine J Turner, Joseph M Fernandez, Daniel Cifuentes, Marcus Ghosh, Sundas Ijaz, Roshan A Jain, Fumi Kubo, Brent R Bill, Herwig Baier,[...]. Neuron 2016
98
12

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
39
12

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
220
12

Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism.
Thomas C Jaramillo, Haley E Speed, Zhong Xuan, Jeremy M Reimers, Shunan Liu, Craig M Powell. Autism Res 2016
95
12

Cacna1c (Cav1.2) Modulates Electroencephalographic Rhythm and Rapid Eye Movement Sleep Recovery.
Deependra Kumar, Nina Dedic, Cornelia Flachskamm, Stephanie Voulé, Jan M Deussing, Mayumi Kimura. Sleep 2015
20
20

Oxytocin improves behavioral and electrophysiological deficits in a novel Shank3-deficient rat.
Hala Harony-Nicolas, Maya Kay, Johann du Hoffmann, Matthew E Klein, Ozlem Bozdagi-Gunal, Mohammed Riad, Nikolaos P Daskalakis, Sankalp Sonar, Pablo E Castillo, Patrick R Hof,[...]. Elife 2017
81
12

Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.
Jacqueline Blundell, Cory A Blaiss, Mark R Etherton, Felipe Espinosa, Katsuhiko Tabuchi, Christopher Walz, Marc F Bolliger, Thomas C Südhof, Craig M Powell. J Neurosci 2010
318
12

Pharmacological modulation of AMPA receptor rescues social impairments in animal models of autism.
Ji-Woon Kim, Kwanghoon Park, Ri Jin Kang, Edson Luck T Gonzales, Do Gyeong Kim, Hyun Ah Oh, Hana Seung, Mee Jung Ko, Kyoung Ja Kwon, Ki Chan Kim,[...]. Neuropsychopharmacology 2019
54
12

Pten regulates neuronal arborization and social interaction in mice.
Chang-Hyuk Kwon, Bryan W Luikart, Craig M Powell, Jing Zhou, Sharon A Matheny, Wei Zhang, Yanjiao Li, Suzanne J Baker, Luis F Parada. Neuron 2006
700
12

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
367
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


CNTNAP2 stabilizes interneuron dendritic arbors through CASK.
Ruoqi Gao, Nicolas H Piguel, Alexandria E Melendez-Zaidi, Maria Dolores Martin-de-Saavedra, Sehyoun Yoon, Marc P Forrest, Kristoffer Myczek, Gefei Zhang, Theron A Russell, John G Csernansky,[...]. Mol Psychiatry 2018
24
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.