A citation-based method for searching scientific literature

Stéphane J Baudouin, Julien Gaudias, Stefan Gerharz, Laetitia Hatstatt, Kuikui Zhou, Pradeep Punnakkal, Kenji F Tanaka, Will Spooren, Rene Hen, Chris I De Zeeuw, Kaspar Vogt, Peter Scheiffele. Science 2012
Times Cited: 196







List of co-cited articles
1507 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
635
35

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
32

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
483
30


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
253
25

Mutations causing syndromic autism define an axis of synaptic pathophysiology.
Benjamin D Auerbach, Emily K Osterweil, Mark F Bear. Nature 2011
413
24

Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function.
Mark Etherton, Csaba Földy, Manu Sharma, Katsuhiko Tabuchi, Xinran Liu, Mehrdad Shamloo, Robert C Malenka, Thomas C Südhof. Proc Natl Acad Sci U S A 2011
211
22

Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.
K Radyushkin, K Hammerschmidt, S Boretius, F Varoqueaux, A El-Kordi, A Ronnenberg, D Winter, J Frahm, J Fischer, N Brose,[...]. Genes Brain Behav 2009
222
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
821
21

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
420
20

Neuroligins determine synapse maturation and function.
Frédérique Varoqueaux, Gayane Aramuni, Randi L Rawson, Ralf Mohrmann, Markus Missler, Kurt Gottmann, Weiqi Zhang, Thomas C Südhof, Nils Brose. Neuron 2006
540
20

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
20

The cerebellum, sensitive periods, and autism.
Samuel S-H Wang, Alexander D Kloth, Aleksandra Badura. Neuron 2014
325
20

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
19

Cerebellar plasticity and motor learning deficits in a copy-number variation mouse model of autism.
Claire Piochon, Alexander D Kloth, Giorgio Grasselli, Heather K Titley, Hisako Nakayama, Kouichi Hashimoto, Vivian Wan, Dana H Simmons, Tahra Eissa, Jin Nakatani,[...]. Nat Commun 2014
90
21

Autism-associated neuroligin-3 mutations commonly disrupt tonic endocannabinoid signaling.
Csaba Földy, Robert C Malenka, Thomas C Südhof. Neuron 2013
174
18

Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome.
S K E Koekkoek, K Yamaguchi, B A Milojkovic, B R Dortland, T J H Ruigrok, R Maex, W De Graaf, A E Smit, F VanderWerf, C E Bakker,[...]. Neuron 2005
297
17

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
815
16



Neuroligins Sculpt Cerebellar Purkinje-Cell Circuits by Differential Control of Distinct Classes of Synapses.
Bo Zhang, Lulu Y Chen, Xinran Liu, Stephan Maxeiner, Sung-Jin Lee, Ozgun Gokce, Thomas C Südhof. Neuron 2015
81
19

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.
Stephane Jamain, Konstantin Radyushkin, Kurt Hammerschmidt, Sylvie Granon, Susann Boretius, Frederique Varoqueaux, Nelina Ramanantsoa, Jorge Gallego, Anja Ronnenberg, Dorina Winter,[...]. Proc Natl Acad Sci U S A 2008
367
15

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
387
15


Neuroligin 2 is exclusively localized to inhibitory synapses.
Frédérique Varoqueaux, Stéphane Jamain, Nils Brose. Eur J Cell Biol 2004
354
15

Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses.
J Y Song, K Ichtchenko, T C Südhof, N Brose. Proc Natl Acad Sci U S A 1999
488
15

Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2.
Alexander A Chubykin, Deniz Atasoy, Mark R Etherton, Nils Brose, Ege T Kavalali, Jay R Gibson, Thomas C Südhof. Neuron 2007
395
14

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
298
14

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
584
14

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
935
14


Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice.
Saša Peter, Michiel M Ten Brinke, Jeffrey Stedehouder, Claudia M Reinelt, Bin Wu, Haibo Zhou, Kuikui Zhou, Henk-Jan Boele, Steven A Kushner, Min Goo Lee,[...]. Nat Commun 2016
95
14

Altered synaptic plasticity in a mouse model of fragile X mental retardation.
Kimberly M Huber, Sean M Gallagher, Stephen T Warren, Mark F Bear. Proc Natl Acad Sci U S A 2002
952
13

Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis.
Dan Ehninger, Sangyeul Han, Carrie Shilyansky, Yu Zhou, Weidong Li, David J Kwiatkowski, Vijaya Ramesh, Alcino J Silva. Nat Med 2008
581
13

Neuroligin 2 drives postsynaptic assembly at perisomatic inhibitory synapses through gephyrin and collybistin.
Alexandros Poulopoulos, Gayane Aramuni, Guido Meyer, Tolga Soykan, Mrinalini Hoon, Theofilos Papadopoulos, Mingyue Zhang, Ingo Paarmann, Céline Fuchs, Kirsten Harvey,[...]. Neuron 2009
315
13


The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
12

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
870
12

Autism-related deficits via dysregulated eIF4E-dependent translational control.
Christos G Gkogkas, Arkady Khoutorsky, Israeli Ran, Emmanouil Rampakakis, Tatiana Nevarko, Daniel B Weatherill, Cristina Vasuta, Stephanie Yee, Morgan Truitt, Paul Dallaire,[...]. Nature 2013
335
12

Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice.
Kathryn K Chadman, Shiaoching Gong, Maria L Scattoni, Sarah E Boltuck, Shruti U Gandhy, Nathaniel Heintz, Jacqueline N Crawley. Autism Res 2008
194
12

Loss of Tsc2 in Purkinje cells is associated with autistic-like behavior in a mouse model of tuberous sclerosis complex.
R Michelle Reith, James McKenna, Henry Wu, S Shahrukh Hashmi, Seo-Hee Cho, Pramod K Dash, Michael J Gambello. Neurobiol Dis 2013
104
12

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
539
12

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.
J Yan, G Oliveira, A Coutinho, C Yang, J Feng, C Katz, J Sram, A Bockholt, I R Jones, N Craddock,[...]. Mol Psychiatry 2005
219
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
341
12

Cerebellar associative sensory learning defects in five mouse autism models.
Alexander D Kloth, Aleksandra Badura, Amy Li, Adriana Cherskov, Sara G Connolly, Andrea Giovannucci, M Ali Bangash, Giorgio Grasselli, Olga Peñagarikano, Claire Piochon,[...]. Elife 2015
69
17

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
191
12

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
11

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Christelle M Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Rastam, I Carina Gillberg, Henrik Anckarsäter,[...]. Nat Genet 2007
964
11

A synaptic trek to autism.
Thomas Bourgeron. Curr Opin Neurobiol 2009
432
11

Neuroligin-1 controls synaptic abundance of NMDA-type glutamate receptors through extracellular coupling.
Elaine C Budreck, Oh-Bin Kwon, Jung Hoon Jung, Stephane Baudouin, Albert Thommen, Hye-Sun Kim, Yugo Fukazawa, Harumi Harada, Katsuhiko Tabuchi, Ryuichi Shigemoto,[...]. Proc Natl Acad Sci U S A 2013
113
11


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.