A citation-based method for searching scientific literature

Claire S Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kevin Mouzat, Dalila Pinto, Jennifer Howe, Nathalie Lemière, Christelle M Durand, Jessica Guibert, Elodie Ey, Roberto Toro, Hugo Peyre, Alexandre Mathieu, Frédérique Amsellem, Maria Rastam, I Carina Gillberg, Gudrun A Rappold, Richard Holt, Anthony P Monaco, Elena Maestrini, Pilar Galan, Delphine Heron, Aurélia Jacquette, Alexandra Afenjar, Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiesa, François Rivier, Dominique Bonneau, Beatrice Regnault, Diana Zelenika, Marc Delepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth-Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J Schmeisser, Tobias M Boeckers, Mary Coleman, Daisuke Sato, Peter Szatmari, Stephen W Scherer, Guy A Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron. PLoS Genet 2014
Times Cited: 316







List of co-cited articles
1009 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
985
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
856
39

SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
270
33

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
368
29

Modeling autism by SHANK gene mutations in mice.
Yong-Hui Jiang, Michael D Ehlers. Neuron 2013
292
28

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).
K Phelan, H E McDermid. Mol Syndromol 2012
244
27

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
350
27

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
165
27

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
729
25

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
204
24

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
166
24

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
160
24

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
440
23

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
21


Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.
Silvia De Rubeis, Paige M Siper, Allison Durkin, Jordana Weissman, François Muratet, Danielle Halpern, Maria Del Pilar Trelles, Yitzchak Frank, Reymundo Lozano, A Ting Wang,[...]. Mol Autism 2018
69
28

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
160
19

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
397
19

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
82
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
437
18

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
137
17

The Shank family of scaffold proteins.
M Sheng, E Kim. J Cell Sci 2000
362
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
358
17

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
86
18

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
164
16

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.
Maria Clara Bonaglia, Roberto Giorda, Silvana Beri, Cristina De Agostini, Francesca Novara, Marco Fichera, Lucia Grillo, Ornella Galesi, Annalisa Vetro, Roberto Ciccone,[...]. PLoS Genet 2011
123
16

Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.
Sara M Sarasua, Luigi Boccuto, Julia L Sharp, Alka Dwivedi, Chin-Fu Chen, Jonathan D Rollins, R Curtis Rogers, Katy Phelan, Barbara R DuPont. Hum Genet 2014
85
18

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
52
28

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
66
22

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome.
M C Bonaglia, R Giorda, R Borgatti, G Felisari, C Gagliardi, A Selicorni, O Zuffardi. Am J Hum Genet 2001
207
15

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
90
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
524
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
225
14

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients.
Aleksandr Shcheglovitov, Olesya Shcheglovitova, Masayuki Yazawa, Thomas Portmann, Rui Shu, Vittorio Sebastiano, Anna Krawisz, Wendy Froehlich, Jonathan A Bernstein, Joachim F Hallmayer,[...]. Nature 2013
305
14

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
249
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
95
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
156
14

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
241
14

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
280
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

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
810
13

Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome).
Sara M Sarasua, Alka Dwivedi, Luigi Boccuto, Jonathan D Rollins, Chin-Fu Chen, R Curtis Rogers, Katy Phelan, Barbara R DuPont, Julianne S Collins. J Med Genet 2011
81
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
168
12

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
75
16

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
227
12

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
46
26

The emerging role of SHANK genes in neuropsychiatric disorders.
Audrey Guilmatre, Guillaume Huguet, Richard Delorme, Thomas Bourgeron. Dev Neurobiol 2014
152
12

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
89
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
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.