A citation-based method for searching scientific literature

Michael J Schmeisser, Elodie Ey, Stephanie Wegener, Juergen Bockmann, A Vanessa Stempel, Angelika Kuebler, Anna-Lena Janssen, Patrick T Udvardi, Ehab Shiban, Christina Spilker, Detlef Balschun, Boris V Skryabin, Susanne tom Dieck, Karl-Heinz Smalla, Dirk Montag, Claire S Leblond, Philippe Faure, Nicolas Torquet, Anne-Marie Le Sourd, Roberto Toro, Andreas M Grabrucker, Sarah A Shoichet, Dietmar Schmitz, Michael R Kreutz, Thomas Bourgeron, Eckart D Gundelfinger, Tobias M Boeckers. Nature 2012
Times Cited: 407







List of co-cited articles
1055 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
53

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
40

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
27

SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
277
26

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
24

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Claire S Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kevin Mouzat,[...]. PLoS Genet 2014
319
22

Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.
Albert Y Hung, Kensuke Futai, Carlo Sala, Juli G Valtschanoff, Jubin Ryu, Mollie A Woodworth, Fleur L Kidd, Clifford C Sung, Tsuyoshi Miyakawa, Mark F Bear,[...]. J Neurosci 2008
251
21

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.
Simone Berkel, Christian R Marshall, Birgit Weiss, Jennifer Howe, Ralph Roeth, Ute Moog, Volker Endris, Wendy Roberts, Peter Szatmari, Dalila Pinto,[...]. Nat Genet 2010
362
21

Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism.
Xiaoming Wang, Alexandra L Bey, Brittany M Katz, Alexandra Badea, Namsoo Kim, Lisa K David, Lara J Duffney, Sunil Kumar, Stephen D Mague, Samuel W Hulbert,[...]. Nat Commun 2016
162
19

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
989
18

Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission.
Mehreen Kouser, Haley E Speed, Colleen M Dewey, Jeremy M Reimers, Allie J Widman, Natasha Gupta, Shunan Liu, Thomas C Jaramillo, Muhammad Bangash, Bo Xiao,[...]. J Neurosci 2013
170
18

Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin.
S Naisbitt, E Kim, J C Tu, B Xiao, C Sala, J Valtschanoff, R J Weinberg, P F Worley, M Sheng. Neuron 1999
732
18

Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice.
Mu Yang, Ozlem Bozdagi, Maria Luisa Scattoni, Markus Wöhr, Florence I Roullet, Adam M Katz, Danielle N Abrams, David Kalikhman, Harrison Simon, Leuk Woldeyohannes,[...]. J Neurosci 2012
245
17

Mice with Shank3 Mutations Associated with ASD and Schizophrenia Display Both Shared and Distinct Defects.
Yang Zhou, Tobias Kaiser, Patrícia Monteiro, Xiangyu Zhang, Marie S Van der Goes, Dongqing Wang, Boaz Barak, Menglong Zeng, Chenchen Li, Congyi Lu,[...]. Neuron 2016
176
16

Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators.
Lara J Duffney, Ping Zhong, Jing Wei, Emmanuel Matas, Jia Cheng, Luye Qin, Kaijie Ma, David M Dietz, Yuji Kajiwara, Joseph D Buxbaum,[...]. Cell Rep 2015
164
15

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
207
15

Modeling autism by SHANK gene mutations in mice.
Yong-Hui Jiang, Michael D Ehlers. Neuron 2013
296
15

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Claire S Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Rastam,[...]. PLoS Genet 2012
282
15

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
911
14

Shank3-mutant mice lacking exon 9 show altered excitation/inhibition balance, enhanced rearing, and spatial memory deficit.
Jiseok Lee, Changuk Chung, Seungmin Ha, Dongmin Lee, Do-Young Kim, Hyun Kim, Eunjoon Kim. Front Cell Neurosci 2015
98
14

The Shank family of scaffold proteins.
M Sheng, E Kim. J Cell Sci 2000
364
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
619
14

Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies.
Andreas M Grabrucker, Michael J Schmeisser, Michael Schoen, Tobias M Boeckers. Trends Cell Biol 2011
158
13

Communication impairments in mice lacking Shank1: reduced levels of ultrasonic vocalizations and scent marking behavior.
Markus Wöhr, Florence I Roullet, Albert Y Hung, Morgan Sheng, Jacqueline N Crawley. PLoS One 2011
146
13

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
88
13

Pharmacological enhancement of mGlu5 receptors rescues behavioral deficits in SHANK3 knock-out mice.
C Vicidomini, L Ponzoni, D Lim, M J Schmeisser, D Reim, N Morello, D Orellana, A Tozzi, V Durante, P Scalmani,[...]. Mol Psychiatry 2017
67
17

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
103
12

Sociability and motor functions in Shank1 mutant mice.
Jill L Silverman, Sarah M Turner, Charlotte L Barkan, Seda S Tolu, Roheeni Saxena, Albert Y Hung, Morgan Sheng, Jacqueline N Crawley. Brain Res 2011
151
12

Autism-like behavioral phenotypes in BTBR T+tf/J mice.
H G McFarlane, G K Kusek, M Yang, J L Phoenix, V J Bolivar, J N Crawley. Genes Brain Behav 2008
516
12


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
11

Regulation of dendritic spine morphology and synaptic function by Shank and Homer.
C Sala, V Piëch, N R Wilson, M Passafaro, G Liu, M Sheng. Neuron 2001
533
11

Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation.
Andreas M Grabrucker, Mary J Knight, Christian Proepper, Juergen Bockmann, Marisa Joubert, Magali Rowan, G Uirich Nienhaus, Craig C Garner, Jim U Bowie, Michael R Kreutz,[...]. EMBO J 2011
146
11

Cell-Type-Specific Shank2 Deletion in Mice Leads to Differential Synaptic and Behavioral Phenotypes.
Ryunhee Kim, Jihye Kim, Changuk Chung, Seungmin Ha, Seungjoon Lee, Eunee Lee, Ye-Eun Yoo, Woohyun Kim, Wangyong Shin, Eunjoon Kim. J Neurosci 2018
24
45

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

Contribution of SHANK3 mutations to autism spectrum disorder.
Rainald Moessner, Christian R Marshall, James S Sutcliffe, Jennifer Skaug, Dalila Pinto, John Vincent, Lonnie Zwaigenbaum, Bridget Fernandez, Wendy Roberts, Peter Szatmari,[...]. Am J Hum Genet 2007
441
10

Shank synaptic scaffold proteins: keys to understanding the pathogenesis of autism and other synaptic disorders.
Carlo Sala, Cinzia Vicidomini, Ilaria Bigi, Adele Mossa, Chiara Verpelli. J Neurochem 2015
89
11

The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations.
Elodie Ey, Nicolas Torquet, Anne-Marie Le Sourd, Claire S Leblond, Tobias M Boeckers, Philippe Faure, Thomas Bourgeron. Behav Brain Res 2013
82
12

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
10

Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
Mark R Etherton, Cory A Blaiss, Craig M Powell, Thomas C Südhof. Proc Natl Acad Sci U S A 2009
301
10

Model of autism: increased ratio of excitation/inhibition in key neural systems.
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
10

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
10

The emerging role of SHANK genes in neuropsychiatric disorders.
Audrey Guilmatre, Guillaume Huguet, Richard Delorme, Thomas Bourgeron. Dev Neurobiol 2014
152
10

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
568
10

SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons.
Kirill Zaslavsky, Wen-Bo Zhang, Fraser P McCready, Deivid C Rodrigues, Eric Deneault, Caitlin Loo, Melody Zhao, P Joel Ross, Joelle El Hajjar, Asli Romm,[...]. Nat Neurosci 2019
66
15

Neurobiology of rodent self-grooming and its value for translational neuroscience.
Allan V Kalueff, Adam Michael Stewart, Cai Song, Kent C Berridge, Ann M Graybiel, John C Fentress. Nat Rev Neurosci 2016
324
9

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
888
9

CLK2 inhibition ameliorates autistic features associated with SHANK3 deficiency.
Michael Bidinosti, Paolo Botta, Sebastian Krüttner, Catia C Proenca, Natacha Stoehr, Mario Bernhard, Isabelle Fruh, Matthias Mueller, Debora Bonenfant, Hans Voshol,[...]. Science 2016
90
10

SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties.
Kihoon Han, J Lloyd Holder, Christian P Schaaf, Hui Lu, Hongmei Chen, Hyojin Kang, Jianrong Tang, Zhenyu Wu, Shuang Hao, Sau Wai Cheung,[...]. Nature 2013
229
9

Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits.
Haley E Speed, Mehreen Kouser, Zhong Xuan, Jeremy M Reimers, Christine F Ochoa, Natasha Gupta, Shunan Liu, Craig M Powell. J Neurosci 2015
84
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.