A citation-based method for searching scientific literature

Yong-Hui Jiang, Michael D Ehlers. Neuron 2013
Times Cited: 313







List of co-cited articles
1191 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
303
47

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
345
43

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
43

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
35

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
30

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
757
30

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
391
28

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
176
26

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
460
24

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
223
23

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
420
23

Social deficits in Shank3-deficient mouse models of autism are rescued by histone deacetylase (HDAC) inhibition.
Luye Qin, Kaijie Ma, Zi-Jun Wang, Zihua Hu, Emmanuel Matas, Jing Wei, Zhen Yan. Nat Neurosci 2018
107
22

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
178
21

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
19

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
175
19

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
455
18

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
95
18

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
949
17

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
17

Coupling of mGluR/Homer and PSD-95 complexes by the Shank family of postsynaptic density proteins.
J C Tu, B Xiao, S Naisbitt, J P Yuan, R S Petralia, P Brakeman, A Doan, V K Aakalu, A A Lanahan, M Sheng,[...]. Neuron 1999
830
17

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
165
17

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
373
16


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
191
16

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
683
16

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
106
15

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
88
17

The Shank family of scaffold proteins.
M Sheng, E Kim. J Cell Sci 2000
374
15

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
238
14


Early hyperactivity and precocious maturation of corticostriatal circuits in Shank3B(-/-) mice.
Rui T Peixoto, Wengang Wang, Donyell M Croney, Yevgenia Kozorovitskiy, Bernardo L Sabatini. Nat Neurosci 2016
123
14

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).
K Phelan, H E McDermid. Mol Syndromol 2012
267
13

Atypical behaviour and connectivity in SHANK3-mutant macaques.
Yang Zhou, Jitendra Sharma, Qiong Ke, Rogier Landman, Jingli Yuan, Hong Chen, David S Hayden, John W Fisher, Minqing Jiang, William Menegas,[...]. Nature 2019
95
13

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
13

Novel de novo SHANK3 mutation in autistic patients.
Julie Gauthier, Dan Spiegelman, Amélie Piton, Ronald G Lafrenière, Sandra Laurent, Judith St-Onge, Line Lapointe, Fadi F Hamdan, Patrick Cossette, Laurent Mottron,[...]. Am J Med Genet B Neuropsychiatr Genet 2009
231
12

SHANK1 Deletions in Males with Autism Spectrum Disorder.
Daisuke Sato, Anath C Lionel, Claire S Leblond, Aparna Prasad, Dalila Pinto, Susan Walker, Irene O'Connor, Carolyn Russell, Irene E Drmic, Fadi F Hamdan,[...]. Am J Hum Genet 2012
231
12

Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
Luigi Boccuto, Maria Lauri, Sara M Sarasua, Cindy D Skinner, Daniela Buccella, Alka Dwivedi, Daniela Orteschi, Julianne S Collins, Marcella Zollino, Paola Visconti,[...]. Eur J Hum Genet 2013
146
12

C-terminal synaptic targeting elements for postsynaptic density proteins ProSAP1/Shank2 and ProSAP2/Shank3.
Tobias M Boeckers, Thomas Liedtke, Christina Spilker, Thomas Dresbach, Jürgen Bockmann, Michael R Kreutz, Eckart D Gundelfinger. J Neurochem 2005
92
13

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms.
H L Wilson, A C C Wong, S R Shaw, W-Y Tse, G A Stapleton, M C Phelan, S Hu, J Marshall, H E McDermid. J Med Genet 2003
259
12

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
12

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
546
12

Novel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function.
Thomas C Jaramillo, Haley E Speed, Zhong Xuan, Jeremy M Reimers, Christine Ochoa Escamilla, Travis P Weaver, Shunan Liu, Irina Filonova, Craig M Powell. Autism Res 2017
56
19

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
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
154
11

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
252
10

Brain region-specific disruption of Shank3 in mice reveals a dissociation for cortical and striatal circuits in autism-related behaviors.
Alexandra L Bey, Xiaoming Wang, Haidun Yan, Namsoo Kim, Rebecca L Passman, Yilin Yang, Xinyu Cao, Aaron J Towers, Samuel W Hulbert, Lara J Duffney,[...]. Transl Psychiatry 2018
53
18

An architectural framework that may lie at the core of the postsynaptic density.
Marisa K Baron, Tobias M Boeckers, Bianca Vaida, Salem Faham, Mari Gingery, Michael R Sawaya, Danielle Salyer, Eckart D Gundelfinger, James U Bowie. Science 2006
215
10

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A Ting Wang, Guiqing Cai, Elena Parkhomenko,[...]. Mol Autism 2013
180
10

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
75
13



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.